I can not answer your question. Dr. Van Allen is part of the Metastatic Prostate Cancer Project. I participated in that. Supported in part by Malecare.
I had an idea early on about comparing my germline mutations to my four brothers, to see why I got PCa and they didn't. The lead doctor at the Prostate Cancer Foundation recommended I discuss the idea with Dr Van Allen.
My only interaction with him was through email, but I found him to be open minded and insightful.
Thanks for the input. I’ve been watching your journey through the LU treatments and am sorry that those have not worked for you as you hoped they would. I have not committed to an MO yet for my own PCa treatment, so I’m researching those in the field and collecting information including geographic locations in New England. All the best.
There are some fabulous MO’s in Boston. I am not familiar with the Dr Van Allen but we see Dr Misha Beltran and she is amazing. We are so fortunate to live within driving distance. Brigham and Womens has excellent surgeons and many doctors are Harvard Professors. Best of luck finding a good fit.
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