A few weeks prior to my lovable, sweet-temped, all out fun Cardigan Welsh Corgi had his second birthday he had his first seizure. It felt like an eternity before it was over when in reality it was probably less than a minute. I took him to the vet the next day and we started with Phenobarbital and a very low level. After 17 seizures in one month several phone calls to the vet and one trip to the neurologist, we upped the Phenobarbital and added Potassium Bromide. Months and months of seizures we have finally been able to reduced them to about one per month, which I think is about as good as we are going to get. It has now been over a year since his first seizure.
Recently we have had a new issue that has sent us back to the vet and then back to the neurologist. Cole started losing the ability to use his back legs. He stumbles, he falls, his back legs are wobbly, he has trouble getting up and sometimes has to drag himself by his front paws. I took him to the vet and had x-rays done of his spine, the vet thought it was a slipped disc but the meds did nothing so we ended up back at the neurologist. The neurologist thinks his potassium bromide might be causing the problem so we stopped it all together and are slowly introducing it back. We have had good days and we have had very bad days, so bad I thought he would be gone when I got up in the morning. He is still having problems with his back legs but there is a sparkle in his eyes again and he has even picking on his bratty big sister Annie a German Shepherd. Since Cole is a Cardigan Corgi the neurologist also recommended we do a DNA test for DM, I should have the results back in about 4 weeks.
I am worried the decrease of the PB will start a new round of seizures so I am having him sleep with me since he seems to have his seizures in the very early morning hours. There is nothing like a wet nose first thing in the morning to wake you up

I have read everything I can get my hands on and I finally found this site. It is comforting to know that you have been in my shoes and you understand the heartbreak and frustration this disease can be.
Thank you
Suzy