Guest guest Posted August 30, 2007 Report Share Posted August 30, 2007 Welcome . Please don't worry about being proper around here. You will quickly find that we are one big family that can be turned to in time of need or for some fun. Yes, there is going to be a gathering in 2008. Haven't narrowed down an area as yet...probably a bit early to do so. Would love to have it in or around Canada. We have one stubborn member there that NEEDS to be at the gathering so what a better way to meet up with her but to head to her neck of the woods. I shall put you on my roll call as a possibility of attending the gathering. Many hugs to you- Sandie Des Moines, IA dad, Merle, passed from LBD 9-20-02, age 65 -- Green wrote: Hello I have just joined your caregivers group, so I am not sure if this is the proper way to start or respond, but I thought I would give it a try. My mother was diagnosed by LBD in February. It is a lengthy story which I would like to share with you at sometime, however, I notice that you are planning a meeting of members in the summer of 2008 and have given Canada consideration. I live in Toronto, and of course for personal reasons would love to have the meeting here. But more importantly I think LBD needs a much higher profile in this country. Obviously as I have just joined, I don't know what other people's experience with the medical profession, or for that matter ordinary people. However I have learned to answer questions re my mother with " Do you want the long answer " or the " short answer " . Oh, bye the way, during a patient's advocate meeting requested by me, the Doctor at a major hospital in Toronto, referred to LBD as a theory. I am not sure whether he was referring to my mother's diagnosis LBD (which they did not make) or the disease itself. Thank you for this opportunity. Quote Link to comment Share on other sites More sharing options...
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