When it comes to relapsing MS, you don’t really “get” it, until you get it. That includes experiencing tough-to-talk-about symptoms like bowel and bladder issues. We’re here to help.
If you’ve experienced increased frequency in urination, urgency to urinate, incontinence, constipation, or other bowel/bladder problems, you’re not alone. That’s because some MS lesions can block or delay nerve messages that control the bladder and bowel. Get tips for dealing with these problems by either talking to your doctor or going to: bit.ly/MSLLsymptoms_bowel_bladderbit.ly/MSLLsymptoms_bowel_bladder
I really hate to harp on this age old theme, just like I am so tired of listening to the rhetoric of the current presidential debates. Unlike the arguments leading up to this year's national election, this issue is pertinent. Today I have the opportunity to do something new and I am very excited about it. I am official "reader" for West Virginia Read Aloud. This morning I will read to a third grade class at our town's elementary school. It is only for twenty minutes and I m relatively comfortable with the "lay of the land", so I shouldn't have an issue with bladder control. Should I? Just thinking about it makes me want to relieve the ol' bag of urine. The problem is...I do not always know when that is going to happen until it is too late.
So, how do I combat this? I do not drink anything prior to attending said event. Sounds like a good idea. Until my body remind me that I am not hydrated with a stinging urge to purge the bladder. Yep. It is that fast. UTI symptoms seem to be just waiting for a chance to taunt me. It's crazy.
I have to leave you now for my reading debut, but I will return to this topic soon. Looking for suggestions. How do you deal with this Multiple Sclerosis Fact #7? (I am also looking for a complete set of these animated MS Facts.) Stay dry, Lisa
With a forecast for rain and cool temperatures, many felt the 2018 Walk for MS might be a sloppy mess; but when I arrives in Morgantown, West Virginia, I found an optimistic, celebratory atmosphere that no storm could dampen. Clouds dispersed and skies cleared, knowing that the heavens could not compete with the storm happening on the ground at the Waterfront.
The true champions had arrived and their name was Warrior.
Tents were erected, tables arranged, team shirt distributed, books stacked, (I got to share I Have MS. What's Your super Power? !!!!)
acknowledgements made, participants in place, and the walk began,
with Team Tiffany in the lead. My new MS friend, Tiffany Albright, is an inspiration. she single-handedly recruited an amazing team of walkers that outnumbered any other congregation in attendance. Her numbers were amazing in monetary contributions and the enthusiasm of her teammates was more than inspiring.
Event though I did not personally join the walkers, my day was fu…
I don't know about you, but sometimes (most of the time) the motivation to exercise is just not there. And that is just plain crazy.
I am more than aware of the positive effects of daily exercise. I always feels better, both physically and mentally, after taking time to stretch, bend, and force my body to meet the challenge of movement. My biggest issue is the accountability. Exercising alone means no one can attest to your commitment. Unfortunately group gym, spa, or class situations are not financially nor logically an option for many of us.
And sometimes, like this morning, it is even an effort to fire up the DVD player in order to access one of my many yoga videos. Even though that cute little blond instructor coos encouraging words my way, her interest in me is purely superficial. We know nothing about one another.
According to healthcare.com the following chart shows the seven best exercises for living with MS. They are easy, doable and require no equipment or additional cost.…
Last evening I attended an area meeting to learn more about Aubagio, one of the three oral MS medications on the market. General MS physician Mark Hospodar provided the informational portion of the session, complete with a slide presentation full of facts about multiple sclerosis. It was very basic and mostly repetitive for those pro-active MS sponges. Not mind-blowing stuff, but pretty heavy on the importance of medicating upon diagnosis. Enough to convince me to take a closer look at my own choice to remain MS drug free.
It was an intimate group of approximately a dozen women plus the doctor. Very relaxed, informal, and free of judgement. We were all there for the same reason with the same goal in mind: to discover the "wonder" drug, or at least something closer to a promised remedy. (In addition to the fantastic Italian cuisine at Muriale's Restaurant. Yum!:)
We heard from Aubagio veteran, Renee, who told her journey with her initial diagnosis s well as her life with …