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Diagnosis: LYME (Possibly have MS-WAIT AND SEE?)
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Diagnosis: LYME (Possibly have MS-WAIT AND SEE?)

I have Lyme Disease. I live in Mississipp and 2 Western Blots are positive for Lyme. Weeks were spent under care of neuro who suspected MS. MRI's show 3 active lesions on the brain. One on the brainstem (pons). All of my symptoms arrived in this order:stiffness of muscles in back an neck (feel very tight) eye muscle weak, drooping of lid, facial tingling around lips and cheek, fainting spell, toes numb over intervals of 6 months with the last occurence of numbess in my chest and abdomen, encircling my upper half and more prominent when I flex my neck ever so slightly. (This upper body numbness began Nov 13th,07 and in the past week-Jan 6th, 08 has become almost unnoticeable). At times this week Ive had a burning sensation stream thru the same spot on the same foot that has numb toes at times. Gets real hot then subsides.
I have great concerns that my Neurologist who was initially confident that I have what he called the beginning of MS -relapse/remitting and even went so far as to discuss the medication Copaxone with myself and husband while we awaited results of Spinal tap. He said diagnosis of MS is 90% MRI  and such lesions, particularly the brain-stem lesion but that the spinal could tell us more. When results arrived there were no 'bands' present in CSF and he completely dismissed his initial believe of MS. - Also, Lyme not present in CSF at time of spinal. He wants to see me for follow ups and sent me on my way to an Infectious Disease doctor because although no lyme was in spinal, 2 blood serum test reveal positives for LYME and also ANA positive. The Infectious disease doctor treats with Doxycycline/amoxicillin as well and says I DO have lyme. Been taking the meds since DEC 5th 07 and am feeling more energy and overall well being increased.  I have had long term fatigue that increased in the last 6 months of 07 with lots of joint/body pain. Knees, elbows, shoulders, shoulder blades, neck stiffness, etc which has reduced as well but still flaring up at times.
My concern are obvious:
Multiple lesions on brain--went from 2 to 3 in 5 weeks on MRI"S (in sept/oct 07)- symptoms indicate clinically MS, with positive MRI"S and radiological interpretation indicating possible MS as well on reports dictated. highly unlikely at age 41 I have small vessel disease...so these things that come and go as if going in and out of remission are tale tale signs that indicate I have MS, why would SPINAL tap be used as his definitive decision maker and him go from saying 90% of MS diagnosis is from MRI? Since no bands present: POOF, NO Multiple Sclerosis. Isn't that a bit incorrect in the present day school of thought---Isn't it possible that there were no bands present because it just hasn't gotten to that point where they are showing up? And do they have to present to diagnose? Or would it just make him more comfortable if the bands were present in order for him to make a definitive diagnosis?
Sounds kind of crazy to me. The infectious disease doctor was speechless upon learning of my lesions on brainstem and reading the reports from radiologists. He is the one that mentioned there are many cases where MS patients are positive for lyme and vice versa....but what do we do, remain sitting ducks, waiting for a disease to progress, what will the next lesion bring? How serious is this? Share any information you would like with me. I'm all ears! Thanks.
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I live in the Lyme capital of the world, right across from Lyme Conn.  in Long Island, NY.  I was diagnosed w/ Lymes in 1989, but first they thought it was MS, then they thought it was AIDS, that was a real scare, then they found the Lymes.  Isn't it awful how they can mess with your head like that? They said I'd probably had Lymes for a long time and hit me hard with antibiotocs and rocefforin which caused my immune system to shut down and caused me to get Lupus (druged induced). Later a homeopathic treatment was found that many said worked miracles.  I will find out the name of it when I go to my chiropractor tomorrow and I will send it to you.  I suggest you take it. It can't hurt. I did and I haven't had a positive Lyme test since.  I still have Lupus though.  You should get on a healthy diet too.  No more white stuff like bread, pasta, rice, sugar, nothing white.  You'll be amazed at how much better you feel. I'll be in touch tomorrow.
Hang in there. Your not alone.
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391038_tn?1298740986
My Chiro wasn't there today, I have to wait till he calls me.  I left him a message.  Hope you're OK today.
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I would love to know the name of the treatment.

I will also steer clear of white foods.

Thanx
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