New electric chair.

[WillyB]

Well as you can see by the many other post PLS and ALS are hard to diagnose. I can tell you for sure I have never had many of the symptoms you are having. It doesn’t sound like ALS to me, but I'm no doctor, just a good ol boy from TN (GO VOLS). The only advice I can give you is; have your GP to refer you to a good neuro doc, and go from there. If it turns out to be one of the above, that don't mean life is over, it just becomes a little bit more interesting....as my 10 year old daughter would say "Remember Dad Slow and Steady wins the race". I don't know if she says that because of my wheelchair incidents or strength for what the future hold. Prob a little of both.

 

[WillyB]

Nothing, I could not find the site that kiwisally was talking about. Not giving up though.

 

[WillyB]

I can't find the site that kiwisally is referring to. So the wheelchair saga continues.

 

[WillyB]

Good to be back. Had to go to the Mayo in Jacksonville to hear the same old story I've been hearing for years. It's a shame you or your insurance co has to pay for that. Here is how it played out.
Doc: Well how’s it been going?
Me: Oh about the same, speech and swallowing has gotten a little worse.
Doc: I noticed you were talking much slower, then does the usual test (check reflexes, strength etc.)
Me: Is anything new going on, research, stem cells anything new?
Doc: Not that I'm aware of.
Doc: Do you have any more questions?
Me: No, I don't guess.
Doc: See you in six months.
It was a nice little vacation, nice weather and good food.
Anything happening on your side?

 

[billbell52]

There are some greats sites for powerchair information that cover tons of interesting stuff like batteries, chargers, PWCs etc...

 

[scotttyna]

It is good for you.

 

[billbell52]

It removed the link I posted

wheelchairdriver (dot) com