Friday, May 16, 2014

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Thursday, May 15, 2014

FW: You have to watch this

Dear salare,

The other day I sent you a very important email that included a video about young Matty Moo. And although he is seizure free at this time, there are countless others who are still searching for their answers.  

salare – we were there for Matty – will you help us be there for the over 2 million other men, women,  and children who are living with epilepsy? Please click here to show your support today. I hope I can count on you to help.

Sincerely,
Philip Gattone


From: Philip M. Gattone, Epilepsy Foundation [mailto:info@efa.org]
Sent: Tuesday, May 13, 2014 2:00 PM
To: maiboaleynaoraa.nahok22@blogger.com
Subject: You have to watch this

This is a remarkable story...and it takes less than 2 minutes to watch.
Click here to be inspired.

ef-logo.gif You have to watch this

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. 

Click here to watch this video

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.

Phil Gattone 2013

Sincerely,
Phil Gattone signature
Philip M. Gattone, M.Ed.
President and CEO

P.S. On behalf of Matty Moo and all kids with epilepsy, thanks again for all you do! Please watch Matty’s video and help us reach more children like Matty with your special gift today. Thank you!

You have to watch this

About Us I Donate Today I Forward to a Friend

Epilepsy Foundation of America ®
www.epilepsy.com I 8301 Professional Place I Landover, MD 20785-2353 I 800-332-1000


Unsubscribe from receiving email, or change your email preferences.

Tuesday, May 13, 2014

You have to watch this

This is a remarkable story...and it takes less than 2 minutes to watch.
Click here to be inspired.

ef-logo.gif You have to watch this

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. 

Click here to watch this video

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.

Phil Gattone 2013

Sincerely,
Phil Gattone signature
Philip M. Gattone, M.Ed.
President and CEO

P.S. On behalf of Matty Moo and all kids with epilepsy, thanks again for all you do! Please watch Matty’s video and help us reach more children like Matty with your special gift today. Thank you!

You have to watch this

About Us I Donate Today I Forward to a Friend

Epilepsy Foundation of America ®
www.epilepsy.com I 8301 Professional Place I Landover, MD 20785-2353 I 800-332-1000


Unsubscribe from receiving email, or change your email preferences.

Ten sizzling summer music festivals in Europe

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The world's best places to dress for success

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Saturday, May 10, 2014

LUXURY WATCHES,JEWELRY and ACCESSORIES

Buy watch or bag in our shop. - http://x.co/4bZTg
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Tuesday, May 6, 2014

The world’s most extreme road trips

Lonely Planet
Travel guides for your next adventure. 3 for 2 across all print and digital guidebooks!
The world's most extreme road trips

Where's the fun in taking the easy route? Rumble a 4WD into the Australian Outback or steer India's needle-sharp mountain passes if you want a road trip to remember. Here are five jaw-dropping journeys to make you grip your steering wheel.

Whiten your knuckles

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