Pain and Endometriosis
March 10th, 2010 | by admin |
The UCSD School of Medicine and the Diana Padelford Binkley Foundation bring you the newest installments of this innovative series targeted at successfully managing pain in women. Studies show women often receive inadequate care as pain manifests uniquely in the sexes and requires distinctive treatment strategies. In this program, Karen Berkley, Ph.D., Distinguished Professor of Neuroscience, Florida State University, talks about pain and endometriosis.
Series: Pain Management in Women Over the Lifecycle [10/2007] [Health and Medicine] [Professional Medical Education] [Show ID: 12601]
Duration : 0:47:43
[youtube IsoC5q81dcw]
11 Responses to “Pain and Endometriosis”
By hormiguitainAms on Mar 10, 2010 | Reply
wish the last slide …
wish the last slide was readable… any idea if this is available somehow?
By hacsince91 on Mar 10, 2010 | Reply
UHMMM i would …
UHMMM i would rather they use a RAT for research rather than myself or my loved ones! use ur brain kid, think!
By Norb1t9 on Mar 10, 2010 | Reply
god you sound like …
god you sound like you’re out of breath! slow down!
By christmas1971 on Mar 10, 2010 | Reply
Thanks Amy, that …
Thanks Amy, that was very sweet of you. I will mail you if I get stuck and confused about all of this. I appreciate it. This is such a hard thing to deal with and misunderstood disease. Thank you.
By amytamez on Mar 10, 2010 | Reply
Well… Hi …
Well… Hi Christmas1971, I was diagnosed by my gynecologist, he is the Director of Reproduction and Fertility in one of the most important hospitals in Mexico City. He told me in 1997 that my endo has spread to my bowel and to my bladder, ureter and may get my colon. So I think it depends in how many organs the endo attacks. I am not sure of it, but after my first surgery he told me so and I go to a check up every 6 months.
Take care and if you need something let me know.
Blessings
By christmas1971 on Mar 10, 2010 | Reply
Hi Amy, I had a dx …
Hi Amy, I had a dx of endo after 10 yrs. of er trips and emergency surgery for a ruptured choc. cyst and a final dx of endo after a partial hysterectomy in 2007. Stupid me, did not educate myself on it because I have been pain fee since UNTIL a week ago. I now have a choc. cyst and have to have a total Hyst. My quest. is how do I know what stage endo I have. My gyno was awesome, Duke grad, sweet. But she never said anything about a stage. Thanks!
By amytamez on Mar 10, 2010 | Reply
You are right, it …
You are right, it is not fair to use them in order to possible get a cure for the ones who have a disease.
I have endometriosis IV, and being honest I am very sorry, but I can’t handle so much pain every month and for more than 15 years I have suffering this, it is urgent for the young women to find a cure. I am 39yo and I couldn’t have babies, but there is a lot of very young women with this.
I know what you mean but we need it.
Blesings
By endometriosis83 on Mar 10, 2010 | Reply
well I’d rather …
well I’d rather they use rats instead of humans
By endometriosis83 on Mar 10, 2010 | Reply
well I’d rather …
well I’d rather they use rats instead of humans
By XrWnMwX on Mar 10, 2010 | Reply
umm…umm…umm…
umm…umm…umm…
By reneechadwick on Mar 10, 2010 | Reply
i don’t agree on …
i don’t agree on useing rats or any other animals for research