Everyone's Blog Posts - Alopecia World2024-03-19T03:36:25Zhttps://alopeciaworld.com/profiles/blog/feed?xn_auth=noThe Secret to Shutting Down Alopecia Haters for Good – One Bold Approach Can Transform Your Confidence!tag:alopeciaworld.com,2024-01-07:2022678:BlogPost:19812312024-01-07T02:29:09.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p>Dealing with unwanted comments about your alopecia can be challenging, and many may suggest responding with a quick comeback. However, diving deeper into the issue reveals a fundamental truth – you cannot control what others say about you. True empowerment comes from within, allowing you to navigate through the comments with grace and confidence.…</p>
<p></p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12347121282?profile=original" rel="noopener" target="_blank"><img class="align-full" src="https://storage.ning.com/topology/rest/1.0/file/get/12347121282?profile=RESIZE_710x"></img></a></p>
<p>Dealing with unwanted comments about your alopecia can be challenging, and many may suggest responding with a quick comeback. However, diving deeper into the issue reveals a fundamental truth – you cannot control what others say about you. True empowerment comes from within, allowing you to navigate through the comments with grace and confidence.</p>
<p></p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12347121282?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12347121282?profile=RESIZE_710x" class="align-full"/></a></p>
<p><span style="font-size: 8pt;"><em>Photo Source: Ad campaign for Dove Soap from quite a few years ago.</em></span></p>
<p></p>
<p><strong>The Illusion of Control:</strong></p>
<p>Attempting to control others' opinions is an exercise in futility. People will always have something to say, whether positive or negative. It’s crucial to recognize when comments are veiled attempts at control, trying to shape your behavior based on someone else's expectations. This phenomenon is known as the "locus of control," where external factors dictate your actions.</p>
<p> </p>
<p><strong>Breaking Free from External Validation:</strong></p>
<p>Relying solely on external validation can be a slippery slope. If your choices are determined by the approval of others, you may find yourself constantly changing to meet their expectations. The commentary on your appearance becomes a never-ending loop leading to a loss of your authentic self.</p>
<p> </p>
<p><strong>Living Through It:</strong></p>
<p>To truly liberate yourself from the burden of unwanted comments, the key is to live through them. While it may, sound easier said than done, experiencing these remarks allows you to build resilience. Over time, you will find that these comments no longer hold power over you. Recognize that these comments stem from others' insecurities, not your own.</p>
<p> </p>
<p><strong>Your Unique Journey:</strong></p>
<p>If you desire the freedom to walk out the door without a wig, wear a head covering, allow your bald patches to show, change up the color and length of your hairpieces whenever you want, get a tattoo on your head, or make any other choice you wish regarding YOUR alopecia, you must learn to handle the comments. Living authentically requires working through the discomfort, facing doubts head-on, and ultimately realizing that the opinions of others do not define you. Your journey with alopecia is unique, and the decision on how to live it should be yours alone.</p>
<p> </p>
<p><strong>Reframing Beauty and Attraction:</strong></p>
<p>Challenge societal norms and redefine what beauty means to you. Your worth is not determined by conforming to someone else's idea of attractiveness. Share your narrative and celebrate the aspects of yourself that make you feel empowered. It’s essential to recognize that true beauty lies in authenticity. </p>
<p><strong>Conclusion:</strong></p>
<p>In navigating the world with alopecia, it’s crucial to work through doubts, challenge societal norms, and let the decision of how to live your alopecia life be entirely yours. Embrace your journey and celebrate your uniqueness.</p>
<p><strong>Question:</strong></p>
<p>Are you letting others dictate how you should live with alopecia, or is it time to reclaim your power?</p>Navigating the Crossroads: Balancing Alopecia Treatments, Self-Acceptance, and Unanswered Questionstag:alopeciaworld.com,2024-01-05:2022678:BlogPost:19813682024-01-05T00:30:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><span>In the ever-evolving narrative of alopecia, a noticeable shift has occurred. Once rooted in the empowering realm of self-acceptance, the conversation now centers around the "promising" developments in alopecia treatments. While these advancements offer a glimmer of hope, I believe we should still tread carefully and maintain a balance between progress and the pursuit of self-acceptance.</span><br></br><br></br><span>The discovery of new alopecia treatments undeniably brings a sense of optimism…</span></p>
<p><span>In the ever-evolving narrative of alopecia, a noticeable shift has occurred. Once rooted in the empowering realm of self-acceptance, the conversation now centers around the "promising" developments in alopecia treatments. While these advancements offer a glimmer of hope, I believe we should still tread carefully and maintain a balance between progress and the pursuit of self-acceptance.</span><br/><br/><span>The discovery of new alopecia treatments undeniably brings a sense of optimism into the community. It's only natural to feel a surge of hope with the prospect of transformative solutions. However, my caution remains. The shift from self-acceptance to a focus on treatments prompts questions, concerns, and considerations that merit our attention.</span><br/><br/><span>There is a big difference between "treatments" and "cures." Are these treatments genuinely transformative in the long run, or do they offer only a temporary fix?</span><br/><br/><span>What are the potential long-term side effects that may accompany these treatments?</span><br/><br/><span>What happens if one discontinues these treatments for medical or financial reasons? Will the results be reversed? Or are individuals signing up for a lifetime dependency on these treatments?</span><br/><br/><span>Then there is the financial aspect. Alopecia treatments, like Olumiant, come at a steep price, $5,244.00 for a 30-day supply! The significant financial investment raises ethical questions about accessibility and affordability. Will these treatments be accessible to everyone, or will financial constraints act as barriers to transformation for some?</span><br/><br/><span>As these treatments keep coming, I think it is important that we retain a sense of control over our choices.</span><br/><br/><span>I firmly believe that the quest for self-acceptance remains important. There is still the 'now' and 'in the meantime' that need to be dealt with. Whether a treatment or cure is on the horizon or not, the importance of continuing to seek self-acceptance is something we should continue to pursue.</span><br/><br/><span>I fear a run for solely a treatment can put an end to the pursuit of self-acceptance, which could be devastating if any of the above scenarios were to happen. My real quest is to be okay whether my hair grows back or not.</span><br/><br/><span>As we think about the evolving advances of alopecia treatments and the delicate dance with self-acceptance, I ask you to share your perspective: What does self-acceptance mean to you in the context of embracing potential transformative treatments? How do you strike a balance between the progress of treatments and maintaining a sense of self-acceptance?</span><br/><br/><span>I stand in the middle, feeling uncomfortable and compelled to speak. These are my concerns when I sit and hear the conversation in support groups, online, and elsewhere.</span></p>Wishing You a Bright and Happy New Year, Alopecia World Members!tag:alopeciaworld.com,2024-01-01:2022678:BlogPost:19810222024-01-01T04:00:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12343641885?profile=original" rel="noopener" target="_blank"><img class="align-right" src="https://storage.ning.com/topology/rest/1.0/file/get/12343641885?profile=RESIZE_710x" width="250"></img></a> Dear Alopecia World Members,</p>
<p>As we bid farewell to the old and embrace the new, We wanted to take a moment to extend my warmest wishes to each and every one of you. As we step into the dawn of a brand new year, may it bring you joy, prosperity, and endless possibilities.</p>
<p>May this year be a canvas of new experiences, filled with moments of…</p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12343641885?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12343641885?profile=RESIZE_710x" width="250" class="align-right"/></a>Dear Alopecia World Members,</p>
<p>As we bid farewell to the old and embrace the new, We wanted to take a moment to extend my warmest wishes to each and every one of you. As we step into the dawn of a brand new year, may it bring you joy, prosperity, and endless possibilities.</p>
<p>May this year be a canvas of new experiences, filled with moments of laughter, love, and personal growth. As members of Alopecia World, you've shown resilience, strength, and unity in facing the challenges that come with alopecia. Your support and understanding have created a community that stands as a testament to the power of solidarity.</p>
<p>Let's carry the spirit of hope into the coming year, celebrating our uniqueness and embracing the beauty that resides in diversity. May 2024 be a year of self-discovery, self-love, and acceptance. Remember that each of you is an essential part of this wonderful community, contributing to its richness and strength.</p>
<p>Thank you for being a part of Alopecia World, and here's to a year filled with kindness, growth, and an abundance of positive moments.</p>
<p></p>
<p>Wishing you a Happy New Year!</p>
<p>Warm regards,</p>
<p></p>
