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Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
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#1 | ||
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Junior Member
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I think it is almost impossible for anyone to understand the pain and limitations we go through on a daily basis. I know even I struggle with it. One day I can do a task the next day I am unable too. One of my biggest struggles have been learning and accepting my limitations I now have.
I know I found myself saying why can't I just do this or that and felt deflated when I was unable to do the thing I wanted. May it be taking my daughter to the park or even going for a small walk around the block. It felt like I was not able to do anything at all and why bother trying anything else.... but I am learning that yes, I may not be able to do what I wanted that day...but it does not mean I can't do anything at all. Instead of going to the park maybe I can manage to set up an obstacle course in my living room for my daughter and I can watch and cheer her on... or instead of that walk I so wanted...maybe I can sit on my front porch and still get the fresh air I wanted and enjoy the nice weather. I guess my point is that your daughter needs to understand that maybe you can not do the things you use too...but instead to appreciate the things you can do. Depending on how old the grand baby is... maybe you can read a stories over the phone to them when you are unable to visit? Or now a days even skype to them. ![]() We may not have the life we want...but that does not mean we still cant have a good quality of life for ourselves! Don't let your limitations make you think you are not holding up your end of being a good grandparent...as I am sure you are a wonderful one.... just when we are faced with limitations we are we just have to be a bit more "creative" to achieve some of the things we would like to do. Take care, Karen (just noticed I repeated a lot of what Sonny had said...sorry didn't read the reply's... Guess great minds think a like Sonny ![]() |
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"Thanks for this!" says: | RSDjaded (05-28-2011) |
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#2 | ||
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Member
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[QUOTE=cndangel;774428]I think it is almost impossible for anyone to understand the pain and limitations we go through on a daily basis. I know even I struggle with it. One day I can do a task the next day I am unable too. One of my biggest struggles have been learning and accepting my limitations I now have.
I know I found myself saying why can't I just do this or that and felt deflated when I was unable to do the thing I wanted. May it be taking my daughter to the park or even going for a small walk around the block. It felt like I was not able to do anything at all and why bother trying anything else.... but I am learning that yes, I may not be able to do what I wanted that day...but it does not mean I can't do anything at all. Instead of going to the park maybe I can manage to set up an obstacle course in my living room for my daughter and I can watch and cheer her on... or instead of that walk I so wanted...maybe I can sit on my front porch and still get the fresh air I wanted and enjoy the nice weather. I guess my point is that your daughter needs to understand that maybe you can not do the things you use too...but instead to appreciate the things you can do. Depending on how old the grand baby is... maybe you can read a ![]() stories over the phone to them when you are unable to visit? Or now a days even skype to them. ![]() able to do more... you will. We may not have the life we want...but that does not mean we still cant have a good quality of life for ourselves! Don't let your limitations make you think you are not holding up your end of being a good grandparent...as I am sure you are a wonderful one.... just when we are faced with limitations we are we just have to be a bit more "creative" to achieve some of the things we would like to do. Take care, Wanna hear something funny?...Oh btw... Your bestest buddy card I sent you...well, just so you know..I got that and sent it bf I got myself in the dog house...timing just worked out that way...good think huh? Karen [Quote] Dear Cindi, I had a real pretty reply going out to you this morning... My suggestion was also using the skippe on the computer.... And never worry as this is such a double edged sword with our loved ones...as they have trouble admitting to our illness cuz their hearts won't let them... We have to hold in there together and share small doses, often of our world with them... None of this is nice for us or them.... You are in my prayers.... Hugz, Kathy |
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#3 | |||
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Senior Member
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I know exactly what you mean...the limitations are SO frustrating and it is hard to explain to people what you are going through...especially because to a lot of people many of us "look fine." When I first got the diagnosis of CRPS...it was so frustrating going through the process of relearning to walk at age 26. I mean...seriously...I have been walking since I was a year old and now I had to retrain my body how to do it. And then there are the things like going up and down stairs...can do it...but it's painful and it's SLOW. I hate having to explain to customers at work every time I go into the stockroom that it's going to take me a little while to get something because I have trouble with stairs. I don't want them to think it's an excuse...but I also don't want people to think I forgot about them because it takes a little while. And then there's the stupid stuff like holding open a door with my foot or pushing a drawer shut with my foot...never gonna happen and I feel like an idiot every time I want to do those things that come so naturally to me. And then there's the simple matter of having to ask for help to do things that I used to be able to do perfectly will on my own before like lift something heavy or move a fixture/furniture. I used to be SO independant before and now I always have to ask for help.
Of course now I REALLY have to ask for help because now I can't even walk at all...but I can crawl. I spent a couple of months just on the couch...and that got old REALLY fast. So now I have a relay of rolling chairs set up on the wood/tile floors is different rooms. I have to crawl everywhere else if I want to get around...talk about frustrating. I love to cross stitch...but it hurts to move my arms or to lean back against the couch like I used to. So I had to figure out a new way to do it where I sit in the kitchen at the table, prop the stitching frame up on the table and my elbow on the arm of the chair so that I don't move as much. Took a while to figure it out...but I got it down now. And I can't concentrate enough to read books anymore...takes forever to just read a couple of pages when I used to be able to read 500 pages an hour. But now I listen to audio books. It's just awful how this condition robs us of our sense of "normal." It takes a lot of effort and hard work to get back a fraction of what we used to have and even then...some days it's not even possible to have that much. Maybe if you can explain some of those things to your daughter she can understand some of your daily frustration and understand that you are doing the best that you can. There's a quote I have always liked...which I am probably going to butcher...but I think it goes something like: Just because someone doesn't give you what you want, doesn't mean they don't give all they have...or something like that. I think that may be the way your daughter will have to think about your relationship now. Of course you WANT to do more...but you can't. Doesn't mean you don't give her and the baby everything you have to give. |
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