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| Topic: Vanishing white matter disease- help find a cure | |
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Please everyone help spread awareness of this disease we need a cure my son has this and he is 12yrs old I've seen stories of children that have not made it and I don't want this to be the story of my son, you can like and share my fb page it's called vanishing white matter disease and other forms of leukodystrophy
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There is no cure or treatment for this disease that's what awareness is so important because it's rare and not a lot of people know about it, I need as many of you as possible to help raise awareness
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I do not know what to say for I have no words...
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PRAYERS for your son and for God to help find a cure! 
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4eva, Prayers for your son and thanks for enlightening us on this disease. I am going to research it.
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prayers for you and your son. I was reading about this and it reminded me of someone I know with ms. they don't have a cure but there appear to be things that slow it down.
im wondering if it could be something similar. sending you a big hug. |
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Best wishes to you
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Thank you everyone and if you could all make copies of my profile pic and share it around as we with maybe some info on it?
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The one that's says find a cure for children
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Best wishes to u..
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Come on over and like and share my fb page it's called vanishing white matter disease and other forms of leukodystrophy
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