Guest guest Posted August 31, 2005 Report Share Posted August 31, 2005 Hi . Sed rate measures inflammation, and it is very common that it is elevated in RA. Liver enzymes often become elevated by the meds we take. Do you know how high your liver enzymes are? What meds are you taking? a On Aug 31, 2005, at 1:55 PM, Climer wrote: > Hi all. I went in Monday to have my blood work done to determine if > I had RA > or not, and they called me with the results today, and the > > nurse told me the doctor was very concerned about some of the > results. The > test they do to check for RA was actually normal, but she > > said they did a sed rate and it was high as well as my liver > enzymes were > high. Are results like these common with RA? I am sooo > > scared I don't know what to do. Can someone please have some > answers for me. > I go into see the doctor friday morning. They wanted to > > see me ASAP. > > Thanks in advance > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 31, 2005 Report Share Posted August 31, 2005 Hi . Sed rate measures inflammation, and it is very common that it is elevated in RA. Liver enzymes often become elevated by the meds we take. Do you know how high your liver enzymes are? What meds are you taking? a On Aug 31, 2005, at 1:55 PM, Climer wrote: > Hi all. I went in Monday to have my blood work done to determine if > I had RA > or not, and they called me with the results today, and the > > nurse told me the doctor was very concerned about some of the > results. The > test they do to check for RA was actually normal, but she > > said they did a sed rate and it was high as well as my liver > enzymes were > high. Are results like these common with RA? I am sooo > > scared I don't know what to do. Can someone please have some > answers for me. > I go into see the doctor friday morning. They wanted to > > see me ASAP. > > Thanks in advance > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2005 Report Share Posted September 1, 2005 I know sed rate means there is an infection, but I have taken no different meds since the last liver profile I had done, and they were ok. Also, the test that checks for RA was normal. Can this test be normal, and still have RA. And as of yesterday afternoon, I have started to loose my voice. I have not been feeling like I have been getting a cold or anything, but by this morning, I sound like Minnie Mouse. Do any of these symptoms make any since to anyone?:? I am totally baffled. And now my husband is worried sick. (You would think he would be happy I lost my voice LOL) -- Re: [ ] Help please! Hi . Sed rate measures inflammation, and it is very common that it is elevated in RA. Liver enzymes often become elevated by the meds we take. Do you know how high your liver enzymes are? What meds are you taking? a On Aug 31, 2005, at 1:55 PM, Climer wrote: > Hi all. I went in Monday to have my blood work done to determine if > I had RA > or not, and they called me with the results today, and the > > nurse told me the doctor was very concerned about some of the > results. The > test they do to check for RA was actually normal, but she > > said they did a sed rate and it was high as well as my liver > enzymes were > high. Are results like these common with RA? I am sooo > > scared I don't know what to do. Can someone please have some > answers for me. > I go into see the doctor friday morning. They wanted to > > see me ASAP. > > Thanks in advance > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2005 Report Share Posted September 1, 2005 I know sed rate means there is an infection, but I have taken no different meds since the last liver profile I had done, and they were ok. Also, the test that checks for RA was normal. Can this test be normal, and still have RA. And as of yesterday afternoon, I have started to loose my voice. I have not been feeling like I have been getting a cold or anything, but by this morning, I sound like Minnie Mouse. Do any of these symptoms make any since to anyone?:? I am totally baffled. And now my husband is worried sick. (You would think he would be happy I lost my voice LOL) -- Re: [ ] Help please! Hi . Sed rate measures inflammation, and it is very common that it is elevated in RA. Liver enzymes often become elevated by the meds we take. Do you know how high your liver enzymes are? What meds are you taking? a On Aug 31, 2005, at 1:55 PM, Climer wrote: > Hi all. I went in Monday to have my blood work done to determine if > I had RA > or not, and they called me with the results today, and the > > nurse told me the doctor was very concerned about some of the > results. The > test they do to check for RA was actually normal, but she > > said they did a sed rate and it was high as well as my liver > enzymes were > high. Are results like these common with RA? I am sooo > > scared I don't know what to do. Can someone please have some > answers for me. > I go into see the doctor friday morning. They wanted to > > see me ASAP. > > Thanks in advance > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2005 Report Share Posted September 1, 2005 , Many here test negative for RA, me included. I have a website