Danielle on living with epilepsy and cerebral palsy
I’m Danielle and I wanted to share a little about my experience living with epilepsy and cerebral palsy as well as some info on epilepsy and CP.
I’m Danielle and I wanted to share a little about my experience living with epilepsy and cerebral palsy as well as some info on epilepsy and CP.
Recently Colleen was sick and hadn’t eaten in days. Jenny shares her experience with practicing gratitude during this difficult time.
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.
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.
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.
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