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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
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
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Hello - I was diagnosed with FFA in 2011 - I've been taking anti-malarial tablet every day as an anti-inflammatory and vitamins for the hair, hair loss is very slow, people often comment on my 'bouncy curls' but freaks me out when I read about how one can go 'almost bald' especially as I went and did the most stupid thing earlier this year. It began a couple of years ago when I went to a tattooist and got him to put some fine lines, like hair, around where my 'sideburns' had gone...the result was amazing!!! Looked almost the real deal and I could tuck my hair behind my ears, and my confidence was back again. Then I went to the same bloke this February and just thought as he had done such a great job before, I just wanting him to fill in the few missing bits that had come in the last couple of years - this time the result was hideous!!!! So on top of everything else, am having laser treatment to get rid of this 'thing' he has tattooed, so I have a double whammy to contend with. On the plus side, as said before, still lots of hair, but on the down side, as I said before, when I hear that others are 'almost bald' I think, if I don't get rid of that tattoo, I am going to look doubly weird!!!!
Kristen P I totally agree! My derm also scoffed at the link to sunscreen and FFA. I would rather lose my hair to FFA than to chemo. I won't stop using sunscreen unless there is a broad long running study which proves otherwise. Then I will be hiding under long hats and shirts so no one will see I have no hair anyway.
Yes, Christi Q, I also put on 15 lbs. All in the stomach. I looked like I was six month pregnant. Dr. Donovan said that there is a 5 - 7 lb. weight gain in the stomach that some women will experience. I have gone back on it, but I have promised myself that if I put on more than 3 lbs., this time, I will go off. I've never been able to lose the 15 lbs.
For those of you on Dutasteride/Avodart, did you notice you gained weight when taking it? I have packed on 15 pounds since I started a few months ago and my weight never fluctuated before. The weight is all in my stomach which I didn't have before. I called my doctor and she basically said it was all in my head. There is a woman in my office though that is on Finasteride, and she is experiencing the same thing. I want to get off this drug, but I'm terrified all my hair will fall out if I do! I'm also on Rogaine/Minoxidil.
5 HTP is a serotonin increases works like Zoloft for those who do not want to take antidepressants - I am currently taking this
Hi Ladies. You all have left a lot of information here. I was interested in the treatment they prescribed to you at Guy's Airam. I have never heard of the medication they prescribed and wonder what the counterpart, if there is one, in the USA would be.
I just came off of using plaquenil for about 6 weeks. My scalp was terribly inflamed. As bad as it has been in at least seven years. That is why I went on plaquenil. It cleared up my scalp to a great degree, but I started having terrible side effects and could not continue using it.
I know use clobetasol solution as needed. Protopic as needed. Minoxidil 5% has been used since January. I did not shed hair or see any increase in redness or flaky spots when I started Minoxidil. I think it helps and I have seen some hair growth. I also saw a great deal of hair loss while I was on Plaquenil.
Just last week, I added dutasteride to my plan. It is the second time I have been on it. I stopped before because of weight gain. I find it stop the hair from falling out, so I am trying it again because of the great loss I've had in the past few month.
I have had FFA as a confirmed condition since 2013. I think I've had it since 2006. I am nearly half way bald and am losing hair at the nape of the neck now. I want to hang on to the hair at the back so I can continue to wear toppers.
I believe that sun screen contributes to this condition. I wore them daily in my moisturizer and makeup for over 25 years. Pauliegirl, what is the brand that you are no using that you think is safe? I find titanium dioxide in everything. Even vitamins have it in them.
I think stress is a factor in causing our bodies to go into overdrive with inflammation. I also think the GI track is part of the problem.
Are any of you a part of the Facebook group: LPP - Put Out The Fire?
I completely understand the stress component as this started for me after two years of dealing with the deaths of both of my parents. For me antidepressants are not an option. I tried them years ago and had terrible side effects. I seem to be very sensitive to all medications. I have also used sunscreen for years in all the facial products I use but so has everyone else I know and they don't have FFA? I am going to look for more natural sunscreen products. I think about all of you lovely courageous women who have dealt with this for so many years. It can be all consuming everyday and I hate it. Honestly I could go about my day so much easier if I didn't constantly have these awful scalp tingling sensations. I don't know if it's the heat, or FFA or how I react to the topical steroids? What do you all do to help relieve that?
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