Tag Archives: Epilepsy

More plodding on.

Life is fairly routine at the moment, not too dull and not too exciting. I have just had my 6 monthly MS clinic appointment during which it was decided we should add another medication (Gabapentin). My Epilepsy has been manageable … Continue reading

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It has been a while.

Having been in hibernation for a while makes it feel like the year is flying past. I have been housebound so far this year with only a few buggy trips out with the woofers. MS symptoms have been a bit … Continue reading

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Not going out.

It has been a few weeks that I have been stuck at home. A little bit of Epilepsy brain and a lot of MS symptoms have made it unsafe to venture far. I have had the joy of going to … Continue reading

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A disappointing day. :-(

In the early days of having MS I found people to be kind, caring, and on the whole understanding. If I had any complaint it would be that some people appeared to pity me? I could live with that. The … Continue reading

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Getting on with Mr Epilepsy.

I am not yet out of the Epilepsy hole but I am getting there. I have had a kind offer from a friend to go out for coffee in a safe environment and I have had a couple of visits … Continue reading

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The little thing called Epilepsy.

I thought that the shock and fear I felt when diagnosed with Epilepsy would be as bad as it gets, it isn’t! Since the seizure I had 3 weeks or so ago I appear to be frozen with a kind … Continue reading

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Not the best week but I’ve had worse.

I’m afraid the dreaded “eppy” has returned! On Monday I spent a few hours doing some gentle gardening (sitting on the ground potting some seedlings) after I got up I remember saying something to Julia and then the lights went … Continue reading

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Not much going on.

Nothing much has happened lately, my foster choice (Pippin) got adopted but there are still lots of adorable pooches at Love Underdogs waiting for a home. We will contact Karine once Julia gets back from Spain tomorrow to see who … Continue reading

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A little under the weather.

I haven’t been on line much for 3 weeks or so, I have been suffering some MS symptoms and some Epilepsy auras! I have had to increase one of my medications and this makes me extremely tired. It is odd … Continue reading

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Doctors Orders.

Almost exactly 2 years ago I was diagnosed with Epilepsy, the first thing my neurologist said to me after my diagnosis was don’t climb ladders and stay away from open water. I thought the open water thing would be the … Continue reading

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