Help us raise awareness of Neurofibromatosis Type 1, this genetic disorder that is causing Ella to lose her vision now in both eyes. For Ella personally, our prayers and positive thoughts are what is needed sent her way. For Ella's wishes of H.O.P.E. we can share everything we learn about Neurofibromatosis and help change the future of NF research and care; AND we can follow Ella's example of helping those around us every chance we get! There is a lot of wisdom in that little 7 year old body.
Please share HopeforElla however you can: verbally, on Facebook, Twitter, by email, regular mail...whatever form, as long as we share we really can change the world!
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