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Started by NorthCarolinaMama. Last reply by lordiron yesterday. 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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I've just joined Celia's group. I've also been prescribed Hydroxcloroquine 200mgs but only once a day. Worried that this may not be enough to be effective.
Rebecca, Dr Harries has told me to take 200mg twice a day to begin with, I know there are other ladies taking it twice a day and some just once. Rebecca are you also taking the doxycycline ?? and having steriod injections into scalp?? Liz, you don't know if the meds are making the FFA slow down/stop or if it would have done so anyway if you did nothing. This is one of the many problems with FFA and why it is so hard for derms to treat because getting evidence of meds that works really is tricky.
Good luck with plaquenil, Rebecca. I'd be interested to know how you get on with it as I have to see my dermatologist next week and if it is now a recognised treatment she might suggest it for me. I'm a terrible coward about taking medication, I'm afraid. I always worry about possible side-effects.
Hi Alice. I dont do it very often because it makes me shudder but every few months I pull on some hair around the hairline (about 30/40 strands). If it falls out without any effort or pain I assume that my condition is still active.
x
This may sound like a stupid question but here goes: How does one know that FFA has stopped progressing? And for that matter, how does one know if a medication is working? Do the bumps along the hairline ever go away? I can tell if my scalp looks red or feels itchy but can't really tell what my hairline is doing from day to day. So, it's hard to judge what may or may not be helping.
When I went to Trendco the hair pieces were far more expensive as they were 'bespoke'. They cost about £700.
Celia I am happy to travel to London :o)
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Simone, if you can find a hair piece that is affordable for you then by all means wear that instead of a full wig, I feel more secure in a wig, that said I have never worn a hair peice so this is just my personal feelings, I would go to a wig shop and try both on, I find that in a full wig I can forget I have it on. This condition means that a full wig isn't necessary to cover up the hair loss but it is whatever you feel most relxed in. Try both and see and weigh up the costs.
Celia it would be super if you could have a get together, it was great when we had a coffee back in November, I am up for that.
Jules, OMG I am astonished that your FFA stopped for 8 years after taking fucidin - yes, please do ask about that too. There are not many wigs that are designed to be slept in, you can sleep in a wig of course but you will find it does not last very long, there are some wigs that you wear non-stop for several weeks at a time (bonded full lace) they are available from online wig shops for about £200 and there are shops in London that sell them. I suggest you go on the www.wigsupport.com site and look at a recent post about sleeping in wigs.
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