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Old 05-04-2012, 10:58 AM #1
Royce Royce is offline
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Default I understand

I understand what you are going through.
My (several specialists) Dr's have made me feel like I was loosing my mind. they need to realize that pt's know their bodies best and to listen to them. I was also told there was nothing wrong with me, advised I may be depressed, chronic fatigue syndrome and fibromyalgia were among some of the wrong Dx. Finally after 2 1/2 years I went to a Neuro again for the second time. But this time I went to a teaching hospital. They did a full neuro exam and said one of my thoughts, poss MG ( I have also been thinking MS or ALS). I went for a EMG and SFEMG both came back abnormal and still waiting for AChR and MUSK to come back. What an exhausting journey. And they say stay away from stress. they are the cause of it!! I hope your journey becomes easier and you can find a Dr who really cares and will listen to your concerns. Good luck to you.
Royce


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Originally Posted by Swallow123 View Post
There seem to be a great deal of autoimmune disorders on my mom's side of the family. 2 aunts (and possibly an uncle) have MG and my mom has Lupus. I ended up with Graves Disease and MG.

After an SFEMG test in 2001, the neurologist decided I had Occular MG and gave me Mestinon. My blood test turned up negative.

The neuro didn't say much, perhaps because she was behind and perhaps because she was ill herself. Anyways, I didn't think anything of it and got my future scripts from my GP. My family isn't that close - especially when it comes to discussing diseases.

A few years later, I thought it might be a good idea to visit the same neuro for a check up, because I was experiencing some weakness in my extremities. Neuro said everything was fine and to increase the Mestinon as needed.

For about 5 years in all, I didn't realize it, but I had been making allowances for things like the long walks I used to take with my husband and neighbour in the evenings and choosing hamburger over steak - because filet was too tough.

In 2006, I started to experience breathing problems and woke up in neuro ICU of the local teaching hospital. Dr's did a course of plasmapharesis and finally removed the breathing tubes and IV's about 5 days later. According to the Endocrinologist, my thyroid levels were dangerously low.

YEARS LATER, I would find out that the Magnesium I was taking for muscle spasms was binding to the synthroid and weakening its efficacy. That, and the MG saw an opportunity to play havoc with my body. To this day, my neuro still believes that I quit taking my synthroid(???).

Anyways, for about 2 yrs, I was in that "Maybe she does / Maybe she doesn't" category that many of us have had to endure. Most times, I was treated with IVIG, Solumedrol, etc. FINALLY, after a Tensilon test, I got re-diagnosed!

Since I don't present in a text book manner, I was given a T/F psychological test that showed I also have CONVERSION DISORDER. Apparently, if you admit that you were sexually abused as a child - your "inner child" can manifest physical disorders to cover up for mental illness.

I was even told I had "drug seeking tendencies" and that I go for the "big guns" instead of a tylenol.

This was brought up, when I went to the ER for burning pain and swelling in my hands and fingers. Try to get ahold of any medical person on a Friday afternoon! None of the drugs I had at home were doing the trick - hence the "big guns" (Percocet). Later, I found out that I have osteoarthritis in my wrists and, were it not for my rheumatologist sending me for a bone scan, I'd be even sicker (mentally) than they first thought!

In the meantime, for MG I'm taking Mestinon 60mg x 3, Mestinon 180SR at night, 200mg Imuran & Prednisone (15mg alternating to 5mg every other day). I take a whole host of other drugs, as well.

As long as I take things easy and rest before a planned day out, I'm okay. The stress part can be tough to handle, but I seem to manage okay. It's only when I overdo it that I get into trouble.

My neuro now says that if I have trouble swallowing, I should go her hosp right away. Yeah - Like that'll EVER happen!

Sorry for the long winded story
Swallow123
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Old 05-04-2012, 01:06 PM #2
BackwardPawn BackwardPawn is offline
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Originally Posted by Royce View Post
I understand what you are going through.
My (several specialists) Dr's have made me feel like I was loosing my mind. they need to realize that pt's know their bodies best and to listen to them. I was also told there was nothing wrong with me, advised I may be depressed, chronic fatigue syndrome and fibromyalgia were among some of the wrong Dx. Finally after 2 1/2 years I went to a Neuro again for the second time. But this time I went to a teaching hospital. They did a full neuro exam and said one of my thoughts, poss MG ( I have also been thinking MS or ALS). I went for a EMG and SFEMG both came back abnormal and still waiting for AChR and MUSK to come back. What an exhausting journey. And they say stay away from stress. they are the cause of it!! I hope your journey becomes easier and you can find a Dr who really cares and will listen to your concerns. Good luck to you.
Royce
I know how that feels. For a long time I was told nothing was wrong with me. I was even sent to see a psychiatrist. Then finally I was given a diagnosis, only it was the wrong one. I was taking all sorts of nasty, cancer causing meds and they weren't doing much. The sad part was that I was seeing a neurologist regularly and had seen a neuro-opthamologist and neither mentioned myasthenia.

