23rd May 2008
Marcia of course I know your right. I have just told pepper the same I would not even consider the SCS with out seeing a good PM, there is to much I don't know yet & PM & CP is something I have to learn alot about. I am not the type to jump into anything but at the same time I will just research. I know I have to research the RSD, I am frustrated that the surgeon is making me wait till the end of the 6months, but really my hands are tied. I am hoping now that Osteo has been tried this will give him a jump start. I am not sure whether to make an appoinmtent of just ask to be put into pm when calling his office this coming week for a refill on my meds. I do know my patience is gone. I am having alot of pain with that shoulder, alot. Can't lift it over my head at all, in fact it hurts to move it at all.
The symptoms are so darn sparatic it confuses the heck out of me. I just know the pain is getting worse & I am at the end of my rope here. I am just starting to feel drained, by the pain & the emotional acceptance of it all. I try so hard to have some what of a normal routine & life but in the back of my mind I wonder how the future will be.
I think its cruel to make me wait much longer, you know? On days like today I will stay in pain all day & to boot my darn stomach hurts because my bowels are acting up. It is definantly time to try some other avenues. I am pretty sure the osteo would agree since she handed me the SCS book, & came right out & said at this point she just don't know if she can help me. She said to call her & then I will ask her some important questions. The thing is these osteos don't really get into drug treatments, but I need some names of PMs I am hoping she will give me at least a name & then of course the surgeons recommendation. I am going to try to follow the advice of cmp & ask for one that specailizes in rehab. or anesth. Of course I am alittle scared because I know this doctor will play a major role in my life. That is when I will address the RSD & mean time I will start researching it.
I do believe for a fact that muscle is involved. Once again I have to get a doctor who will be treating me, not one just passing through. Its difficult right now. I am in limbo.
To be honest I am ready to up my meds abit, I have been holding back & I am tired of the pain. That is something I am going to go over with the surgeon. Man I hope he continues to treat this while I am waiting to get into a PM, if not he should have started that along time ago. I have to trust he knows what he is doing. I still can't believe this is my life. Called my sister in Florida & just cried on the phone. She knows how active I am & knows how hard it is, she has a muscle desease & understands how hard it is to accept it. Hers does not cause her cp but almost cost her life. I told her I am finding it hard to get used to the changes I will have to make, it is just so ironic for a person like me who has ADHD to find themselves physcially limited. Work calms me & is so rewarding. I am not a women who likes to sit & watch tv or just ignore work & wait for hubby. Oddly I know so many women like that & I could never figure out how they could stand it. I always found it rewarding to accomplish things like yard work, even love my house to be clean, I just love to tackle things. This is the hardest thing for me to get used to. I hope PM will give me some of that back. That is my only hope left. Right now on days like today I can't do hardly anything, even putting dishes away or folding clothes is painful. I wish I was lazy sometimes (ha). I keep telling myself keep a good attitude, find something to laugh at, even if it is myself. I want my old life back, want ot play ball with my girls, clean my windows, heck I wont even complain about scrubbing the foors, which I hate. I have been real quite since the doctors opinion, have been avoiding people, you know? Heck what do you say? I told my husband he is not to discuss my condition or meds with anyone, I have seen peoples reactions to CPers & I will tell you I would loose it with anyone & their stupid uneducated opinions. So easy for them to talk. I have already kind of lost it with my husband who of course does not like the meds, told him if he wants to vomit & all that good stuff on a daily basis due to the pain be my guest but I will not go back to that for anyone. I am so careful with meds I am undermedicating, I know it, but always have to worry about obtaining the refills. Next call I am telling them I am taking them if need be, according the the instructions 1-2 every four to six hrs. On days like today no more waiting in pain all day. I try to stay at no more then 3 all day with motrin in between, not working anymore, & the compound cream, I need a different muscle relaxer to. I will try the skelaxin again but did nothing before surgery. I have some, so might as well try them. I'll tell you I will not rest easy till I am in PM.
