Is this MS/ waiting is hard.

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Is this MS/ waiting is hard.

Postby simpy1 » Sat Mar 16, 2013 9:28 am

I am new here and new to even the concept of MS...

I had an "attack" last week that sent me to the ER...I had left sided "pins and needles" in my face, arm and leg that last about two hours. It started in my arm and then spread to my face and leg. I thought I was having a stroke. After all the usual tests, no stroke was seen, but I have always known I have had bright spots on my brain (due to MRI's for another issue), but never thought of MS until I was reading about some of the symptoms I have. I was told the white spots were probably because of migraines.

Whatever this attack was last week has left me COMPLETELY exhausted. My left leg, although not like it was that night, does not feel "right" ....almost heavy or something. Sometimes when trying to write with my right hand, things just dont seem to be right and I have a hard time controlling it, or it just seems to be extremely slow for some reason.

My doctor has asked my husband and I to come and "talk about my MRI results" next week. He has said its NOT cancer, but wants to go over somethings and I am thinking it might be MS.

For the past few years I have been having some unusual symptoms that have been on my mind, but I keep chalking them up to something else. I have had a numbness, burning, itching in my left thigh that has been present for about 2 years. At one point, I could not have anything touch my skin there...even the sheets on my bed rubbing would cause a very uncomfortable heat and burning sensation even though it was completely numb. Strange enough, is almost gone and seemed to go away the other night when these other symptoms popped up.

After doing anything strenuous with my arms I frequently have tremors for a day or two...these are noticable when drinking or holding my arms up to my face etc. I also have a general feeling of shakiness inside my body that I can't explain.

Feels like my legs are heavy now and then.

I am horribly off balance...I frequently cannot walk in the dark and bump into walls. I have been known to fall for absolutely no apparent reason and this was a frequent joke between my best friend and I. This is probably my most noticable symptom.

I also have an issue with missing steps...its like my brain isnt coordinating when my leg should step up...I have to think about this sometimes and it seems strange to me.

My eyes are blurry...I have had a few episodes when I wake up in the mornings and I just cannot see well....I rub and rub my eyes but they seem to stay blurry for hours. I have a general foggy feeling to my vision that I can't really explain...almost a haze...I thought maybe it was just that I am in my 40's now.

Anyways, if I do have MS....these things have been going on for years and have never been severe enough until the last year with numbness etc. I am scared to belong to this club, but it seems there is a lot of support and knowledge here and I would appreciate everyone's input greatly.

Thank you!
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Re: Is this MS/ waiting is hard.

Postby lyndacarol » Sat Mar 16, 2013 3:35 pm

Welcome to ThisIsMS, simpy1. Since you seek "everyone's input," I offer you my standard action plan recommendation – we cannot answer your question, "Is this MS?":

First, you may not have MS at all, but there is a possibility; it is a differential diagnosis – made by ruling out other possibilities, as you may know. Very often, it is not easy or quick to diagnose. Before expensive tests even existed to diagnose MS, doctors used to diagnose MS on the basis of symptoms and if they temporarily worsened when the patient sat in a hot bath for a while. IF you do have MS, you have found many supportive friends at this site. Don't be "scared to belong to this club." In general, we are a friendly group. We come from diverse experiences and hold diverse ideas. We do not agree necessarily in our thoughts on MS – my personal suspicion is that excess insulin (and resulting insulin resistance) is responsible for many MS (or "neurological") symptoms. You will probably not agree with some of us either; we only ask for tolerance when we express unconventional ideas.

Second, I hope the doctor you and your husband are meeting with next week is a good GP or internist, that he is compassionate and enjoys being a "disease detective." I am not sure that a neurologist would consider ordering the following blood tests. I tend to believe that if you see a surgeon about a problem, he will find a solution in surgery; if you see a neuro, he will only see the problem/solution in neurology. I just read an article that summed this up well: "doctors are experts in, and only test for, those parts of the body in which they specialize."

A GP can order the tests necessary to rule out some non-MS possibilities. If you and your physician have not already started your investigation, start at the beginning with your symptoms list and with a thorough physical baseline examination including blood tests for your (#1) cortisol level, which can be elevated with stress and cause blood sugar to rise; (#2)glucose AND (#3) insulin levels (these are two DIFFERENT tests – I think the "fasting blood insulin test" is the most important and one of the least expensive tests; your level may be above the optimal 3 UU/ML; (#4) thyroid hormone levels (TSH, Free T4, Free T3, Total T3, Reserve T3, and antithyroid antibodies). The (#5) CRP (C-reactive protein) test (testing for inflammation) and (#6) liver tests are also a good idea. Ask for a copy of all your test results for your own file.

I suspect insulin involvement and resulting insulin resistance in skeletal muscles causes many symptoms, such as you describe (excess insulin is known to thicken and stiffen smooth muscles; skeletal muscles, too). I believe the burning sensation in my feet and legs is actually due to the strongly irritating hormone insulin damaging the inside of my blood vessels or affecting the muscles in the blood vessel walls (and not initially the nerves).

Third, if you like to read and if you do have MS, start your reading with two books: Multiple Sclerosis: The History of a Disease by T. Jock Murray, OC, MD, and I think The Multiple Sclerosis Diet Book by Roy Swank, MD, PhD and Barbara Dugan is a good second book to read or even have. You may be able to get these through your local library.

Fourth, since I believe insulin is a major player, from this day forward, I encourage you to eat a healthy diet (a good idea whether or not you have MS,) – a diet that will not trigger insulin production. Many people find that diet can influence the symptoms of MS. In my opinion, this means a low-carb diet -- remove all trans fats (These increase insulin.) remove all sugar (including beer, wine, etc. which have sugar), remove all artificial sweeteners, including sugar alcohols like sorbitol, xylitol, etc. (These promote insulin production, too.), and white flour, white bread, white potatoes, white rice (in fact, all carbs so far as possible) from your diet.

My suspicion is that Fatty Liver Disease is also involved in MS, since visceral fat (belly fat) secretes cytokines (like poison to the internal organs), which lead to increased insulin, which leads to inflammation which leads to more visceral fat… And the cycle goes round and round. Diet is important; in fact, you may find the account of Dr. Terry Wahls and her dramatic improvement in MS interesting (http://www.TerryWahls.com).

All the best to you.
My hypothesis: excess insulin (hyperinsulinemia) plays a major role in MS, as developed in my initial post: http://www.thisisms.com/forum/general-discussion-f1/topic1878.html "Insulin – Could This Be the Key?"
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