<p>Cheryl Carvery-Jones<br/> Co-Founder<br/> AlopeciaWorld.com</p>How Do You Slay Holiday Fashion with Alopecia?tag:alopeciaworld.com,2023-11-29:2022678:BlogPost:19800692023-11-29T19:00:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12305369059?profile=original" rel="noopener" target="_blank"><img class="align-right" height="294" src="https://storage.ning.com/topology/rest/1.0/file/get/12305369059?profile=RESIZE_710x" width="294"></img></a> The holiday season has always been a time of joy, laughter, and the challenge of finding the perfect festive outfit. However, for someone navigating the twists and turns of alopecia, getting dressed up takes on a whole new layer of complexity. Alopecia, with its unpredictable hair loss, throws a unique set of challenges into the mix when deciding what to…</p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12305369059?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12305369059?profile=RESIZE_710x" width="294" class="align-right" height="294"/></a>The holiday season has always been a time of joy, laughter, and the challenge of finding the perfect festive outfit. However, for someone navigating the twists and turns of alopecia, getting dressed up takes on a whole new layer of complexity. Alopecia, with its unpredictable hair loss, throws a unique set of challenges into the mix when deciding what to wear for those special holiday gatherings. The choice between a trusty wig, stylish hats or scarves, or boldly embracing baldness becomes a journey filled with both societal expectations and deeply personal considerations.</p>
<p> </p>
<p>For someone who usually relies on wigs, the holiday season becomes a unique puzzle. The question arises: Should they stick with their tried-and-true favorite, or is it time to switch things up with a different style or color to mark the festivities? The pressure to conform to beauty norms feels like a spotlight, making this decision a deeply personal journey.</p>
<p>On the flip side, there are occasions where they may opt for stylish hats or scarves during the holidays. These not only add a fashionable touch but also offer a comforting shield. Yet, going hat or scarf-clad brings its own set of questions. How do they seamlessly coordinate these accessories with their holiday outfit? And, truth be told, the worry about drawing attention to themselves or feeling self-conscious about standing out is always in the back of their mind.</p>
<p>Then, there are those moments when they may choose to embrace their baldness during the holidays. While it is empowering, it's not without its challenges. How do they handle the inevitable questions or comments from those who might not be aware of their condition? This choice demands a level of self-assurance that, fortunately, is bolstered by the support of friends and family. This was my situation; the first time my co-workers saw me without a wig was at the company holiday party. At that time, I was only wearing the wig at work, and I felt that a company holiday party was more personal time, so I took that opportunity to take the step.</p>
<p><strong>Here are a few questions that we can help each other with:</strong></p>
<ol>
<li>How do you personally navigate the decision of what to wear during the holiday season with alopecia?</li>
<li>Do you find comfort in sticking to the same wig, or do you enjoy experimenting with different styles and colors for festive occasions?</li>
<li>Are there hat or scarf styles that you have found particularly empowering or festive for holiday events?</li>
<li>For those who choose to go bald during the holidays, what tips do you have for embracing this choice with confidence?</li>
</ol>
<p></p>
<p>The stress behind getting dressed up for the holidays with alopecia is undeniably personal. It's a journey filled with both the expectations of the world around us and the deep, internal desire to feel comfortable in our own skin. By sharing our stories and seeking advice from the supportive community of Alopecia World, perhaps we can help others navigate this holiday season more confidently. Let's celebrate the diversity and resilience within the alopecia community during this special time of year, remembering that the most important thing is to feel comfortable and authentic, no matter the choice made.</p>
<p></p>
<p><strong>Share your struggles, solutions and pictures with Alopecia World!</strong></p>
<p></p>Webinar: Men & Alopecia Areata: Our unique experiencestag:alopeciaworld.com,2023-11-13:2022678:BlogPost:19795792023-11-13T07:28:13.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<div class="event-details"><strong><span class="c2">Webinar - Virtual Event</span></strong></div>
<div class="event-details"></div>
<div class="event-details"><span class="c1">Organizer: </span><span class="c2">NAAF</span></div>
<p></p>
<p></p>
<p>
</p>
<div class="left-column"><div class="image-date-block"><div class="date-time-block"><p class="date">Wednesday, November 15</p>
<p class="time">4:00 PM, PST</p>
<p class="time">7:00 PM, EST…</p>
</div>
</div>
</div>
<div class="event-details"><strong><span class="c2">Webinar - Virtual Event</span></strong></div>
<div class="event-details"></div>
<div class="event-details"><span class="c1">Organizer: </span><span class="c2">NAAF</span></div>
<p></p>
<p></p>
<p>
<br />
</p>
<div class="left-column"><div class="image-date-block"><div class="date-time-block"><p class="date">Wednesday, November 15</p>
<p class="time">4:00 PM, PST</p>
<p class="time">7:00 PM, EST</p>
</div>
</div>
<div class="event-details"></div>
</div>
<div class="description"><p><span>It’s time to talk about how alopecia areata affects men. Hear from a group of men to learn about some of the challenges they have faced living with this disease. This webinar will be moderated by NAAF Board member, Tyrone Folliard-Olson, and will be an honest discussion by panel members of experiences, struggles, and coping strategies – as well as answers to your questions.</span></p>
</div>
<br />
<div class="button-container"></div>
<div class="button-container">Register here:</div>
<div class="button-container"></div>
<br />
<p></p>
<br />
<div class="widgets-footer"><div class="footer-widget"></div>
<div class="footer-widget footer-widget-flex"></div>
</div>
<br />
<p><a href="https://www.naaf.org/events/men-alopecia-areata-our-unique-experiences/">https://www.naaf.org/events/men-alopecia-areata-our-unique-experiences/</a></p>Your not alone!tag:alopeciaworld.com,2023-11-13:2022678:BlogPost:19795782023-11-13T07:04:14.000Z559Courtneyhttps://alopeciaworld.com/profile/559Courtney
<p>It is essential to recognize that you are not alone in this, as there are 6.5 million people in the US affected by Alopecia. Embrace your new bald appearance and find happiness within yourself, appreciating the journey you have undertaken. Allow Alopecia to be your beautiful cure</p>
<p>It is essential to recognize that you are not alone in this, as there are 6.5 million people in the US affected by Alopecia. Embrace your new bald appearance and find happiness within yourself, appreciating the journey you have undertaken. Allow Alopecia to be your beautiful cure</p>Your Personal Path to Embracing Self-Acceptancetag:alopeciaworld.com,2023-10-25:2022678:BlogPost:19787312023-10-25T05:14:14.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12264798457?profile=original" rel="noopener" target="_blank"><img class="align-left" src="https://storage.ning.com/topology/rest/1.0/file/get/12264798457?profile=RESIZE_710x" width="250"></img></a> When I was first diagnosed alopecia, the idea of self-acceptance felt like an impossible mountain to climb. There were no quick fixes or easy solutions. I didn't wake up one morning, glance at my bald reflection, and suddenly embrace it with unwavering courage. It took me years of struggling with my insecurities, facing my fears head-on, and gradually…</p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12264798457?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12264798457?profile=RESIZE_710x" width="250" class="align-left"/></a>When I was first diagnosed alopecia, the idea of self-acceptance felt like an impossible mountain to climb. There were no quick fixes or easy solutions. I didn't wake up one morning, glance at my bald reflection, and suddenly embrace it with unwavering courage. It took me years of struggling with my insecurities, facing my fears head-on, and gradually learning to love the person staring back at me in the mirror. <br/> <br/> Avoiding my reflection would be easier but one day, I mustered the strength to stand there and truly see myself. It was a small step, but it marked the beginning of my journey towards self-acceptance. I wish I could pinpoint the exact moment when the shift occurred, but it was more like a slow, steady realization that I was tired of hiding who I really was. <br/> <br/> I wanted to be authentic, to have the freedom to choose how I presented myself to the world. Whether it was wearing a wig, a scarf, or living my life as a bald woman, I wanted to make that choice for myself. It wasn't about conforming to societal expectations; it was about reclaiming my identity. <br/> <br/> My journey towards self-acceptance wasn't a one-size-fits-all experience. It involved stepping out of my comfort zone in ways that felt right for me. It meant revealing my alopecia to my closest friends, experimenting with different fashion styles, and even sharing my story with others. Every small step I took, every choice I made, was a conscious effort to reclaim my sense of self and be myself. <br/> <br/> Through this journey, I realized that self-acceptance isn't about reaching a destination; it's about embracing the process, the ups, and the downs, and allowing yourself the space to evolve and change. It's about understanding that you alopecia is just one part of who you are. <br/> <br/> Your journey toward self-acceptance may not look like anyone else's, you need to make your decisions decide how you want to live your alopecia. Keeping in mind that any decision you make, you have the freedom to change it at any time if you find it does not suit you. </p>
<p></p>
<p style="text-align: center;">If you are in a place of self-acceptance, what advice can you give to others trying to get there? And for those still navigating the path, what poses the greatest challenge to overcome?</p>
<p></p>Embracing Empowerment: Sharing Your Alopecia Journeytag:alopeciaworld.com,2023-10-16:2022678:BlogPost:19784162023-10-16T07:00:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12258008295?profile=original" rel="noopener" target="_blank"><img class="align-right" src="https://storage.ning.com/topology/rest/1.0/file/get/12258008295?profile=RESIZE_710x" width="250"></img></a> Living with alopecia presents a unique set of challenges. The emotional turmoil, the physical changes, and the constant search for acceptance can challenging. However, I believe that every individual's experience is a testament to strength and resilience. By sharing your personal alopecia story, you have the power to inspire and support others who may be…</p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12258008295?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12258008295?profile=RESIZE_710x" width="250" class="align-right"/></a>Living with alopecia presents a unique set of challenges. The emotional turmoil, the physical changes, and the constant search for acceptance can challenging. However, I believe that every individual's experience is a testament to strength and resilience. By sharing your personal alopecia story, you have the power to inspire and support others who may be embarking on a similar path.</p>
