I am now 50 and finally diagnosed last year with Congenital Myasthenia Gravis. I am finding everyones input so helpful. I do not meet much criteria test wise (only the nerve muscle conduction), ha, but my body doesn't really care, it still has the symptoms anyway. I have been in trouble for symptoms since I was a child. I am finally not in trouble, whew.
I have alot of questions and look forward to learning from all of you thruout this site.

Welcome! This is a great place to meet folks with MG and to share info about it.

What type of CMS do you have, and what treatment are you getting for it?

why was it diagnosed just now, if you were having symptoms and EMGs for many years. ( or did I get it wrong?).

alice

I have had symptoms since birth (orphanage til 6mo). It hit very hard when I was 25. I come up neg in the blood tests, so I was told it was psychogenic/conversion. Once that is in your records...............
I would try about every 3-5 yrs to dare get help. Finally I demanded to be diagnosed psychogenic/conversion by a real psychiatrist. The psychiatrist was impressed with the work I have done (massive counselling) , diagnosed no Psy/conv and was so concerned with my symptoms referred me to Wa Univ Med center. They also ruled out mental, leaned toward MG but no diagnoses was given.
I went back to a neurologist who had worked with me years back (he had temp quit his practice for health reasons). He had given me the nerve muscle cond test which was positive. That is the only criteria I meet besides many symptoms. He diagnosed me CMG. I had not realized there were different, forms?, I have no idea. The mestinon did not do anything. He said he felt mine was not treatable and said we would treat the symptoms as we go. He sent in therapists. I am amazed at how many things I had not realized were symptoms! Even chewing! Oh, I would get in so much trouble as a kid with the not being able to chew! Oh my.
My neurologist sadly has quit his practice again so I will have to go back to the Wa Univ Med. I will ask more. I had not asked my Dr anything, to be honest. My daught and I did not even breathe til we were out of the office and were in shock I was given any diagnoses!
There is, of course alot more to it all, but that is the 'short' reason it took so long. It affects all my muscles. The psychiatrist gave me my dignity back. I really appreciat her and will share some of her advice some time.

First, I am so glad that you were finally given a proper diagnosis.

Second, I am so sorry to hear of what you have been through.

Third, there are many types of congenital myasthenias, and some can be treated very effectively. And they are constantly finding new mutations.

If you have a diagnostic EMG (I still find it hard to believe that no one thought of doing this test before!), then you may want to try and get to Dr. Andrew Engel at Mayo clinic.

I do hope you get a more accurate diagnosis and the proper treatment you deserve (and have deserved for many years).

And keep fighting for your dignity and proper medical treatment.

You are not the only one that has to deal with this.

An excellent psychiatrist (probably similar to the one you saw) said this years ago-

"In the main the diagnosis of ‘hysteria’ applies to a disorder of the doctor–patient relationship. It is evidence of non-communication, of a mutual misunderstanding ... We are, often, unwilling to tell the full truth or to admit to ignorance ... Evasions, even untruths, on the doctor’s side are among the most powerful and frequently used methods he has for bringing about an efflorescence of ‘hysteria’... The diagnosis of ‘hysteria’ is a disguise for ignorance and a fertile source of clinical error. It is, in fact, not only a delusion but also a snare.”

Eliot Slater, ‘Diagnosis of “Hysteria”’, British Medical Journal, 29 May, 1965, p. 1399


alice

I really do appreciate your reply. I see your responses and involvement with others and you are amazing! Thank you for the Dr's name at the Mayo, I will keep it in my paperwork. This neurologist wanted me to go. Had me set up with an appointment and everything, but, my disability does not cover it. Felt like my neurologist was as let down as I was. I still wish I could go.
The quote is so true. I had read while looking up the psychogenic/conversion that this is what doctors call hysteria. Interesting. They seem to cause it.

I read some of the threads of ones not diagnosed yet, oh, what a painful spot. It really wears on you. I feel so bad for them. I hope they all get their diagnoses, atleast close enough to get the help they need.

One factor that held back getting help was I was in Alaska for half of that time. My general practitioner was so encouraging. He hung in there with me thru alot of years. He always said he tought it was either MG or MD. He was seeing me when it hit so hard.

Many neurologists tested me in the past for MS. Everyone has thought I had MS. So, I get tested for MS. I do not meet the criteria and I am dismissed. 'Let me know if you get any worse' I am told. Ha! If I come back, worse, I am told it is mental.
Truely it only takes one report saying it is mental and this stops many from being willing to go any further.
I had gotten to where I only went in to the neurologist when I was doing better. That didnt go over well, but I could no longer bear being treated so awful while at my worst.
I also realized many have assumed it is my legs that make it hard for me to walk. But actually it is more my hips. I clarify this now and insist the physical therapist reports are actually read and considered!

The psychiatrist I had seen answered alot of my questions and her response to why all the overboard diagnosing of conversion/psychogenic, etc, made alot of sense. My friends kept telling me it must be my insurance, I did not agree. She said the doctors have a reputaion. Alot of their reputation is their percentage of diagnoses. They want to maintain a high ratio, 98/99%. If you are not text book and will take time, this will lower their diagnoses ratio. So...they throw out the easy 'mental' diagnoses. Voila', they maintain their high ratio, sadly the patient suffers. Sure explained alot to me and helped me look at them different.

