Guest guest Posted January 23, 2001 Report Share Posted January 23, 2001 a: I too have short term memory loss, Dr. Lawson says it is associated with RA for not getting enough rest and FM. It does get frustrating, I write notes but then forget to take them with me or forget where I put them.....I try to rest each afternoon and it does help. Of course, I don't have small children at home and it is easier for me. Jan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2001 Report Share Posted January 23, 2001 a, Have you ever heard of a child having FM. The more i read about FM from all of you and seeing what (jason's mom) goes through, i see some of the similiarities in . Sometime he complains that his muscles hurt in his thighs and arms. Some times its almost impossible to give him his injection. He also is very forgetful which i thought was normal kid stuff or that he was just playing it up which he is good at. I mean sometimes he seems to use his illness to get away with things which the dr says is normal for children with a illness but iam wondering if its something else cause most of the time he just seems different then when he is playing it up. I can tell when he isn't telling me the truth. an example of him forgetting: he and his brother were fighting over the big screen tv in the living room. had come out of his room and turned the channel while his brother was watching a show. I said jesse why don't you just watch tv in your room. he told me that he forgot they had a tv in there. They just got it for christmas. Anyway he seemed embrassed and try to cover it all up by saying jake always got to watch what he wanted on the big screen. When and go back pensacola i will ask him if its possible for a child to have it but i wanted your imput too. seems so young to have FM but then again he seems to young for arthritis too. I just want to know so that i can do the best for him that i can. shelly Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2001 Report Share Posted January 23, 2001 Good afternoon Barb. Sorry your house got hit with the flu. I hope everyone is feeling better. It may be a good idea to let your doctor look at that lymph node. I hope you get your homeschooling caught up. I can imagine it is a lot of work, but it is worth it. I also have a bad memory, and it seems to be getting worse. Do you have FM too? I don't think memory problems are associated with RA, but many people with RA also have FM. Are you still seeing improvements from Remicade? Are you on your 3rd treatment? is doing ok thanks. I am blessed to have such a great guy. Sometimes I wonder how he puts up with all my problems. I hope you have a good day. a ----- Original Message ----- From: Kendall <bbkendall@...> < egroups> Sent: Monday, January 22, 2001 8:42 PM Subject: [ ] Good Morning a > Good Morning a, > just stopped in for a minute to say thanks again for all the info. We have > had the flu here. Mines been weird, just muscle aches down the back side of > me and I feel a little off. oh ya, have a swollen, hard lymph node under > chin on left. I have a busy week, need to catch my daughter up in school. > Homeschooling's great, but it's alot of work when they are sick and we have > to play catch-me-up!! > > I hope you're feeling well. How's ? I think you two are together, I get > so confused sometimes, I wish I could blame in on fibro fog, but no such > luck. I have noticed a large decrease in memory since having RA. Anyway, > just wanted to say good morning!! > Barb in CA > -----Original Message----- > From: a <aA@...> > egroups <egroups> > Date: Tuesday, January 23, 2001 8:29 AM > Subject: [ ] Today's Topic: Is Caffeine Bad For Bones? > > > >January 23, 2001 > >NUTRITION NEWS FOCUS > > " Nutrition news is important. We help you understand it! " > > > >Today's Topic: Is Caffeine Bad For Bones? > > > >Some, but not all, studies have found caffeine increases excretion of > >calcium in the urine. Most previous experiments have studied bones > >of postmenopausal women. A new study looked at 177 young adult women > >at a university in the U.S. and found average caffeine intake of 100 > >mg a day. > > > >Since many factors are known to influence bone density, these were > >adjusted for statistically. After adjusting for height, body-mass > >index, age at menarche, calcium intake, protein consumption, alcohol > >intake, and tobacco use, caffeine did not predict bone mineral > >density of the hip or spine. No source of caffeine (coffee, tea, > >cola) was associated with lower bone density. The article appeared > >in the November 2000 issue of Preventive Medicine. > > > >HERE'S WHAT YOU NEED TO KNOW: There seemed to be a > >decrease of density of the spine with high caffeine intake only when > >combined with low calcium intake. However, there was no effect on > >the hip. Some studies have found a detrimental effect of high > >caffeine intake on bone density in older women, but the majority of > >studies have not. Remember that this type of study is limited in its > >ability to show cause and effect. > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2001 Report Share Posted January 24, 2001 a: Thanks for understanding. Had a relatively good night last , slept fairly well, unfortunately my poodle had his days and nights mixed up and wanted to play....just like a child. I see the dr today again, hopefully, he will give me some marvelous insight and solve it all...ha,ha.... anyway, hope you have a good day, will keep you all in my thoughts. jan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2001 Report Share Posted January 24, 2001 Dear all in the Group: Shirley from Wyoming still suffering severely, went back to Dr. today, still have high white blood count of over 14,000 and normal is about 700, they do not know what to do with me the rheumatologist can't see me until Fri. so went to reg. Dr. today, evry joint in my rheumatoid body hurts severely, my husband has to help me up and down and I cry all the time, don't know what that is from, maybe depression and effects of the pain medications. The rheumatologist wnats to start me on remmicade or bump the prednisone up over 60 and I amafraid of that, please anyone let me know how you feel about remmicade, as I am at my whits end, can't function and can't stnad the pain any longer, they talk about morning stiffness, well it is not stiffness, IT IS PAIN< , and morning, huh, it lasts all day and night, even with the pain patch and pain pills and now they gave me antiinflamitory pills today, it only just takes the edge off, and I sleep in 15 to 20 minute intervals. Please anyone with any news on bumping prednisone up high or getting on remmicade let me know what you think and is the remmicade working? Love and prayers to all of you PS: I couldn't even go to physical therapy today (had rotator cuff surg), had to cancell my therapy as I am in just too much pain to get on the CATC bus and go to therapy, plus they don't just work one side of my body for the surgical shoulder I have to uto both sides and I can't even raise my other arm so thought it would v be best to rest today. Love and Prayers to all ov of you and please pray for me, this has been a God send Group for me to belong to, it has helped me so much. Shirley from Wyoming Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2001 Report Share Posted January 24, 2001 Jan, Probably the lack of sleep from the pain of RA causes FM. That may be why so many of us with arthritis wind up with FM. The constant pain increases the stress level, which also is probably a contributing fact. I hope as pain meds improve and doctors aren't so reluctant to treat pain, less people will develop FM. Whenever I don't sleep, I have a much higher pain level. It is hard to concentrate on anything when in pain. a ----- Original Message ----- From: <burnettaljanb@...> < egroups> Sent: Tuesday, January 23, 2001 12:22 PM Subject: Re: [ ] Good Morning a > a: > > I too have short term memory loss, Dr. Lawson says it is associated with RA > for not getting enough rest and FM. It does get frustrating, I write notes > but then forget to take them with me or forget where I put them.....I try to > rest each afternoon and it does help. Of course, I don't have small children > at home and it is easier for me. > > Jan > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2001 Report Share Posted January 24, 2001 Shirley: So very sorry to hear of your flare-up. I have, in the past had to bump up Prednisone to 65 mg per day. I was not pleased with it but I guess it eventually did help. At times like this, we need to trust our drs. and believe they have our best interest in heart. As for the pain, I wish with all my heart someone could wave a magic wand and make it go away. I am going through a flare-up myself and the Ultram 50.. 2 q hrs, didn't help, Vioxx, tears up my stomach and doesn't really help that much. I'm taking Lortab now, cautiously, as I have a hx of substance abuse in the past. I try to alter heat and cold packs and just rest as much as I can. I am scheduled to start Remicade once I work out the fees with my budget,etc so can offer no advice regarding that. I do know that if it wasn't for the Lord giving me the daily strength to deal with the pain I don't know what I would do, I cry too from the pain, get depressed, that's normal to a degree. Keep talking about how you feel to those of us who understand. I'm sending you Psalm 68:19, to comfort you. I will pray for you and keep you in my thoughts. Remember, you are not alone... Jan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 24, 2001 Report Share Posted