<p></p>
<p><strong><em>Here at AlopeciaWorld.com we would love to hear your story! Consider sharing your story with the community as a blog:</em></strong></p>
<p></p>
<p></p>
<p>Here are a few pointers when recounting your journey with alopecia to help guide you:</p>
<ol>
<li><strong>The Beginning:</strong> Reflect on the initial moments when you noticed changes in your body or appearance. How did you feel? What were your immediate thoughts and concerns? Sharing these raw emotions can create a connection with others who may be going through a similar experience.</li>
<li><strong>Challenges Faced:</strong> Discuss the challenges you encountered along the way. This could include struggles with self-confidence, societal stigmas, or the emotional toll of navigating a world that often values conventional beauty standards. By shedding light on these difficulties, you can help others understand that they are not alone in their struggles.</li>
<li><strong>Triumphs and Coping Mechanisms:</strong> Share the strategies and coping mechanisms that helped you navigate the hurdles. Whether it was seeking professional support, embracing self-care practices, or finding solace in a supportive community, detailing these triumphs can provide hope and encouragement to those seeking guidance.</li>
<li><strong>Embracing Self-Acceptance and Empowerment</strong>: Illustrate how you cultivated self-acceptance and embraced your unique beauty. Discuss the turning points and the journey towards realizing that true beauty can transcend hair. Your story can serve as a beacon of hope for others striving to find peace and self-love.</li>
</ol>
<p>Through sharing your alopecia journey, you are not only advocating for awareness and understanding but also fostering a sense of solidarity within the alopecia community. Your story has the power to inspire and uplift others who may be struggling to find their own sense of confidence and self-acceptance.</p>
<p>Let’s celebrate the diversity of human experiences and champion a world where others feel seen, heard, and embraced for who they are. Your story matters, and it has the potential to ignite a spark of hope and resilience in the hearts of others.</p>Embracing the Journey and the Challenge Aheadtag:alopeciaworld.com,2023-10-03:2022678:BlogPost:19781432023-10-03T22:42:42.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12239125077?profile=original" rel="noopener" target="_blank"><img class="align-right" height="251" src="https://storage.ning.com/topology/rest/1.0/file/get/12239125077?profile=RESIZE_710x" width="251"></img></a> The "Call to Adventure" in the world of alopecia is undeniably daunting, but it is also a call to self-discovery, resilience, and personal growth. It's a journey that no one chooses, but it can be transformed into a path of empowerment and acceptance. As you navigate the challenges, emotions, and uncertainties that come with living with alopecia, I leave you…</p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12239125077?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12239125077?profile=RESIZE_710x" width="251" class="align-right" height="251"/></a>The "Call to Adventure" in the world of alopecia is undeniably daunting, but it is also a call to self-discovery, resilience, and personal growth. It's a journey that no one chooses, but it can be transformed into a path of empowerment and acceptance. As you navigate the challenges, emotions, and uncertainties that come with living with alopecia, I leave you with a challenge:</p>
<p><strong>Embrace Your Unique Journey:</strong> Instead of dwelling on the aspects of your appearance that have changed, focus on the qualities that make you unique. Celebrate the strength, courage, and resilience that you embody as you face this journey head-on.</p>
<p><strong>Share Your Story:</strong> Your journey with alopecia can inspire and support others who are just beginning theirs. Consider sharing your experiences, challenges, and triumphs with your community, Alopecia World or other online platforms. By doing so, you can create awareness and foster a sense of solidarity among those on similar journeys.</p>
<p><strong>Educate and Advocate:</strong> Challenge misconceptions and stigmas associated with alopecia by educating those around you about the condition. Advocate for greater understanding and empathy, encouraging a more inclusive and accepting society.</p>
<p><strong>Seek Support:</strong> Remember that you don't have to face this journey alone. Reach out to Alopecia World, in-person support groups, organizations like NAAF, or mental health professionals who specialize in helping individuals with alopecia. Connecting with others who understand your experiences can be incredibly empowering.</p>
<p><strong>Embrace Self-Love:</strong> Perhaps the most important challenge is to practice self-love and self-acceptance daily. Recognize that your worth is not defined by your follicles on your head, and that true beauty radiates regardless. Embrace your alopecia journey as an opportunity for personal growth and self-discovery.</p>
<p>In the face of adversity, you have the power to transform your journey with alopecia into a story of courage and inspiration. Remember, you are not defined by your hair, but by your resilience, strength, and the unique qualities that make you who you are. Embrace the call to adventure, face its challenges, and emerge as a hero in your own story.</p>The reason I am bald . Ok I had fire an some of my hair was burnt off...tag:alopeciaworld.com,2023-10-03:2022678:BlogPost:19782062023-10-03T14:30:00.000ZGuphttps://alopeciaworld.com/profile/Gup
<p>The reason I am bald . Ok I had fire an some of my hair was burnt off . So I decided to keep shaved off smooth. Then I decided to tattoo my head . From them on I go an an shaved every two weeks. Wow I really love it bald . I really prefer bald any day of the week . I really the the people are bald because of alopecia or some else . I really love women are bald an some day I would love date a lady with a bald head then I probably want to get married to her . But I will promise her I will keep…</p>
<p>The reason I am bald . Ok I had fire an some of my hair was burnt off . So I decided to keep shaved off smooth. Then I decided to tattoo my head . From them on I go an an shaved every two weeks. Wow I really love it bald . I really prefer bald any day of the week . I really the the people are bald because of alopecia or some else . I really love women are bald an some day I would love date a lady with a bald head then I probably want to get married to her . But I will promise her I will keep my head shaved smooth every day then an I never wear a hat again. I really love the bald head look an I always will. BALD IS VERY BEAUTIFUL. </p>"To all those living with alopecia,
I am one of you, and I want to share some words with you. We all face common challenges, but you are not alone on this journey.
Alopecia may be a part of our liv…tag:alopeciaworld.com,2023-09-29:2022678:BlogPost:19781192023-09-29T01:28:28.000ZAbdehttps://alopeciaworld.com/profile/Abde
<p>"To all those living with alopecia,</p>
<p></p>
<p>I am one of you, and I want to share some words with you. We all face common challenges, but you are not alone on this journey.</p>
<p></p>
<p>Alopecia may be a part of our lives, but it does not define us. We are capable of achieving our dreams and goals, regardless of this condition.</p>
<p></p>
<p>There will be no limits to what we can do. We are here to prove to the world that we are strong and resilient. Despite the challenging…</p>
<p>"To all those living with alopecia,</p>
<p></p>
<p>I am one of you, and I want to share some words with you. We all face common challenges, but you are not alone on this journey.</p>
<p></p>
<p>Alopecia may be a part of our lives, but it does not define us. We are capable of achieving our dreams and goals, regardless of this condition.</p>
<p></p>
<p>There will be no limits to what we can do. We are here to prove to the world that we are strong and resilient. Despite the challenging environment we may live in, especially in Morocco with limited support, we are ready to face challenges and succeed.</p>
<p></p>
<p>We will never stop fighting against the odds and achieving our aspirations. Let's create our own successes and live our lives with confidence and pride.</p>
<p></p>
<p>We are here to support each other and share this journey. With love and solidarity,</p>
<p></p>
<p>Abderahman from Morocco</p>CBD and hair growthtag:alopeciaworld.com,2023-09-21:2022678:BlogPost:19776862023-09-21T19:00:00.000ZJeannie Terrelhttps://alopeciaworld.com/profile/JeannieTerrel
<p>Has anyone had any luck with using CBD to help with hair regrowth. My peach fuzz is starting to grow back thicker and it just might turn into actual hair. The only thing I have changed is consuming small dose of CBD daily.</p>
<p></p>
<p>---------------------------</p>
<p></p>
<p></p>
<p>AW: Other Post across Alopecia World on CBD Oil:</p>
<p><a href="https://alopeciaworld.com/main/search/search?q=cbd+oil">https://alopeciaworld.com/main/search/search?q=cbd+oil</a></p>
<p>Has anyone had any luck with using CBD to help with hair regrowth. My peach fuzz is starting to grow back thicker and it just might turn into actual hair. The only thing I have changed is consuming small dose of CBD daily.</p>
<p></p>
<p>---------------------------</p>
<p></p>
<p></p>
<p>AW: Other Post across Alopecia World on CBD Oil:</p>
<p><a href="https://alopeciaworld.com/main/search/search?q=cbd+oil">https://alopeciaworld.com/main/search/search?q=cbd+oil</a></p>Week 3 - Alopecia Awareness Month - 30 Days, 30 Facts: Spreading Alopecia Awarenesstag:alopeciaworld.com,2023-09-15:2022678:BlogPost:19777492023-09-15T15:00:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><span><strong>30 Days, 30 Facts: A Social Media Initiative</strong></span></p>
<p>One innovative way to participate in Alopecia Awareness Month is by joining the "30 Days, 30 Facts" campaign. This initiative involves sharing graphics that feature a different alopecia-related fact each day of the month. </p>
