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Started by NorthCarolinaMama. Last reply by lordiron on Monday. 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. 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 all, I wanted to share that I went to get a second opinion of my hair loss yesterday to a different dermatologist than my previous one. He was a bit more optimistic which made me feel better. When I was diagnosed in March 2012, my other derm did a biopsy on one section of hair and said it was FFA, and offered no other treatment and I was too much in shock to think of any questions to ask. So after a year of agonizing over it and losing more hair, I saw a new doctor now. He looked at my hair more thoroughly and said he's not entirely convinced I have FFA and may be Alopecia Areata instead, or a combination of both. He said FFA primarily only occured in women of African-American descent which I am not, but I'm not sure I agree with that since I've come to know all of you here. But he is going to look over all my previous dermatology records and then probably do another biopsy. One reason I hadn't gone back to the derm is my health insurance says they don't cover treatment for alopecia and my other appointments in the past got very expensive. But I decided I needed to go back for some answers, whether it's covered or not. A few things he did recommend for hair loss was Rogaine 5% and Biotin 5000 mcg a day. He will get back to me in a few weeks and let me know what to do next, and I feel better about him as a doctor than I did the previous one. I know the parts above my ears and forehead that are very bald probably won't grow back, but if I can save more hair on the sides and back at least it will look better in general. I'm interested in the Buffs that were mentioned, I just wonder how hot it would be, but at least I could wear one as a headband over my bald spots and when the wind blows I won't look so weird. I'm not really a hat person, although I have become one. Celia, good luck at your appointment!
Paula - I rather stupidly because of security risk, deleted my inbox - you need to invite me as a friend and then I can give you directions via this internal e mail. Look forward to seeing you.
Hello all - I see Dr Harries in the morning and will ask him the q about DNA testing and what would they be looking to identify. I am going with rather a lack of optimism, I'm afraid, but that's partly my mindset at the moment - I will be very upbeat when I see you all though - I promise ! We are collecting Martyn's 92 year old aunt (she has a fine head of hair !!!) from near Manchester after my appt. and having her to stay for a week - feed her up, cheer her up and take her back happy - she is very lonely. Debs - I think I said a few days ago - truly every time I go to the DIY store B & Q I see at least one person with significant hairloss - even 2 cashiers and I end up nudging Martyn. Perhaps this thing has always been around and you don't notice it until it affects you personally.
Liz , I have worked with youngsters with Aspergers Syndrome in mainstream school and I am sure this must be very hard to deal with at home, cannot help your stress levels at times. I hope your school is helpful. See you soon - any other questions - I will check this website in the morning before I set off. Have a good day - sunshine ! x
I saw a woman at work at couple of days ago that most definately has FFA, I have never met her before and I decided not to approach her in case I caused offence. Her hair loss is about the same as mine (which I think is about the same as Liz) and she was wearing her hair long and up in a pony tail. Looking at her straight on was OK but from the side view the FFA was evident. I saw 2 ladies in the waiting area at the hospital the other week when I saw Dr Harries, both had FFA and were trying to style their hair without using supplemental hair. I can see that it is possible to brush it forwards and wear a fringe to a certain extent but the hair loss notices sideways on more than when you look at yourself in a mirror from the front view. Pam's suggestion of getting a fringe piece would work as would Celia's suggestion of having a fringe cut in from further back if your hair will allow. I would just say having seen these 3 ladies and their hair styles do just check yourselves out from the side view when deciding how you will manage your hairdos because from the side view the recession is more noticeable than from the front.
Pam - I too have no idea why days are different - could be diet/stress or something we do not know about...... I am using the Philip Kingsley dandruff treatment and it worked the other day - I use Kerastase shampoo and also the Kerastase Bain Satin conditioner - the latter is making a difference to dryness - it actually feels like hair again ! For how long who knows ? Of to run around the gym - escape a bit ! x
Hi Celia. I dont wear the hairband much, only when I want to forget about the hairloss. I wear it now several times a week and sometimes in the evening. I have a son with Aspegers who is facinated by my hairloss and not in a good way. A few days back he told me that 'it looks like a scar around your head'. I said to him 'Are you being horrible about my hair?' He looked at me and said, 'No, I'm being horrible about the bit that has no hair'. He also keeps asking if I have cancer. He thinks that losing my hair is a symptom of cancer even though I have tried to explain that it's not...And so, that is why I am wearing the headband more! And, alas, I dont have enough decent hair to make a fringe. The hair on the top of my head is thin and has gone frizzy. I asked the hairdresser and she said there is not enough hair. I may try some Philip Kingsley shampoo. My hair is so dry. I went to the doctors yesterday with itchy sore ears and she mentioned anti inflammitory drops for them or almond oil. I wonder if that would help my head.
xx
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