| This is a remarkable story...and it takes less than 2 minutes to watch.
Click here to be inspired.  
| | Dear salare, As President & CEO of the Epilepsy Foundation, I hear personal stories every day of children and families affected by epilepsy and other seizure disorders. Each of these stories is special, but it is not often that I receive a video that is so moving and personal, that I feel compelled to share it with our most committed supporters like you. Recently, I had such an experience. You see, Derrick Rumenapp sent me this moving video he created to document his son, Mattys’ journey with epilepsy. | 
| | Young ‘Matty Moo’ (as he is affectionately nicknamed) was diagnosed with a severe form of epilepsy at 2½ and his family has fought tirelessly to find relief from his aggressive seizures. Luckily for him, Matty and his family found the resources and support they were looking for through their local Epilepsy Foundation affiliate, and Matty is now seizure free. But unfortunately there are countless more kids who are not seizure free yet. And for that reason, we will not rest until not another moment is lost to seizures. salare, please continue helping us provide children and families like Matty’s with the information and resources they need to live to their fullest potential. The fact is, we were there for Matty Moo because you’ve been there for us. For all you do, thank you. |  | Sincerely,
Philip M. Gattone, M.Ed.
President and CEO |  |
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