<p>Alopecia Awareness Month is an annual campaign that takes place in September, dedicated to raising awareness about alopecia, a condition that affects millions of people worldwide.…</p>
<p><span><strong>30 Days, 30 Facts: A Social Media Initiative</strong></span></p>
<p>One innovative way to participate in Alopecia Awareness Month is by joining the "30 Days, 30 Facts" campaign. This initiative involves sharing graphics that feature a different alopecia-related fact each day of the month. </p>
<p>Alopecia Awareness Month is an annual campaign that takes place in September, dedicated to raising awareness about alopecia, a condition that affects millions of people worldwide. While some people may be familiar with the term alopecia, many are unaware of the various forms it can take and the profound impact it has on our lives.</p>
<p><strong>Informative:</strong></p>
<p>These graphics serve as bite-sized pieces of information about alopecia, covering various aspects of the condition. They educate the public on what alopecia is, its different forms, and the challenges individuals with alopecia face.</p>
<p></p>
<p></p>
<p><span><strong>Getting involved in the "30 Days, 30 Facts" campaign is easy:</strong></span></p>
<p></p>
<p><strong>Download and share the Graphics.</strong> </p>
<p>Below are 7 graphics for September 15 – 21, we will be uploading 7 graphics each week. Be sure to use the hashtags #AlopeciaAwarenessMonth, #alopeciaworld to connect with others participating in the campaign. And don’t forget to Alopecia World (@alopeciaworld) in your posts too! </p>
<p></p>
<p><strong>Conclusion:</strong></p>
<p>Alopecia Awareness Month is a crucial opportunity to shed light on a condition that affects millions of us. By participating in the "30 Days, 30 Facts" campaign and sharing on social media, you can play a vital role in dispelling myths, reducing stigma, and showing support for those with alopecia. Let's come together to make a difference and spread awareness about alopecia throughout the month of September and beyond. Together, we can make a positive impact on the lives of those living with alopecia.</p>
<p></p>
<p>You do not need to go in order! If there is one that you like from a previous week, you can find them here:</p>
<p></p>
<p><strong>Week 1:</strong></p>
<p><a href="https://alopeciaworld.com/profiles/blogs/september-is-alopecia-awareness-month-30-days-30-facts-spreading-">https://alopeciaworld.com/profiles/blogs/september-is-alopecia-awareness-month-30-days-30-facts-spreading-</a></p>
<p></p>
<p><strong>Week 2:</strong></p>
<p><a href="https://alopeciaworld.com/profiles/blogs/week-2-alopecia-awareness-month-30-days-30-facts-spreading-alopec">https://alopeciaworld.com/profiles/blogs/week-2-alopecia-awareness-month-30-days-30-facts-spreading-alopec</a></p>
<p></p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12224677298?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12224677298?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12224677668?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12224677668?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12224677496?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12224677496?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12224677887?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12224677887?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12224678283?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12224678283?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12224678474?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12224678474?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12224678490?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12224678490?profile=RESIZE_710x" width="180" class="align-left"/></a></p>Eve Betts, Alopecian and Former Reality TV Star, faces online abusetag:alopeciaworld.com,2023-09-09:2022678:BlogPost:19772332023-09-09T00:00:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><strong>Alopecian, Eve Betts, a reality TV contestant from the show First Dates from 2007 says she receives abuse and sexually explicit material over social media.</strong></p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12219681464?profile=original" rel="noopener" target="_blank"><img class="align-right" height="241" src="https://storage.ning.com/topology/rest/1.0/file/get/12219681464?profile=RESIZE_710x" width="241"></img></a> Eve shared, "I get a lot of death threats. People saying that I should just die because of the way that I look." Her decision to remove her wig on camera during the show made her a…</p>
<p><strong>Alopecian, Eve Betts, a reality TV contestant from the show First Dates from 2007 says she receives abuse and sexually explicit material over social media.</strong></p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12219681464?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12219681464?profile=RESIZE_710x" width="241" class="align-right" height="241"/></a>Eve shared, "I get a lot of death threats. People saying that I should just die because of the way that I look." Her decision to remove her wig on camera during the show made her a target for hurtful comments about her appearance.</p>
<p>"I get quite a lot of personal comments on my appearance, comparing me to the worst things like an alien or a robot," Eve said.</p>
<p>"My experience with online abuse has been distressing," she added. "The barrage of hateful messages, threats, and explicit content really is not pleasant."</p>
<p><span style="font-size: 12pt;"><strong>Question:</strong></span></p>
<p>As someone who may have encountered online abuse, mean comments, bullying, or unwanted advances due to your experience with alopecia, what personal insights and strategies have you discovered to navigate these difficult situations effectively? By sharing your firsthand wisdom, we can collectively empower and support one another within the alopecia community.</p>
<p> </p>
<p><em><strong>You can watch a snippet of the episode of "First Date" here:</strong></em></p>
<p><a href="https://alopeciaworld.com/video/eve-removes-her-wig-during-dinner-first-dates">https://alopeciaworld.com/video/eve-removes-her-wig-during-dinner-first-dates</a></p>
<p></p>
<p><em><strong>Source BBC Article Here:</strong></em></p>
<p><a href="https://www.bbc.com/news/uk-wales-66747165">https://www.bbc.com/news/uk-wales-66747165</a></p>
<p> </p>
<p> </p>
<p> </p>
<p> </p>Week 2 - Alopecia Awareness Month - 30 Days, 30 Facts: Spreading Alopecia Awarenesstag:alopeciaworld.com,2023-09-08:2022678:BlogPost:19772302023-09-08T20:05:21.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><span><strong>30 Days, 30 Facts: A Social Media Initiative</strong></span></p>
<p>One innovative way to participate in Alopecia Awareness Month is by joining the "30 Days, 30 Facts" campaign. This initiative involves sharing graphics that feature a different alopecia-related fact each day of the month. Here's why this campaign is so impactful:</p>
<p></p>
<p>Alopecia Awareness Month is an annual campaign that takes place in September, dedicated to raising awareness about alopecia, a…</p>
<p><span><strong>30 Days, 30 Facts: A Social Media Initiative</strong></span></p>
<p>One innovative way to participate in Alopecia Awareness Month is by joining the "30 Days, 30 Facts" campaign. This initiative involves sharing graphics that feature a different alopecia-related fact each day of the month. Here's why this campaign is so impactful:</p>
<p></p>
<p>Alopecia Awareness Month is an annual campaign that takes place in September, dedicated to raising awareness about alopecia, a condition that affects millions of people worldwide. While some people may be familiar with the term alopecia, many are unaware of the various forms it can take and the profound impact it has on our lives.</p>
<p></p>
<p><strong>Informative:</strong></p>
<p>These graphics serve as bite-sized pieces of information about alopecia, covering various aspects of the condition. They educate the public on what alopecia is, its different forms, and the challenges individuals with alopecia face.</p>
<p></p>
<p><strong>Engaging:</strong></p>
<p>Visual content is highly engaging on social media. People are more likely to interact with and share graphics, which can lead to a broader reach and more significant impact.</p>
<p></p>
<p><strong>Conversation Starter:</strong></p>
<p>Sharing these graphics can spark conversations about alopecia. People may ask questions, seek more information, or express their support for those affected by the condition. This dialogue is essential for dispelling myths and promoting understanding.</p>
<p></p>
<p><strong>Unity:</strong></p>
<p>When people across the world share these graphics simultaneously, it creates a sense of unity and solidarity within the alopecia community. It shows that people from diverse backgrounds care about this cause.</p>
<p></p>
<p><span><strong>Getting involved in the "30 Days, 30 Facts" campaign is easy:</strong></span></p>
<p></p>
<p><strong>Download and share the Graphics.</strong> </p>
<p>Below are 7 graphics for September 8 – 14, we will be uploading 7 graphics each week. Be sure to use the hashtags #AlopeciaAwarenessMonth, #alopeciaworld to connect with others participating in the campaign. And don’t forget to Alopecia World (@alopeciaworld) in your posts too! </p>
<p></p>
<p><strong>Conclusion:</strong></p>
<p>Alopecia Awareness Month is a crucial opportunity to shed light on a condition that affects millions of us. By participating in the "30 Days, 30 Facts" campaign and sharing on social media, you can play a vital role in dispelling myths, reducing stigma, and showing support for those with alopecia. Let's come together to make a difference and spread awareness about alopecia throughout the month of September and beyond. Together, we can make a positive impact on the lives of those living with alopecia.</p>
<p></p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12219609879?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12219609879?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12219609695?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12219609695?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12219610094?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12219610094?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12219610290?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12219610290?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12219610666?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12219610666?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12219610496?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12219610496?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12219610874?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12219610874?profile=RESIZE_710x" width="180" class="align-left"/></a></p>Hair is growing in...Olumianttag:alopeciaworld.com,2023-09-04:2022678:BlogPost:19773532023-09-04T22:00:00.000ZJRChttps://alopeciaworld.com/profile/JRC
