Hello fellow Canadians, specifically Torontonians. Any one aware of a CLL support group that meets together on a weekly/monthly basis?
CLL Support group in Toronto canada: Hello... - CLL Support
CLL Support group in Toronto canada
Hi there I am also from Ontario, about an 1 1/2 east of Toronto. I have not heard of any CLL support groups in the area. However I would be very interested in joining one. For me this site is a great support group but it would be nice to have a small local group where you could meet people face to face who are dealing with the same issues.
Chris
Hi Curling123
I live in Toronto and am not aware of any current groups.
There was a survey that came out from the CLL Society late last year that was gathering info on who would be interested in attending meetings but I have not heard anything more about it since I responded.
I indicated that I was interested and would welcome the opportunity to meet with fellow Cll’ers
I was surprised that in a city of this size that we don’t have any groups. There is one in Montreal
Regards
Heather
We are actively pursuing starting a CLL Society sponsored support group in Toronto. We had some issues after the survey data was collected but I am confident there will be a group started in the next few months. From what we saw, there is a great deal of interest in forming a group.
Terry Evans
Director of Support Services
CLL Society
How will we find out when it will be up and running?
We will be posting information on Health Unlocked as soon as we have a meeting time and location identified. Be patient because the process generally moves slowly. We have found just getting a meeting location can be a long process. The day and the time of the meeting has to meet the majorities schedule as well. But it will happen. This will be our 32nd CLL Society CLL Support group, and are anxious to get it going.
Thanks for reply. Hopefully if and when one is up and running, we will be notified quickly. Looks like the CLL Society is on it’s way to creating one. Certainly the interest is there.
Hi Curling
I noticed you mentioned you had an appointment with your Cll specialist on April 26. If you don’t mind my asking. How did it go?
Regards
Heather
Yes, I did with Dr Spaner at Sunnybrooke. He went over my FISH results. 17p, 11q, 13q. Not the best, but it is what it is. Have no symptoms. Diagnosed in February this year. A few small nodes in neck, had one biopsied. Result CLL. Awaiting a CT scan and had blood tests at appointment with Dr. Spaner. Lymphocytes up a bit from February, 3.2 in February, now 4.00. Was just finishing with a cold so hoping that is why it was higher. Scheduled to go back in June for more blood tests. Guess I am on W&W for now.
Hi, We are in the process of forming a CLL Society patient and care giver support group in Toronto, but the folks who were going to help facilitate have had some health challenges. We have several signed up and ready to go. If you are interested in facilitating (we train you and fly you down to Orange County, CA), please reach out to me and fill out the interest survey on our website (toronto-cll.questionpro.com) . Let's make this happen soon. Stay strong. We are all in this together. Brian Koffman CLLSociety.org
Hi, I am new to all this, just diagnosed with CLL in September 2019. I live in Oakville and would be interested in joining a support group based in Toronto. Please pass on any information about one. My email is laldoroty@gmail.com
Thanks
Hi,
Joining a CLL specific support group is a smart move. It has sure helped me.
Here are the details on the CLL Society's Toronto Support Group for the last meeting and contact info. Mark is a great group leader: cllsociety.org/event/toront...
We have 30 groups in the US and one in Montreal and Toronto. Maybe Vancouver next?
Stay strong. We are all in this together
Brian Koffman (CLLSociety.org)