with links to many articles that may help you understand. http://rheumatoid.arthritis.freehosting.net/Lab%20Tests.html Unfortunately lab tests are only a part of the diagnosis of RA. Lab tests can't confirm RA. I hope this website helps. I hope you feel better. Do you think you have a cold? a On Sep 1, 2005, at 9:14 AM, Climer wrote: > I know sed rate means there is an infection, but I have taken no > different > meds since the last liver profile I had done, and they were ok. > > Also, the test that checks for RA was normal. Can this test be > normal, and > still have RA. > > And as of yesterday afternoon, I have started to loose my voice. I > have not > been feeling like I have been getting a cold or anything, but by this > morning, I sound like Minnie Mouse. Do any of these symptoms make > any since > to anyone?:? I am totally baffled. And now my husband is worried > sick. (You > would think he would be happy I lost my voice LOL) > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2005 Report Share Posted September 1, 2005 , Many here test negative for RA, me included. I have a website with links to many articles that may help you understand. http://rheumatoid.arthritis.freehosting.net/Lab%20Tests.html Unfortunately lab tests are only a part of the diagnosis of RA. Lab tests can't confirm RA. I hope this website helps. I hope you feel better. Do you think you have a cold? a On Sep 1, 2005, at 9:14 AM, Climer wrote: > I know sed rate means there is an infection, but I have taken no > different > meds since the last liver profile I had done, and they were ok. > > Also, the test that checks for RA was normal. Can this test be > normal, and > still have RA. > > And as of yesterday afternoon, I have started to loose my voice. I > have not > been feeling like I have been getting a cold or anything, but by this > morning, I sound like Minnie Mouse. Do any of these symptoms make > any since > to anyone?:? I am totally baffled. And now my husband is worried > sick. (You > would think he would be happy I lost my voice LOL) > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2005 Report Share Posted September 1, 2005 No I don't have a cold. I don't feel like I usually do when I get a cold. And my hands and feet are still extremely swollen and painful. I hope to goodness they can diagnose me soon. Not knowing whats going on is the worse -- Re: [ ] Help please! , Many here test negative for RA, me included. I have a website with links to many articles that may help you understand. http://rheumatoid.arthritis.freehosting.net/Lab%20Tests.html Unfortunately lab tests are only a part of the diagnosis of RA. Lab tests can't confirm RA. I hope this website helps. I hope you feel better. Do you think you have a cold? a On Sep 1, 2005, at 9:14 AM, Climer wrote: > I know sed rate means there is an infection, but I have taken no > different > meds since the last liver profile I had done, and they were ok. > > Also, the test that checks for RA was normal. Can this test be > normal, and > still have RA. > > And as of yesterday afternoon, I have started to loose my voice. I > have not > been feeling like I have been getting a cold or anything, but by this > morning, I sound like Minnie Mouse. Do any of these symptoms make > any since > to anyone?:? I am totally baffled. And now my husband is worried > sick. (You > would think he would be happy I lost my voice LOL) > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2005 Report Share Posted September 1, 2005 No I don't have a cold. I don't feel like I usually do when I get a cold. And my hands and feet are still extremely swollen and painful. I hope to goodness they can diagnose me soon. Not knowing whats going on is the worse -- Re: [ ] Help please! , Many here test negative for RA, me included. I have a website with links to many articles that may help you understand. http://rheumatoid.arthritis.freehosting.net/Lab%20Tests.html Unfortunately lab tests are only a part of the diagnosis of RA. Lab tests can't confirm RA. I hope this website helps. I hope you feel better. Do you think you have a cold? a On Sep 1, 2005, at 9:14 AM, Climer wrote: > I know sed rate means there is an infection, but I have taken no > different > meds since the last liver profile I had done, and they were ok. > > Also, the test that checks for RA was normal. Can this test be > normal, and > still have RA. > > And as of yesterday afternoon, I have started to loose my voice. I > have not > been feeling like I have been getting a cold or anything, but by this > morning, I sound like Minnie Mouse. Do any of these symptoms make > any since > to anyone?:? I am totally baffled. And now my husband is worried > sick. (You > would think he would be happy I lost my voice LOL) > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2005 Report Share Posted September 1, 2005 , I will be glad when you get to the doctor. Let us know how it goes, I'm worried about you. My prayers are with you, Tawny > > > > > I know sed rate means there is an infection, but I have taken no > > > different > > > meds since the last liver profile I had done, and they were ok. > > > > > > Also, the test