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Riley's Journey with Epilepsy

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Uploaded by on Apr 11, 2008

This video is meant to show the many sides of epilepsy. The seizures are only the medical component of epilepsy. Social stigma, learning delays, and the strain on the entire family are part of the day to day battle of epilepsy. If you are new to epilepsy or feel like you have been battling this on your own, you are not alone. I encourage you to find a support group in your area. A great example is www.epilepsyalliance.org

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Uploader Comments (krcr4)

  • i just want to say that i have a baby that has epilepsy 2 and i dond know what to doo every time that she has an seisure i want to die i feel so bad pleasse let me know how did u manage this cuz i dnt know

  • I take it one day at a time and don't let the doctors stop trying to find a better drug combination or other ways of treating the epilepsy. I also try to really enjoy the times we aren't dealing with the seizures. Hang in there. Find a support group in your area. My support group Epilepsy Support Network of Orange County has been a life saver.

    Prayers for your baby.

Top Comments

  • What a beautiful daughter you have!

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All Comments (168)

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  • Great Vid Mr. Kish Thnx for showing it to us.

  • poor girl, is so cute, I love his eyes

  • We can all hope for health care for all. Some day there will be a true cure for diseases such as this. What a beautiful daughter you have.

  • I can't imagine how strong parents of children suffering with epilepsy must be. Once the part of Riley on the floor up close to her face, looking into those eyes.. my eyes watered. :/

  • Hi I would like to know how has been  riley? I hope she is well blessings

  • i have been epileptic for 10 years and its so hard to live with. your daughter has a great life and great parents so keep up the good work xxx

  • @krcr4 @krcr Hi my name is katrina Murrin I have a daughter that has G.E.F.S.+ epilepsy disorder and she is the same age as Riley her name is Emma born july 30 2004.I have not been dealing with her her seizures well at all.I fell apart at one point,Emma stops breathing on her seizures and we almost lost her 3 times.She is getting better with them but it is still really hard how do you do it.You can reach me on face book would love to talk Katrina Murrin from Newfoundland.

  • @krcr4 @krcr Hi my name is katrina Murrin I have a daughter that has G.E.F.S.+ epilepsy disorder and she is the same age as Riley her name is Emma born july 30 2004.I have not been dealing with her her seizures well at all.I fell apart at one point,Emma stops breathing on her seizures and we almost lost her 3 times.She is getting better with them but it is still really hard how do you do it.

  • @TheMopardude Ima hata fool eeee what now fool in mexican accent

  • @TheMopardude Ima hata fool eeee what now fool

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