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Interesting artice for seronegative MG'ers

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Old 03-13-2014, 06:13 PM #1
catie catie is offline
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Default Interesting article for seronegative MG'ers
I found this letter to the editor in the Cleveland Clinic Journal of Medicine responding to an article on Myasthenia Gravis that was published this past November. As a patient with seronegative and EMG negative MG, I am grateful to my neurologist for treating me based on a clinical presentation of MG.

The MG letter is on page 2.

Cate
Attached Files
File Type: pdf 144.full.pdf (61.7 KB, 447 views)
Last edited by catie; 03-13-2014 at 08:11 PM. Reason: Misspelling
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AnnieB3 (03-13-2014), Bipedal Primate (03-15-2014), cait24 (03-13-2014), Needananswer (03-14-2014), Panorama (10-18-2014), rach73 (03-15-2014), southblues (03-13-2014)

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Old 03-13-2014, 09:30 PM #2
MaureenNY MaureenNY is offline
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Originally Posted by catie View Post
I found this letter to the editor in the Cleveland Clinic Journal of Medicine responding to an article on Myasthenia Gravis that was published this past November. As a patient with seronegative and EMG negative MG, I am grateful to my neurologist for treating me based on a clinical presentation of MG.

The MG letter is on page 2.

Cate
I saw this on another blog. Looks like they are starting to "get it"...
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Old 03-14-2014, 07:50 AM #3
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Thanks dr posting the PDF, Catie.

There are so many seronegative MGers suffering and then being told it is all in their head. Not sure why clinical symptoms are so often overlooked, particularly those that have such a neg impact on activities of daily living.

I'm pleased to see this getting air time!
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Old 03-15-2014, 03:35 AM #4
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So there is hope that maybe some day in the future I can add a positive MG diagnosis to my already long list of ailments!

Thank you for posting this.

Rach
__________________
Diagnosed with:
Postural Orthostatic Tachycardia Syndrome,Post Prandial Hypotension, Orthostatic Intolerance, Arrythmia, unstable blood pressure, severe autonomic nervous system dysfunction ,Ehlers Danlos Syndrome Type 3,Gastroparesis,IBS,Hidradenitis supprativa
And Myasthenia is still a possible diagnosis depending on which Dr I see.

My blog address is
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Lord, grant me the serenity to acceptThe things I cannot change,The courage to change The things I can,
And the wisdom to hideThe bodies of Doctors I shot
When they said,"You're perfectly healthy,
It's All In Your Head."
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Old 10-18-2014, 02:52 AM #5
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Quote:
Originally Posted by catie View Post
I found this letter to the editor in the Cleveland Clinic Journal of Medicine responding to an article on Myasthenia Gravis that was published this past November. As a patient with seronegative and EMG negative MG, I am grateful to my neurologist for treating me based on a clinical presentation of MG.

The MG letter is on page 2.

Cate
They found a new antibody to diagnose Myasthenia, for at least some of us seronegatives. I tested negative for the AcTh and MuSK, but I have not been tested for this one.. guess I should get in line! I have no diagnosis, despite many of the symptoms, most of which have thankfully settled now (thanks to daily Kundalini yoga, I believe!). Check out the article below:


http://www.sciencedaily.com/releases...1111112641.htm
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