that checks for RA was normal. Can this test be > > > normal, and > > > still have RA. > > > > > > And as of yesterday afternoon, I have started to loose my voice. I > > > have not > > > been feeling like I have been getting a cold or anything, but by this > > > morning, I sound like Minnie Mouse. Do any of these symptoms make > > > any since > > > to anyone?:? I am totally baffled. And now my husband is worried > > > sick. (You > > > would think he would be happy I lost my voice LOL) > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 1, 2005 Report Share Posted September 1, 2005 , I will be glad when you get to the doctor. Let us know how it goes, I'm worried about you. My prayers are with you, Tawny > > > > > I know sed rate means there is an infection, but I have taken no > > > different > > > meds since the last liver profile I had done, and they were ok. > > > > > > Also, the test that checks for RA was normal. Can this test be > > > normal, and > > > still have RA. > > > > > > And as of yesterday afternoon, I have started to loose my voice. I > > > have not > > > been feeling like I have been getting a cold or anything, but by this > > > morning, I sound like Minnie Mouse. Do any of these symptoms make > > > any since > > > to anyone?:? I am totally baffled. And now my husband is worried > > > sick. (You > > > would think he would be happy I lost my voice LOL) > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 22, 2007 Report Share Posted March 22, 2007 > > my son has diarrhea since yesterday. i think it's caused by virus since > his preschool advised that there's been 2 kids already that was sent > home last week due to gastro virus. i gave him kirkman's probio > yesterday and today, since it firms up his stool most of the time that > he's taking it. don't know if i should give him vitc though since it > might aggravate his diarrhea. what should we do? Give a small amount of vitamin C, no more than 500mg, see if that helps. I use vitamin C, Virastop enzyme, and olive leaf extract to eliminate viral illnesses for my kids. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 21, 2007 Report Share Posted April 21, 2007 , did you get a copy of the report and a copy of the MRI? If you didn't, get them. If you did, do you understand what the report said? In any case, you will want to have copies of both in case you feel the need to get a second opinion. I don't know the extent or the degree of your spinal arthritis, but it is a very common place for arthritis to strike. There are lots of conservative measures you can try before you go for surgery, so don't rush that, that SHOULD be a last resort. There are medications like Celebrex that might be able to help, and of course, other pain meds. You might want to try physical therapy. There are cortisone injections, and there are epidurals. There really are a lot of things you can try before you think about a surgical fix. In my case, I don't have a choice. I am now facing surgery, with no certain outcome, but I'm out of options. Carol In a message dated 4/21/2007 4:43:46 P.M. Pacific Daylight Time, espivey@... writes: Before I begin searching for another group with this specific topic, can anyone tell me anything about degenerative disc disease and/or anular tears? Since February my lower back has been killing me and I finally got the ortho to do an mri and he says that is the problem. He further said all I can do is to take pain meds or shots. I find that hard to believe. Anyone with any experience? Thanks! ************************************** See what's free at http://www.aol.com. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2007 Report Share Posted April 22, 2007 , I found out last summer I have degenerative disc disease. It is also called Osteoarthritis. My Dr. did an MRI and on the orders for the MRI, he has RA and Osteoarthritis as a DX. I already knew I had RA. I just didn't know about the OA. Take my word for it, I know exactly what you are going through. The MRI showed that I have three pinched nerves and four bulges in my lower back. What did your MRI show? I'll tell you the treatments that was done to me then you can decide what you want to do for youself. I was sent to a pain clinic and the first thing the Dr. did was give me three epidural shots which didn't help at all. Then he decided he'd have to go into the nerves. I had to go to the hospital as an outpatient then he gave me six or seven prednison shots which didn't help in the least. Two weeks later he told me that he had to go in and do more to those nerves. I found out that he was going to do a Rizotomy. I asked a Dr if it were him would he let them do that treatment to him. The DO said that he wasn't me but if it were him he would not let them do that treatment to him. So I talked myself out of that one. I read of the side effects that could happen with the TX. One of the side effects could possibly be incontinence and the other may be numbness in the lower part of your body. It's not a sure thing you'll have these side effects but I'm not going to risk it. My Dr has me on Morphine now which helps. Has your Ortho suggested PT or Water