Write me: eva@evagremmert.com
Don’t underestimate what is possible.

Don’t underestimate what is possible.

A couple of years ago we decided to add on a few days in Paris to our usual trip to Ireland.  Both Arden and I had wanted to visit the City of Lights, so we asked Nick if he wanted to go to Paris.  He said “Yes, we see the sights.”...... Read More

Regular visits to the Doctors.

Regular visits to the Doctors.

Today we had our semi-annual visit with Nick’s neurologist at Swedish.  His name is Dr. Doherty.  We think that he is awesome, and not only just  because of his name.  I was thinking today as we left his office how grateful I am for medical...... Read More

Information about seizures.

Information about seizures.

Our son Nick has epilepsy.  He has an epilepsy syndrome called Lennox Gastaut Syndrome, or LGS.  It is a type of epilepsy with multiple different types of seizures that begins in childhood.  The seizures are hard to control and require life-long...... Read More

“I am walking now.”

“I am walking now.”

We got some great news today.  After reviewing new x-rays, the doctor said that Nick’s ankle is healed up and he can retire his walking air cast.  I thought that Nick would show more excitement when he heard the news.  I think that the...... Read More

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