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We are most definitely wired weird :-)
Sherry
I have had burning sensations for 3 & 1/2 years. It began in my legs, top of feet, thighs. Some days it feels like a bad sunburn, other days it feels like a blowtorch, and the worst days it feels like a trillion bees stinging me. It progressed to my spine last Dec., and the nerves sting. Yes, you can trust what you are feeling. Push for a diagnosis. It only gets worse without treatment.
I'm so sorry this is happening to you. I empathize.
Sheila
Welcome to the world of weirdness!
Moki
There is a song like that though
Feels like I've been rubbed with too much methyl salicylate (bengay, dencorub etc)...
My tongue is burning at the moment and my lip.... along with a spot on my thigh... and on my shoulder, and a few other spots....... and so the weirdness goes on... :(
But I tend too get an icy feelings in my toes even when I were my bunny boots, I can feel my toes are freezing but when I remove them my feet are just sweaty and warm and trust me you don't want to be around when I take them off
Cowboy
I've also had the burning sensation feel similiar to when something is really cold. My left arm and leg will feel cold to me, but to other people they are the same temperature.
Rena
I have just found this forum and can I say "thank God I found it."
I live in Australia and am a 50 yr old female.
I have been going through the very long process of an unconfirmed diagnosis now for the past 3 years. Nobody can make their mind up what is wrong with me, the opinion just keeps changing...yes it is MS, no it isn't, yes it is, no it isn't...........aaahhhh!
I have had 2 MRI's both with contrast a year apart and both showed multiple scattered lesions of different sizes and shapes and in both hemispheres of my brain but mostly adjacent to the corpus callosum with no changes within that time frame.
I have also had a lumbar puncture, (negative) and a spinal MRI (also negative). I have had multiple blood tests all negative, no B12 deficiency, Lupus, Lyme, Thyroid problems. Nerve tests, visual tests, all normal.
I have pursued a second opinion and didn't get any sense out of that neuro either both saying "they are not sure." The 2nd neuro did say I have no active lesions at present,
how reassuring!
I asked my Dr to send me off to a psychologist in case I am going loopy and because
I am getting nowhere fast with my diagnosis and I feel that my symptoms are increasing and my disability is also.
How refreshing to read the opening articles with the information on MS, MRI's and how they don't necessarily show up every lesion, symptoms and diagnosis of same.
I now know I am not going nuts and I really truly don't consider that my symptoms are all "psychological."
I thought I had found an ally in the psychologist who initially was great but nope, after taking in my MRI's ( he asked to see them ) he is no better than the others and is another text book junkie!
He said "your brain lesions could not possibly be producing any of your symptoms and it doesn't make physiological sense!"
I don't fit into the "text book diagnosis" and my lesions don't match my symptoms so therefore they are all now of the opinion that I have just conjured them up to get attention?
Oh please!
Do they really think I want to feel this way? Do they think I have nothing better to do than to surf the internet looking for symptoms so that I can run back and forward and have medical procedures that I hate to get attention?
The psychologist suggested that because I am not in a close relationship with a partner ( I don't have one ) I am compensating by making all of this up so that I feel that somebody cares about me.
Is he for real? I mean, come on!
If you had of asked me what symptoms I had 3 years ago I can only remember telling the neuro I was tired all the time, had become clumsy, was dropping small objects and of course the reason I went there in the first place was because of my facial pain and I was looking to get some type of better pain