"I have been on Dutasteride 0.5mg for 4 years with no side effects. It stopped my attack in its tracks and no new follicles became inflamed. The original inflamed follicles are very slowly still falling out four years later. I am in burn out right…"
"I’m 24, female and basing fast. My whole life has been a struggle. My family was dysfunctional, my mother had severe alcohol dependency issues, I suffered sexual abuse from a family friend, and again when I was older. As a teen I went through…"
I have just his week begun taking 0.5mg of Dutasteride/Avodart this week. I was hoping to come across other ladies with experience using this medication for their hairloss, and if so, what your dose was and how effective you found it.…"
I saw your story when reading through comments and wanted to write because I too am young like you and was just diagnosed. Not quite as young as I am 31 but still feel too young to be losing my hair. our stories sound similar too,…"
"I agree with Jen, your eyebrows look thick and normal, and your hairline , temples and in front of your ears is still mostly intact. You need to see some different doctors if they are unwilling to help you. I do hate wind also, so I usually try to…"
I have been on Dutasteride 0.5mg for 4 years with no side effects. It stopped my attack in its tracks and no new follicles became inflamed. The original inflamed follicles are very slowly still falling out four years later. I am in burn out right now.
I saw your story when reading through comments and wanted to write because I too am young like you and was just diagnosed. Not quite as young as I am 31 but still feel too young to be losing my hair. our stories sound similar too, I felt my hairline had changed but it was not enough for anyone else to notice so everyone, family, drs, etc. told me that basically it was just in my head and if there was any due to the stress of my husband walking out on me out of the blue. Anyways, a year and tons of obsessing later a therapist felt that I had Body dysmorphyic disorder and then what do you know my biopsy came back as FFA. I feel that it has worsened around the area where I had the biopsy but still my family says its not noticeable. I don't ever wear my hair pulled back. Mine recession is almost opposite of yours as I never used to have widows peak but I do now because one side has receded so much!!I also wanted to tell you that even though you notice it and it really bothers you, you still look great and it really does look like a normal hairline for now. I've decided that's what I have to tell myself since nobody else seems to notice and tells me that everyone has a different hairline. It just doesn't look normal to us because it is definitely different than how we've always seen ourselves and I think that is the hardest thing to adjust to. Seeing yourself differently than how you know you looked. Stay positive. If it gets bad enough there are solutions, not ones we want to have to deal with but just a reality none the less. Definitely helps to have a website such as this where people are going through the same thing. Hope to hear from you about how you are doing.
I am so sorry that this is happening to you. I do believe that this disease has something to do with menopause. Your hair loss looks different from mine so I am wondering if it really is ffa. You say that there are no white shiny spots where the hair was before and also it does not seem like you have spots. If it is not the scarring type then your hair may grow back. I had this happen when I was in my 20's. I am now 59.
I have had ffa for 4 years and my hair loss consists of bald spots about 1.5 inches in diameter. Lots of bald spots on the hairline that have joined together making a complete band of hairless scalp. Yours seems a little different. It seems like more diffuse loss along the hairline. I am using some dark eye shadow along the hairline then I pull the hair over the affected area. I am wearing my hair curly now. It seems very unusual that someone so young is suffering from this condition.
Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.
AlopeciaWorld.com: It's hair loss support at its best!