My biggest concern when I was diagnosed with Multiple Sclerosis waaaaaay back in 1997 was what the disease would do to my ability to walk. I started working with a physical therapist quickly after my diagnosis because I knew the important role PT would play in managing my disease.
I completely underestimated the chunk of my future that would deal with something just as pivotal in managing my MS: controlling urological issues.
Bladder dysfunction occurs in at least 80% of people with MS, affecting everything from frequent urination to the inability to urinate. It took me some time to realize that while we’ve all “gotta go,” my newly discovered chronic illness was going to challenge my abilities to stop and start. So much like PT, I enlisted the help of an awesome urologist.
I’m grateful that over the course of my time with MS I’ve been able to regularly connect with fantastic specialists. Their insights, perspectives and expertise have helped me to better understand MS and what I can do to better manage its symptoms.
That is why Dan and I were so excited when AnCan had the opportunity to host an open and honest dialogue about MS and urological issues with the outstanding Dr. Rachel Rubin, a Board-Certified urologist and sexual medicine specialist.
The AnCan webinar with Dr. Rubin, which was cosponsored by MS4MS, gave those in attendance an opportunity to ask questions, and to speak openly and honestly about urological issues that are not often discussed.
In fact, I could tell by the look on Dan’s face that Dr. Rubin’s answer to his online chat question blew him away. Yes, Dr. Rubin explained, men can and do get urinary tract infections.
We’re thrilled to share the video recording of this webinar with Dr. Rubin to help increase your understanding of MS and bladder issues.