www.alopeciaworld.com
Started by CurlyK. Last reply by kevinsstelly Jul 14. 32 Replies 14 Likes
CARF 2018 Conference Notes:First of all, I am so glad I went to the CARF Conference! It was worth every dime I spent – a true investment in myself, but hopefully I can bless and encourage others from what I learned.The CARF staff and volunteers are…Continue
Started by 2Dachshunds. Last reply by Shawnaynay Jul 8, 2023. 18 Replies 0 Likes
Hi Everyone: I remember there is a women on here who connected Botox to FFA. I was given the article, Frontal Alopecia after Repeated BotulinumToxin Type A Injections for Forehead Wrinkles:An Underestimated Entity?Antonino Di Pietro a Bianca Maria…Continue
Started by Robin. Last reply by anettemandell Apr 20, 2023. 31 Replies 0 Likes
Hello All, I am venturing into new territory. It just dawned on me that a good experiment would be to try a medical grade CBD oil tincture on my hairline and see if it affects the redness. CBD is the nonpsychoactive part of marijuana that is being…Continue
Started by Thomas. Last reply by Thomas Nov 23, 2022. 27 Replies 4 Likes
Hello,Thought I’d share my experience, as one of the few men with FFA, in the hope that it will be useful to others. It’s possible that the condition progresses and responds differently in men. I’m 40, live in London and otherwise healthy.I first…Continue
Comment
Sounds great ! Well done !
Hello ladies, having just got back on this site I am hoping I haven't lost contact again since I cannot view any posts after Jen's on April 25. Best wishes, Celia.
Hi Celia,
Thank you for starting this for starting this online group. It has been very informative for me. reading these stories has made me feel less alone and more calm.
Thank you Celia, I found the get together a real help last time so would definitely like to come again.
Hi Meme it was good to meet with you albeit ages ago over in my home. So sorry to hear that your air loss is continuing I hope to have another get together soon and would love you to be here..
Great to hear from you Celia. I to havent posted for a while. My hair loss has got worse and is noticeable and I am undecided as to whether to have a hair piece or go down the wig route. But like you I am just trying to get on with life and enjoy it. Hope you are well.
Thank you, Liz. I've been able to see how you are, but unable to comment until today when I was given a new password. What is noticeable is how many younger women are experiencing FFA.
I haven't kept up for a very long time, but I hope there are some people out there who may remember me ! I haven't taken any medication for at least a year. I didn't want to trigger anything else !
I was diagnosed in 2011 at a . time after an illness that meant that I took serious antibiotics.
I've lost hair above my ears and about3cm from my hairline. I have my eyebrows tattooed thanks to Deb who introduced me to Belinda Hayley in Chertsey.- she does my brows every 18 months.
I see Dr Ali at Charing Cross Hospital periodically.
All stressful but try to enjoy life anyway.
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.
© 2024 Created by Alopecia World. Powered by
You need to be a member of Frontal Fibrosing Alopecia to add comments!