January 24, 2001 ouch!!!! i hope your doc figures this out soon... rhoda --- Edmis3@... wrote: > Dear all in the Group: Shirley from Wyoming still > suffering severely, went > back to Dr. today, still have high white blood count > of over 14,000 and > normal is about 700, they do not know what to do > with me the rheumatologist > can't see me until Fri. so went to reg. Dr. today, > evry joint in my > rheumatoid body hurts severely, my husband has to > help me up and down and I > cry all the time, don't know what that is from, > maybe depression and effects > of the pain medications. The rheumatologist wnats > to start me on remmicade > or bump the prednisone up over 60 and I amafraid of > that, please anyone let > me know how you feel about remmicade, as I am at my > whits end, can't function > and can't stnad the pain any longer, they talk > about morning stiffness, well > it is not stiffness, IT IS PAIN< , and morning, > huh, it lasts all day and > night, even with the pain patch and pain pills and > now they gave me > antiinflamitory pills today, it only just takes the > edge off, and I sleep in > 15 to 20 minute intervals. Please anyone with any > news on bumping > prednisone up high or getting on remmicade let me > know what you think and is > the remmicade working? Love and prayers to all of > you > PS: I couldn't even go to physical therapy today > (had rotator cuff surg), > had to cancell my therapy as I am in just too much > pain to get on the CATC > bus and go to therapy, plus they don't just work one > side of my body for the > surgical shoulder I have to uto both sides and I > can't even raise my other > arm so thought it would v be best to rest today. > Love and Prayers to all ov of you and please pray > for me, this has been a God > send Group for me to belong to, it has helped me so > much. > Shirley from Wyoming > > > [Non-text portions of this message have been > removed] > > > Chat room: chat/ > Web pages for our group: > http://rheumatoid.arthritis.freehosting.net/ > http://www.rasupport.webprovider.com/ > Change subscription options: > > ===== contact: ICQ 14328968 , plantjunkie page http://www.angelfire.com/on3/rhodasbusinesspage _______________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 25, 2001 Report Share Posted January 25, 2001 Hi Shirley, I tried remicade and it did help. I didn't notice anything with the first infusion. I had trouble sitting for the three hours. The second infusion I could sit with no problem and when I went to leave I could move my hand better. Rainy Sue has had a lot of luck with it. I would love to take it again but they are not going to let me. My immune system is in bad shape, so I can't take it. I would tell you though that it is well worth you trying it. It was nice after the second time, I really could move around better. Hope this helps. Me Mom ---------- > From: Edmis3@... > egroups > Subject: Re: [ ] Good Morning a > Date: Wednesday, January 24, 2001 4:51 PM > > Dear all in the Group: Shirley from Wyoming still suffering severely, went > back to Dr. today, still have high white blood count of over 14,000 and > normal is about 700, they do not know what to do with me the rheumatologist > can't see me until Fri. so went to reg. Dr. today, evry joint in my > rheumatoid body hurts severely, my husband has to help me up and down and I > cry all the time, don't know what that is from, maybe depression and effects > of the pain medications. The rheumatologist wnats to start me on remmicade > or bump the prednisone up over 60 and I amafraid of that, please anyone let > me know how you feel about remmicade, as I am at my whits end, can't function > and can't stnad the pain any longer, they talk about morning stiffness, well > it is not stiffness, IT IS PAIN< , and morning, huh, it lasts all day and > night, even with the pain patch and pain pills and now they gave me > antiinflamitory pills today, it only just takes the edge off, and I sleep in > 15 to 20 minute intervals. Please anyone with any news on bumping > prednisone up high or getting on remmicade let me know what you think and is > the remmicade working? Love and prayers to all of you > PS: I couldn't even go to physical therapy today (had rotator cuff surg), > had to cancell my therapy as I am in just too much pain to get on the CATC > bus and go to therapy, plus they don't just work one side of my body for the > surgical shoulder I have to uto both sides and I can't even raise my other > arm so thought it would v be best to rest today. > Love and Prayers to all ov of you and please pray for me, this has been a God > send Group for me to belong to, it has helped me so much. > Shirley from Wyoming > > > Quote Link to comment Share on other sites More sharing options...
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