I am hoping to start a support group in Toronto - we could meet every couple weeks? It would be so nice. We can speak with others who are going through the same things, and maybe that will mean less venting and education about Lyme to unsuspecting strangers, and our ever so patient friends

Really though, it would be great. I certainly could use some live Lymies to interface with, call on from time to time, because this, as you know, is really difficult at times - and for so many reasons, which you also know (including limited treatment options in Canada reasons - few LL MDs). You can e-mail me off list if you are interested. My address is: [email protected]

remove (delete) the NOSPAM from the address.

Thanks, and best,

Alyssa. (Toronto)