If you would
like to post a comment or provide feedback, please forward to
james@cycleforlyme.com.
Inappropriate comments or language will not be posted.
_____________________________________________________
It took my common-law
husband to figure out what I had, and I have about 95% of
the symptoms. I just wanted you to know that I admire what
you are doing and think this is a great way to get awareness
out there, if I could, I would join you, lol... I used to be
very athletic, always on the go and doing something and now
have been forced to use a cane and rarely am able to leave
my house. I am slowly seeing improvement with the IV, but I
still have a long way to go... not different from a lot of
stories of Lyme. I hate that we have to suffer so much and
get told that we're crazy and Lyme doesn't exist. I have to
go to the U.S. in order to get treatment, even though I
tested positive twice here in our own country with the
horrible testing we have. Once I had the tests done through
my LLMD I brought that report in for my appointment with one
of the Infectious Disease Dr.'s here, and she told me that I
had Irritable Bowel, not Lyme.
I just thought I would
give you a little piece of my story... something needs to be
done about the lack of health care and knowledge, and it's nice
to see that you have the strength to do all of this! I'd like
to thank-you for that!
Take care and all the best,
Trudy B.
Ottawa, Ontario.
_____________________________________________________
To find out more,
- view the Let's Target Lyme
brochure,
Click Here.
-
view the Let's Target Lyme (FRENCH)
brochure,
Click Here.
- from the
Chief Medical Officer of Health,
Click Here.
- from the
Ministry of Health and
Long-Term Care,
Click Here.
CycleForLyme.blogspot.com
