Guest guest Posted November 25, 2002 Report Share Posted November 25, 2002 > I think if we allowed dr's access to our little group they'd > undermine what we're trying to do here. Just my humble opinion. FWIW, physicians may join if they care to, and none of us would be the wiser. The only way to prevent it would be to restrict membership and screen everyone trying to join up. But my thought on this, aside from not wanting to screen joiners, is that any physician joining up would be doing so to gain perspective from MA sufferers rather than to dispense advice. A physician would probably lurk very lightly, this not being a peer/professional forum. About hearing from doctors: I have this web page on PCOS, and part of the narrative crabs about my having gotten rather superficial treatment in the past from my doctors. I complained that OB-GYNs tended to dismiss the seriousness of PCOS, offer mere cosmetic solutions, etc. I wrote that in 1999, when it was truer than it is today. In spite of the frustration I expressed on that page, I have received some really nice e-mail from several REs over the years . . . and one really sarcastic one from an OB-GYN, which he finished up by offering me cosmetic advice, LOL. From my perspective, it just served to reinforce my high opinion of REs. :-) Beth SU Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2002 Report Share Posted November 26, 2002 >In spite of the frustration I expressed on that page, I have > received some really nice e-mail from several REs over the > years . . . and one really sarcastic one from an OB-GYN, which he > finished up by offering me cosmetic advice, LOL. > That's pretty cool that some MDs wrote to you for your PCOS website. Have any sent you an email about this site? Dr. Valle kept telling me that he wants one of his med students to do a project on the support that women receive on the internet. I was wary to give him this website, but I had mentioned it to him. In retrospect, after his failed handiwork, I'm glad that I can speak freely here about my experience. Although it would be nice to have a professional opinion when we are uncertain, I think that my most burning questions have been able to be answered here by other women who have already experienced it and I am able to hear how different each dr approaches a certain problem. Sara Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2002 Report Share Posted November 26, 2002 >In spite of the frustration I expressed on that page, I have > received some really nice e-mail from several REs over the > years . . . and one really sarcastic one from an OB-GYN, which he > finished up by offering me cosmetic advice, LOL. > That's pretty cool that some MDs wrote to you for your PCOS website. Have any sent you an email about this site? Dr. Valle kept telling me that he wants one of his med students to do a project on the support that women receive on the internet. I was wary to give him this website, but I had mentioned it to him. In retrospect, after his failed handiwork, I'm glad that I can speak freely here about my experience. Although it would be nice to have a professional opinion when we are uncertain, I think that my most burning questions have been able to be answered here by other women who have already experienced it and I am able to hear how different each dr approaches a certain problem. Sara Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2002 Report Share Posted November 26, 2002 Well, I should probably follow up my post from yesterday by saying I have yet to see an RE (my appt is Dec 11!), so I may have a bit of a jaded view here. I mean, I like my OB, but it's been a bit frustrating, asking for tests he's saying " no " to, etc. Beth, you make a good point that anyone can sign up for the group, so for all any of us know, we already have doctors in our midsts! I think it might actually be helpful for OBs and even REs to read what we write, and to hear our perspective on things. Maybe it would help them as they give care to other women with MA's. Tina 31, 2 m/c, dx BU Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2002 Report Share Posted November 26, 2002 Well, I should probably follow up my post from yesterday by saying I have yet to see an RE (my appt is Dec 11!), so I may have a bit of a jaded view here. I mean, I like my OB, but it's been a bit frustrating, asking for tests he's saying " no " to, etc. Beth, you make a good point that anyone can sign up for the group, so for all any of us know, we already have doctors in our midsts! I think it might actually be helpful for OBs and even REs to read what we write, and to hear our perspective on things. Maybe it would help them as they give care to other women with MA's. Tina 31, 2 m/c, dx BU Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2002 Report Share Posted November 26, 2002 > That's pretty cool that some MDs wrote to you for your PCOS website. > Have any sent you an email about this site? A UK OB-GYN (Danny Tucker) wanted to list this as a resource link on his web page, intended for patients. He did not join, just approached me for more information. His consuming interest right now seems to be to encourage fellow physicians how to deal with net citations and how to communicate with patients in a better way than is currently happening. He thinks too many alienated women are turning away from consulting doctors to consulting " junk " information on the web. I agree. It's really too bad when people trust sources that go no deeper than a teenager typing in her room, or take anecdotes from bulletin boards to their doctors as " proof " of what they need. My impression was that Tucker wanted better Dr./Pt. communications and greater recognition of genuinely solid medical information to be found on the web. Beth SU Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2002 Report Share Posted November 26, 2002 > That's pretty cool that some MDs wrote to you for your PCOS website. > Have any sent you an email about this site? A UK OB-GYN (Danny Tucker) wanted to list this as a resource link on his web page, intended for patients. He did not join, just approached me for more information. His consuming interest right now seems to be to encourage fellow physicians how to deal with net citations and how to communicate with patients in a better way than is currently happening. He thinks too many alienated women are turning away from consulting doctors to consulting " junk " information on the web. I agree. It's really too bad when people trust sources that go no deeper than a teenager typing in her room, or take anecdotes from bulletin boards to their doctors as " proof " of what they need. My impression was that Tucker wanted better Dr./Pt. communications and greater recognition of genuinely solid medical information to be found on the web. Beth SU Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 26, 2002 Report Share Posted November 26, 2002 > > My impression was that Tucker wanted better Dr./Pt. communications > and greater recognition of genuinely solid medical information to be > found on the web. > I found this site by searching on Uterine Septum, finding one of those " ask the doc " sites where people were e-mailing in questions to a doctor. A doctor recommended this site as a good support network to someone who had discovered they had a septum. I assumed the doctor had been to this group, and I also assume there may be a few lurking in the group already. It's not that docs aren't welcome, I think, as much as the imbalance or alienation it might cause if anyone felt that they were being overruled or belittled by a medical professional, which seems to be a sore spot with many of us here. It seems logical that this forum is mainly meant for women who suffer from this congenital condition, with the aim to better manage our situations as patients and find support from other women who understand our pain. We all have our own docs whom we have searched for and found mainly due to their experience and knowledge and understanding of our conditions. We can share both our good and bad experiences with others who may or may not be getting the care they need. In this group we genuinely profit from hearing what other people's docs have done, how they've managed things, surgical techniques, etc. I am certainly not for banning docs from the group. But I certainly don't feel that there's a need for a resident doc dispensing advice either, because in my opinion the ladies here have collectively covered more of the bases than any one doc could ever cover. Mes deux centimes ... xo, p.s. This group is one of the blessings I am counting this year! Quote Link to comment Share on other sites More sharing options...
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