Megan Adair
  • Female
  • Norfolk, VA
  • United States
Share

Megan Adair's Friends

  • claudiaclaude
  • mhart04843
  • Sarah
  • Toni
  • You can do it : )
  • Hannah Dennis
  • Frank Pratt
  • Pedro Costa
  • Pam Fitros

Gifts Received

Gift

Megan Adair has not received any gifts yet

Give a Gift

 

Megan Adair's Page

Profile Information

Relationship Status:
In a Relationship
About Me:
I have had Alopecia since I was 9 years old. I am very proud to be one of the many people diagnosed with this disease, I truly believe Alopecia brings out raw beauty tucked away inside the soul's of those diagnosed. I have had this disease for nine years now and I have realized that Alopecia is a blessing in disguise. It has shaped me into the woman I am today and I am so thankful that I can share my story with the world. We are more than this disease. We are Bald and Beautiful.
Do you have alopecia?
Alopecia totalis
Are you age 18 or older?
Yes - I am 18 or older

Megan Adair's Photos

  • Add Photos
  • View All

Megan Adair's Blog

My memoir "Split Ends"

Posted on July 29, 2012 at 9:38pm 13 Comments

It was a Tuesday. I was 15 years old, and like every Tuesday, I would go to the doctor, receive my treatment, and then go home. On that particular Tuesday, however, something different occurred. I didn’t follow my normal routine. It was a strange day for me. I had that routine memorized like the back of my hand, but that Tuesday was the day it all changed.

I sat in the waiting room of the doctor’s office. I had always hated the plain gray walls that began to blur when you stared at…

Continue

Comment Wall (5 comments)

You need to be a member of Alopecia World to add comments!

Join Alopecia World

At 11:11pm on December 5, 2016, eva said…
Pam are you the lady in the video I'm not an oddity? If so,can we be friends? I love that video.it did so much for me.
At 2:04pm on August 15, 2012, LeslieAnn Butler said…

Hello and welcome, Megan!
How are you today?
Leslie Ann

At 1:01pm on August 10, 2012, claudiaclaude said…

Thank you for adding me!

At 11:36am on August 3, 2012, Pam Fitros said…

How lovely! I am so thrilled at the generous responses of so many women. It is as though the timing I thought had gone so wrong as to stop writing was actually just perfect. We are the Pioneers of Bald. And we have so very, very much to offer our sisters and brothers who share the path of alopecia. I cannot wait for this to be published. Our collective stories are so poignant and compelling. What a tapestry of courage and character these stories weave. Those of you who are praying folk, whatever your faith may be, please pray this book gets into the hands of the people who need it. That is my prayer for this effort of mine - to reach as many as possible with the message of hope and community and acceptance and courage we all contribute to. I'd better stop now and get back to writing or I think I might explode with excitement all over this posting! God bless us, each and every one.

At 8:26pm on August 2, 2012, Sarah said…

Hi there Megan, your story is truly inspirational. Thank you for posting it and taking the time to write it. There are many days where I think of doing away with myself because this world is cruel, but someone recently told me, "if you can change your situation, do it, if you can't change it, change your attuide." I agree, but like you were in high school, I'm severely depressed and miss my long, beautifully curly thick hair... it's a shame that's how we all describe people; 'the lady with the red poufy hair' or whatever, now I try to find other ways of describing people. If you'd like to, I'd love to chat with you. -Sarah K.

 
 
 

Disclaimer

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!

© 2019   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service