An Answer From ASCO, Sort Of
As I mentioned the other day, I didn't receive a grant to go to Chicago for the ASCO annual meeting as a patient advocate. Maybe I have a huge ego, but I really thought I wrote a good application and I would get a grant.
So that was disappointing. I still plan to go, but it's a lot of money for me, since my income is primarily from SS Disability. Anyway, for future reference, and because I was curious, I e-mailed and asked what kind of patient advocates they gave grants to, and how many they gave this year.
Here was my e-mail, to Jeannine M. Salamone, who is senior program manager, Communications & Patient Information, for ASCO, the American Society of Clinical Oncology:
Jeannine—Hi. I was wondering what kind of patient advocates you gave grants to—were they “professional” patient advocates like social workers and people who work full time for cancer-related nonprofits? Also, how many grants did you give this year?
She didn't answer my last question, about how many grants they gave, but here's her answer:
Dear Jeanne,
Please accept my apologies for not getting back to you sooner. We look at a lot of different factors when evaluating patient advocate scholarship applications. We look at financial need, timing of the application, involvement in research advocacy, and affiliation with non-profit cancer associations/organizations (either as staff or volunteer). Many scholarship recipients work as volunteers on SPOREs, IRBs, research panels, grant review panels, they review clinical trial consent forms, etc. This is the second year that we were able to provide patient advocate scholarships for our Annual Meeting and next year we hope to secure even more funding.
I look forward to seeing you in Chicago. Please be sure to utilize our Patient Advocate Lounge (room S402) and attend our Research Review Sessions for Patient Advocates, in the Patient Advocate Lounge on Saturday, May 31 and Sunday, June 1 from 5:15 to 6:30 PM. Once we receive your registration form, you will be placed on our patient advocate list and will receive more information about these Annual Meeting Patient Advocate Programs.
Best Regards,
Jeannine
If my reading of that is correct, they were leaning towards people involved in "research advocacy," and it's true that that is not a primary focus of mine.
I care less about the latest and greatest cancer treatment breakthroughs than I do about issues like doctor/patient communication, making decisions about treatment, and the whole "psychosocial" side of living with cancer, which includes support, coping, stress, and all of that.
I will be going to the meeting, and blogging about it each day that I am there. If you are a cancer patient who is also planning to go, please let me know. Maybe we can join forces while we're there.
@ Jeanne Sather 2008.
