Guest guest Posted January 8, 2002 Report Share Posted January 8, 2002 Eleanor, Years ago, before I was truly diagnosed, I experienced long periods of remission & wasn't on any meds, or at least meds for Stills. My flares each & every time were brought on by an infection of some sort: bacillery dystentry, staph, amoeba, & can't remember the last one. The last one pushed me into a chronic disease pattern though. Perhaps my age & changing hormones has something to do with it being chronic, or maybe eventually it just happens. I don't know why & neither do the doctors. My body was stressed each time though, so in a sense " stress " triggered the flares, but I think you are probably asking about emotional stress. For me, emotional stress has not been the trigger. Blessings, Teri _________________________________________________________________ MSN Photos is the easiest way to share and print your photos: http://photos.msn.com/support/worldwide.aspx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2002 Report Share Posted January 8, 2002 Eleanor, Years ago, before I was truly diagnosed, I experienced long periods of remission & wasn't on any meds, or at least meds for Stills. My flares each & every time were brought on by an infection of some sort: bacillery dystentry, staph, amoeba, & can't remember the last one. The last one pushed me into a chronic disease pattern though. Perhaps my age & changing hormones has something to do with it being chronic, or maybe eventually it just happens. I don't know why & neither do the doctors. My body was stressed each time though, so in a sense " stress " triggered the flares, but I think you are probably asking about emotional stress. For me, emotional stress has not been the trigger. Blessings, Teri _________________________________________________________________ MSN Photos is the easiest way to share and print your photos: http://photos.msn.com/support/worldwide.aspx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2002 Report Share Posted January 8, 2002 Eleanor, Years ago, before I was truly diagnosed, I experienced long periods of remission & wasn't on any meds, or at least meds for Stills. My flares each & every time were brought on by an infection of some sort: bacillery dystentry, staph, amoeba, & can't remember the last one. The last one pushed me into a chronic disease pattern though. Perhaps my age & changing hormones has something to do with it being chronic, or maybe eventually it just happens. I don't know why & neither do the doctors. My body was stressed each time though, so in a sense " stress " triggered the flares, but I think you are probably asking about emotional stress. For me, emotional stress has not been the trigger. Blessings, Teri _________________________________________________________________ MSN Photos is the easiest way to share and print your photos: http://photos.msn.com/support/worldwide.aspx Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2002 Report Share Posted January 8, 2002 Beth, I agree with you that stress must play a major role in this disease, as with stress comes flares (for me). Also, doing stress reduction exercises is a wonderful habit to get into...I would be happy to get into any type of exercise. I have gotten totally out of my routine since the holidays and I need exercise bad. I'm afraid of a flare though because I don't feel really strong right now. I thought I had been flaring but my Primary Care Physician called to say that all my blood work looked good except that my white blood cell count was really high...indicating to him that I have some sort of infection???? It would be the first infection I have had since having Still's. I would almost welcome an infection because to me that means that maybe my immune system is somewhat back to normal. I have not had a cold, infection or even a fever blister since my onset. My immune system has been in such overdrive. Anyway... Much Love, Kim --- eg4@... wrote: > I personally (my opinion only!) believe that after a > stressful event symptoms > can come on strong-but I really believe it is a deep > seated immune or other > problem that causes things to get out of control. I > will also say, that when > I take the time to practice stress reduction > exercises I am really better for > it- I just need to remind myself of that so that I > do them! > > I have always felt that probably everyone has the > potential to get some sort > of disease (don't know if that is right word), but > it is a series of things > that determine whether or not your body comes down > with the illness. > > My grandmother had lupus and I have some speculation > of what caused me then > to come down with an autoimmune illness- like I > said, an outside agent like a > virus or vaccination that pushed my system over the > edge. > > Beth > > > [Non-text portions of this message have been > removed] > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2002 Report Share Posted January 8, 2002 Beth, I agree with you that stress must play a major role in this disease, as with stress comes flares (for me). Also, doing stress reduction exercises is a wonderful habit to get into...I would be happy to get into any type of exercise. I have gotten