Guest guest Posted October 30, 2011 Report Share Posted October 30, 2011 I have met on more than one occasion, sat with him at LRF conferences, and attended the CLL support group he is a member of (and he is a member equal to the others, not the leader of the group). is not a retired doctor. He is a CLL patient who is also a family practice doctor. His medical training, obviously, gives him a step up over most of us when it comes to understanding much of the information and literature about CLL, but he pursues that information as a patient, looking for the best options for himself and others. He is very willing to share information he has found, just as some of the other good researchers involved with online groups do, or explain technical information in layman's terms, but very careful to not diagnose or suggest treatment for anyone who he has not seen as a patient. He is, as a doctor, active nationally as a speaker about his areas of interest and expertise. and spends a great deal of time attending medical conferences and keeping up with current medical information related to those areas, as well as CLL. Suggesting that is diagnosing, based on posted information, or telling people which treatments they should try puts his medical license at risk. It is dangerous to assume. There is a reason signs his posts the way he does and we do not have the right to tell him to do otherwise. I believe that you will find that Dr. Furman and Dr. Hamblin, while they are listed as doctors, follow the same rules about not diagnosing or dictating treatment on the lists. It would be a shame if the lists lost as a contributor because he is put in the position of dropping out to protect his medical license! Pat K Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2011 Report Share Posted October 31, 2011 Well said! None of the doctors on this list or any other are dispensing advice for individual patients. We are trying to ensure that any information that is published on the lists is accurate and not misleading. It is impossible to second guess a patient's own doctor; we just do not have enough information. WE can suggest alternative strategies but these should always be put before a patient's own doctor and we are not upset if our suggestions are not followed. We are another internet resource, which we hope is a safeguard against some of the wilder suggestions that are out there. Terry Hamblin MD Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2011 Report Share Posted October 31, 2011 Thank you, Dr. Hamblin, for all your good advice. Do you know any good CLL doctors in Providence? I travel to Boston monthly for treatment, which is getting hard at my age. On the other hand a very nice doctor at Miriam Hospital in Providence told me to continue in Boston because I also have Merkel Cell Carcinoma, which not many doctors know about, including those at Dana Farber as well as in Providence. Carolyn Swift, age 83, Providence, Ri Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2011 Report Share Posted October 31, 2011 Carolyn I am not familiar with the American scene. Terry Hamblin Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 31, 2011 Report Share Posted October 31, 2011 Pat, Thanks again to you and others for your kind words. As everyone knows, I am not a hematologists or oncologist, but a practicing family doctor who does a lot of teaching of other docs and who has his own skin in the CLL game. My practice is limited due my risk of infection from my patients. I am no CLL expert, I get things wrong and I am highly opinionated. My medical training and experience sometimes allows me to offer different perspectives and insights than that of a lay person, though I am constantly being blown away by the clarity of vision of some of the non-MD CLL savants we are blessed to have in our midst. would be at the top of my pyramid. I learn more from all of you than I could ever teach. No MD, myself included, can treat a patient by email or phone, but we can provide information to help guide you with your attending doctors. That is the only way I can help. BTW, my next CME lecturing trip (my topics will be sleep issues and migraines, nothing to do with leukemia) is in Dearborn Michigan, so if you are in that area, let me know and we can share a cup of tea and war stories. So while I love all these comments, let's get back to the business at hand of helping each other navigate our way through the CLL maze. Be strong. We are all in this together. And that's the real truth. Quote Link to comment Share on other sites More sharing options...
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