therapy? I went through those therapies too. I agree with you, it feels like your lower back is going to kill you. I too have been in excruciating pain before starting on morphine. I'd have to hold on to the wall to go from one room to the other. =================================================================== > > Before I begin searching for another group with this specific topic, > can anyone tell me anything about degenerative disc disease and/or > anular tears? Since February my lower back has been killing me and I > finally got the ortho to do an mri and he says that is the problem. > He further said all I can do is to take pain meds or shots. I find > that hard to believe. Anyone with any experience? > Thanks! > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2007 Report Share Posted April 22, 2007 I'm suffering from it, too. What I started doing was to drape myself over a step ladder right at the hips and it stretched my back into place. I had to do it as much as 3 times a day, every day for a week or so, and it did solve the problem for me. Now when I feel it coming on, I drape myself over the ladder for about 20 minutes and it goes away enough for me to keep going. It's either that or an epidural, not much of a choice. Dennis in Eastexas " It's not Rocket Surgery " [ ] Help Please! > Before I begin searching for another group with this specific topic, > can anyone tell me anything about degenerative disc disease and/or > anular tears? Since February my lower back has been killing me and I > finally got the ortho to do an mri and he says that is the problem. > He further said all I can do is to take pain meds or shots. I find > that hard to believe. Anyone with any experience? > Thanks! > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2007 Report Share Posted April 22, 2007 Thanks for the response. I'm so confused. I knew I had OA and RA and DDD but didn't realize the two were the same. Different docs use different terms. He said I had a large anular tear ( which he said is the sac around the disk) and severe degeneration in L5. On the mri the whole disk was black where all the others were bright white, in varying degrees. The tear was bright white and the size of the side of the disk. He said pain meds or shots were my only options! He did say to walk all I could which I will but it is difficult with my right leg being weak and half-numb! I've seen on the net where surgery is an option for ddd and I know it is for " ruptured " disks, if that's what I have. I wish I had asked him to talk to me in " my " terms so I understood more. I think i'm going to look for a second opinion. I am still working full time because I have to but I can't like this. They've given me Darvocet, Ultram and Lortab for pain and it doesn't faze it. I also saw on the net that this is the greatest cause of disability in the US. That's not encouraging! I'm only 46 and have 3 small granddaughters! Thanks again. > > > > Before I begin searching for another group with this specific > topic, > > can anyone tell me anything about degenerative disc disease and/or > > anular tears? Since February my lower back has been killing me > and I > > finally got the ortho to do an mri and he says that is the > problem. > > He further said all I can do is to take pain meds or shots. I find > > that hard to believe. Anyone with any experience? > > Thanks! > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2007 Report Share Posted April 22, 2007 Hi and Carol, When first diagnosed with DDD in 2000 I did the epidurals, trigger point injections, nerve blocks, physical therapy, even chiropractic adjsutments with heat packs and tens massage. I took so many doses of steroids I gained 40 lbs. Nothing changed. Neuro went in and shaved off bulging parts of herniated discs. L-4 L-5. Same day surgery, no big deal. He said I had DDD and would most likely be back. After recovery (3-4) weeks, I had 18 months pain free. When it came back it was with a vengance. Like before went thru everything again. Steroids put another 40 lbs. on me. I went from 140 to 220 lb in 3 years. This time fusion was next step. L-3,L-4,L-5,S-1. Went to different neuro, same diagnosis but was informed that meds I was taking would cause kidney and liver failure. SOOO,I opted for fusion. After 9 hours of surgery, 5 days in hospital, 8 weeks of recovery went back to work part time. (Office manager) Pain still so bad sent to pain mgmt. I held on until December 2005 and the pain won. I quit work so I could work on hopefully a routine to where I could have a life. Some days I get out of bed and some I don't. I don't know until I get up in the morning how my day will be. My husband is very supportive and takes care of what I can't. I know this is not the story you wanted to read but it is my life with DDD. Hang in there. Hugs and Prayers, Fayray. >From: boomer6454@... >Reply- > >Subject: Re: [ ] Help Please! >Date: Sat, 21 Apr 2007 20:04:05 EDT > > >, did you get a copy of the report and a copy of the MRI? If you >didn't, get them. If you did, do you understand what the report said? > >In any case, you will want to have copies of both in case