Guest guest Posted November 16, 2004 Report Share Posted November 16, 2004 Hello! I have not posted anything in awhile but I do read and learn a lot from all of you. Thanks for all the information. My son is actually doing great over all. He only has a few days left on Orapred. He has done fine through the taper. He is on Methotrexate and will go on Nambumetone when he goes off the Orapred this Friday. Here is my first dilema. My son will run around just fine, then when I need him to say walk to the bath tub he says that his legs hurt and he wants me to carry him. He just seems to be doing so well most of the time now that we wonder if sometimes he is trying to take advantage of the situation. The other day in a store he did not want to walk one minute because his legs hurt but the next minute he was running after his sister. He told me that they were hurting still he was just not complaining about it. I think in that situation he just did not want to walk. However, I know that after a lot of running around his legs do still seem to get sore. We are just having trouble distinguishing from real pain and sympathy pain. Dilema # 2 I will not bore you with all the details but the bottom line is that I am very frustrated with our PT and OT visits. What should I expect from PT and OT visits? I really do not think that they have benefited us very much especially for the amount they have charged. They charge twice as much as the pediatric rheumatologist. ( Sorry to complain but I could not believe the charges.) The doctor asked them to give us a home exercise program, information on joint protection, etc. but I am not really sure that we got all that. The PT gave us a few excercises but the OT said we really do not need to do them because at his age he will move around enough. As far as joint protection she told us to take breaks when traveling long distances in the car and when he colors a lot. That was it. When your children are doing O.K. except for maybe a little pain at the end of a very active day what type of exercises do you do, if any? What activites do you keep your children from doing, if any? Do you have any suggestions for questions that I should ask the PT and OT? What do you do for joint protection? I appreciate any advice/suggestions you can give. Thanks, Christi (Logan, systemic, 4) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 17, 2004 Report Share Posted November 17, 2004 Hi Christy, Can't help with dilema #2 but #1 I have my own stories. was 4 when Enbrel was added to the mix of drugs and it changed everything.He was able to do everything any other child could do.He finaly breezed through the pred tapers instead of being slamed with severe pain and swelling. He would play hard every single day then in the evening he would creep on his belly saying he couldn't walk.Something would catch his attention and he would be up and out of there.This happened every single night and we thought he was faking because duiring the day he was fine.At his next trip to the rheumy we brought this matter up and how we thought he was faking it because he wasn't getting all the sick child attention anymore.The rheumy tweaked his Enbrel dose just a smidgen and the belly creaping never happened again. realy was haveing pain but he was also being overdramatic. My guess is Logan is haveing some minor pain and not faking it but he is a bright boy and useing it to his advantage.I would just very calmly tell him that you understand that he is haveing pain but that he can walk.If he insists on crawling then let him crawl but no more carrying him.That is his reward and thats what he is looking for.Try and help him understand how lucky he is that he can walk now and how happy you are for him.Try and find some special time together because my gut says he just misses the attention and knows that crawling and saying he can't walk gets it.Ok off my Dr.Phil soap box,lol Hugs Becki and 6 systemic Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 17, 2004 Report Share Posted November 17, 2004 Hi Christi...all kids are different and so are their reactions and I can only speak for myself. When I was a child say 4-10 I did not fake my pain or my ability or lack of. If anything when I was moving well and appearing to be fine it was me trying to forget I had pain I am still guilty of this at 39! If I say it hurts now just like as a child then it hurt. Now as I got older things may have changed but not much. I did learn to use the arthritis as I got older but it was not often. I have since realized that often when I thought I was " faking " it, there were some underlying issues other than simply not wanting to do something. Often there was pain but becoming so use to the pain makes it harder to see (and feel) sometimes....even now I may move slower or have more of a limp which is obvious before I even recognize the pain....I am hoping some adults who have been there can chime in with me on this one..hugs to all! Donna Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 17, 2004 Report Share Posted November 17, 2004 It does seem sometimes that they must be faking the pain whe they are whining one minute and running the next. It isn't always the case, however. Some things just have higher priority for them. Just remember that to a 4 yr old, chasing a sister is more important than walking to the bathtub lol It is easier to put up with pain when you're doing something you want to do. Both my hubby and I have joint problems that flare up in similar circumstances as 's jra, so we often know when he will have a bad day. I do still carry him at times. He is 60 lbs now, so it's not easy, but I do what I can when I know he's hurting. We also have a jogging stroller rated for 75 lbs that we use for long trips, like to the zoo. It was expensive, but worth it. I don't have an answer for your 2nd dilemma. has not been prescribed even any exercises. His dr says basically he'll move around enough just playing. Misty and (6, systemic) Quote Link to comment Share on other sites More sharing options...
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