WOBBLY FEET FOUNDATION INC

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WFF promotes awareness of A-T and contributes to advancement in life improving therapies & a cure. Wobbly Feet Foundation, Inc. was created to provide education, an internet based support group and financial support to medical professionals who conduct scientific research for the improvement of symptoms or cure of Ataxia Telangiectasia, as well as, to provide financial support to families of a child diagnosed with Ataxia Telangiectasia for benificial medical equipment and treatment.

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Address: 6014 Winchester Place, SarasotaWeb: Sign in to see organisation websiteFacebook: fundraisersICO: 271068774

Home - Wobbly Feet Foundation Social tags teamconnor cureforataxiatelangiectasia CureATnow ATWarrior Wobbly Feet Foundation Inc. was created to provide education an internet based support group and financial support to medical professionals who conduct scientific research for the improvement of symptoms or cure of Ataxia Telangiectasia as well as to provide financial support to families of a child diagnosed with Ataxia Telangiectasia for beneficial medical equipment and treatment. 10th Annual Pasta Bar for a Cure of AT. DonateFundraise Create a Facebook Fundraiser Donate Direct via Paypal 800000 out of 1000000 Latest News Archives Recent Post Wobbly Feet FoundationCommunity Partners sdzembogmail.

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Natalie

🍝 Excited for the 10th Annual Pasta Bar for a Cure! Let’s come together to raise awareness and funds for this important cause! Every little bit helps! #teamconnor #WobblyFeetFoundation

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Jennifer

💙 So inspired by the incredible work Wobbly Feet Foundation is doing to support families affected by Ataxia Telangiectasia! Let's keep pushing for a cure together! 🙌 #CureATnow #ATWarrior

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Michaela

1. What innovative fundraising strategies could Wobbly Feet Foundation implement to increase awareness and financial support for Ataxia Telangiectasia research and families affected by the condition?

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Alan

2. How can online support groups enhance the emotional and informational resources available to families dealing with Ataxia Telangiectasia, and what role should Wobbly Feet Foundation play in facilitating these connections?

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