These are two separate problems: The first has been discussed in a previous thread. After nearly 40 yrs. of voiding on my own, dealing with bladder spasms and lower extremity spasticity, my uro urged me to try intermittent catheterization. I had resisted it for many years, because I wanted to be "normal". Within days of starting IC I found that I did not leak (ditropan helps), output increased from less than 200 cc's to 500 cc's, and bladder function was greatly improved. Urodynamic testing showed a very calm bladder and discomfort (I have full sensation in my bladder.) was reduced by at least 95%. The only downside is increased number of UTI's as IC introduces a foreign body to the urethra.
The second problem is generalized spasticity due to bladder issues; infection and bladder pressure. For years when I was working and up in my w/c for 12-14 hrs. a day I experienced severe spasticity in my legs. It was worst at mid-day and bedtime. Twenty mg baclofen wasn't enough and forty mg baclofen made me too drowsy the next day. I thought I had UTI's and kept asking my doc to send scripts to the lab for urinalysis. They always came back negative. The culprit was bladder pressure, but no medication worked effectively for me. In desperation I asked my doc to prescribe pressure mapping. This entails sitting on a grid that is hooked up to a computer. The hottest areas with the most pressure will be red, the potential problem areas will be yellow, and the safe areas will be blue or green. In my case one of the hot areas was directly under the bladder. Since I was sitting for so many hours each day, pressure would build in the bladder causing uncontrollable spasticity. I changed to a Deep Contour Jay cushion with extra gel. The gel not only provided protection but served to cool the bladder area. Within a week the spasticity problem was eliminated.
The moral of the story is that SCI is a unique experience for each of us. As I stated previously, you are the most important member of the medical team. Never stop trying to improve your own situation with education and creativity. Participate on boards like this, including CareCure and Apparalyzed. The I'net provides so many resources that would be out of reach to all of us from previous generations. Good luck.
hobo, thankyou so much for sharing this with us...its been a revelation for me personally reading this. I have found it so interesting. My spasm in my legs and ankles have worsened lately. Ive spoken to my urologist, my physio and my consultant..all at my unit.
Ive had special insoles made for my shoes to help keep my feet more balanced to help with the ankle ones. Ive also tried more exercise for the spasms in my thighs and then tried less. They are always at night and are driving me crazy!
The spasm in my thighs are at the back in the hamstring. I also get bladder spasms but ditropan helps a little but not enough. I tend to get spasms as the catheter enters the bladder, pretty much due to the reaction to something 'foreign' being inserted there.
But this pressure mapping sounds interesting....im using a different seat for several hours a day and it dosent have cushioning as my chair has so i may be getting issues from this pressure. My butt area is mostly numb so its likely and to be honest i hadnt thought of this..so thankyou because il ask about this pressure mapping to be carried out,.
hobo your bladder issues sound a lot like mine! The pressure mapping is a great idea and it's incredible how proper seating corrected the spasm issue in your bladder! I've never heard of anything like that but I'm going to talk to me seating clinic next time I'm there.