Where acceptance is all there is!
Started by Leni. Last reply by Lang Bozic May 22. 10 Replies 0 Likes
I am interested in getting a topper but don't know where to go for one. Having one of those weeks when the hair keeps falling and I am not feeling very comfortable. I don't want to spend a lot of money. Thinking of ordering off the internet. Please…Continue
Started by Liz. Last reply by Carol Aug 7, 2025. 11 Replies 1 Like
Hi I don't post on here much so I may well be giving information which you might have been discussing already. Are any of you in the UK going to the Get Ahead of Hairloss event in London at the end of September? It has been organised by Dr Wong who…Continue
Started by NorthCarolinaMama. Last reply by lordiron Nov 25, 2024. 10 Replies 0 Likes
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
Started by CurlyK. Last reply by kevinsstelly Jul 14, 2024. 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
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In defense of STEROID INJECTIONS
Good news, Ladies! I just want to emphasize the positive effect they have had on me. With my complicated medical history and heavy load of maintenance prescriptions, very few options were safe for me in dealing with the scalp biopsy diagnosis of FFA. And understanding that no one has yet been able to medically stop, let alone reverse the progression, I chose to reject postponing the inevitable with additional medications to the pharmaceutical soup already in my GI and bloodstream. But the superficial corticosteroid scalp injections have no systemic effect, they are simply localized in the affected scalp. My only goal has been to slow the ebbing tide of my receding hairline. Like any ending relationship -- this one, with my hair -- I want to be let down easy, please.
And it absolutely MUST be working. I have had the full blown scalp involvement -- red, inflamed follicles and nasty itching -- for well over a year. But I have never lost more than a few hairs a day [maybe 15-20; with shampooing at most about 75 hairs: I actually counted yesterday morning, an exercise in futility and frustration]. The injections relieve both the visible inflammation and the itching, and I can always tell when I'm due for another round. Yesterday afternoon I had my 7th session, and my Derm was very pleased, finding almost no visible inflammation at all. I definitely felt the ramp up in itching a few days before the appt. But she studied my scalp under her lighted magnifying glass and declared surprisingly little progress in the hairline recession.
In all, my frontal hairline has receded just a little over 1/2 inch [I just measured the pale, smooth area] and is getting sparse for the next 3/4 inch. The temples have receded closer to one inch, but that was almost the full extent of loss before I even began treatment 10 months ago. Looking back, I know the disease was active at least 2 years ago. But my total loss since then is remarkably slow, and I am increasingly grateful. And it must be said, since I have taken no other treatment, that the injections are working!
The only side effect that others find troubling is a sort of indented furrow on the forehead which can result from a poorly placed injection [they need to be within the affected area, not on the edge of the hairline or on the balding area]. Some may have several "dents", but we are told by many that they disappear after treatment ends. I have one visible furrow, about 1/8 inch wide and 1 inch long, at a diagonal where my Widow's Peak used to be. I can easily feel it with my fingers, but I doubt anyone would see it, even if I pulled my hair back -- and why would I ever do that?!
My invisible eyebrows are another story. They were at least 75% missing before FFA diagnosis last summer. They are now 90% gone. Injections there were never discussed, though today's comments by others have me pondering. I have recently begun using Rogaine just on my eyebrows, but it will be many months before I see much progress there, I fear. And I enjoy the artistic challenge of creating them with make-up anyway. But I no longer work and have no morning rush day after day. If the Rogaine is not successful, I will probably join the ranks of the happy tattooed.
As many have said of their experience with this disease, it's hard to know what's working when you're trying several treatments at once. I may be the only one on this forum that is taking injections and no other treatment. Not sure why my comments always end up so long, but I suspect you all enjoy a success story.
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Hi All. I just thought I would share with you that I have been using rogaine on my eyebrows and have finally noticed some regrowth. Its painfully slow, but it is there! I had lost all but 7 hairs on my left eyebrow and on the right Id lost everything. I read somewhere on the net that eyebrow hair is able to grow back as it does not experience the scarring. Iv'e been applying it to my brows for around 2 months now, and I am so pleased to see new "sprouts" appearing! The lose of my brows was very depressing, more depressing than my full head of hair.
MJ, I read a study about eyebrow regrowth after intralesional triamcinolone injections. I asked my dermatologist about it. She sees a LOT of alopecia patients - all different types of alopecia. She will NOT give eyebrow injections due to a risk of blindness from injections in that area. She was surprised to hear that there are dermatologists giving those injections.
Welcome to Caro ! We already have a Caro - so maybe you would like to be New Caro or a name of your choice - perhaps where you live. Sorry you have this - we shall hear your story soon I hope. x
Pam, I sent you a message about your hairpieces. I am very curious about them...
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