Don't worry I am listening to your advice, heck where would I be with out you? I am just trying to be patient. I asked the osteo about the RSD but she pretty much just blew it off. She is really nice, every doctor has there specility & that is not her area. Let me know what you think about whether to try to get into the surgeon or just request the start of getting into pm via phone, I should probably try to get in, to many questions & I am worried about the shoulder, perhaps I can get into pt when I get the right PM, what do you think? Talk to you soon, Sammy
The symptoms are so darn sparatic it confuses the heck out of me. I just know the pain is getting worse & I am at the end of my rope here. I am just starting to feel drained, by the pain & the emotional acceptance of it all. I try so hard to have some what of a normal routine & life but in the back of my mind I wonder how the future will be.
I think its cruel to make me wait much longer, you know? On days like today I will stay in pain all day & to boot my darn stomach hurts because my bowels are acting up. It is definantly time to try some other avenues. I am pretty sure the osteo would agree since she handed me the SCS book, & came right out & said at this point she just don't know if she can help me. She said to call her & then I will ask her some important questions. The thing is these osteos don't really get into drug treatments, but I need some names of PMs I am hoping she will give me at least a name & then of course the surgeons recommendation. I am going to try to follow the advice of cmp & ask for one that specailizes in rehab. or anesth. Of course I am alittle scared because I know this doctor will play a major role in my life. That is when I will address the RSD & mean time I will start researching it.
I do believe for a fact that muscle is involved. Once again I have to get a doctor who will be treating me, not one just passing through. Its difficult right now. I am in limbo.
To be honest I am ready to up my meds abit, I have been holding back & I am tired of the pain. That is something I am going to go over with the surgeon. Man I hope he continues to treat this while I am waiting to get into a PM, if not he should have started that along time ago. I have to trust he knows what he is doing. I still can't believe this is my life. Called my sister in Florida & just cried on the phone. She knows how active I am & knows how hard it is, she has a muscle desease & understands how hard it is to accept it. Hers does not cause her cp but almost cost her life. I told her I am finding it hard to get used to the changes I will have to make, it is just so ironic for a person like me who has ADHD to find themselves physcially limited. Work calms me & is so rewarding. I am not a women who likes to sit & watch tv or just ignore work & wait for hubby. Oddly I know so many women like that & I could never figure out how they could stand it. I always found it rewarding to accomplish things like yard work, even love my house to be clean, I just love to tackle things. This is the hardest thing for me to get used to. I hope PM will give me some of that back. That is my only hope left. Right now on days like today I can't do hardly anything, even putting dishes away or folding clothes is painful. I wish I was lazy sometimes (ha). I keep telling myself keep a good attitude, find something to laugh at, even if it is myself. I want my old life back, want ot play ball with my girls, clean my windows, heck I wont even complain about scrubbing the foors, which I hate. I have been real quite since the doctors opinion, have been avoiding people, you know? Heck what do you say? I told my husband he is not to discuss my condition or meds with anyone, I have seen peoples reactions to CPers & I will tell you I would loose it with anyone & their stupid uneducated opinions. So easy for them to talk. I have already kind of lost it with my husband who of course does not like the meds, told him if he wants to vomit & all that good stuff on a daily basis due to the pain be my guest but I will not go back to that for anyone. I am so careful with meds I am undermedicating, I know it, but always have to worry about obtaining the refills. Next call I am telling them I am taking them if need be, according the the instructions 1-2 every four to six hrs. On days like today no more waiting in pain all day. I try to stay at no more then 3 all day with motrin in between, not working anymore, & the compound cream, I need a different muscle relaxer to. I will try the skelaxin again but did nothing before surgery. I have some, so might as well try them. I'll tell you I will not rest easy till I am in PM.
Don't worry I am listening to your advice, heck where would I be with out you? I am just trying to be patient. I asked the osteo about the RSD but she pretty much just blew it off. She is really nice, every doctor has there specility & that is not her area. Let me know what you think about whether to try to get into the surgeon or just request the start of getting into pm via phone, I should probably try to get in, to many questions & I am worried about the shoulder, perhaps I can get into pt when I get the right PM, what do you think? Talk to you soon, Sammy
