Guest guest Posted September 30, 2004 Report Share Posted September 30, 2004 Sandy, Have you ever been tested for autoimmune diseases such as lupus, rheumatoid arthritis, autoimmune thyroid disease, etc.? Most autoimmune diseases can cause debilitating fatigue and many cause joint pain. When you say your fnp is going to some nuclear tests, I assume you mean she is going to do a blood test called an ANA or anti-nuclear antibody along with probably some of the 'sub' antibody tests. Those can help to determine if you have an autoimmune disease (or maybe multiple autoimmune diseases). Hang in there as many autoimmune diseases are quite illusive and hard to diagnose. In answer to your question, NO - you don't sound depressed to me, but I'm not a doctor. However, I would not be quick to let them simply chalk your new symptoms off as depression without thoroughly ruling out other potential problems. Many autoimmune diseases can be improved drastically with the right medications. I have lupus and without taking plaquenil (an anti malaria drug that helps with the joint pain, fatigue, and skin rashes that go with lupus) my fatigue and joint pain are unbearable. I still have a lot of fatigue, but the plaquenil makes it much better! take care and listen to your body - you know it better than anyone else. W Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2004 Report Share Posted October 1, 2004 Sandy, I am glad I was able to help offer things that your doctor should look for. I hope you get some answers soon. The debilitating fatigue is often worse than dealing with pain. Even now, when I am so tired that even showering is tough, I sometimes think that maybe I am just being lazy and if I pushed myself I'd be able to all I used to do. The logical side of my brain knows that if I do not rest when my body screams for rest, I will end up in the hospital. However, there's that other side that says 'the doctors are all wrong- there's really nothing at all wrong with you except that you are lazy'. I'm much better at pushing that away now than I used to be, but, still it creeps in my head now and again. Must be those red roots of my hair or maybe the fact that until I got sick I thought that I could control everything. Accepting limitations is hard for everyone, but it is especially hard for those of us who tend to be perfectionists and think that we are responsible for the world. W Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 1, 2004 Report Share Posted October 1, 2004 Sandy, have you started any new medications recently? Some medications have sore joints as a side effect. Zocor is one such medication. Also, have you looked into the option that you may have arthritis. It can start fairly young you know. I have arthritis in both hands and I'm only 34. For the tiredness, have you been tested for anemia? If you've already thought of these things, my apologies, I'm just trying to think of anything that deals with these symptoms and I'm not a doctor, so I'm sure i only see the obvious things. What about mono? The other option, if you are that tired, has anyone ever thought to test you for sleep apnea (stop breathing in the middle of the night)? I was that tired to at one point and my mom, who just found out she had sleep apnea, went with me on a trip somewhere and she said she thought I had stopped breathing briefly during the night. So, I got test, and yep, I had it. So, I got my CPAP machine (helps you provide air throughout the night), and the difference was amazing. Before, I had been so tired that at one point, I started to fall asleep in mid talk. Not Kidding, it really happened. I was with a coworker at the time. Have you thought of possibly seeing the doctor and not the FNP? Sometimes NP's miss things that a doctor would think of. And Sandy, it's healthy to complain once in a while too. Kimber -- Kimber Vallejo, CA hominid2@... Note: All advice given is personal opinion, not equal to that of a licensed physician or health care professional. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 2, 2004 Report Share Posted October 2, 2004 Sandy, I can have empathy for you, because I am in the same situation. I do know that what you discribe like me is a form of depression and maybe not true clinical depression as defined by textbook. I am a nurse and have cystic fibrosis in addition to the cp. They can not seem to get my enzymes down lipase still 1400 and amylase 400 and I continue to have difficulty in eating and pain with nausea. I am very weak, tired, and fatigued althought most of mine is due to my staph and pseudomonous infections that have not cleared since May. I am on Zoloft and fought it for a long time. Initially, it really helped then they had to back up the dosage and it is less helpful now. Once they get me back up there I'm sure I will feel better. I can not tell you what to do but yes you do have the right to feel as you do but I know at 50 and having struggled with cf for all those years that you need to listen toyour body and your physicians for the needed help and trust in the Lord for all else. I will pray for you and please write back. Deb with cp and cf. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 2, 2004 Report Share Posted October 2, 2004 Sandy, sounds like you need to get another doctor if she continues to push the anti-depressants and the doctor is such an ass. A test to see if the thyroid mediction is working won't tell anyone if it is causing joint pain as a side effect, only that it's doing what it's supposed to be doing. A medication can be doing what it's supposed to AND cause severe side effect that no one would ever want.. Have you checked the listed side effects online at http://www.rxlist.com ? Please check the medication on there, it will only take a few minutes of your time. At this point, I don't trust the FNP to check up the listed side effects, just because the medication IS working and she doesn't want to look for a new medication. I also saw that you thought it might be chronic fatigue syndrome. That sounds like a definite one to look into as well. As for your sore joints, has your FNP looked into fibromyalgia? It also tends to occur with Chronic Fatigue Syndrome. Unfortunately, I don't know personally of any other things to suggest, but if this FNP and doctor aren't working out for you, get another one. Don't feel bad about posting, that's what we are here for, to help and support people through any problems they are having, answer any questions, etc. And since you are in the group we are here to help you in any way we can, even if it's to vent. I just wish I could be of more help. Kimber -- Kimber Vallejo, CA hominid2@... Note: All advice given is personal opinion, not equal to that of a licensed physician or health care professional. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 4, 2004 Report Share Posted October 4, 2004 Sandy, I can understand that you don't want to have to re-establish yourself with a new doctor. I also understand what you mean about some doctors only believing what they want to. I'm sorry you still have all those symptoms still. I'll be waiting to hear what happens on wednesday and what the FNP says with your friend there. Kimber -- Kimber Vallejo, CA hominid2@... Note: All advice given is personal opinion, not equal to that of a licensed physician or health care professional. Quote Link to comment Share on other sites More sharing options...
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