totally out of my routine since the holidays and I need exercise bad. I'm afraid of a flare though because I don't feel really strong right now. I thought I had been flaring but my Primary Care Physician called to say that all my blood work looked good except that my white blood cell count was really high...indicating to him that I have some sort of infection???? It would be the first infection I have had since having Still's. I would almost welcome an infection because to me that means that maybe my immune system is somewhat back to normal. I have not had a cold, infection or even a fever blister since my onset. My immune system has been in such overdrive. Anyway... Much Love, Kim --- eg4@... wrote: > I personally (my opinion only!) believe that after a > stressful event symptoms > can come on strong-but I really believe it is a deep > seated immune or other > problem that causes things to get out of control. I > will also say, that when > I take the time to practice stress reduction > exercises I am really better for > it- I just need to remind myself of that so that I > do them! > > I have always felt that probably everyone has the > potential to get some sort > of disease (don't know if that is right word), but > it is a series of things > that determine whether or not your body comes down > with the illness. > > My grandmother had lupus and I have some speculation > of what caused me then > to come down with an autoimmune illness- like I > said, an outside agent like a > virus or vaccination that pushed my system over the > edge. > > Beth > > > [Non-text portions of this message have been > removed] > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 8, 2002 Report Share Posted January 8, 2002 Beth, I agree with you that stress must play a major role in this disease, as with stress comes flares (for me). Also, doing stress reduction exercises is a wonderful habit to get into...I would be happy to get into any type of exercise. I have gotten totally out of my routine since the holidays and I need exercise bad. I'm afraid of a flare though because I don't feel really strong right now. I thought I had been flaring but my Primary Care Physician called to say that all my blood work looked good except that my white blood cell count was really high...indicating to him that I have some sort of infection???? It would be the first infection I have had since having Still's. I would almost welcome an infection because to me that means that maybe my immune system is somewhat back to normal. I have not had a cold, infection or even a fever blister since my onset. My immune system has been in such overdrive. Anyway... Much Love, Kim --- eg4@... wrote: > I personally (my opinion only!) believe that after a > stressful event symptoms > can come on strong-but I really believe it is a deep > seated immune or other > problem that causes things to get out of control. I > will also say, that when > I take the time to practice stress reduction > exercises I am really better for > it- I just need to remind myself of that so that I > do them! > > I have always felt that probably everyone has the > potential to get some sort > of disease (don't know if that is right word), but > it is a series of things > that determine whether or not your body comes down > with the illness. > > My grandmother had lupus and I have some speculation > of what caused me then > to come down with an autoimmune illness- like I > said, an outside agent like a > virus or vaccination that pushed my system over the > edge. > > Beth > > > [Non-text portions of this message have been > removed] > > __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2002 Report Share Posted January 10, 2002 In a message dated 1/10/2002 10:10:47 PM Eastern Standard Time, Henbane2@... writes: > Randy had sever excema as a young child. So bad that he couldn't start > kindergarten. The rheumy thinks it is was related or was Still's then. I > need to grill him more on this. > This makes sense to me. When I was first diagnosed with SD, the idiot rheumy I had back then would write JRA on my paper work. I had a skin problem back then too. They called it winter skin back then. I have no idea what it was. Now a days I get the rash, but I don't remember if the rash as a kid was the same as the rashes I get now. The SD rash comes and go. But I do have another form of rash that comes up and when it does, I become lizard woman. It's awful. The dermatologist gave me a special cortisone cream and shampoo that I have to use when that happens. In addition, it also itches like the dickens and if I start to sweat, it really gets agitated. Hopefully, it won't come back for a long time, if ever. It sure won't hurt my feelings. Hang in there. Much love, Terry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2002 Report Share Posted January 10, 2002 In a message dated 1/10/2002 10:10:47 PM Eastern Standard Time, Henbane2@... writes: > Randy had sever excema as a young child. So bad that he couldn't start > kindergarten. The rheumy thinks it is was related or was Still's then. I > need to grill him more on this. > This makes sense to me. When I was first diagnosed with SD, the idiot rheumy I had back then would write JRA on