From newly diagnosed patients to several patients diagnosed more than 10 years ago, we share what we know with each other so that we can all be educated as much as possible about myeloma diagnosis, symptoms, markers, treatments, side-effects, clinical trials, quality of life, and many other topics of interest including invited speakers on occasion. Most of all, we believe that myeloma should be not be treated as a death sentence but rather as a disease to be managed…and education & support are key.  From time to time we invite speakers who are experts in various areas such as oncologists, nutritionists, naturopathic physicians, integrative/alternative specialists, etc.  See Meeting Dates and monthly meeting mailers/emails for information on speakers.   

Click on any of the following items of interest:

1) How to get started click here

2) Meeting Calendar for 2 years click here

3) Meeting Locations click here

4) Directions/Maps to Meeting Locations click here

5) Support Group Leaders & other Key Personnel click here

6) Clinical Trials Resource click here

7) Other Links to Multiple Myeloma Patient Support/Research/Education click here 

8) You can be an Advocate click here

9) Need a ride to support group mtg? click here

 

To add, delete, or update your contact information on our Support Group Roster: click here  (signify e-mail, regular mail, or both and provide addresses) 

 

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