you feel the >need >to get a second opinion. I don't know the extent or the degree of your >spinal >arthritis, but it is a very common place for arthritis to strike. There >are >lots of conservative measures you can try before you go for surgery, so >don't >rush that, that SHOULD be a last resort. > >There are medications like Celebrex that might be able to help, and of >course, other pain meds. You might want to try physical therapy. There are >cortisone injections, and there are epidurals. There really are a lot of >things you >can try before you think about a surgical fix. In my case, I don't have a >choice. I am now facing surgery, with no certain outcome, but I'm out of >options. > >Carol > >In a message dated 4/21/2007 4:43:46 P.M. Pacific Daylight Time, >espivey@... writes: > >Before I begin searching for another group with this specific topic, >can anyone tell me anything about degenerative disc disease and/or >anular tears? Since February my lower back has been killing me and I >finally got the ortho to do an mri and he says that is the problem. >He further said all I can do is to take pain meds or shots. I find >that hard to believe. Anyone with any experience? >Thanks! > > > > > > > > >************************************** See what's free at >http://www.aol.com. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2007 Report Share Posted April 22, 2007 You are correct. Degenerative Disk Disease is not the same as Osteoarthritis of the spine, but the two things often go hand in hand. I just did a good bit of web researching and discovered that my RD over simplified things when I asked him about this. He told me " it's basically arthritis of the spine " . I guess he didn't want to go into it.... Yes, I know. I need a new doctor. Carol In a message dated 4/22/2007 4:07:12 P.M. Pacific Daylight Time, drack2@... writes: Correct me if I'm wrong, but OA and DDD are not the same thing! ************************************** See what's free at http://www.aol.com. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2007 Report Share Posted April 22, 2007 For reasons unknown, DDD is attacking both cervical and lumbar regions of my spine. We haven't looked at the thorasic, but I'm sure if we did, it would be affected too. , you said your regular neurosurgeon wouldn't touch your back. Did he say why? I had the same problem. My ortho wants to do surgery. I'm going in tomorrow for a second opinion with a Doctor that specializes in minimally invasive surgeries. I'm beginning to think I want to wait on this back surgery until I'm sure about what can and can't be done, and what the prognosis is. My back is a very serious MESS. Carol In a message dated 4/22/2007 4:10:14 P.M. Pacific Daylight Time, drack2@... writes: , I have degenerative disc disease as well. Mine is in my neck. The way my surgeon explained it to me is this: as we age, our discs begin to " dry out " slowly and flatten out. Thus, there are annular tears in the outer covering of the disc. If these tears become too big, the inside disc material may squish out and do all kinds of damage. With the disease, our discs age way too early. I am 34 and have had this disease for 5 years that I know of (when I had my first surgery). In essence, my discs are that of about a 65 year old person. Unfortunately, there is not much that can be done unless a disc actually ruptures and entraps a nerve or pushes too much on the spinal cord. I've had 2 surgeries, been thru physical therapy a dozen times, pain management, you name it. I take pain meds daily or I'd be in the ER every other day. I am so sorry to hear about your disc disease. Pardon my language but it sucks. I am going to a new ortho May 1st, as a regular neurosurgeon won't touch me any longer due to my degenerative disc disease and degenerative joint disease in my neck. [ ] Help Please! Before I begin searching for another group with this specific topic, can anyone tell me anything about degenerative disc disease and/or anular tears? Since February my lower back has been killing me and I finally got the ortho to do an mri and he says that is the problem. He further said all I can do is to take pain meds or shots. I find that hard to believe. Anyone with any experience? Thanks! ************************************** See what's free at http://www.aol.com. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2007 Report Share Posted April 22, 2007 Dennis, Could you tell me what you mean be a step ladder and how do you go about stretching your back into place? Will it help pinched nerves and bulges? I'm sorry I sound so dumb but I've never heard of this. Joyce from Texas Re: [ ] Help Please! I'm suffering from it, too. What I started doing was to drape myself over a step ladder right at the hips and it stretched my back into place. I had to do it as much as 3 times a day, every day for a week or so, and it did solve the problem for me. Now when I feel it coming on, I drape myself over the ladder for about 20 minutes and it goes away enough for me to keep going. It's either that or an epidural, not much of a choice. Dennis in Eastexas " It's not Rocket Surgery " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2007 Report Share Posted April 23, 2007 , I have degenerative disc disease as well. Mine is in my neck. The way my surgeon explained it to me is this: as we age, our discs begin to " dry out " slowly and flatten out. Thus, there are annular tears in the outer covering of the disc. If these tears become too big, the inside disc material may squish out and do all kinds of damage. With the disease, our discs age way too early. I am 34 and have had this disease for 5 years that I know of (when I had my first surgery). In essence, my discs are that of about a 65 year old person. Unfortunately, there is not much that can be done unless a disc actually ruptures and entraps a nerve or pushes too much on the spinal cord. I've had 2 surgeries, been thru physical therapy a dozen times, pain management, you name it. I take pain meds daily or I'd be in the ER every other day. I am so sorry to hear about your disc disease. Pardon my language but it sucks. I am going to a new ortho May 1st, as a regular neurosurgeon won't touch me any longer due to my degenerative disc disease and degenerative joint disease in my neck. [ ] Help Please! Before I begin searching for another group with this specific topic, can anyone tell me anything about degenerative disc disease and/or anular tears? Since February my lower back has been killing me and I finally got the ortho to do an mri and he says that is the problem. He further said all I can do is to take pain meds or shots. I find that hard to believe. Anyone with any experience? Thanks! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2007 Report Share Posted April 23, 2007 Correct me if I'm wrong, but OA and DDD are not the same thing! [ ] Re: Help Please! Thanks for the response. I'm so confused. I knew I had OA and RA and DDD but didn't realize the two were the same. Different docs use different terms. He said I had a large anular tear ( which he said is the sac around the disk) and severe degeneration in L5. On the mri the whole disk was black where all the others were bright white, in varying degrees. The tear was bright white and the size of the side of the disk. He said pain meds or shots were my only options! He did say to walk all I could which I will but it is difficult with my right leg being weak and half-numb! I've seen on the net where surgery is an option for ddd and I know it is for " ruptured " disks, if that's what I have. I wish I had asked him to talk to me in " my " terms so I understood more. I think i'm going to look for a second opinion. I am still working full time because I have to but I can't like this. They've given me Darvocet, Ultram and Lortab for pain and it doesn't faze it. I also saw on the net that this is the greatest cause of disability in the US. That's not encouraging! I'm only 46 and have 3 small granddaughters! Thanks again. > > > > Before I begin searching for another group with this specific > topic, > > can anyone tell me anything about degenerative disc disease and/or > > anular tears? Since February my lower back has been killing me > and I > > finally got the ortho to do an mri and he says that is the > problem. > > He further said all I can do is to take pain meds or shots. I find > > that hard to believe. Anyone with any experience? > > Thanks! > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2007 Report Share Posted April 23, 2007 I just happened to have a 6 foot ladder on the porch, so I brought it inside to stretch off of. My sister had a chance to get on an 'inverter' where you stand in it and strap your feet and then rotate it so you're upside down. She liked hanging by her heels, so my daughter and I devised the ladder thing, and it worked. Later, I cut the legs down so I didn't have to climb, just lay over it. It pulls your back out as you droop over, taking all the weight off your back, similar to what the cervical traction device does for the neck, and right where stretching is needed, the small of your back. The top of the folding ladder was a little wide, but I took a pillow and put it on the top to soften it. Then I laid over it with the pillow right at groin height, and could use my arms to straighten or move for better control. And, I made sure Liz was with me for the first try, something I would recommend. The only thing I had to worry about was my sinuses, they drain when you're upside down. lol Dennis in Eastexas " It's not Rocket Surgery " Re: [ ] Help Please! > > > I'm suffering from it, too. What I started doing was to drape myself over > a > step ladder right at the hips and it stretched my back into place. I had > to > do it as much as 3 times a day, every day for a week or so, and it did > solve > the problem for me. Now when I feel it coming on, I drape myself over the > ladder for about 20 minutes and it goes away enough for me to keep going. > It's either that or an epidural, not much of a choice. > > Dennis in Eastexas > " It's not Rocket Surgery " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 25, 2007 Report Share Posted April 25, 2007 Hi Carol. The reason my neurosurgeon won't touch my neck is that the more he fuses, the