Stem Cell Therapy - is it possible?
Started by Tracey on 02/19/2010
Last update 2 days ago by Catherine
Welcome!! Since starting in February 2009 Epilepsy Awareness 2009 has been on Circle of Moms offering support to families and individuals living with epilepsy. In March of 2010 we expanded, opening another support site on Facebook. To join us at one or both of these sites please go to http://www.circleofmoms.com/epilepsy-awareness-2009 or http://www.facebook.com/epilepsyawareness2009 Seizure disorders can sometimes be extremely difficult for family and friends alike to understand. I witnessed my first seizure at the age of 4 and I was 12 when I lost a family member with Epilepsy to suicide. Now, ironically, I too have Epilepsy. At the age of 29 I experienced my first seizure and for the last 15 years, I have had my own personal challenges with uncontrolled complex partial and tonic clonic (grand mal) seizures. For over 13 years, I was a volunteer with the Epilepsy Huron-Perth Organization. And I was President for their Organization for almost 4 years. Presently I am focusing more on speaking in public, research, and writing my first book. As well, I am always working to support people with epilepsy through various awareness projects and by continuing to work with many Epilepsy Organizations, including The United Way. Our goal on these sites is to provide quality information and support to the many families, friends, and individuals living with seizure disorders. It is also our hope that we can be helpful in clearing any confusion concerning the myths about epilepsy, as well as provide answers to commonly asked questions, and also to provide information about seizures to people within the community. My interest for Epilepsy Awareness 2009 is to share factual information on what I know. And when I can, direct those who have questions that should be handled professionally to a more appropriate source. For those wanting more information about seizure disorders and/or education programs available within the local schools and communities, please feel free to contact me here at E.A.2009. or email me at epilepsyhppresident@hotmail.com You can also keep in touch with our blogs on typepad at http://profile.typepad.com/traceyalderson or if you're curious to see what we have in the way of custom awareness products available for sale, check out the store at http://www.zazzle.com/t_alderson?rf=238130066563660814 Also, if you need to find your local Epilepsy Organization you can go to www.epilepsyontario.org in Canada or www.epilepsyfoundation.org in the U.S. Please note; This site is intended for informational purposes only. Anyone with a seizure disorder should always consult a specialist about the available options for their individual needs when taking anti convulsants or trying to gain seizure control. Thanks for your support! Sincerely, Tracey Alderson Administrator, Epilepsy Awareness 2009
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