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Dear Friends,

I am working to raise funds with two major brain tumor research organizations, The Brad Kaminsky Foundation and The Musella Foundation for brain tumor research-for UCLA department of neuro surgery and oncology, to find a cure for brain cancer. Together TBKF and The Musella Foundation are hosting the Heroes of Hope Race for Research on November 23 at Dockweiler State Beach. I would love for you to be a part of this inaugural event.

Please contact me if your business in California would like to be a sponsor for the Heroes of Hope Race for Research. You may receive a Sponsor Packet via email or postal mail, it is up to you. Send an email to:JenniferJAlves@gmail.com. Learn more about The Brad Kaminsky Foundation and Heroes of Hope Race for Research at www.TBKF.org. With your generous support for brain tumor research, medical students, doctors and scientists continue to learn and advance towards better treatments and cures. Please help support research for the leading cause of cancer death in children and young men.

Thank you for being our Hero of Hope and for becoming a part of the united forces against brain tumors. Together in Hope, we will win the war against this disease!

Have a great day,

Jennifer Alves

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Hello Jennifer,

I'm a pretty new Puzzlenut, and I was just browsing through the old forum topics. I noticed that you and I seem to have a second interest in commom...brain tumors.
I'm familar with The Musella Foundation, and have heard of Brad Kaminsky Foundation. In August of 2007 I had a brain MRI, doctors were looking for MS, but instead found a lesion of some kind in my left frontal lobe. To this date, this lesion has remained unchanged, and I have never had it biopsied, and I have no symptoms that can be directly related to this lesion. So, since that time, I have been getting and keeping myself educated about the latest treatments for brain tumors, and my doctors believe there is a pretty good chance that what is in my brain is malignant, and will at some point in the future need treatment. There is also the chance that what is in my brain has been there for ages, and will never change and never need treatment. My doctor reports having a patient like me who has been getting MRIs for ten years now with no changes.

So, I am on The Musella Foundation's email list and on a few brain tumor yahoo groups.

Just curious....how and when were you welcomed into the brain tumor world?

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