Eventually I just stopped going to the doctor. Fast forward about two years and I got to the point that I couldn't walk, so I see a new neurologist, he looks at my eyes and says, "I know what you have." Then he sends me to have hip surgery (as I hadn't connected the walking issues with MG, yet, knowing nothing about it, yet I have impinged hips). So I stop breathing on the table and when the neurologist hears about it, he's like, "You definately have MG, but I need to do some tests to confirm it." I was like, "Thanks, but did I have to almost die to get a dx."

But then he refused to treat it until I had a thymectomy. I wasn't about to have my chest cut open right after I stopped breathing in surgery. I switched neurologists again and my new neurologist has been overly cautious about surgery, though, and has insisted I put off the thymectomy twice now, as she didn't think I was stable enough. I'd really just like to get it over with, though.
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Old 06-19-2012, 02:23 AM #3
music girl music girl is offline
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Originally Posted by radarmomma View Post
I am having a lot of trouble with balance, muscle sensation, brain fog, memory, exhaustion. I dont know what to do anymore
Did you get any answers?
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Old 06-19-2012, 02:24 AM #4
music girl music girl is offline
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Did you get any answers?
Did you get a diagnosis?
I have some similar symptoms. My Neuro-Surgeon said my problem was Neuromuscular.
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Old 01-23-2014, 11:00 AM #5
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Originally Posted by radarmomma View Post
I am having a lot of trouble with balance, muscle sensation, brain fog, memory, exhaustion. I dont know what to do anymore
I am having all of these symptoms and negative blood work for mg but neuro sending me to another neuro, he wants muscle biopsy.
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Old 05-10-2015, 05:13 PM #6
michaelunty michaelunty is offline
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Originally Posted by radarmomma View Post
I am having a lot of trouble with balance, muscle sensation, brain fog, memory, exhaustion. I dont know what to do anymore
Hi, did you ever find/get answers to your symtoms? So similar to mine.
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Old 05-15-2015, 08:55 AM #7
davew41 davew41 is offline
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Hi, did you ever find/get answers to your symtoms? So similar to mine.

get vitamin d3 checked asap
dr calls it vitamin d 25 hydroxy test
bet its under 30 actually guarantee it is..
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Old 03-14-2016, 05:54 PM #8
Glenmeadowfarm Glenmeadowfarm is offline
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Smile resting aggressively

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Originally Posted by radarmomma View Post
I am having a lot of trouble with balance, muscle sensation, brain fog, memory, exhaustion. I dont know what to do anymore
I tell my son I am "very very busy" because I am resting aggressively! You have to get flat, get gravity off your body and really rest it. Put pillows under anything where there is muscle tension until you can float like a jelly fish. Pool floating works great, too! I rebound faster if I truly, truly rest my muscles, my mind, my emotions. Have to have the quiet in the room, the lights not bothering me, truly restful. The other thing I have done with good results is just go to my primary care doctor and tell her I am having a flare. She prescribes what I call a "poison ivy pack", a ten day thing where you are tapering down, of prednisone. For me, it's often enough to just hit the reset button and pull me up.
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Old 07-14-2018, 07:58 PM #9
LeeMac LeeMac is offline
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Default New to MG and How much variation is "normal"

Greetings,

I've recently been diagnosed with MG. Honestly my neurologist is still a bit skeptical because I tested negative for AChr antibodies and the symptoms came on after a bad concussion. However, my response to Mestinon is like night and day for resolving double vision, tension headaches, and overall fatigue.

My question is how much variability is "normal?" The double vision is fairly consistent but other muscles seem to vary greatly from day to day. Some days it's my legs, others my arms, and recently breathing which eventually passed. I understand it can vary, but I guess I expected that at least which muscles would be affected would be somewhat consistent.

Does anyone else experience MG this way or should I be considering asking the Dr. about other Dx?

Thanks, Lee
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Old 10-29-2018, 03:41 AM #10
aielwen aielwen is offline
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Originally Posted by LeeMac View Post
Greetings,

I've recently been diagnosed with MG. Honestly my neurologist is still a bit skeptical because I tested negative for AChr antibodies and the symptoms came on after a bad concussion. However, my response to Mestinon is like night and day for resolving double vision, tension headaches, and overall fatigue.

My question is how much variability is "normal?" The double vision is fairly consistent but other muscles seem to vary greatly from day to day. Some days it's my legs, others my arms, and recently breathing which eventually passed. I understand it can vary, but I guess I expected that at least which muscles would be affected would be somewhat consistent.

Does anyone else experience MG this way or should I be considering asking the Dr. about other Dx?

Thanks, Lee
Hi Lee, please feel free to read my introduction post on this thread. I am triple seronegative, but also find it's night and day with mestinon. Get a Single Fiber Electromyelogram (SFEMG) test done. It is considered the gold standard for MG for those who are seronegative. You should also get tested for LRP4 which is the latest antibody discovered to cause MG. Unfortunately, there are likely MANY antibodies that cause MG, but we only have tests for 3. If you are like me and test negative for LRP4, welcome to the small club.
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