This is topic Any Canadians out there on IV treatment? in forum Medical Questions at LymeNet Flash.


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Posted by lymekuda (Member # 23972) on :
 
Just wondering about this. From my knowledge living on the west coast of Canada it is impossible. The only way I know of doing it is to get an ID Doc to sign off on it. Everyone I have spoken to who has gone to an ID Doc has been told they are crazy... "Sadly".

So has anyone accomplished the impossible?

Thanks,

Kuda
 
Posted by Dania84 (Member # 26278) on :
 
There was an ID doc that wanted me to go on IV but I don't think I need to be on that quite yet. I also live in western Canada.
 
Posted by JOLA (Member # 23498) on :
 
No luck for me in Vanc. Dr R in WA will be puting me on IMBilcilin shots next visit if there is no improvement. PM and let me know who you see and what you are currently doing
 
Posted by Dania84 (Member # 26278) on :
 
Its very unfortunate there are no LLMD's in this part of Canada [Frown]
 
Posted by JOLA (Member # 23498) on :
 
thats b/c they are in denial that we have LD here. I guess the ticks need a passport to cross the border???
 
Posted by lymekuda (Member # 23972) on :
 
Ahahaha very true, good one JOLA!

Thank you everyone for replying!

Kuda
 
Posted by momofthree (Member # 19490) on :
 
I heard there is going to be a class action lawsuit in Canada....at least you have someone starting something up there!
 
Posted by lymekuda (Member # 23972) on :
 
Hey Mom,

Really? Where did you hear that? How do I get in on that lol. They first diagnosed me with MS and really messed me up with the drugs [Frown] ! I now go to the US for treatment...

Glad to see something is happening well I hope so!

Take care,

Kuda
 


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