The numbness started going away from the chest down. The feeling in my feet were the last to return. Considering my numbness started in my left arm ran down my left side and up the right til it reached my chest how it returned didn't seem that odd. I really think you need a new neuro. who specializes in MS. However, even some who say they specialize aren't always the most knowledgeable. Do your homework. I have had 4 neuro in 14 yrs, 2 were in the same office who I saw for 12yrs. I only switched due to insurance. I now travel an hour to a MS clinic....which I love. I get a complete neuro exam which even with an MS specialist I had never received in the yr and a half I saw him. You can also have nerve damage from MS. Good luck and keep us informed.View Thread
I also had the numbness from the chest down. I was on IV steroids for 5 days. To be honest it took about 4 months for total feeling to return. I was in PT & OT 3 times a week for 2 months. I am not saying this will be the same for you....as others have stated everyone is different. My concern is if your neuro doesn't think its MS has he indicated what he does think it could be? Has he sent you for additional testing or to another dr? I will say that I had a very large lesion on my cervical spine. I hope that if your dr. isn't trying to find out what is going on you will at least do so. Best of luck to you.View Thread
I have suffered and treated for severe frequent migraines since I was 12. I was diag. with RRMS at 40 and started taking Copaxone. After about 6 mos. on Copaxone the migraines became less frequent and eventually I would only have a mild one every 6 mos. My neuro at the time said there wasn't any connection between migraines and MS and the Copaxone couldn't have helped with my migraines. Well I know differently. Especially now that I have had to switch to Avonex....my migraines are back...not as severe but they are definately returning. I think the bottom line is we are learning so much about MS that we really can't rule anything out. I also thank God for this site where we can all share different experiences and make a connection with the symptoms that might otherwise go unnoticed as a part of MS. Case in point....MS Hug....I have had this for years and never knew it was from MS.
I find it interesting that I have only recently heard of the MS hug....I have experienced this for years and never made the connection and even the drs never made the connection. Warm compresses do help as hacker says. You may want to try wearing a sports bra...I tried wearing one about a month ago when the pain was intense and it does help somewhat.View Thread
I am so very confused right now....I saw a new neuro yesterday after seeing the same one for 10yrs. The new neuro told me my MRIs of the brain from 2009 and 2011 were clear not typical of a person who was diag. 12yrs ago with symptoms of MS dating back 30 yrs. The exascerbation which led to my diag. was from a very large lesion on my spine which led to numbness from the chest down. At that time the MRI of my brain was normal, MRI of spine showed dimylating plaque. I also had a spinal tap which showed the bands were present. I was on solu medrol for 5 days and immediately started on Copaxone. All previous MRI show lesions including an MRI done in 1997, with the exception of the the last 2 which only show 2 small areas. Is it possible to have an MRI of the brain with no new lesions after all these years?View Thread
I went yesterday for my OCT testing to check optical nerve damage. My neuro had suggested this test because some MS patients who have been diagnosed for many years have damage to these nerves. I am happy to say I do not have any damage. However, I was very confused when the technician told me that the Dr. will usually send his patients for the OCT when there will be a treatment change. So confusion sets in again. Well should have some answers..hopefully soon. MRI of cervical and thoracic spine tomorrow and MRI of brain on Saturday.View Thread
I do give credit to Copaxone, although my new neuro doesn't have alot of faith in it. Unfortunately, after 12 yrs on Copaxone I had to go off of it due to hives at injection sites. The hives gradually increased in size and I ended up with them every day. I was off treatment for 2 weeks before gradually starting on Avonex. Neuro did mention that the recent MRI's were done in the Open MRI due to claustrophobia, which might explain the lack of new lesions. I am scheduled for MRI's of brain, cervical and thoracic in the closed MRI to see if that shows more lesions. He also mentioned NMO, which is a type of MS that involves the T17 cells. If that is the case my research shows being on Avonex would cause MS symptoms to become worse. Believe me I am very pleased my MRI looks good, and I attribute that to Copaxone! I was treated for migraines from 12yrs to 21 yrs old. Then I was treated for TIA's for 10yrs. Then back to migraine treatment. I was finally diag. with MS. Now after 12 yrs of treatment I am told I may not have MS after all....I am in a whirlwind of emotions. Hopefully after new MRI's, NMO antibody blood tests and OCT testing I will have some idea of what is going on.
Thank you everyone for your responses and I would greatly appreciate any other comments, info, and suggests anyone has for me.View Thread
I too was diag. with TIA 29 yrs ago with basically the same symptoms. In 2000 I was finally diag. with MS after being treated for the TIA and migraines for 18 yrs. I was also sent to see a neuro and cardio. The MS diag was made after my left arm went numb which eventually led to being numb from the chest down. My primary had mention several times over the years it could be MS. I wish now I had insisted on more testing. I have been on Copaxone as well as numerous other meds for 11yrs and it has controlled my symptoms. But my point is...I feel if I had been diag. 29 yrs ago I may still be working instead of on disability. All research shows the sooner you start therapy the better chances you have to live a productive life. Do not stop searching for the answers!!! Best of luck to you both!!!!View Thread
I have been on Copaxone for 11yrs. Approx 2 months into starting the injections I started having an occasional reaction right after the shot, which has been listed in the pamplet: palpitation, heavy chest, constriction of the throat, flushing and not being able to speak. They would only last about 10 minutes, and then I was fine. My last reaction was approx. 5yrs ago....until this morning. But this one was a little different. It started with my scalp feeling like it was on fire in different areas, then the palpitations with the usual array of reactions. But the difference was the scalp burning and then I got a massive headache covering my whole head and my inner ears were burning. I took 2 vicotin for the headache and in about 10 mins everything was back to normal mostly.
Has anyone experienced the burning scalp, massive headache and burning inner ears from the Copaxone injection? Since I have never experienced these reactions before I thought maybe someone would have a similar experience.
Thank you for your responses. Copaxone has been very effective for me. I haven't had any severe flare-ups since I began my injections only minor episodes that last a few weeks. I would hate to switch therapy since it has worked so well for me. In my experience I have found that other MS patients are better sources of info then the Drs. as far as symptoms go. for instance, after I started Copaxone my migraines went away, which I had suffered with since I was 12. My Neuro said there was no connection between the two. Now they say migraines are connected with MS.
I will speak with my neuro about this episode, so far it only occurred once.
56shorty - You really do need to be on some type of therapy please continue to talk to your dr. to find the best fit for you.