<p>I have been lucky enough to get on Olumiant. I’n five weeks I have a mustache and patches of hair growing. Im 68 and been dealing with my hair growing in a falling out. This drug has some serious side effects that you need to monitor. <br></br> My sense is that alopecia is IS a “systemic disease” process. I have had a bowel resection, mitro valve repair, of course episodic stomach issues and eye issues, recently retina repair… I.E. everything related to human anatomy and hairlike structures…</p>
<p>I have been lucky enough to get on Olumiant. I’n five weeks I have a mustache and patches of hair growing. Im 68 and been dealing with my hair growing in a falling out. This drug has some serious side effects that you need to monitor. <br/> My sense is that alopecia is IS a “systemic disease” process. I have had a bowel resection, mitro valve repair, of course episodic stomach issues and eye issues, recently retina repair… I.E. everything related to human anatomy and hairlike structures such as peristalsis, and honestly everything dealing with “hairlike structures” inside and out. Just my own opinion.</p>
<p></p>
<p>Other discussions on Olumiant:</p>
<p><a href="https://alopeciaworld.com/main/search/search?q=Olumiant">https://alopeciaworld.com/main/search/search?q=Olumiant</a></p>Truthfulness and Alopecia: Confronting the Fear of Feeling Uglytag:alopeciaworld.com,2023-09-04:2022678:BlogPost:19771232023-09-04T19:17:16.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p></p>
<p><span><a href="https://storage.ning.com/topology/rest/1.0/file/get/12217109269?profile=original" rel="noopener" target="_blank"><img class="align-right" src="https://storage.ning.com/topology/rest/1.0/file/get/12217109269?profile=RESIZE_710x" width="250"></img></a> Do you ever struggle with feeling unattractive due to alopecia? How has it affected your self-image and how do you deal with those emotions?</span></p>
<p></p>
<p>Living with alopecia, a condition characterized by hair loss, can challenge our self-esteem and self-image in profound ways. It's okay to acknowledge the feelings of vulnerability and…</p>
<p></p>
<p><span><a href="https://storage.ning.com/topology/rest/1.0/file/get/12217109269?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12217109269?profile=RESIZE_710x" width="250" class="align-right"/></a>Do you ever struggle with feeling unattractive due to alopecia? How has it affected your self-image and how do you deal with those emotions?</span></p>
<p></p>
<p>Living with alopecia, a condition characterized by hair loss, can challenge our self-esteem and self-image in profound ways. It's okay to acknowledge the feelings of vulnerability and insecurity that come with it. In this blog, we will address the complex issue of confronting the fear of feeling ugly when dealing with alopecia, and why it's essential to have honest conversations about these emotions.</p>
<p><strong>The Unfiltered Reality</strong></p>
<p>Let's face it – living with alopecia can sometimes lead to feeling unattractive. The reflection in the mirror may not align with the conventional beauty standards that society often glorifies. It's crucial to create a safe space for honest conversations about these feelings without resorting to clichés like <em>"beauty is within."</em></p>
<p><strong>Facing the Fear</strong></p>
<p>It's okay to confront the fear of feeling ugly due to alopecia. Pretending that these feelings don't exist or trying to convince yourself that inner beauty is all that matters isn't always helpful. Instead, embrace your emotions and use them as a catalyst for self-discovery and growth.</p>
<p><strong>Seeking Validation</strong></p>
<p>Feeling ugly with alopecia doesn't make you weak or vain. Seeking validation is a natural human desire, and there's nothing wrong with wanting to feel attractive. It's essential to acknowledge this need and find healthy ways to fulfill it.</p>
<p><strong>Reframing Beauty</strong></p>
<p>While it's crucial to acknowledge your feelings of insecurity, it's also essential to reframe your understanding of beauty. Beauty isn't a one-size-fits-all concept. It's subjective and varies from person to person. Explore what beauty means to you beyond conventional standards, and don't be afraid to challenge those standards.</p>
<p><strong>Acceptance vs. Transformation</strong></p>
<p>Acceptance doesn't mean resignation. It's about embracing your authentic self while leaving room for growth and transformation. If you want to explore options like wigs, scarves, or other hair alternatives, do it. It's not a betrayal of your true self but an expression of your autonomy.</p>
<p><strong>Finding Strength in Vulnerability</strong></p>
<p>Being truthful about your feelings of ugliness with alopecia can be empowering. It allows you to connect with others who share similar experiences, fostering a sense of community and mutual support. Vulnerability can be a source of strength.</p>
<p><strong>Building Confidence</strong></p>
<p>Working on your self-esteem and self-confidence is a lifelong journey. Challenge negative self-talk and surround yourself with people who uplift and support you. Seek professional help if needed, as therapy can provide valuable tools for building self-esteem.</p>
<p><strong>Conclusion</strong></p>
<p>In the world of alopecia, it's essential to have candid conversations about the fear of feeling ugly. Pretending that these feelings don't exist or promoting the idea that inner beauty is all that matters can be dismissive. Your journey with alopecia can lead to personal growth, strength, and self-acceptance.</p>September is Alopecia Awareness Month - 30 Days, 30 Facts: Spreading Alopecia Awarenesstag:alopeciaworld.com,2023-08-31:2022678:BlogPost:19772762023-08-31T16:30:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><span style="font-size: 12pt;"><strong>30 Days, 30 Facts: A Social Media Initiative</strong></span></p>
<p>One innovative way to participate in Alopecia Awareness Month is by joining the "30 Days, 30 Facts" campaign. This initiative involves sharing graphics that feature a different alopecia-related fact each day of the month. Here's why this campaign is so impactful:</p>
<p></p>
<p>Alopecia Awareness Month is an annual campaign that takes place in September, dedicated to raising awareness…</p>
<p><span style="font-size: 12pt;"><strong>30 Days, 30 Facts: A Social Media Initiative</strong></span></p>
<p>One innovative way to participate in Alopecia Awareness Month is by joining the "30 Days, 30 Facts" campaign. This initiative involves sharing graphics that feature a different alopecia-related fact each day of the month. Here's why this campaign is so impactful:</p>
<p></p>
<p>Alopecia Awareness Month is an annual campaign that takes place in September, dedicated to raising awareness about alopecia, a condition that affects millions of people worldwide. While some people may be familiar with the term alopecia, many are unaware of the various forms it can take and the profound impact it has on our lives.</p>
<p></p>
<p><strong>Informative:</strong></p>
<p>These graphics serve as bite-sized pieces of information about alopecia, covering various aspects of the condition. They educate the public on what alopecia is, its different forms, and the challenges individuals with alopecia face.</p>
<p></p>
<p><strong>Engaging:</strong></p>
<p>Visual content is highly engaging on social media. People are more likely to interact with and share graphics, which can lead to a broader reach and more significant impact.</p>
<p></p>
<p><strong>Conversation Starter:</strong></p>
<p>Sharing these graphics can spark conversations about alopecia. People may ask questions, seek more information, or express their support for those affected by the condition. This dialogue is essential for dispelling myths and promoting understanding.</p>
<p></p>
<p><strong>Unity:</strong></p>
<p>When people across the world share these graphics simultaneously, it creates a sense of unity and solidarity within the alopecia community. It shows that people from diverse backgrounds care about this cause.</p>
<p></p>
<p style="text-align: center;"><span style="font-size: 14pt;"><strong>Getting involved in the "30 Days, 30 Facts" campaign is easy:</strong></span></p>
<p style="text-align: center;"></p>
<p><strong>Download and share the Graphics.</strong> </p>
<p>Below are 7 graphics for September 1 – 7, we will be uploading 7 graphics each week. Be sure to use the hashtags #AlopeciaAwarenessMonth, #alopeciaworld to connect with others participating in the campaign. And don’t forget to Alopecia World (@alopeciaworld) in your posts too! </p>
<p></p>
<p><strong>Conclusion:</strong></p>
<p>Alopecia Awareness Month is a crucial opportunity to shed light on a condition that affects millions of us. By participating in the "30 Days, 30 Facts" campaign and sharing on social media, you can play a vital role in dispelling myths, reducing stigma, and showing support for those with alopecia. Let's come together to make a difference and spread awareness about alopecia throughout the month of September and beyond. Together, we can make a positive impact on the lives of those living with alopecia.</p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12214540670?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12214540670?profile=RESIZE_710x" width="180" class="align-left"/></a></p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12214540875?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12214540875?profile=RESIZE_710x" width="180" class="align-left"/></a></p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12214541067?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12214541067?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12214540901?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12214540901?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12214541275?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12214541275?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12214541300?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12214541300?profile=RESIZE_710x" width="180" class="align-left"/></a><a href="https://storage.ning.com/topology/rest/1.0/file/get/12214542062?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12214542062?profile=RESIZE_710x" width="180" class="align-left"/></a></p>WALK FOR ALOPECIA™ - NAAF Awareness Event - Ways to join in!tag:alopeciaworld.com,2023-08-31:2022678:BlogPost:19772752023-08-31T14:30:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><a href="https://assets.classy.org/1824718/4961e662-858b-11ea-ba99-0e4f8324fcdb.jpg" rel="noopener" target="_blank"><img class="align-right" height="190" src="https://assets.classy.org/1824718/4961e662-858b-11ea-ba99-0e4f8324fcdb.jpg?profile=RESIZE_710x" width="286"></img></a></p>
