I just received the latest e-newsletter from the Epilepsy Foundation; the organization has announced that a new website targeted at parents of children with epilepsy has just been launched. The Epilepsy and my child website has several sections:
- Just Diagnosed
- About Epilepsy
- Treatment
- Living With Epilepsy
- Raising Awareness
- Resources & Connections
- Letters from Parents
- and much more
I wish that this information was available in such an easy to navigate format when Alexander was undergoing the diagnostic process last summer. I Googled my behind off to find this type of information and now, it is all available in one location. I’m glad that the Epilepsy Foundation created the website, though. It will still help me but I imagine it will be a tremendous research for parents just beginning the journey.
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