Anyway, thank you for your response. I am so glad your friends and you are on here. All of you are obv very intelligent, caring and full of useful information.

There is a type of myasthenia called limb-girdle= DOK7.

The way you describe your walking sounds as if this might be your diagnosis.

This is important, because there is pretty effective treatment for it.

Maybe if they can't send you to Mayo, they could at least send some tests?

Or they could try treating you with Ephedrine/ Albuterol.

Could you give more details of your symptoms?

alice

Oh my, my symptoms. I am still learning what they all are. Sounds silly but I was never told something was a symptom. Even the eyelids. My son looked up MS symptoms years back and we fell over laughing at the picture of the guy with his eyelids low. Unbelievable. Just something that happened. My kids always thought I was just grumpy or really mad as my eyebrow lowered also.

Of course, drooping eyelid. Alot of drooping in my face, eyebrow as the day goes on (mostly on the right side). Effects my speech, severe at times. Tremors, hoarse with exertion-even standing. Breathing (they just got me a hosp bed to sit up) All my muscles fatigue from exertion, sitting-using my torso really is hard on me. effects breathing alot. Neck fatigue. bladdar at times.
Walking is harder as I go. Therapist showed me I use the muscle inside my thigh to walk, that is why my feet turn out first. Very unsteady hips, gate. feet drag the more I go. I am easier walking sideways. I use an elecwheechair for any distance. (Just got it now that I am not 'crazy')
I had trouble chewing since child. Trouble swallowing.
Here they looked and my esophagus is not moving the food thru. They stretched it twice, that lasts about a month for me (was great to eat! and feel it go down, I had no idea) I have had food come up after I fell asleep since I was a teenager. Guess it just sits there. Have to grind my food now-ewwww!
I appreciated the input of the therapists of the fatigue effecting thinking and memory. I struggle there. I struggled thru school. This is a big one all the time.

thats all i can think of right now.

I had not realized tests could be sent to the Mayo. I will ask about that at my visit to Wa Univ. I will ask what kind of CMG is diagnosed in my records. Tho, I am having a hard time finding my records to have them sent.

Many mention the nerve muscle tests causing pain. I did not feel much, had it twice. I feel that electrical feeling alot. The neurologist kept apologizing like it should hurt but it did'nt.

I was wondering, have you heard of anyone having symptoms with their heart along with their muscles with MG? Just wondering.

Did they do any respiratory tests? or a sleep study?

It sounds like you may benefit from non-invasive respiratory support.

I am not an expert on CMS, so can't say which type it is (they are also constantly finding new ones), but I don't think its reasonable not to try and find some treatment that could work.

I do not like the pulmanologist and looking for a new one. He does not answer questions and does not listen at all. My oxygen level stays acceptable, just the labor to breathe is exhausting.
The respiratory tests, he says I have COPD. He insists is from asthma. My speech therapist was here one day I was having a very hard time breathing. I would not have said a thing, I have always had it happen. She was very concerned, said I was having a,oh I forget the name when your symptoms onset. I had been holding my grandson, he is a big baby! We call him Chubba Bubba for a reason, ha. This is what made it come on.

The pulmanologist had me do the sleep study as he was convinced I have sleep apnea. I do not. The people who did the study said they saw a few things, like restless leg, but I would have to find all the things out when I saw my pulmanologist. Well, he said there was nothign else! He did not even mention the restless leg. I have to have to the records sent to my reg. dr.

I told him the breathing is onset by anything, holding something heavy for me. He referred to MG, not CMG and said this would be from muscle problem if it was like Lou gehrigs (sp?) or somethng like that.
I dont know. I just dont understand any of this. I am overwhelmed that suddenly 'I have symptoms' and they are serious. Ha. I was looked at like a looney for even havign a cane.
I get so tired, add on the stress of a doctor, I am toast. I am afraid of them now. I have been yelled at, spit raspberries at, it is unbelievable. I am so use to just being sent out, now I have all this information to try and keep up with.

When my last neurologist sent the team of therapsits, I was so scared. They turned out to be so nice, kind and informative. The physical therapist came. He did not say much at first, just asked questions. Did the strength tests, etc. I was so stressed. When he was done, he said words to me i could not believe. he told me I have done amazing for what I am dealing with! liek that was not enough, he said he was not going to give me exercises! No way! He said my treatment was energy conservation and that is what he would work with me with. He said I did a great job figuring out how to walk with my cane. ..........it was all I could do not to fall on the floor and blubber...Bohoohoo, ha! Blaahhaha! I still laugh at the control I had to use to not really do that!

So much had been cut for the disability here. but your idea of having tests sent to the Mayo I will def talk to this next neurologist. I had seen her before adn she treats eveyone with dignity.

I have to say, all the help from the therapists has benefitted so much. I am not as hoarse. i was all the time. I stop now when I am tired, which is pretty regular. But i see changes and no longer feel bad our guilty about it.



I