<p><strong>Source: <a href="http://www.naaf.org">www.naaf.org</a></strong></p>
<p><br></br> "Imagine waking up to clumps of hair on your pillow.</p>
<p><br></br> Or turning off the shower only to find a pile of your hair on the drain.</p>
<p><br></br> And that you have numerous bald spots on your head that are so big they can no longer be hidden.</p>
<p>Millions of…</p>
<p><a href="https://assets.classy.org/1824718/4961e662-858b-11ea-ba99-0e4f8324fcdb.jpg" target="_blank" rel="noopener"><img src="https://assets.classy.org/1824718/4961e662-858b-11ea-ba99-0e4f8324fcdb.jpg?profile=RESIZE_710x" width="286" class="align-right" height="190"/></a></p>
<p><strong>Source: <a href="http://www.naaf.org">www.naaf.org</a></strong></p>
<p><br/> "Imagine waking up to clumps of hair on your pillow.</p>
<p><br/> Or turning off the shower only to find a pile of your hair on the drain.</p>
<p><br/> And that you have numerous bald spots on your head that are so big they can no longer be hidden.</p>
<p>Millions of Americans don’t have to imagine. This is their reality.</p>
<p><br/> A chronic, lifelong skin disease, alopecia areata causes the immune system to mistake healthy hair follicles as dangerous and begins attacking them. The result is hair loss ranging from patchy spots on the head to complete loss of hair over the whole body. Nearly 7 million Americans are affected by this common autoimmune disease.</p>
<p></p>
<p style="text-align: center;"><span style="font-size: 14pt;"><strong>Let’s Do Something About Alopecia Areata,</strong></span></p>
<p style="text-align: center;"><span style="font-size: 14pt;"><strong> Let’s WALK FOR ALOPECIA™!</strong></span></p>
<p></p>
<p>On Saturday, September 30th, 2023 we will rally coast to coast to raise funds, support our community, educate the public and empower people living with alopecia areata everywhere. This year we will host one Walk site at Lake Merced in San Francisco, CA, honoring the community where NAAF was established more than four decades ago. At the same time, do it yourself “Walk Where You Are” teams will step-off in communities all over the country providing an opportunity for anyone, anywhere to do something about alopecia areata."</p>
<p></p>
<p>To join a team, donate or get more information click the link below:</p>
<p><a href="https://support.naaf.org/campaign/2023-walk-for-alopecia-tm/c481771"></a><a href="https://support.naaf.org/campaign/2023-walk-for-alopecia-tm/c481771">2023 WALK FOR ALOPECIA™ - Campaign (naaf.org)</a><a href="https://support.naaf.org/campaign/2023-walk-for-alopecia-tm/c481771"></a></p>
<p></p>Generic Xeljanztag:alopeciaworld.com,2023-08-20:2022678:BlogPost:19770122023-08-20T22:04:47.000ZApplehttps://alopeciaworld.com/profile/Apple
<p>Guys my medication arrived yesterday from Wellworld. I am so happy right now, yay! I can breathe… in between looking for a job, family illness, and about to run out of meds for Alopecia I can say this one little thing is the biggest thing ever. Thank you guys for your support if anyone needs info send me text.</p>
<p>Guys my medication arrived yesterday from Wellworld. I am so happy right now, yay! I can breathe… in between looking for a job, family illness, and about to run out of meds for Alopecia I can say this one little thing is the biggest thing ever. Thank you guys for your support if anyone needs info send me text.</p>Is This Video About Bald Women: Beautiful or Offensive? Share Your Thoughts!tag:alopeciaworld.com,2023-08-12:2022678:BlogPost:19764402023-08-12T14:30:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><span>Let's have a discussion AlopeciaWorld.com. Do you find the contents and lyrics to this video about bald women beautiful or offensive.</span></p>
<p></p>
<p><em>*All perspectives are welcome on Alopecia World, but please try to be respectful.</em></p>
<p></p>
<p><em><iframe width="560" height="315" src="https://www.youtube.com/embed/SBW0VQ4sXtA?wmode=opaque" frameborder="0" allowfullscreen=""></iframe>
</em></p>
<p></p>
<p><span>Let's have a discussion AlopeciaWorld.com. Do you find the contents and lyrics to this video about bald women beautiful or offensive.</span></p>
<p></p>
<p><em>*All perspectives are welcome on Alopecia World, but please try to be respectful.</em></p>
<p></p>
<p><em><iframe width="560" height="315" src="https://www.youtube.com/embed/SBW0VQ4sXtA?wmode=opaque" frameborder="0" allowfullscreen=""></iframe>
</em></p>
<p></p>10 Clever Comebacks: Handling Offensive Bald Commentstag:alopeciaworld.com,2023-08-11:2022678:BlogPost:19765502023-08-11T15:30:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p></p>
<p>Dealing with offensive comments can be challenging, but responding with humor and grace can often diffuse the situation. Here are 10 comebacks to offensive bald comments:</p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12187396874?profile=original" rel="noopener" target="_blank"><img class="align-left" src="https://storage.ning.com/topology/rest/1.0/file/get/12187396874?profile=RESIZE_710x" width="250"></img></a></p>
<p>1. "Bald and bold – a combo that obviously intimidates some."</p>
<p>2. "I'm too busy living life to worry about my hair. How about you?"</p>
<p>3. "Being bald…</p>
<p></p>
<p>Dealing with offensive comments can be challenging, but responding with humor and grace can often diffuse the situation. Here are 10 comebacks to offensive bald comments:</p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/12187396874?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/12187396874?profile=RESIZE_710x" width="250" class="align-left"/></a></p>
<p>1. "Bald and bold – a combo that obviously intimidates some."</p>
<p>2. "I'm too busy living life to worry about my hair. How about you?"</p>
<p>3. "Being bald doesn't define me, but your comment says a lot about you."</p>
<p>4. "Funny how my hair loss is more interesting to you than your manners."</p>
<p>5. "Oh, you noticed? Congratulations on your detective skills!"</p>
<p>6. "I may be bald, but I've got a thick skin."</p>
<p>7. "Let's talk about something as irrelevant as your comment – like the weather."</p>
<p>8. "You must be an expert on hairstyles. What other profound insights do you have?"</p>
<p>9. "My baldness may be temporary, but being rude seems to be a lifelong commitment."</p>
<p>10. "Remember, kindness is free, but your comments could cost you some friends."</p>
<p></p>
<p>Add some of your own or do have other ways that you can share with the community that may have help you in these situations.</p>International Alopecia Day - August 5th, 2023 - How to Participate!tag:alopeciaworld.com,2023-07-23:2022678:BlogPost:19757092023-07-23T18:00:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><img class="align-center" src="https://storage.ning.com/topology/rest/1.0/file/get/12161949269?profile=RESIZE_710x" width="500"></img></p>
<p>People all around the world will be having parties, celebrations and awareness events. You’ll see IAD selfies popping up all day on social media.</p>
<p>YOU can be part of the annual International Alopecia Day YouTube slide show!</p>
<p>HOW YOU CAN BE IN THE 2023 IAD VIDEO:</p>
<p>1. Take your photos ON International Alopecia Day, August 5. This is meant to be a snapshot of Alopecians around the world on this ONE day.</p>
<p>2. Please don’t send in professional “studio”…</p>
<p><img src="https://storage.ning.com/topology/rest/1.0/file/get/12161949269?profile=RESIZE_710x" width="500" class="align-center"/></p>
<p>People all around the world will be having parties, celebrations and awareness events. You’ll see IAD selfies popping up all day on social media.</p>
<p>YOU can be part of the annual International Alopecia Day YouTube slide show!</p>
<p>HOW YOU CAN BE IN THE 2023 IAD VIDEO:</p>
<p>1. Take your photos ON International Alopecia Day, August 5. This is meant to be a snapshot of Alopecians around the world on this ONE day.</p>
<p>2. Please don’t send in professional “studio” portraits OR photos that you’ve posted on your Facebook page before IAD.</p>
<p>3. You can be in a wig, bald, with patches or lots of hair, or in a hat or scarf. THIS IS ALL OF US, AS WE ARE! It’s your choice.</p>
<p>4. You can include non-Alopecian family or friends in the photo.</p>
<p>5. If you have a GROUP event, make sure that everyone in your IAD photo understands it will be in a Public YouTube video and agrees to that.</p>
<p>6. It’s great if you make and hold a SIGN saying where you live – and, you can write the sign in your LANGUAGE. Posing in front of a local LANDMARK or scene adds to the international theme.</p>
<p>7. If you make a sign or banner that includes the name of the holiday, please make sure you use the official NAME: “INTERNATIONAL ALOPECIA DAY”, and NOT “Alopecia Awareness Day” or other variations. We’re trying to raise awareness with this annual event, so the name needs to be consistent.</p>
<p>8. Send only ONE photo per person or family - your best and favorite. BUT, if you’re having a GROUP event and need more than one photo to show everyone, you can send in more than one. Can’t decide which photo to send? You can make a COLLAGE in one image. BUT, remember that your photos will look smaller in the finished video if they’re part of a collage.</p>
<p>9. TO GUARANTEE THAT YOUR PHOTO IS IN THIS YEAR’S YOUTUBE IAD VIDEO, YOU MUST SEND IT TO: internationalalopeciaday@gmail.com Do not send BEFORE August 5. Emailing your photo to me is how I can be sure I have your PERMISSION to put it in the video.</p>
<p>10. Please give me your COUNTRY in the email you send with the photo so that I can put it in the correct place in the video.</p>
<p>11. The deadline to submit photos is August 31, 2023, so there’s plenty of time after IAD. The finished video will be online in September.</p>
<p>WATCH the previous years' videos on YouTube under "International Alopecia Day" to get ideas for your event or photo.</p>
<p></p>
<center><iframe width="560" height="315" src="https://www.youtube.com/embed/4Z8DGjuY4d4?wmode=opaque" frameborder="0" allowfullscreen=""></iframe>
</center>
<p></p>
