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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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I've had this piece of hair for six months now (the System remains in place on your head for two years before it needs replacing, but the hair that is attached obviously deteriorates, as it receives no nutrients other than through products you put on it). That's longer than I was told it would be, so I am very pleased.
It's definitely faded and is less shiny, but I would expect that.Still looks natural though.
So this morning my own hairdresser (not a personal one you understand! I'm not that rich!) coloured my hair (yes, I need it to cover the grey), plus, for the first time, the hair piece. It's brought back the shine and looks much better, but is slightly different in colour to my own.
Not a problem, as it's nothing major and also next month I am having the hair replaced (at Lucinda Ellory clinic) and they will match to my own hair. But it is useful to know that I don't need to go to them (about 1.5 hours away) to have colour applied.
I am now quite comfortable with the whole thing, and can't imagine being a baldie again (well, not a baldie completely, as I have plenty of hair on my crown - it's just the classic band across my forehead and above my ears that is sadly lacking). It's not cheap and you definitely need to go every six weeks to have it adjusted as your own hair grows and pushes the System up a bit.
But WORTH it!
Denise
DeniceC, I finally took a look at the intralace system, I think, that when it comes time, that is what I will do also. I had thought, other then my hairline that my hair wasn't too bad! But as I have been putting the Clobetasol on every night and lifting up different sections of hair and finally taking a good look at my scalp, I see it is really getting very thin in patches :-(
Oh and I finally have figured out how this comment wall works :-) , I always thought it was comments made on threads that are posted, but then couldn't figure out why I was not finding these comments on the actual threads, duh, no, it is just comments!
I don't have hair extensions, but I do have an Intralace System, which is similar. It comprises a fine webbing with full hair, attached to my own hair (on the crown and sides) by my own hair being threaded through and extensions woven into it.
Ordinary extensions wouldn't work for me, as all they would do would be to thicken the hair that I still have, and it's thick anyway. The issue (in my case) is the fact that however thick (or long) my hair is, it won't attach to the bald bits, so I will always have those seemingly acres of scalp showing once my carefully arranged hair moves from place!
So the Intralace works for me - and looks great. Very pleased.
As for the long term impact of having it (or extensions), I really do not know. I asked those questions, and of course, no one can tell you. But, again for me, that was a risk worth taking, as I felt I just didn't want to go on feeling as I did about my hair loss. And this was the best solution I could find.
So my advice would be to stop adding to the stress by worrying about it. If the extensions look great, enjoy them, and you will, by default, reduce your levels of stress as your confidence returns.
Good luck to you!
Denise
I have not commented in a while but try to keep up with all the new news - I am so confused as to why I stopped losing hair as I hate that so many of you have not - I have gone back to the retinol night cream and serum from Roc as an experiment and have had no problem but I do not use anything with spf in it. I have still been using mineral makeup but mostly as it does not seem to bother anything and I simply have not had time to do additional research. I still take milk thistle and 4 b-complex stress formula daily and will say for those of you that are stressed that it is extremely helpful. I also have been experimenting with rogaine 5% again - I had avoided putting it on the hairline above my forehead as the lichen simply never totally clears up - never does anything - no hair loss - no itching - just there - but this time I thought what the heck - much to my surprise it has almost totally cleared up the lichen - go figure - so I actually have started using it twice a day and putting it on my eyebrows - or where they used to be - as well - I am over three years from the shedding of hair and medication nightmare - for those of you that are just starting the lichen loves stress so please all take care of yourselves. Maybe the lichen is just an indication that the hair follicles are starting to die and perhaps the rogaine stops that from happening - will report back later to let you all know what happens
I am noticing people with FFA more and more now. I would venture to guess USA Olympic Gold Swimmer, young Katy Ladecki has FFA. She's showing signs of male pattern baldness. What I find so interesting is, I bet she does not even realize it. :( Maybe they will find a cure sooner than later with so many people now being diagnosed.
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