I can definitely understand....throughout highschool, I was a cheerleader (captain I might add), in drill team, drama club, gospel choir, yearbook committee, ski club, etc.....& my vit appeared during the summer rite b4 I started 9th grade & was transferring 2 a new school (tramatic rite?). I've learned that judgement is what people do best..especially when noticing differences about others. I encourage you to do more research & look at the pictures on the site of us who have children....my son, for example, is the very same age I was when my vit started, but @ no time while I was pregnant w/ him, did I ever fear I wud "pass on" somthing I knew was not hereditary. Just take it 1 day at a time......
Im about 14 as of december 20th..I got vit when i was 8 years old since then its covering about 35% of my body eyes the corners of my mouth legs elbows ankels under arms nd around my waist the randomly tiny spots of them all over my body..I hate facing gym each day I actually go! I love sports but Im so afraid to dress out cause kids can be so cruel and stare. I also have vit on my scalp so it causes white hair! I constantly dye my hair but trying not to as much, Im afraid its gnna fall out ha!;). Im starting to see vit coming in on my hands. Im always doubting I'll ever make it famous,(Im a singer people say Ill go far?) but Im afraid people will judge and that ill never get married and I wouldnt wanna have kids..I mean I do someday would lke to be a mother but I wouldnt have the heart to risk passing on my diesese to my child..:/ Support from people that go through the same obstacles as well as myself is whhat I think we all need<3 God Bless!
your a brave woman. I use makeup on my face. I have vitiligo over 60% of my body. I don't mind/care anymore about my hands, feet, legs, arms, etc. but, my face !!! It's really hard because I have, kind of, a public job so I am constantly traveling and meeting people. So, like I said, for the past 40 years I have worn makeup.
Now I am trying a combination of new treatments. I'll post the results and see if any good comes from it.
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Now I am trying a combination of new treatments. I'll post the results and see if any good comes from it.