burning sensation

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beannie
Regular Member


Date Joined Jun 2006
Total Posts : 50
   Posted 9/11/2009 5:11 AM (GMT -6)   
Hi, I was just wondering if anyone has ever had a severe burning sensation around the diaphragm? It goes around the back and sometimes my skin is very sensitive to the touch on my side. It is very strange....Sometimes it feels like someone has their elbow digging it in my back...Just annoying....thanks ....Beannie mad confused

dianna30
Regular Member


Date Joined Mar 2009
Total Posts : 90
   Posted 9/13/2009 8:33 PM (GMT -6)   
I am not exactly sure of what you are describing.  I do get a burning feeling in my lower back, which I assume is due to my herniated disc.  Skin sensitivity can be neuropathy, that is when a section of skin feels weird-tingly, sensitive, buzzing, etc.  It's probably best if you mention it the next time you see your doctor.

Be joyful in hope, patient in affliction, faithful in prayer (Romans 12:12).

http://diannaschnabel.blogspot.com/


Buff Dominator
New Member


Date Joined Sep 2009
Total Posts : 3
   Posted 9/14/2009 1:08 PM (GMT -6)   
Yes, I get very intense burning in my arms, shoulders, and neck. I have cervical lesions C1 to C5, so the communication brain to arms is poor and it extends down stream to my back, abs an legs. It is caused by communication to those muscles being disrupted due to a lesion(s). I had similar sensations in my back a few years before I was diagnosed with MS. Over the following 5 years, I had those sensations in various parts of my body, but the worst was in my legs ( quads on side). They were so bad I would drop to the floor. It felt like a hot knife was being stuck in my leg. At that time I used lidocaine patches. They work, but very toxic.

The burning I have now is fairly consistent and I control it with neurontin, stretching, light weights, acupuncture, and cannabis. I have found cannabis works the best for immediate relief of skin pain and sensitivity. Acupuncture takes a few visits to kick in, and you must consistently go, but also calms the nerves more long term. On occasion my pain doctor will do a combination of trigger point injections and needling. Not fun, but last for a few weeks. I have tried Oxycontin, vicodin, lyrica, cymbalta, and others, but the side effects were not worth the varied pain relief they provided. I do take neurontin and found it to be tolerable. I try to keep my dosage low, but sometimes I get tempted to go higher because it hurts so bad sometimes. It is usually tied to activity. It is highly important to exercise those muscles, as this keeps the communication active and muscles working. I have a long list of other alternative treatments I have tried, but these have worked the best for me to date. I hope you are on a MS therapy i.e. interferon, tysabri,... and would suggest a MRI to make sure lesion activity is under control.

I hope this helps. Hang in there!

BD

Gretchen1
Forum Moderator


Date Joined Jan 2007
Total Posts : 3539
   Posted 9/14/2009 7:48 PM (GMT -6)   
Hey BD,
 
Good advice.  You have a great response on the other thread as well.  It is nice to have you here.  Welcome! 
Gretchen  ~  diagnosed with MS July 2006
 
I have no lesions on my soul and so I will live with no limits.

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