<p>Make sure YOUR country is represented!</p>Breaking News: US FDA approves another hair loss drug by Pfizer this timetag:alopeciaworld.com,2023-06-27:2022678:BlogPost:19748822023-06-27T14:30:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><strong>Recent Stories from ABCNews.com"</strong></p>
<p></p>
<p><em><strong>"The U.S. Food and Drug Administration on Friday approved an alopecia treatment for kids..</strong></em></p>
<p><a href="https://www.empr.com/wp-content/uploads/sites/7/2023/06/Litfulo-Pfizer.jpg" rel="noopener" target="_blank"><img class="align-right" height="236" src="https://www.empr.com/wp-content/uploads/sites/7/2023/06/Litfulo-Pfizer.jpg?profile=RESIZE_710x" width="353"></img></a></p>
<p>The drug, ritlecitinib, is a once-daily pill for kids ages 12 and older with severe alopecia areata, a disease that develops when the body attacks the hair follicles,…</p>
<p><strong>Recent Stories from ABCNews.com"</strong></p>
<p></p>
<p><em><strong>"The U.S. Food and Drug Administration on Friday approved an alopecia treatment for kids..</strong></em></p>
<p><a href="https://www.empr.com/wp-content/uploads/sites/7/2023/06/Litfulo-Pfizer.jpg" target="_blank" rel="noopener"><img src="https://www.empr.com/wp-content/uploads/sites/7/2023/06/Litfulo-Pfizer.jpg?profile=RESIZE_710x" width="353" class="align-right" height="236"/></a></p>
<p>The drug, ritlecitinib, is a once-daily pill for kids ages 12 and older with severe alopecia areata, a disease that develops when the body attacks the hair follicles, causing hair loss.</p>
<p>The medication will be sold under the brand name Litfulo, and is manufactured by Pfizer.</p>
<p>Pfizer said Litfulo will be available for consumers "in the coming weeks."</p>
<p><strong>According to Pfizer, a full year supply of Litfulo has a list price of $49,000,</strong> similar to other specialty dermatologic treatments. The company said the actual cost to patients will vary based on individual health care plans.</p>
<p><br/> "We are committed to helping patients access the treatments they need," Pfizer said in a statement.</p>
<p>"There will be copay savings for commercially insured patients and a patient assistance program for eligible patients to help achieve this. Through the Pfizer Dermatology Patient Access Program, eligible patients will be able to get support with access to LITFULO."</p>
<p>The medication has already been a game-changer for Maria Strattner, an 18-year-old with alopecia who took part in the clinical trial that led to the FDA's approval.</p>
<p><br/> Within months of taking the medication, Maria Strattner's hair started to regrow, according to her mom, who said of her daughter's persistence, "Thank God that kid was smart enough not to give up."</p>
<p></p>
<p>Dr. Brett King, associate professor of dermatology at Yale School of Medicine and principal investigator of the clinical trial of ritlecitinib, described the FDA's approval of ritlecitinib as a "huge advancement" in the treatment of alopecia, describing the drug's effect as "nothing short of transformative."</p>
<p><br/> "Over 24 weeks of treatment, about 30% of people participating in the trials regrew their hair. Remember, these are patients who at the start had 50% to 100% scalp hair loss. Often they had no scalp hair," King told ABC News. "And 24 weeks later, 30% of them have less than 20% [scalp hair loss] or complete scalp hair regrowth, and up to 48 weeks, that number rises to 40% of people achieving dramatic regrowth of hair."</p>
<p></p>
<p>Would you try it?</p>
<p></p>
<p>Read more on <a href="https://alopeciaworld.com/main/search/search?q=Oluminant" target="_blank" rel="noopener">Oluminant</a> here:</p>
<p>Check back here for more stories on <a href="https://alopeciaworld.com/main/search/search?q=Litfulo" target="_blank" rel="noopener">Litfulo</a> as our community starts talking about it.</p>
<p></p>
<p><em><strong>My opinion on whether I would take these drug or not to come.</strong></em></p>
<p></p>
<p>Source: <a href="https://abcnews.go.com/GMA/Wellness/fda-approves-1st-treatment-grow-back-hair-teens/story?id=100325718" target="_blank" rel="noopener">ABCNews.com</a></p>"Leah Hayes wants to bring alopecia awareness to the Olympics"tag:alopeciaworld.com,2023-06-15:2022678:BlogPost:19744242023-06-15T13:35:27.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p></p>
<p><a href="https://bvmsports.com/wp-content/uploads/2023/06/USATSI_19365188-e1686259689229-1366x768.jpg" rel="noopener" target="_blank"><img class="align-full" height="316" src="https://bvmsports.com/wp-content/uploads/2023/06/USATSI_19365188-e1686259689229-1366x768.jpg?profile=RESIZE_710x" width="562"></img></a></p>
<p><span style="font-size: 8pt;"><em>Photo credit: Grace Hollars-USA TODAY Sports</em></span></p>
<p></p>
<p>Leah Hayes, a high school senior and competitive swimmer, has set her sights on making it to the 2024 Olympics in Paris. However, her goal goes beyond competing; she also wants to raise awareness about alopecia, an autoimmune…</p>
<p></p>
<p><a href="https://bvmsports.com/wp-content/uploads/2023/06/USATSI_19365188-e1686259689229-1366x768.jpg" target="_blank" rel="noopener"><img src="https://bvmsports.com/wp-content/uploads/2023/06/USATSI_19365188-e1686259689229-1366x768.jpg?profile=RESIZE_710x" width="562" class="align-full" height="316"/></a></p>
<p><span style="font-size: 8pt;"><em>Photo credit: Grace Hollars-USA TODAY Sports</em></span></p>
<p></p>
<p>Leah Hayes, a high school senior and competitive swimmer, has set her sights on making it to the 2024 Olympics in Paris. However, her goal goes beyond competing; she also wants to raise awareness about alopecia, an autoimmune disease that causes her hair loss. </p>
<p></p>
<p>Hayes, who was diagnosed with alopecia at the age of 7, found solace in swimming, where she felt comfortable not wearing a wig or swim cap due to her hair loss. Over time, swimming helped her gain confidence, and she now wants to use her platform as an athlete to bring attention to alopecia.</p>
<p></p>
<p><span>Hayes has already made significant strides in her swimming career. She won a bronze medal in the 200m individual medley (IM) at the world championships and made her Team USA debut. Despite dealing with a stress fracture in her foot, she achieved a time almost four seconds better than her previous Olympic trials time. Hayes's accomplishments also include being named SportsKid of the Year by Sports Illustrated in 2018.</span></p>
<p></p>
<p>Her journey has inspired others with alopecia and autoimmune diseases, as she has become a role model for those looking to embrace their true selves. Hayes is training for upcoming events such as the world championships and the Olympic trials, with the hope of reaching the Olympics and using the international platform to spread awareness about alopecia.</p>
<p></p>
<p>To read more about Leah Hayes you can read the full article here:</p>
<p>SOURCE: <a href="https://bvmsports.com/2023/06/08/leah-hayes-wants-to-bring-alopecia-awareness-to-the-olympics/">https://bvmsports.com/2023/06/08/leah-hayes-wants-to-bring-alopecia-awareness-to-the-olympics/</a></p>
<p></p>Clinical Trial Opportunitytag:alopeciaworld.com,2023-06-05:2022678:BlogPost:19743712023-06-05T23:31:05.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><a href="https://www.naaf.org/wp-content/uploads/2023/05/Fast-AA-Color-logo-300x62.png" rel="noopener" target="_blank"><img class="align-center" src="https://www.naaf.org/wp-content/uploads/2023/05/Fast-AA-Color-logo-300x62.png?profile=RESIZE_710x"></img></a> A clinical research study is looking for adults (18+) diagnosed with alopecia areata with 50% or more scalp hair loss. This study is investigating an oral (taken by mouth) study drug called farudodstat. The main purpose of the study is to see whether farudodstat, when taken twice a day for 12 weeks, can help people with alopecia areata grow hair and to find out…</p>
<p><a href="https://www.naaf.org/wp-content/uploads/2023/05/Fast-AA-Color-logo-300x62.png" target="_blank" rel="noopener"><img src="https://www.naaf.org/wp-content/uploads/2023/05/Fast-AA-Color-logo-300x62.png?profile=RESIZE_710x" class="align-center"/></a>A clinical research study is looking for adults (18+) diagnosed with alopecia areata with 50% or more scalp hair loss. This study is investigating an oral (taken by mouth) study drug called farudodstat. The main purpose of the study is to see whether farudodstat, when taken twice a day for 12 weeks, can help people with alopecia areata grow hair and to find out if farudodstat is safe when compared to placebo (a pill that looks like the farudodstat tablet but has no drug or other active ingredient in it).</p>
<p>Eligible participants will receive study drug for 12 weeks and placebo for 12 weeks. The study will last approximately 8 months and you will have to go to the study center for 11 scheduled visits. Participation in this study is at no cost to you.</p>
<p></p>
<p style="text-align: center;"><span style="font-size: 12pt;"><strong>This study will occur at multiple clinical trial sites throughout the United States.</strong></span></p>
<p style="text-align: center;"><span style="font-size: 12pt;"><strong>Click here to learn more:</strong></span></p>
<p style="text-align: left;"><strong><a href="https://www.naaf.org/studies/phase-2a-study-to-investigate-farudodstat-in-adults-with-alopecia-areata/">https://www.naaf.org/studies/phase-2a-study-to-investigate-farudodstat-in-adults-with-alopecia-areata/</a></strong></p>An Open-Label Subpopulation Study to Evaluate Efficacy and Safety of Baricitinib in Participants that Identify as Black or African Americantag:alopeciaworld.com,2023-06-05:2022678:BlogPost:19743732023-06-05T23:30:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p></p>
<p><span style="font-size: 12pt;"><strong>CLINICAL TRIAL:</strong></span></p>
<p><a href="https://www.naaf.org/wp-content/uploads/2023/03/Eli_Lilly_and_Company-Logo.wine_-300x200.png" rel="noopener" target="_blank"><img class="align-left" src="https://www.naaf.org/wp-content/uploads/2023/03/Eli_Lilly_and_Company-Logo.wine_-300x200.png?profile=RESIZE_710x" width="198"></img></a></p>
<p><span>An ongoing clinical research study is currently recruiting Black and African American patients with alopecia areata for a study that evaluates the safety and effectiveness of an oral drug. Would you like to know more about this study? This study…</span></p>
<p></p>
<p><span style="font-size: 12pt;"><strong>CLINICAL TRIAL:</strong></span></p>
<p><a href="https://www.naaf.org/wp-content/uploads/2023/03/Eli_Lilly_and_Company-Logo.wine_-300x200.png" target="_blank" rel="noopener"><img src="https://www.naaf.org/wp-content/uploads/2023/03/Eli_Lilly_and_Company-Logo.wine_-300x200.png?profile=RESIZE_710x" width="198" class="align-left"/></a></p>
