Each year we walk for our daughter Maggie who has epilepsy...

This is our third year of walking for Maggie. We will be walking virtually with thousands of others on October 3rd.

This year has been difficult and full of seizures unfortunately. We are still after 3 years trying to find the perfect drug to cure Maggie of these miserable seizures. 

Some of them, are small others leave half of her body paralyzed for hours before some how (by a miracle of God) she regains movement in her extremities. 

Because of these seizures, what comes easy to most, doesn't for Maggie.  She attends special education classes as well as Speech, OT and PT weekly.

I know that with Cov-id things have been difficult but if you are able to donate to the MN epilepsy foundation on Maggie's behalf, we would greatly appreciate it.

Click the purple donate now button below