Hello you guys!! i hope you all are doing well and are staying beautiful!! So I've been a member since 2010 after i was diagnosed with vitiligo in 2009, and after trying with dermatologist with no success i gave up and lost hope, i became very depres
I just now remembered about Ms. Sarah Cooper who was the first person I talked to here when I joined www.vitiligofriends.org. It's hard to exactly remember what we discussed then but I remember we talked something about 'methylation'. The last words
I just thought I'd share my really positive experience.
I have suffered from vitiligo for 10 years and until last November 2013 I had white patches spread across sections of my whole body, mainly hands, wrists, under arms, face, neck,
I was checking recently my medical paper library (384 papers) and I thought it could be helpful to select the 3 most important ones according to my opinion.
Please find them attached.
Read them deeply if you have time. Awareness is de
Quick background, I was diagnosed with generalized vitiligo last August so this is still relatively new for me. Anyway, today my girlfriend of 6 years broke up with me. She was truly my best friend and strongest emotional support outlet. It wasn't in
Im 16 and I never see anyone my age who has vitiligo! It kind of upsets me. I see older and younger people, but never in between. I would live to have someone my age to talk to about it, but I can never find anyone
Since joining this group a couple years ago, I've yet to come across anyone who has experienced extensive and permanent repigmentation. Prior to joining, I contacted Steve Hargadon, and my feeling was there is no such person.
This is all new to me. I have a 6 and 7 year old who do not have this disease yet my 5 month old was just diagnosed with it. I am scared, don't know what to expect, how bad and how fast it gets worse what the options are. Please help to enlighten me!
HI everyone ,I have not been to this site since I was 21.I am 25 now and my vitiligo is almost all gone.I have had vitiligo since I was 13 and know how painful it is to be different.I have been using a medicine called Elidel (pimecrolimus) 1%.The med
I am UK based and have suffered with vitiligo since I was about 14. It is only over the last 3 years that it has begun to rapidly spread across my body and now I am very self conscious and it is a constant daily battle.
If you have patches on face or if you think they might spread to there, I've realized one good and easy prevention action that can really help you. Please take it seriously.