my paper work. I had a skin problem back then too. They called it winter skin back then. I have no idea what it was. Now a days I get the rash, but I don't remember if the rash as a kid was the same as the rashes I get now. The SD rash comes and go. But I do have another form of rash that comes up and when it does, I become lizard woman. It's awful. The dermatologist gave me a special cortisone cream and shampoo that I have to use when that happens. In addition, it also itches like the dickens and if I start to sweat, it really gets agitated. Hopefully, it won't come back for a long time, if ever. It sure won't hurt my feelings. Hang in there. Much love, Terry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2002 Report Share Posted January 10, 2002 In a message dated 1/10/2002 10:10:47 PM Eastern Standard Time, Henbane2@... writes: > Randy had sever excema as a young child. So bad that he couldn't start > kindergarten. The rheumy thinks it is was related or was Still's then. I > need to grill him more on this. > This makes sense to me. When I was first diagnosed with SD, the idiot rheumy I had back then would write JRA on my paper work. I had a skin problem back then too. They called it winter skin back then. I have no idea what it was. Now a days I get the rash, but I don't remember if the rash as a kid was the same as the rashes I get now. The SD rash comes and go. But I do have another form of rash that comes up and when it does, I become lizard woman. It's awful. The dermatologist gave me a special cortisone cream and shampoo that I have to use when that happens. In addition, it also itches like the dickens and if I start to sweat, it really gets agitated. Hopefully, it won't come back for a long time, if ever. It sure won't hurt my feelings. Hang in there. Much love, Terry Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2002 Report Share Posted January 10, 2002 Randy had sever excema as a young child. So bad that he couldn't start kindergarten. The rheumy thinks it is was related or was Still's then. I need to grill him more on this. Anyway, for Randy it was physical stress. He hurt his knee jumping off a stage when he was in his 20's. A musician, showing off. The knee gave him grief on and off over the years. But last Christmas, when he came home from rehearsal in the wee hours of the morning, his knee gave out. He was down on the floor 20 minutes. Well, that was how it started. His symptoms are much different than most of other Still's patients. But indeed, Still's. I have mentioned this before, his rheumy treats 14 Still's patients. We are in the out skirts of Seattle. Seems like a lot to me. Steph Wouldn't be surprised if he needs a knee replacement soon. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2002 Report Share Posted January 10, 2002 Weird, as we talk about the rash. Well, guess who is breaking out! On his behind. Deep rash too. And he wants me to check it out. OWWW! Randy came home looking soo tired, actually the last two days. I asked him if he thought he was in a flare. The rash on the ass, and lethargic behavior. but the plaquenil works. But he is being a total pain in the you now where. No more fevers, or Clyde and wilber, the imanginary friends when he hits 104. This sucks! Steph Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2002 Report Share Posted January 10, 2002 Weird, as we talk about the rash. Well, guess who is breaking out! On his behind. Deep rash too. And he wants me to check it out. OWWW! Randy came home looking soo tired, actually the last two days. I asked him if he thought he was in a flare. The rash on the ass, and lethargic behavior. but the plaquenil works. But he is being a total pain in the you now where. No more fevers, or Clyde and wilber, the imanginary friends when he hits 104. This sucks! Steph Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 10, 2002 Report Share Posted January 10, 2002 Weird, as we talk about the rash. Well, guess who is breaking out! On his behind. Deep rash too. And he wants me to check it out. OWWW! Randy came home looking soo tired, actually the last two days. I asked him if he thought he was in a flare. The rash on the ass, and lethargic behavior. but the plaquenil works. But he is being a total pain in the you now where. No more fevers, or Clyde and wilber, the imanginary friends when he hits 104. This sucks! Steph Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2002 Report Share Posted March 3, 2002 Connie, I've been on Effexor XR 37.5 mg for about two years now. At first, my doc did the same thing by upping the dose to 75 mg. He then upped it to 125 mg! I didn't notice a difference in feeling any different. However, I had awful dry mouth, eyes, and thought I had Sjorgren's. They tested for that and found I didn't have that. Then it dawned on my doc that maybe it was all side effects of the Effexor XR. After I was dropped back down to 37.5 mg, I have had no side effects. The " XR " in the name means " extended release, " so you might want to ask your doc about staying at a lower dose. It does take a while for the drug to build up in your system. Then you will start to see any good or bad effects. All I know is that I wish my doc had just stuck