Let me ask the experts...people who have MS...Could it be MS???

Here is my list of symptoms...Sorry it is long..waiting to see the Neuro.  This site has already helped me with 3 recent dx's with auto immune diseases so I come to you the experts...Patients who actually have MS...Thank You kindly!  fatigue visual disorders …I have had blurriness Numbness, tingling all over, vibration feelings…tingling moving sensations on my head…very weird feeling! burning sensations dizziness/vertigo/loss of coordination bladder and bowel dysfunction – I have had incontinence urgency sometimes with retention other times and constipation weakness tremor – hand tremors impaired mobility Sexual dysfunction – No desire which is extremely uncommon for me! spasticity (leg stiffness) Involuntary Leg Movements, especially bothersome at night swallowing disorders – a little chronic aching pain depression mild cognitive and memory difficulties - Short-term memory problems, forgetfulness, slow word recall Acid Reflux Shortness of breath…chest pains Inappropriately cold body parts - always cold hands even with gloves and feet even with 2-3 pairs of thick socks and shoes…most all of the time have a heating pad on them at home! SEVERE pins and needles in feet!   I am concerned about losing my limbs due to lack of circulation!!! Although no real heat sensitivity.. although I have noticed in the last couple of weeks my cheeks being very flushed looking and have had a low grade fever consistently over the last several months. So what do you think??? Christie

I have suffered from quintalone antibiotic toxicity...aka cipro, levaquin, and alelox numerous times of the last several years and never connected the dots.

Thank you for your time!  :)

Looking at your symptoms added to your conditions listed, I would say you should also look into whether you have a long-held Lyme disease infection.

Whatever it is, there is something going on and you shouldn't let your doctors stop looking until they find a diagnosis and treatment that helps you regain your health.

Good luck!

The testing isn't very accurate, beach lover. If you don't get any joy from this new doctor, you could look into seeing a Lyme Literate Doctor.

Come on over to the Lyme forum if you want to talk about this more.

Hope you get some answers soon!

I have most of those symptoms and a brain lesion so the next stop is a lumbar puncture on the fifteenth..no diagnosis of ms yet..hopefully I don't have it.