Post by fishkybizniz on Jun 14, 2014 13:51:42 GMT -8
I don't use my chair in my home, just the Walker. I'm being assaulted with severe spasticity right now. My week day care giver and husband are with me when I need to get up. Zaps all my strength. Cheats all my peeps I know and those I don't out of compliments, well wishes, being goofy and anything I can do to make their day a better one. Speaking of, I need to tune out. My body insists on a nap. I do not remember being voted off the board??
wavewolf & Butiki, do you think it's still risky to get into a pool with the bowel and bladder issues?
For me, yes. Flaccid bowel and bladder (lower motor neuron problem) means that I cannot control exit, and efficacy of diapers or pads in pool is most doubtful.
Dear wavewolf, I used crutches before I went into the hospital with my body under non stop assault I believe the doctors called a hyper spastic escaperation. Not sure if I have that name right. After I was too weak for the crutches so I used a Walker. Hospital docs told me it would be a minimum of of six months maybe more before I could qualify to get off some of the meds. They explained the spasticity makes recovery difficult because the spasticity uses up my energy going 24/7. I keep pushing and get knocked on my butt. The good news, my set backs don't take away my strength. Stamina is what we're working on now. It's a bit of a dance to guess what I can get away with. Right now I'm on bed rest from over doing it. It's obvious my nerves are not ready to be seeing doctors 3 times a week with physical therapy on top. We're exploring what in home therapy is available. The hospital I go to for out patient will open a nuro science wing this fall. I'm looking forward to that guessing my pain management doctor will have a treasure of talent we can tap to help me along.
I have learned that moving between various assistive devices improves my stamina and gives some body parts a break while taxing others, so the energy drain is less or maybe just better spread around. Spasticity can have a benefit, which is maintaining muscle tone. But if nerves are firing so hard that it causes pain, or you're constantly trying to control weird movements so your friends aren't scared (been there, done that!), then it's probably time to try some meds. I found that a low dose of Baclofen has given me a balance of less pain and physical stress, without weakening my muscles so I cannot do the most possible. I started taking Bovine Colostrum supplement for immune support and healing of GI tract, and a very lovely side effect was greater muscle strength. I mention these two things as relatively inexpensive and quite helpful.
BTW, to tag another forum member in a reply, type "@" before the user name. It will show up as fishkybizniz, and you will get a notification then.
For me, yes. Flaccid bowel and bladder (lower motor neuron problem) means that I cannot control exit, and efficacy of diapers or pads in pool is most doubtful.
Post by fishkybizniz on Jun 15, 2014 16:41:02 GMT -8
Hi all, sorry for the late reply. I'm a mess right now. As I shared when joining, I'm a rookie. Just suffered a set back. My cord thew a hissy fit much like (too much like! ) my eight days of hell in the hospital. Had to see my primary doc and my dumb luck to have a kidney infection joining in to make it as pitiful as possible.
"Everything is OK in the end. If it's not OK, then it's not the end. " author : I forgot. Must be the drugs!
fishkybizniz, So sorry to hear of these medical trials you are going through. Hope you can get the infection and pain under control very soon. Please, no worries about "rookiness"--we all had to learn!!!!
Hi all, sorry for the late reply. I'm a mess right now. As I shared when joining, I'm a rookie. Just suffered a set back. My cord thew a hissy fit much like (too much like! ) my eight days of hell in the hospital. Had to see my primary doc and my dumb luck to have a kidney infection joining in to make it as pitiful as possible.
"Everything is OK in the end. If it's not OK, then it's not the end. " author : I forgot. Must be the drugs!
Oh dear..not good! I hope you feel better soon. fishkybizniz, why dont you post up an introduction so members can welcome you to the forum Introductions
wavewolf & Butiki, do you think it's still risky to get into a pool with the bowel and bladder issues?
For me, yes. Flaccid bowel and bladder (lower motor neuron problem) means that I cannot control exit, and efficacy of diapers or pads in pool is most doubtful.
Ok, I am inspired to get back in the pool. Thanks to everyone who has posted and who helps keep the site so we can post. Thank you.
I have been going to the gym for 3 months, and saying that I wanted to get in the pool as soon as I can figure out how to physically do that. Screw waiting. I am going to try something and see if it works. My rt side is much weaker than left and my gait/posture awful. Standing in water sounds perfect, and has sounded perfect for a while. You guys have made me realize, I need to try, not just think about trying.
I too have issues with feeling pretty good, then immediately overdoing. My friends say I will learn , but ........
Anyway, good luck to all, and don't stop trying something....Doing anything that might improve your situation will be good for your mental health, and thus your physical health.
Ok, I am inspired to get back in the pool. Thanks to everyone who has posted and who helps keep the site so we can post. Thank you.
I have been going to the gym for 3 months, and saying that I wanted to get in the pool as soon as I can figure out how to physically do that. Screw waiting. I am going to try something and see if it works. My rt side is much weaker than left and my gait/posture awful. Standing in water sounds perfect, and has sounded perfect for a while. You guys have made me realize, I need to try, not just think about trying.
I too have issues with feeling pretty good, then immediately overdoing. My friends say I will learn , but ........
Anyway, good luck to all, and don't stop trying something....Doing anything that might improve your situation will be good for your mental health, and thus your physical health.
This is so good to hear dodahman! Let us know how you get on You go for it!!
well that was in Oct of last year I promised ya'll (and myself) that I was going to the pool. OK with SCI, sometimes the clocks stands still , or even turn backwards for me, if only measuring progress. 'There will be setbacks' I was told by a trusted physical therapy person. She was right. And it is good to know there will be, so you don't get discouraged too terribly when it happens.
The good news: I finally made it today to the pool. I was able to get back in the car when I was through. I only stayed 15 minutes, but did about what I had hoped to the first visit. I have been going to this gym for a long while(prior to injury) and it was good to see folks who were encouraging and supportive. I think it will be very positive for me as long as I don't try too much too soon.
Best Regards to all, I get lots of inspiration and information from this forum. thanks to everyone who has contributed in both large and small ways.
Congrats dodahman, that's excellent news! There'll always be setbacks with spinal cord injuries but we have to keep pushing forward and that's what you've done.
I think I'm ready to get into a pool/beach this year too!