Anyone from Montreal?
If you're from Montreal, let me know! There aren't as many resources for lupus patients in Montreal than in other Canadian cities, so let's get together! My friends and I are doing a fundraiser for lupus research on Saturday August 23, 2008 at the Leonardo da Vinci Centre (Saint-Leonard) in Montreal and I would like to invite any lupus patients and friends and family members of patients to come join us for a great night of hope.
I am near Montreal all summer long ...cottage. If you get a support group going I would be interested.
I am in NH just a few hours away and try to get up there 2x a year.
There does not seem to be anything in NH for support. I am new to all this and still waiting for final dx but all signs pointing to seronegative lupus and looking for answers and support.