more wear and tear on the discs above and below the fusion site. I know what is going to eventually happen: my entire neck will end up fused. At 34, I just can't bring myself to do it yet. Plus, my surgeon told me that a fusion only lasts so long, 15 years is about the max. So I know I will need that area fixed in about 13 years again if it holds that long. I'm actually lucky because my fusion was with my own hip bone, and no metal was used to hold it. That way there is no metal to remove the next time, which would wear away even more of my joints, etc. I do feel for you. My first surgery was an emergency surgery; it was either that or I was gonna cut my arm off (seriously) or worse. My second surgery was a scheduled one to try to minimize the nerve damage that was taking place and that was almost 2 years ago now. I'm hoping to avoid any more as long as I can. But I do know what it's like, the recoveries are long and very painful, etc. Sorry to hear you are having these problems! [ ] Help Please! Before I begin searching for another group with this specific topic, can anyone tell me anything about degenerative disc disease and/or anular tears? Since February my lower back has been killing me and I finally got the ortho to do an mri and he says that is the problem. He further said all I can do is to take pain meds or shots. I find that hard to believe. Anyone with any experience? Thanks! ************************************** See what's free at http://www.aol.com. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 3, 2007 Report Share Posted December 3, 2007 We just moved to a new school district. We used in Deptford,NJ. Now we moved to Voorhees, NJ. We had IEP in our old school district. My son is PDD. He has been fully mainstreamed in a regular class with an one to one aide since 1st grade. He also has 8 hours after school tutor hours which paid by township. Now the new school doesn't want to give any of this service. They doesn't want to give one-to opne aide and doesn't want to give in-home service. They just want to fit my son in their existing pull out program which is not one to one. They claimed to change my son's IEP to cut all these programs. What can I do to protect my son's right? Do they have right to change my son's IEP in the middle of year? Any suggestions are appreciated. Lan ________________________________________________________________________________\ ____ Be a better friend, newshound, and know-it-all with Mobile. Try it now. http://mobile./;_ylt=Ahu06i62sR8HDtDypao8Wcj9tAcJ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 4, 2007 Report Share Posted December 4, 2007 Hi Jackie, Thanks very much for your response. I really got very dismay after I met with new school special service people yesterday. They don't respect my current IEP at all. The new school district is better in regular education, but definitely worser in special education program. We moved to this new school district is because I have a daughter who is in 8th grade now. She is very smart and has a very good academic skill. We want to give her a better environment to study. But now I have a strong feeling that this moving is definitely a lose to my son. Deptford, NJ is only about 10 miles away from Voorhees, NJ. Lan RE: [ ] help please! Lan, Unfortunately, this happens to a lot of people. My advice to you would be to get evaluations done by experts in the field i..e BCBA, neurologist etc. Present this information to them. If they are not accomodating, then you will need a good attorney who can defend your case. If you do not know any attorneys, you can call Cosac for some recommendations. Join parent support groups and you can learn from other parents. Lan Gao wrote: > We just moved to a new school district. We used in Deptford,NJ. Now we moved to Voorhees, NJ. We had IEP in our old school district. My son is PDD. He has been fully mainstreamed in a regular class with an one to one aide since 1st grade. He also has 8 hours after school tutor hours which paid by township. Now the new school doesn't want to give any of this service. They doesn't want to give one-to opne aide and doesn't want to give in-home service. They just want to fit my son in their existing pull out program which is not one to one. They claimed to change my son's IEP to cut all these programs. What can I do to protect my son's right? Do they have right to change my son's IEP in the middle of year? > Any suggestions are appreciated. > Lan > ____________ _________ _________ _________ _________ _________ _ > Be a better friend, newshound, and > know-it-all with Mobile. Try it now. http://mobile. / ;_ylt=Ahu06i62sR 8HDtDypao8Wcj9tA cJ > ________________________________________________________________________________\ ____ Be a better sports nut! Let your teams follow you with Mobile. Try it now. http://mobile./sports;_ylt=At9_qDKvtAbMuh1G1SQtBI7ntAcJ ________________________________________________________________________________\ ____ Never miss a thing. Make your home page. http://www./r/hs Quote Link to comment Share on other sites More sharing options...
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