with the 37.5 mg dose and let me stay on that for a while before increasing it. I really didn't like the side effects, especially the nasty " dry mouth. " That's my 2 cents. Hope you find the right dosage for you! All my heart, Jul (lilac_rose@... ) Re: question Hi gang iam back and will be posting or bugging everyone more with my posts.LOL the energy level is getting better every day. I have one question i was on zoloft for depression and that seemed to help but after the insurance quite paying for it its was eithe paxil or prozac and i have heard so many horrror stories regarding the paxil i said pass on it so i tried prozac have been on it a couple months and it didnt seem like it was helping my rheumy said also it was understandable to have the depression i have with everythig that i have been thru since november. so she changed my antidepression meds to Effexor XR starting out at 37.5 ,g then increasing to 75mg in a week. of course after i get it filled my insurance doesnt pay for this one either. This damn HMO is getting to be a big pain in the u know what. If anyone has taken the Effexor XR could you please let me know your sucesss or non sucesss of this drug. Iam back to the shop alsmost full time now the pneumonia set me back about 2 weeks to where i wanted to be so this bad weather came at a great time. i went to the the big dealer show with my hubby for the weekend and we walked 2 days straight i made it barley my legs and body was so run down and hurting it took me a week to recover but it was well worth getting away from home and being with my hubby alone we had a great time. We still have issues but we seem to both be trying to work on them. My mom had to remind me that during a marriage there will be rough patches this is our first in 8 years and u cant just leave and get a divorce because things get bad. You stay and work them out. Especially when you have a good husband like i have. She said thats whats wrong with my generation we dont stick things out when things get tough we just divorce. so we are working on us. just wanted to let everyone know iam alive and well for a change. love connie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 3, 2002 Report Share Posted March 3, 2002 Connie, I've been on Effexor XR 37.5 mg for about two years now. At first, my doc did the same thing by upping the dose to 75 mg. He then upped it to 125 mg! I didn't notice a difference in feeling any different. However, I had awful dry mouth, eyes, and thought I had Sjorgren's. They tested for that and found I didn't have that. Then it dawned on my doc that maybe it was all side effects of the Effexor XR. After I was dropped back down to 37.5 mg, I have had no side effects. The " XR " in the name means " extended release, " so you might want to ask your doc about staying at a lower dose. It does take a while for the drug to build up in your system. Then you will start to see any good or bad effects. All I know is that I wish my doc had just stuck with the 37.5 mg dose and let me stay on that for a while before increasing it. I really didn't like the side effects, especially the nasty " dry mouth. " That's my 2 cents. Hope you find the right dosage for you! All my heart, Jul (lilac_rose@... ) Re: question Hi gang iam back and will be posting or bugging everyone more with my posts.LOL the energy level is getting better every day. I have one question i was on zoloft for depression and that seemed to help but after the insurance quite paying for it its was eithe paxil or prozac and i have heard so many horrror stories regarding the paxil i said pass on it so i tried prozac have been on it a couple months and it didnt seem like it was helping my rheumy said also it was understandable to have the depression i have with everythig that i have been thru since november. so she changed my antidepression meds to Effexor XR starting out at 37.5 ,g then increasing to 75mg in a week. of course after i get it filled my insurance doesnt pay for this one either. This damn HMO is getting to be a big pain in the u know what. If anyone has taken the Effexor XR could you please let me know your sucesss or non sucesss of this drug. Iam back to the shop alsmost full time now the pneumonia set me back about 2 weeks to where i wanted to be so this bad weather came at a great time. i went to the the big dealer show with my hubby for the weekend and we walked 2 days straight i made it barley my legs and body was so run down and hurting it took me a week to recover but it was well worth getting away from home and being with my hubby alone we had a great time. We still have issues but we seem to both be trying to work on them. My mom had to remind me that during a marriage there will be rough patches this is our first in 8 years and u cant just leave and get a divorce because things get bad. You stay and work them out. Especially when you have a good husband like i have. She said thats whats wrong with my generation we dont stick things out when things get tough we just divorce. so we are working on us. just wanted to let everyone know iam alive and well for a change. love connie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 5, 2002 Report Share Posted March 5, 2002 Is my