Guest guest Posted July 25, 2006 Report Share Posted July 25, 2006 Hi (BTW - The way your messages begin makes me laugh every time you send a post...) I had my last one (I think) about eighteen months ago, maybe two years ago? I've had chemical meningitis with one, two very large spinal fluid leaks...one completely under the skin, the other leaked to the outside for three long months before surgery was done..both needed long surgeries to correct. I woke up from one surgery unable to move my leg - not one movement at all for a few days, then it was back as quickly as lost. My first one...no pain at all previous to it. Well, some lower leg pain. But, nothing to really write home about. Never stopped one thing except walking once in a great while. It would just lock up - the muscles. Weird, but after the surgery, I had horrible pain and it never left. My bladder went completely and I had to self-cath. That was why I kept having more and more untetherings. The decline kept coming and coming... I too have Chiari, no surgery thankfully though (only one nsg out of all I've seen over the years recommended it...I'm very fortunate.) The only thing about this that is sad for me is my youngest...he's my only son. We have three girls also. They were in high school when I was diagnosed and started the decline. I had already done the backyard baseball games with them and the driveway hoops, running around the block four times a week with a couple, diving into the water from boards and boats, snowmobiling, cross country skiing, you name it, I had already done it with our daughters. Our son though was only nine. Extremely sensitive to what I went through, although silent about it until a few years ago. When I asked him once about him and me playing catch at the beach (we were looking at old pictures), he said it was funny, he couldn't remember me " healthy " or playing hard with him. He has absolutely no recollection of me doing anything vigorous, rigorous or breath-enducing. I find that the saddest, that he only remembers me as " sick " . Always having doctors' appt.s, although he admits when it first started he didn't understand it (in the beginning I wouldn't allow anyone in our house to tell anyone outside of the house that I was dealing with anything, which in turn, made it impossible for anyone in the house to admit what they were dealing with...my one life regret...) That's truly the only thing that bothers me about having this stupid thing. Well, that and my grandchildren will not know any different either. I know I can do a million other things with them, but activity was so important in my life before this came along, it's hard to change stripes when it's ingrained. But, there are so many people that have it so much worse than me with physical problems. (Although their attitudes toward what they go through is better than mine...a thousand times better.) I had a normal childhood, not having clue-one that anything was wrong with me. Didn't everyone pee when they laughed? Wear two left shoes for four years because of feet problems? Have constant bladder/kidney infections until I reached the impossible height of 5'10 " . But, honestly, strangely, once I reached full height...all the problems I had that no doctor could diagnose, stopped almost overnight. No more problems until about eight years before my diagnosis, I was running down my cellar stairs (oak) and fell, landing on my butt on one,- landed so hard that the stair broke in half (not due to my weight, I'm not over-weight.) The pain was unbearable for quite a while, but I didn't go to a doctor because my husband kept telling me that if I broke my tailbone there was nothing that could be done. So, for eight years I declined not knowing that all my strange problems were one big problem. I never complained about one of my strange symptoms to a doctor (the leaking, the fact that I was doing aerobics 4-8 times a week and couldn't get a muscle in my left leg to even flex, etc.) But, all that aside. I am so very grateful for not knowing I had this when I was pregnant with all four of my children. I probably wouldn't have become pregnant four times knowing what the pregnancy and birth can do to us (right ? Well, actually, like , I probably would have done it and just hoped and prayed for the best...I really wanted a large family desperately to be honest.) I'm terrible in some respects. I don't think about my condition. The pain is something that stops me from doing certain things. It keeps me from wanting to walk on carpets barefoot because the pain from my feet touching the carpet is completely unbearable at times (that's what I'm dealing with today, that and vomiting so it's what is on my mind, but in isolation if that makes sense). But, it's an isolated thing...I don't think of this during the day the way I think of other things. Strange...I always wonder if other people are the same. I wake up in the morning feeling completely normal until I go to move, or if was woken by the pain. My mind hasn't changed at all...I still want to do cartwheels at times! Kathy Re: 5 untetherings?? Sumchyk was found muttering these words: > My diagnosis was very strange and not typical. > Kathy, you poor thing! I was mis-diagnosed for years. I was so sure I had polio/post polio I was secretary of the Illinois Post Polio Surviors LOL Funny how they can overlook the hole in my back and every other classic sign of spina bifida and tethered cord. I have only had 2 untetherings and I truly hope the last one was my last one. With Chiari on top of everything else, I lost short term memory, had horrible drug reactions, depressions and all sorts of weird brain reactions along with the recovery experience. I don't think I could do it again. When was your last one Kathy? ********************************* ces, tcs, acm, sbo Aim Name = sumchyk ********************************* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 25, 2006 Report Share Posted July 25, 2006 You really said exactly what I feel! The hardest thing is not the pain or the decline, it's not being able to do the fun things with my kids (age 3 and 5 when this all started...6 and 8 now). They won't know that I used to be a very physically fit person who loved biking, rollerblading, running, dancing yada yada yada. They will just remember the mother who never played soccer or baseball with them and only went swimmimg once in a blue moon. That is really the hardest part for me! Re: 5 untetherings?? Sumchyk was found muttering these words: > My diagnosis was very strange and not typical. > Kathy, you poor thing! I was mis-diagnosed for years. I was so sure I had polio/post polio I was secretary of the Illinois Post Polio Surviors LOL Funny how they can overlook the hole in my back and every other classic sign of spina bifida and tethered cord. I have only had 2 untetherings and I truly hope the last one was my last one. With Chiari on top of everything else, I lost short term memory, had horrible drug reactions, depressions and all sorts of weird brain reactions along with the recovery experience. I don't think I could do it again. When was your last one Kathy? ********************************* ces, tcs, acm, sbo Aim Name = sumchyk ********************************* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 26, 2006 Report Share Posted July 26, 2006 Sumchyk was found muttering these words: That is so sad about your youngest. I have 5 kids from 3 marriages (1st hubby died, 1 divorce and remarriage). The 3 youngest are boys and they have seen me both not-so-good and recovering. I am 6 months from my last surgery and I am walking/bike riding etc... so I am hoping the surgery will work at least long enough to get the last of the little chicks launched (they are 14). Like you, I would have never had them if the docs had known what was wrong with me. And I had twins! I agree there are so many people with so many more extreme problems. We just found out my oldest and only daughter has to have surgery. She had several bad PAP smears as a result of HPV and will be going in for a consultation this week since the freezing procedure failed to address the problem. Keep your fingers crossed for us. << hugs to all >> ********************************* ces, tcs, acm, sbo Aim Name = sumchyk ********************************* Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 26, 2006 Report Share Posted July 26, 2006 Do you all think that pregnancies make TCS worse? I know that the lithotomy postition isn't good. But I had my son C-section and still later developed problems? Peace, Linds Re: 5 untetherings?? Sumchyk was found muttering these words: That is so sad about your youngest. I have 5 kids from 3 marriages (1st hubby died, 1 divorce and remarriage). The 3 youngest are boys and they have seen me both not-so-good and recovering. I am 6 months from my last surgery and I am walking/bike riding etc... so I am hoping the surgery will work at least long enough to get the last of the little chicks launched (they are 14). Like you, I would have never had them if the docs had known what was wrong with me. And I had twins! I agree there are so many people with so many more extreme problems. We just found out my oldest and only daughter has to have surgery. She had several bad PAP smears as a result of HPV and will be going in for a consultation this week since the freezing procedure failed to address the problem. Keep your fingers crossed for us. << hugs to all >> ********************************* ces, tcs, acm, sbo Aim Name = sumchyk ********************************* Quote Link to comment Share on other sites More sharing options...
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