<p><span>An ongoing clinical research study is currently recruiting Black and African American patients with alopecia areata for a study that evaluates the safety and effectiveness of an oral drug. Would you like to know more about this study? This study is testing a drug called baricitinib (the “study drug”) in people with alopecia areata. The purpose of the study is to learn how the study drug can help patients, particularly Black and African American patients with alopecia areata regrow their hair .You may qualify to participate in this study if you are 18 to 60 years for males (70 years of age for females), self identify as Black or African American in race, have at least 50% scalp hair loss, and have been diagnosed with alopecia areata for at least 6 months.</span></p>
<p></p>
<p><span>This study will occur at multiple clinical trial sites throughout the United States. Click here to learn more:</span></p>
<p><span><a href="https://naaf.cmail19.com/t/d-l-vljjthl-mtkkidrf-b/" rel="noopener noreferrer" target="_blank"> </a></span><strong><span><a href="https://naaf.cmail19.com/t/d-l-vljjthl-mtkkidrf-n/" rel="noopener noreferrer" target="_blank">https://www.naaf.org/studies/an-open-label-subpopulation-study-to-evaluate-efficacy-and-safety-of-baricitinib-in-participants-with-alopecia-areata-that-self-identify-as-black-or-african-american-in-race/</a>.</span></strong></p>
<p></p>
<p></p>
<p>To read posts and experiences from member on Alopecia World about <span>baricitinib, click below.</span></p>
<p><a href="https://alopeciaworld.com/main/search/search?q=baricitinib" target="_self">baricitinib on Alopecia World</a></p>
<p></p>
<p></p>
<p></p>
<p></p>Do we need heroes like Jada Pinkett Smith?tag:alopeciaworld.com,2023-03-26:2022678:BlogPost:19712672023-03-26T03:00:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/11004822899?profile=original" rel="noopener" target="_blank"><img class="align-full" height="340" src="https://storage.ning.com/topology/rest/1.0/file/get/11004822899?profile=RESIZE_710x" width="584"></img></a> It's true, sometimes it's comforting to know that someone famous is going through the same thing you are, like Jada Pinkett Smith and Ayanna Pressley, both of whom have opened up about their struggles with alopecia. It's reassuring to know that you're not alone. However, it's important to remember that these celebrities are just people, like you and me. They…</p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/11004822899?profile=original" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/11004822899?profile=RESIZE_710x" width="584" class="align-full" height="340"/></a>It's true, sometimes it's comforting to know that someone famous is going through the same thing you are, like Jada Pinkett Smith and Ayanna Pressley, both of whom have opened up about their struggles with alopecia. It's reassuring to know that you're not alone. However, it's important to remember that these celebrities are just people, like you and me. They have their own struggles and challenges, and while they may be inspiring, they're not necessarily the only source of inspiration.</p>
<p>As much as we may admire these hero’s, we don't necessarily need them to make a difference in the world. Each one of us has the potential to become a hero ourselves, in our own unique way.</p>
<p>What does it mean to be your own hero? It means recognizing your own strength and courage in the face of adversity. It means being willing to step out of your comfort zone and take risks. It means being willing to fail, but getting back up and trying again. It means having the confidence to believe in yourself, even when others may doubt you.</p>
<p>One way to think about being your own hero is to consider the hero's journey. This is a concept that comes from storytelling, but it can be applied to our own lives. The hero's journey involves leaving the familiar, facing challenges and obstacles, and ultimately achieving a goal or transformation. A journey requires courage, perseverance, and a willingness to take risks.</p>
<p>When we apply the hero's journey to our own lives, we can see ourselves as the hero of our own story. We can recognize the challenges we have faced and the obstacles we have overcome. We can celebrate our successes and learn from our failures and most importantly, we can inspire others by sharing our own story and encouraging them to do the same.</p>
<p>Being your own hero is not always easy. It does requires we take risks, face challenges, and stepping out of our comfort zone. There may be moments of doubt, fear, and uncertainty. But despite these obstacles, being your own hero is always worthwhile. It means living a life of purpose, passion, and authenticity. It means creating a future for yourself and it means inspiring others to do the same. So while being your own hero may not be easy, the rewards are immeasurable.</p>
<p>Now my challenge to you is to go out and be your own hero!</p>The Power of AlopeciaWorld.com: Finding Strength and Encouragement in Like-Minded Connectionstag:alopeciaworld.com,2023-03-12:2022678:BlogPost:19697532023-03-12T20:30:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/2117027938?profile=RESIZE_710x&height=394" rel="noopener" target="_blank"><img class="align-left" src="https://storage.ning.com/topology/rest/1.0/file/get/2117027938?height=394&profile=RESIZE_710x" width="221"></img></a> Hey there, fellow members of Alopecia World. Today, let's talk about the importance of our community and what it means to us.</p>
<p> </p>
<p>Living with alopecia can be incredibly isolating and challenging. But by joining Alopecia World, we have found a place where we can share our experiences, struggles, and victories with others who truly…</p>
<p><a href="https://storage.ning.com/topology/rest/1.0/file/get/2117027938?profile=RESIZE_710x&height=394" target="_blank" rel="noopener"><img src="https://storage.ning.com/topology/rest/1.0/file/get/2117027938?height=394&profile=RESIZE_710x" width="221" class="align-left"/></a>Hey there, fellow members of Alopecia World. Today, let's talk about the importance of our community and what it means to us.</p>
<p> </p>
<p>Living with alopecia can be incredibly isolating and challenging. But by joining Alopecia World, we have found a place where we can share our experiences, struggles, and victories with others who truly understand what we're going through. We have formed a community of like-minded people who offer advice, support, and encouragement whenever we need it. <span>And the best part is that Alopecia World is available 24/7. No matter what time of day or night it is, or what time zone you live in, there is always someone there to listen and offer support.</span></p>
<p> </p>
<p>For me personally, being a part of this community has been life-changing. The support and encouragement I've received from everyone has helped me overcome many obstacles and cope with my alopecia in ways I never thought possible. I've learned so much from all of you and I'm grateful for the connection and friendships I've formed here.</p>
<p></p>
<p>However, it's not just about receiving help. It's about giving back too. By sharing our own experiences, offering advice, and supporting others who are going through the same thing, we are creating a community of people who truly care about one another. And that is a beautiful thing.</p>
<p></p>
<p>I know that life can get busy, and it's easy to lose touch with our community. So if you haven't visited our online support community in a while, I want to encourage you to come back. We miss you, and we want you to know that you are always welcome here. Whether you are having a bad day or a great day, or you just need someone to talk to, we are here for you.</p>
<p> </p>
<p>So let's continue to support one another, to share our stories, and to offer encouragement whenever and wherever we can. Together, we can continue to create a community that is strong, supportive, and uplifting. And for those who haven't been here in a while, we hope to see you soon!</p>
<p></p>
<p>What has Alopecia World has meant to you? We would love to hear from you!</p>Olaplex hair products sued for allegedly causing hair loss and bald spotstag:alopeciaworld.com,2023-02-22:2022678:BlogPost:19687242023-02-22T01:30:00.000ZCheryl, Co-founderhttps://alopeciaworld.com/profile/cherylcarvery
<p>According to an article on CNN.com:</p>
<p>"Olaplex, a beauty brand favored by TikTok and Instagram influencers, sells hair products that dozens of customers allege caused “serious injury,” according to a lawsuit filed last week. Olaplex denies the claims, saying independent test results prove the allegations to be false."</p>
<p>'<span>Nearly 30 women joined together to file a lawsuit against Olaplex on February 9, specifically targeting its No. 0 to No. 9 products. They allege the products…</span></p>
<p>According to an article on CNN.com:</p>
<p>"Olaplex, a beauty brand favored by TikTok and Instagram influencers, sells hair products that dozens of customers allege caused “serious injury,” according to a lawsuit filed last week. Olaplex denies the claims, saying independent test results prove the allegations to be false."</p>
<p>'<span>Nearly 30 women joined together to file a lawsuit against Olaplex on February 9, specifically targeting its No. 0 to No. 9 products. They allege the products caused hair loss, breakage, brittle hair, bald spots and scalp irritation."</span></p>
<p><img src="https://media.cnn.com/api/v1/images/stellar/prod/230215081152-olaplex-products-restricted.jpg?c=16x9&q=h_270,w_480,c_fill" alt="Bottles of Olaplex hair care products"/></p>
<p><span style="font-size: 8pt;"><em>Photo Credit: David Williams/Bloomberg/Getty Images</em></span></p>
<p></p>
<p>"<span>The customers say in the lawsuit that Olaplex use ingredients that can cause allergic reactions and are banned in Europe"</span></p>
<p></p>
<p class="paragraph inline-placeholder">In response to the lawsuit, an company spokesperson for Olaplex said “We have publicly released test results from independent third-party laboratories, going above and beyond industry standards, to demonstrate this. We have full confidence and believe in the safety and efficacy of our products,” </p>
<p>"<span>The plaintiffs are seeking more than $75,000 in damages."</span></p>
<p></p>
<p>Source: CNN.com - Olaplex Hair Product Lawsuit </p>
<p></p>
<p></p>
<p><span><a href="https://www.cnn.com/2023/02/15/business/olaplex-hair-products-lawsuit/index.html"></a></span></p>
<p></p>
<p></p>