@4evababy | ||
Vanishing white matter disease is a rare genetic brain degeneration eating all the white matter protecting the brain, it affects the central nervous system and the spinal chord putting these children in wheelchairs for the rest of their short lives,most children diagnosed with this condition don't make it to adulthood, there is no treatment and no cure because not a lot of people know that it exists, we call on the publics help to make a cure possible Thank you |
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@1clivey1 | 28 September 14 | |
wish you all the best with this cause hun |
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@4evababy | 29 September 14 | |
Thanx clivey
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@flossi | 29 September 14 | |
what an awful time for you, im so sorry. I really hope you get enough awareness to allow funding for this.
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@4evababy | 30 September 14 | |
Thank you flossi, me too
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@reallyu | 30 September 14 | |
sorry about ur son.....i do pray dat all ur prayers will b answer and ur son return to his normal self...ders nutrin geater dan God, so keep strong continue to be da best mum and keep ur hope..hugs
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@4evababy | 1 October 14 | |
Thank you reallyu
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@prismf | 12 October 14 | |
i wish you all the luck in raising awareness of this condition and prompting research into it. such a cruel condition.
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@4evababy | 14 October 14 | |
Thank you prismf
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