Guest guest Posted June 28, 2006 Report Share Posted June 28, 2006 It must be in the air as I had an attack of rib cage crunches earlier this month. Of course I think my body is just coming up with creative new ways to cause me pain around the time of my cycle. Tomorrow I get tested again for cholesterol levels and thyroid. It certainly sounds like her medications are helping her. Sounds like she was having a flare which sometimes takes awhile to recover from. When I had my flare it took about a week to recover, once I got out of the hospital. Shandi [ ] Update on rib cage pain My daughter saw her rheumy Monday and he sent her for a high resolution CT scan of her chest which showed nothing which would cause the pain she has experienced. He thinks her pain was part of an overall flare she has experienced because of all the stormy weather these past several days here on the east coast. She is feeling a bit better today. But we got some great news I think. He sent her for blood work Monday and her RF which was 405 back in February is now 33. Her sed rate which was something like 86 in February is now 9. This is encouraging to me. It should be, right? Lori Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 28, 2006 Report Share Posted June 28, 2006 Lori, this sounds extremely encouraging, I am so happy to read your news. Hugs June ----- Original Message ----- From: Lori Maynard My daughter saw her rheumy Monday and he sent her for a high resolution CT scan of her chest which showed nothing which would cause the pain she has experienced. He thinks her pain was part of an overall flare she has experienced because of all the stormy weather these past several days here on the east coast. She is feeling a bit better today. But we got some great news I think. He sent her for blood work Monday and her RF which was 405 back in February is now 33. Her sed rate which was something like 86 in February is now 9. This is encouraging to me. It should be, right? Lori Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 28, 2006 Report Share Posted June 28, 2006 Lori, I am so happy to hear such wonderful news about your daughter. I was praying that she would be okay. Hugs Lori Maynard <lorimaynard@...> wrote: My daughter saw her rheumy Monday and he sent her for a high resolution CT scan of her chest which showed nothing which would cause the pain she has experienced. He thinks her pain was part of an overall flare she has experienced because of all the stormy weather these past several days here on the east coast. She is feeling a bit better today. But we got some great news I think. He sent her for blood work Monday and her RF which was 405 back in February is now 33. Her sed rate which was something like 86 in February is now 9. This is encouraging to me. It should be, right? Lori Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 28, 2006 Report Share Posted June 28, 2006 Great news, Lori. Yes, you should be encouraged. I'm hoping that she will continue to improve. Sue On Wednesday, June 28, 2006, at 08:11 PM, Lori Maynard wrote: > She is feeling a bit better today. But we got some great news I > think. He > sent her for blood work Monday and her RF which was 405 back in > February is > now 33. Her sed rate which was something like 86 in February is now 9. > This is encouraging to me. It should be, right? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 28, 2006 Report Share Posted June 28, 2006 Hi, new here. Are you talking severe muscle spasms around the rib cage? I get those and they are frightening! The first time, it happened while I was in the tub and I couldn't breathe! I saw my rheumatologist today and he was NOT helpful!! He doesn't think this is RA since my Sed rate is 11. He thinks this is fibro. Now my ANA is >160 but he isn't sure about Lupus. My ortho thinks this may all be MS, but the MRI of the brain doesn't show big enough lesions..........I don't really care what the heck they call it, but I would like to be able to control my pain!!! For the past 19 days I've had a nerve in my arm that is giving me EXTREME pain. Ortho put me on a prednisone pack and it didn't even touch the pain. I was still taking 2 Celebrex each day, a muscle relaxer and Tylenol 3 and none of it stopped the pain. The easiest way to describe it is to hit your funny bone and have that pain continually!! I could literally see the muscle jumping in my arm and can't pick up anything with my left hand. The rheumy told me to just take a muscle relaxer and it should help..........well it hasn't in the last 19 days!! I just had a huge blood work up with an oncologist and a lymph node biopsy (which was neg for lymphoma) but did show I have the anti bodies for EBV. The rheumy was suprised by the negative