reply going thru? just checking, Melt Re: question > > > > Visit the Still's Disease Message Board > http://disc.server.com/Indices/148599.html > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 5, 2002 Report Share Posted March 5, 2002 Is my reply going thru? just checking, Melt Re: question > > > > Visit the Still's Disease Message Board > http://disc.server.com/Indices/148599.html > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 5, 2002 Report Share Posted March 5, 2002 Is my reply going thru? just checking, Melt Re: question > > > > Visit the Still's Disease Message Board > http://disc.server.com/Indices/148599.html > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2002 Report Share Posted April 14, 2002 Hi gang... Do any of you ever feel foggy in the head to the point where you feel a real pressure in your head that that advil/ aspirin can't relieve? I also get dizzy and spaced out as a result of this. I know I've probably been overdoing it lately, but not sure if this is from my previous Lymes/ chronic fatigue or Stills. Thanks, Eleanor Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2002 Report Share Posted April 14, 2002 Hi gang... Do any of you ever feel foggy in the head to the point where you feel a real pressure in your head that that advil/ aspirin can't relieve? I also get dizzy and spaced out as a result of this. I know I've probably been overdoing it lately, but not sure if this is from my previous Lymes/ chronic fatigue or Stills. Thanks, Eleanor Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2002 Report Share Posted April 14, 2002 Hi gang... Do any of you ever feel foggy in the head to the point where you feel a real pressure in your head that that advil/ aspirin can't relieve? I also get dizzy and spaced out as a result of this. I know I've probably been overdoing it lately, but not sure if this is from my previous Lymes/ chronic fatigue or Stills. Thanks, Eleanor Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2002 Report Share Posted April 14, 2002 Dear Eleanore; I used to feel this way after extremely high fevers. Of course, these days who knows why, lol. I am extremely forgetfull but have been told this can happen because I take an anti-depressent. I hope you mention this to your doctor and have releif soon, thinking of you, Patty Re: question > Hi gang... > Do any of you ever feel foggy in the head to the point where you feel a real > pressure in your head that that advil/ aspirin can't relieve? I also get > dizzy and spaced out as a result of this. I know I've probably been overdoing > it lately, but not sure if this is from my previous Lymes/ chronic fatigue or > Stills. > > Thanks, > Eleanor > > > Visit the Still's Disease Message Board > http://disc.server.com/Indices/148599.html > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2002 Report Share Posted April 14, 2002 Dear Eleanore; I used to feel this way after extremely high fevers. Of course, these days who knows why, lol. I am extremely forgetfull but have been told this can happen because I take an anti-depressent. I hope you mention this to your doctor and have releif soon, thinking of you, Patty Re: question > Hi gang... > Do any of you ever feel foggy in the head to the point where you feel a real > pressure in your head that that advil/ aspirin can't relieve? I also get > dizzy and spaced out as a result of this. I know I've probably been overdoing > it lately, but not sure if this is from my previous Lymes/ chronic fatigue or > Stills. > > Thanks, > Eleanor > > > Visit the Still's Disease Message Board > http://disc.server.com/Indices/148599.html > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 14, 2002 Report Share Posted April 14, 2002 Dear Eleanore; I used to feel this way after extremely high fevers. Of course, these days who knows why, lol. I am extremely forgetfull but have been told this can happen because I take an anti-depressent. I hope you mention this to your doctor and have releif soon, thinking of you, Patty Re: question > Hi gang... > Do any of you ever feel foggy in the head to the point where you feel a real > pressure in your head that that advil/ aspirin can't relieve? I also get > dizzy and spaced out as a result of this. I know I've probably been overdoing > it lately, but not sure if this is from my previous Lymes/ chronic fatigue or > Stills. > > Thanks, > Eleanor > > > Visit the Still's Disease Message Board > http://disc.server.com/Indices/148599.html > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 2, 2002 Report Share Posted May 2, 2002 Elly, please do not feel that you have to come here and apologize for being absent. We all have our problems and reasons why we can't always be reading and responding to posts and everyone, I'm sure, completely understands. Sorry to hear that you were diagnosed with Osteoarthrosis. I hope the pain gets better. Here are a few sites for you to look at: Marilyn a.. 1.. Osteoarthritis (osteoarthrosis) 1.. Osteoarthritis (osteoarthrosis) With age, injury or overuse, cartilage covering articulating surfaces of bones breaks down; underlying bone becomes thickened and distorted, restricting joint movement and sometimes causing episodes of