Archive for May, 2010
We all Must do our Part to Bring Epilepsy “Out of the Shadows”
May
24 ,
2010 | Posted by
Alysse | In:
Being a Parent with Epilepsy, Epilepsy Advocates, Epilepsy Community, Living with Epilepsy, New Posts, SUDEP Awareness, Talking About Epilepsy
‘The Doctors’…and the Vagus Nerve Stimulator
May
20 ,
2010 | Posted by
Alysse | In:
Epilepsy Advocates, Epilepsy Community, Epilepsy Medications, Epilepsy Treatments, Living with Epilepsy, Neurologists, New Posts, Vagus Nerve Stimulator
Air Date for ‘The Doctors’ is set!
May
17 ,
2010 | Posted by
Alysse | In:
Epilepsy Advocates, Epilepsy Community, Epilepsy Treatments, Living with Epilepsy, New Posts, Seizures, Vagus Nerve Stimulator
Sharing our Seizure Experiences to Boost Knowledge…
May
13 ,
2010 | Posted by
Alysse | In:
Being a Parent with Epilepsy, Epilepsy Advocates, Epilepsy and Facebook, Family, Kids and Epilepsy, Living with Epilepsy, New Posts, Seizures, Talking About Epilepsy
Your Seizure Log can help All of us…
May
11 ,
2010 | Posted by
Alysse | In:
Epilepsy Advocates, Epilepsy Community, Epilepsy Medications, Epilepsy Websites, Epileptologists, Living with Epilepsy, New Posts, Seizures, Tracking Seizures
When you are the One Living with a Disease, but your Child is Healthy…How do you Cope?
May
9 ,
2010 | Posted by
Alysse | In:
Being a Parent with Epilepsy, Childcare, Driving with Epilepsy, Epilepsy Advocates, Epilepsy and Pregnancy, Epilepsy Community, Epilepsy Surgery, Epilepsy Treatments, Family, Living with Epilepsy, New Posts, Seizures, Talking About Epilepsy
Epilepsy…the More we Talk, the More People will Learn!
May
7 ,
2010 | Posted by
Alysse | In:
Epilepsy Advocates, Epilepsy Community, Epilepsy Legislation, Epilepsy Medication Switching, Living with Epilepsy, Neurologists, New Posts, Seizures, Talking About Epilepsy
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