biopsy but said it should be redone in about 6 months. Do any of you all have any insights? I am sick of waking up with pain every day and not knowing which body part is not going to work! Heck, I won't even be 40 til next month. Sorry, I didn't mean to go on and on, just having a really rough day. Hugs [ ] Update on rib cage pain My daughter saw her rheumy Monday and he sent her for a high resolution CT scan of her chest which showed nothing which would cause the pain she has experienced. He thinks her pain was part of an overall flare she has experienced because of all the stormy weather these past several days here on the east coast. She is feeling a bit better today. But we got some great news I think. He sent her for blood work Monday and her RF which was 405 back in February is now 33. Her sed rate which was something like 86 in February is now 9. This is encouraging to me. It should be, right? Lori Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2006 Report Share Posted June 29, 2006 I had the same problems. Had an mri of my spine and found I had bulging discs. Pressing on nerve. I was put on percocet and within two days was in no pain. Was told to do stretching only. In two weeks I was able to stop percocet. Good Luck Bickford <Bickfordla@...> wrote: Hi, new here. Are you talking severe muscle spasms around the rib cage? I get those and they are frightening! The first time, it happened while I was in the tub and I couldn't breathe! I saw my rheumatologist today and he was NOT helpful!! He doesn't think this is RA since my Sed rate is 11. He thinks this is fibro. Now my ANA is >160 but he isn't sure about Lupus. My ortho thinks this may all be MS, but the MRI of the brain doesn't show big enough lesions..........I don't really care what the heck they call it, but I would like to be able to control my pain!!! For the past 19 days I've had a nerve in my arm that is giving me EXTREME pain. Ortho put me on a prednisone pack and it didn't even touch the pain. I was still taking 2 Celebrex each day, a muscle relaxer and Tylenol 3 and none of it stopped the pain. The easiest way to describe it is to hit your funny bone and have that pain continually!! I could literally see the muscle jumping in my arm and can't pick up anything with my left hand. The rheumy told me to just take a muscle relaxer and it should help..........well it hasn't in the last 19 days!! I just had a huge blood work up with an oncologist and a lymph node biopsy (which was neg for lymphoma) but did show I have the anti bodies for EBV. The rheumy was suprised by the negative biopsy but said it should be redone in about 6 months. Do any of you all have any insights? I am sick of waking up with pain every day and not knowing which body part is not going to work! Heck, I won't even be 40 til next month. Sorry, I didn't mean to go on and on, just having a really rough day. Hugs [ ] Update on rib cage pain My daughter saw her rheumy Monday and he sent her for a high resolution CT scan of her chest which showed nothing which would cause the pain she has experienced. He thinks her pain was part of an overall flare she has experienced because of all the stormy weather these past several days here on the east coast. She is feeling a bit better today. But we got some great news I think. He sent her for blood work Monday and her RF which was 405 back in February is now 33. Her sed rate which was something like 86 in February is now 9. This is encouraging to me. It should be, right? Lori Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2006 Report Share Posted June 29, 2006 My MRI also shows 3 herniated disks, C3,C4, C5. I broke C2 when I was 18 when I got broadsided by a drunk driver, and they couldn't fix it or they would paralyze me. That is where I thought all my pain was coming from, but dr doesn't think so. It is such a difficult thing when there are no absolutes with autoimmune. Another day.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2006 Report Share Posted June 29, 2006 For it it felt like I had one of my heavier cats sitting on my chest. I could breathe but I had to dig deeper to get a good breath. Then I just got so tired from having to work extra hard at breathing. Every so often I would have a shooting pain that would radiate from my breastbone. A lot of MS patients get that feeling, around their ribcage like they are being hugged tightly. So you didn't have a large glowing spot....a lot of MS patients don't have those. Many small lesions can mean something if they are in the right place. You are certainly young enough that you shouldn't have lesions showing up unless there is something going on or you are a chronic migraine sufferer. There is a strong link between MS and EBV. From visiting