Glut1DS
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check out the video that ran in the Boston Herald today
5:09 AM Feb 22nd, 2011
via RockMelt
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Since the campaign started, we have heard from two families whose children were recently diagnosed w Glut1DS. Spread the word. @
4:41 PM Feb 16th, 2011
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Click here to hear one mother's story of her son's diagnosis: Milestones for Children (5):
5:15 PM Feb 9th, 2011
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Day 2: 626 clicks on the video so far! Thanks for spreading the word! Donations from 25/50 States & the UK! Let's keep the momentum going!
5:10 PM Feb 8th, 2011
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Check it out! Bobby is the face of Rare Disease Day! Thx @ Bobby’s Story « Rare Disease Day USA:
4:20 PM Feb 7th, 2011
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Read the story about the adorable little boy featured on the rare disease day website by clicking here:
9:50 AM Feb 7th, 2011
via web
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@ : check out Bobby Allen & our campaign for Glut1DS & Rare Disease Day!
5:20 AM Feb 7th, 2011
via RockMelt
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@
5:18 AM Feb 7th, 2011
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in reply to RareDiseases
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@
5:18 AM Feb 7th, 2011
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in reply to RareDiseases
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hoping that @ might pick up our campaign & retweet! 21 Days. $21. Join the Movement.:
5:55 PM Feb 6th, 2011
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21 Days. $21. Join the Movement. Click here to see our campaign! :
5:03 PM Feb 6th, 2011
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Launching the 21 day Campaign for a Cure at 1/2 time of the Super Bowl! Stay tuned!
2:49 PM Feb 6th, 2011
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We kick off our 21 Days 21 Dollars campaign next week! Stay tuned for details.
1:22 PM Feb 5th, 2011
via web
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Check us out on FB! Like our page!
Milestones for Children (1):
3:11 PM Feb 1st, 2011
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We are gearing up for a massive fundraising campaign that will end on @
5:40 PM Jan 31st, 2011
via RockMelt
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- Name Milestones4Children
- Web http://www.milest...
- Bio We raise funds to support finding cures for rare pediatric diseases one disease at a time. Our first is Glucose Transporter Deficiency Syndrome, Glut1DS.
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