Frontal Fibrosing Alopecia

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Frontal Fibrosing Alopecia

This is specifically for frontal fibrosing alopecia sufferers. To share information and support each other.

Location: Dubai UAE
Members: 601
Latest Activity: Jul 8, 2023

Discussion Forum

Botox and FFA

Started by 2Dachshunds. Last reply by Shawnaynay Jul 8, 2023. 18 Replies

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

Tags: Botox, FFA

Trying a new approach with CBD oil...

Started by Robin. Last reply by anettemandell Apr 20, 2023. 31 Replies

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

Man with FFA. New member.

Started by Thomas. Last reply by Thomas Nov 23, 2022. 27 Replies

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

Dermatologists who specialize in alopecia?

Started by NorthCarolinaMama. Last reply by tcasal Nov 2, 2022. 1 Reply

Hope everyone is having a great weekend!I'm a freelance writer working on a story about alopecia. I need to find a dermatologist at major hospital or teaching institution to interview -- any suggestions?I've already reached to physicians at Duke,…Continue

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Comment by Liz on November 28, 2012 at 4:37pm

All the best for tomorrow Celia xx

Comment by MairiM on November 28, 2012 at 4:29pm

Like everyone else, looking forward to what you and Pam can find out for us. All the best for tomorrow, Celia - hope it goes well.

Comment by Heidi Short UK on November 28, 2012 at 1:10pm

Celia and Pam just a quick note to wish you both a sucessful or informative meetings with your doctors. We are all looking forward to hearing any new revelations, although I think us as a group are quite knowledgable on FFA, and fast becoming experts ourselves!!! Best of luck we will be thinking of you!x

Comment by CJ- Christine from Ottawa Canada on November 28, 2012 at 8:01am
Hi all,
In a way, having all these different treatments makes perverse sense. They don't know much about the disease, so they are using agents that have worked somewhat for some people.... That' s the first thing. Secondly, even if they knew lots about the disease, in the same way they know lots about psoriasis, different treatments work differently on each patient... Which is why it's so important to have all options known and available...not always the case.
I am often disheartened that so little is known and that there is so little research happening. On the bright side for us, our numbers are growing, which is too bad for the new folks being diagnosed but better for us all. More patients means more commercial interest in finding a treatment or cure. But of course it will take time.
We are starting a cicatricial alopecia support organization in Canada with our second meeting next month. Are any of you part of local/ national groups?
Comment by Debs on November 28, 2012 at 2:49am

I agree totally with you Pam, we are all on different medication and even when we have the same drug we are being given different instructions on how often to use it... Look fowards to hearing from yourself and Celia and see if there can be some definitive treatment plans for us all to follow. Best of luck to you Pam & Celia. XX

Comment by PamW San Diego, CA, USA on November 27, 2012 at 10:10pm

Celia, good luck to you on Thursday! Wishing you all the best. One thing that I find amazing is that there are 20 members in this group and there aren't two of us who are getting the same treatment. Some doing nothing, some using clobestasol, some on plaquenil, some using minoxidyl, some taking finestaride, some on prednizone. No wonder we can't figure out what works and what doesn't! I am seeing a new dermatologist at UCSD on Friday morning. It will be interesting to compare what he says with what Dr. Harries says. In any event, can't wait to hear from you Celia!

Comment by Debs on November 27, 2012 at 9:23am

Celia, good luck on Thursday. Thank you for taking our questions with you to Dr Harries. I hope you are given something to help you with FFA. Thinking of you. XXXX

Comment by CJ- Christine from Ottawa Canada on November 27, 2012 at 12:04am
Also I'm now on finasteride, which my insurance company won't cover since it is a drug for men.I just started so it's too early to tell if it helps.
The whole thing is just too much somemes, it's hard not to feel stressed. That said, I'm at a conference with a bunch of other patient advocates from organizations repressenting a broad spectrum of diseases and I can honestly say that if I had to choose a disease in the room, I'd choose ours.
Comment by CJ- Christine from Ottawa Canada on November 27, 2012 at 12:01am
Hi all,
I've been too busy with work lately. I'm not sure if I posted that sometimes people with FFA also have the texture of the skin on their face change... It's gets bumpy. I've got this happening to me. I've had two different docs prescribe two different things. For that .. Metrogel and retinol a . I'm alternating.... Also I had one candadian hair expert tell me minoxidil 5% foam is a good idea and another told me not to bother, yet there is some research that suggests it could help. I'm about to start to try it.

My eyelashes are thinning,and my eyebrows are essentially gone. I'm having them tattooed this coming Friday. I am excited ( perverse, I know) by this.
Comment by Judy on November 26, 2012 at 9:54pm

Anabela, I agree that trying to be calmer and less stresed helps. The internet keeps recommends: Sleep, Good diet, excercise and LESS STRESS. Of course that is recommended for eaverything. My dermatologist said FAA usually happenned to post-menopausal women??

Liz, my hair is also getting thinner but not frizzy

Anyone have eyelashes getting thinner???

Celia, if you are still home my question is about shampoos-
It seems to me that shampoo would be a major treatment.
Good luck on your trip and many thanks for representing us.

 

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