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McMaster Association of Lyme Disease Awareness

 
Old 10-12-2011
RockerSocker
This message has been removed by a moderator. .
Old 10-17-2011 at 01:18 PM   #16
terrafirma
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Quote:
Originally Posted by garveygirl2 View Post
Greetings everyone, new to the post and not a student at McM , but someone who believes she is suffering from Lyme. I have been sufffering from the symptoms for almost 6 weeks now (strangely after a visit to VA where Lyme is endemic). I also live in Muskoka. However, still receive blank looks and dismissals from my gp to the respiralogist to the rheumatotgist. I figure you have heard of www.ilads.org website which I have found helpful. Persuiing treatment in the US.As you know expensive and time comsuming. Thank you for setting up MALDA. It is so reassuring. It is tough trying to be your own advocate when you feel lousy. Peace
Hi Maria,

Thanks for sharing your story. We know that it is difficult to get treatment and that is why it is so important for our club to raise awareness for Lyme, so it can get recognition as a serious disease.

We wish you the best in finding an appropriate treatment, and please let us know how it goes!



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