inflammation, http://www.drlockie.com/disease/osteoar.htm a.. 1.. Wiley :: Studies in Osteoarthrosis: Pathogenesis, Intervention, Assessment 1.. Shopping Cart My Account Help Contact Us By Keyword By Title By Author By ISBN By ISSN Wiley > Life & Medical Sciences > Medical Sciences > Endocrinology > General Endocrinology > Studies in Osteoarthrosis: Pathogenesis, Intervention, Assessment http://www.wiley.com/Corporate/Website/Objects/Products/0%2C9049%2C89737%2C00.ht\ ml a.. 1.. Knee products for Osteoarthrosis 1.. Indications: mild strains, sprains, joint swelling and joint pain, subpatellar burstis, meniscus tear, osteoarthrosis, and patellar tendonitis. http://www.kneesupport.com/osteoarthrosis a.. 1.. Arbete och Hälsa 1999:12 Knee osteoarthrosis in relation to physical workload and lifestyle factors - epidemiological s 1.. Arbete och Hälsa 1999:12 Knee osteoarthrosis in relation to physical workload and lifestyle factors - epidemiological studies http://www.niwl.se/ah/1999-12.html a.. 1.. Read Reviews and Compare Prices on The Arthritis Bible: A Comprehensive Guide to Alternative Therapies & Conventional T 1.. Epinions has the best comparison shopping information on The Arthritis Bible: A Comprehensive Guide to Alternative Therapies & Conventional Treatments for Arthritic Diseases Including Osteoarthrosis, Rheumatoid Arthritis, Gout, Fibromyalgia & More. http://www.epinions.com/book_mu-3566332?sp=ink a.. 1.. Thyroid functions in patients with primary deformative osteoarthrosis and laserotherapy treatment efficiency 1.. Thyroid functions in patients with primary deformative osteoarthrosis and laserotherapy treatment efficiency Name L.A. Lepilina, L.R. Gabitova, O.V. Minyaeva, R.G.Kamalova Address Bashkir State Medical University, Ufa, Russia We have observed 34 http://www.icmart.org/icmabs/p82.html a.. 1.. e-MDs | Services | ICD-9 Search | 715 - Osteoarthrosis and allied disorders 1.. e-MDs' ICD-9 Search. 715 - Osteoarthrosis and allied disorders http://www.amt-solutions.com/icd9/715 a.. 1.. ICL-Osteotomies About the Hip for the Prevention and Treatment of Osteoarthrosis (Congress Center Room 202) 1.. American Academy of Orthopaedic Surgeons 1996 Annual Meeting Instructional Course Lectures and Lecture Demonstration Courses Osteotomies About the Hip for the Prevention and Treatment of Osteoarthrosis Course Number: 392 TLD: Three hour Lecture http://www.aaos.org/wordhtml/anmeet96/icl96/392.htm a.. 1.. THE MERCK MANUAL, Sec. 5, Ch. 52, Osteoarthritis And Neurogenic Arthropathy 1.. This Publication Is Searchable The Merck Manual of Diagnosis and Therapy Section 5. Musculoskeletal And Connective Tissue Disorders Chapter 52. Osteoarthritis And Neurogenic Arthropathy Topics Osteoarthritis Neurogenic Arthropathy Osteoarthritis http://www.merck.com/pubs/mmanual/section5/chapter52/52a.htm a.. 1.. Lei Wei: Doctor´sThesis from Karolinska Institutet 1.. search / help / search staff Doctor´s Thesis from Karolinska Institutet Wei, Lei Guinea pig osteoarthrosis: morphological and biochemical studies Thursday, February 25, 1999 Thesis Frame Original [PDF] Acrobat Reader ISBN: 91-628-3361-8 Diss: 99:37 http://diss.kib.ki.se/1999/91-628-3361-8 a.. 1.. Wheeless' Textbook of Orthopaedics 1.. Main Menu Home Page Glenohumeral osteoarthrosis. A late complication of the Putti-Platt repair. Hawkins-RJ; Angelo-RL J-Bone-Joint-Surg-Am. 1990 Sep; 72(8): 1193-7 Osteoarthrosis of the glenohumeral joint is a potential late complication of anterior http://www.medmedia.com/lib6/12.htm a.. 1.. Wheeless' Textbook of Orthopaedics 1.. Main Menu Home Page Heterotopic bone after hip arthroplasty. Defining the patient at risk. Ahrengart L. Lindgren U. Clinical Orthopaedics & Related Research. [JC:dfy] (293):153-9, 1993 Aug. Periarticular heterotopic bone (HB) formation after hip http://www.medmedia.com/a5/129.htm a.. 1.. Knee support for mild strains, sprains and joint swelling 1.. Indications: mild strains, sprains, joint swelling and joint pain, contusion, effusion, infrapatellar, subpatellar burstis, meniscus tear, osteoarthrosis, patellar tendonitis, per anserinus tendonitis, prepatellar tendonitis, and sprain. http://www.kneesupport.com/bioskin/universal_buttress.htm question Dear Friends, I'm so sorry I haven't been posting lately,I have been in alot of pain for some time now,which isn't a good excuse for ignoring my friends,but hopefully explains a little and I ask you to forgive me.Welcome to all the new members and I am so glad you found us,but so sad you needed to. Now on to my question,as some of you know I have been having a problem with my left arm and shoulder.I had an Mri two weeks ago and the diagnosis was Osteo-Arthrosis of the ACjoint.I was wondering if anyone else has been diagnosed with this and what the treatment(s) is? I am totally in the dark and only hope it's fixable!I have to make an appt. with an Orthopedic Doc as soon as possible according to my Rheumy. I've had physical therapy which my rheumy said only irritated the problem.So any input into this problem would sure be helpful.Thanks for listening and try to have a physically and mentally happy day. Love Elly Quote Link to comment Share on other sites More sharing options...
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