Epilepsy Blog Relay: On the importance of questioning side effects
I now know I need to question all the potential side effects a medication causes, even the rare ones.
Special Needs Parenting: When it’s okay to be a helicopter parent
Jennifer shares that sometimes being a helicopter parent is just being a good parent.
The journey to practicing gratitude during difficult times
Recently Colleen was sick and hadn’t eaten in days. Jenny shares her experience with practicing gratitude during this difficult time.
Epilepsy Blog Relay: Life with Cerebral Palsy and Epilepsy Gets Real
Having a child with cerebral palsy and epilepsy has been a ‘learn-as-I-go’ experience, and I’ve really had to decide what is most important. To me, that is sticking to Colleen’s schedule, no matter what.
Epilepsy Blog Relay: Advocating for a non-verbal child
Jen knew something had changed drastically with Colleen’s health, but she had no answers. Jen shares tips for advocating for a non-verbal child.
Epilepsy Blog Relay: Colleen’s mom reminds us that knowledge is power
If my child hadn’t been diagnosed with epilepsy, I’m not sure if I would know how to help during a seizure. Knowledge is power when it comes to first aid.
Epilepsy Blog Relay: Colleen takes on cerebral palsy and epilepsy with a smile
This post is part of the Epilepsy Blog Relay™, which will run from June 1 to June 30, 2018. Follow along! The beginning After Colleen’s birth and being transferred to a nearby hospital’s NICU, we got the phone call that she had had two very big seizures and would need a blood … Read More