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: 602
Latest Activity: Nov 25, 2024

Discussion Forum

Food Allergy Testing question

Started by NorthCarolinaMama. Last reply by lordiron Nov 25, 2024. 10 Replies

Hello!I was wondering if anyone has been tested for food allergies to determine if a particular food is causing inflammation, which in turn could exacerbate FFA. I had the skin test a couple of years ago at an allergy clinic, and it came back…Continue

CARF Conference 2018 Notes

Started by CurlyK. Last reply by kevinsstelly Jul 14, 2024. 32 Replies

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

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

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Comment by MJ on January 8, 2014 at 5:05pm
Annie,
I was on Tamoxifen for breast cancer from age 47 to age 50. I had assumed all my hair changes were from estrogen deprivation. When I stopped taking it this April, I thought my hair would start to improve. Looking back, I probably started losing the frontal wispies about 2 years ago. As it turns out, based on recent bloodwork, I am now in menapause. The only redness I had was after having my hair colored in November. The first derm said it was from hair color. I haven't had my hair colored again and my gray roots are really bad. Want to wait to see what the new doc says on Friday. I really don't want to go gray as I have two young daughters and still blend in with their friend's younger moms...at least while I can still camouflage the hair loss! I will post an update after my appt on Friday.
Comment by Annie on January 8, 2014 at 2:25pm

MJ, I believe I had ffa for at least 2 years before I ever had a painful flareup.  I started out losing the wispy hairs around my hairline when I was about 48.  I just thought it was part of the aging process.  I never even noticed any extra shedding during that time.  It was only after I had a painful flareup & went to a doctor that I started to notice of the hairs in the shower and sink.  I've never had extreme shedding with ffa.  I usually notice between 20 & 30 hairs in the sink on the days I blow dry my hair.  The problem is that many of those hairs aren't growing back.  I'm still able to camouflage my hairloss with the help of a Rogaine & a good hairdresser, but the hair around my face is definitely getting thinner. 

Comment by MJ on January 8, 2014 at 11:27am
I am curious about Zyrtec as well. I am going to an appointment at the Cleveland Clinic on Friday and plan to ask about this also. Also, since I am in the category where I have no rash or itching, my hair just seems to be slowly thinning and disappearing. I was wondering how i can tell if I am "active" or not. Several mention about continuing to "shed." Is is actual hair in your hands that comes out? I am so grateful for all of you in this group. I feel so better informed than I ever could ever have imagined, and so much better prepared for my appointment this Friday.
Comment by Annie on January 8, 2014 at 11:01am

Hi all, just wondering how those taking Zyrtec are getting along.  Are you taking 3 times the daily recommended dose like the case study?  I switched my usual Claritin allergy meds for the recommended daily dose of Zyrtec each night about a month ago.  I've also been on Plaquenil for six months The redness and pain has lessened considerably.  I don't know if the Plaquenil is finally kicking in or the Zyrtec is helping.  I feel much better, but the shedding continues.  I'll discuss it with my doctor at my 3 month appointment on Friday.

Comment by Debs on January 5, 2014 at 3:43am

Brenda I have just sent you a personal message with a 'friends' request, if you don't see it then please see my post above 'FACTSHEET FOR FRONTAL FIBROSING ALOPECIA', please read it and you can get my email address. If you contact me I can send you that factsheet which contains wig website addresses so you can get yourself properly iinformed. You dont have to drive 4 hours to find a wig shop you can safely order online if you know what you are doing. The webiste addresses in the factsheet will give you everything you need. Wigs are a new product for most of us, myself included, so we do need to do our research and take advise from people that are experienced wig wearers. All this is in the factsheet. Happy New Year.

Comment by Brenda, IL US on January 2, 2014 at 4:33pm

KarenGinny the first generic for plaquenil that i took caused a rash all over my body.  my Dr. said to find a different manufacturer or take true plaquenil.  I havent had a rash since.  

Comment by KarenGinny - Iowa, US on January 2, 2014 at 4:09pm

Happy New Year everyone!  I have been seeing a new dermatologist and tried the plaquenil but ended up with a rash from it and had to stop it. He now wants me to take methotrexate which I have started today. Hopefully I will be able to tolerate it. Has anyone else tried this before? It is supposed to be an anti-inflammatory drug sometimes used for rheumatoid arthritis and cancer. I hope it will help my scalp which is always dry and itchy. My hairline has receded more in the past year, but seems to be staying the same for now, although my bangs are very thin, and it's hard to hide the bald patches.

Comment by Brenda, IL US on January 2, 2014 at 11:27am

Happy New Year to all!  Celia my hairline is still receding horribly.  Zyrtec has taken care of the itching.  I'm using clobetasol twice a day now and the inflammation  seems to be lessening.  or it may be the doxy helping.  It's all such a puzzle.  i need to check into wigs but i dont know where to go.  My dermatologist told me to go to a guy in Chicago but its a four hour trip one way and i'd have to go at least twice.

Comment by Polly UK on January 1, 2014 at 1:49pm
Hi everyone hope you had a good Christmas and I wish you all a very Happy New Year xxx

Celia - I've had more aches and pains than usual since taking Hydroxy but it's probably a coincidence. I saw a physio in December because my knee was now very painful and she said the muscles and tendons were in spasm and I had some muscle wastage! It's feeling a bit better now after treatment and following her exercises. I'm going again next week. I also have painful hands but I think it's the nerves in the backs of my hands, not the joints. When I knock them even gently the pain can be excruciating!
I tried cutting down a little on my hydroxy dosage and after one week my forehead and hairline was sore and sensitive and the hair felt singed. Consequently lots of hair fell out over a couple of days and I've returned to 2 tablets daily. It all feels fine now and again could have been a coincidence or over indulgence at Christmas! I'm still taking anti-histamine every night.
Comment by Kath UK on January 1, 2014 at 11:44am

Happy New Year to everyone!

 

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