MS boards in support of my DH the pain they experience sounds very different than what I experience as a RA patient. From your description it sounds like nerve pain is what you may be experiencing. I am going to assume that your doctors know what they are doing but if you have multiple lesions I would always have MS is the back of my mind. My DH has a very mild case (and I hope it stays that way) of MS as he as only had episodes of optic neuritis and case of numbness in his face before I met him. Knock on wood it has been over 2 years since his last optic neuritis episode. Hopefully someone else can help you with the lymph node biopsy. The only things I can think of is looking for cancer, enlargement that may suggest infection or sarcoidosis which you don't show symptoms of. Good luck Shandi Re: [ ] Update on rib cage pain Hi, new here. Are you talking severe muscle spasms around the rib cage? I get those and they are frightening! The first time, it happened while I was in the tub and I couldn't breathe! I saw my rheumatologist today and he was NOT helpful!! He doesn't think this is RA since my Sed rate is 11. He thinks this is fibro. Now my ANA is >160 but he isn't sure about Lupus. My ortho thinks this may all be MS, but the MRI of the brain doesn't show big enough lesions..........I don't really care what the heck they call it, but I would like to be able to control my pain!!! For the past 19 days I've had a nerve in my arm that is giving me EXTREME pain. Ortho put me on a prednisone pack and it didn't even touch the pain. I was still taking 2 Celebrex each day, a muscle relaxer and Tylenol 3 and none of it stopped the pain. The easiest way to describe it is to hit your funny bone and have that pain continually!! I could literally see the muscle jumping in my arm and can't pick up anything with my left hand. The rheumy told me to just take a muscle relaxer and it should help..........well it hasn't in the last 19 days!! I just had a huge blood work up with an oncologist and a lymph node biopsy (which was neg for lymphoma) but did show I have the anti bodies for EBV. The rheumy was suprised by the negative biopsy but said it should be redone in about 6 months. Do any of you all have any insights? I am sick of waking up with pain every day and not knowing which body part is not going to work! Heck, I won't even be 40 til next month. Sorry, I didn't mean to go on and on, just having a really rough day. Hugs We Made Changes Your email is all new. Learn More Share Feedback Recent Activity a.. 26New Members Visit Your Group Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2006 Report Share Posted June 29, 2006 I should have read all the posts before posting Did they do the T2 weighted MRI study on your spine or just the brain? Did that show lesions on your spine? That is a lot of herniated disks in your cervical spine. My Dh has a bulging disk in his lumbar and it gives him trouble. Shandi Re: [ ] Update on rib cage pain My MRI also shows 3 herniated disks, C3,C4, C5. I broke C2 when I was 18 when I got broadsided by a drunk driver, and they couldn't fix it or they would paralyze me. That is where I thought all my pain was coming from, but dr doesn't think so. It is such a difficult thing when there are no absolutes with autoimmune. Another day.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2006 Report Share Posted June 29, 2006 Shandi I had MRI of brain, cervical spine, and left shoulder. Then just recently I had CT's of neck, chest, abdomen and groin. The hernia at C3 is the most pronounced, but they don't want to do anything about it unless the other two start getting larger. I'm not sure I want them messing around in my cervical spine either......I kinda like being able to walk! lol Even if I have to do it in pain. I'm still thinking that alot of this nerve pain may be from the compressions in the spine.........I'd rather think it was that, rather than MS. Hugs Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 29, 2006 Report Share Posted June 29, 2006 Shandi Yes, I do think this is much more MS rather than RA. I guess I had hoped it to be fibro, lupus, or RA rather than MS, but most of what I have is very classic to MS. I don't have much problem with my legs, yet, it seems to stay in my upper body and only occasionally do I have problems in my knees or ankles. I do still have problems when I first get up with my ankles not wanting to flex. I have to sleep with my feet pointed down off the end of the bed or they really hurt the next day. I hope someday to have some complete answers.......maybe I'll go back to the neuro and see what he says. Hugs Quote Link to comment Share on other sites More sharing options...
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