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Polymiocitis and MM (Read 6170 times)
alamo7300
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San Antonio, USA, TX, Texas
Gender: male
Polymiocitis and MM
May 1st, 2005 at 6:53pm
 
I was diagnosed with MM in 1987. In 1992, I was diagnosed with polymiocitis (muscle inflammation causing weakness, only in my legs). Doctors I am seeing now are wondering if there could be some correlation. Also, this past July I was found to have a spastic coronary artery. My cardio Dr, is perplexed by it and is wondering if there is a poly/MM correlation. I have 3 rare conditions, you think I could hit the lottery with these odds. Undecided
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alamo73_99  
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kotipup
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My daughter, Daphne, has
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Posts: 247
Landenberg, USA, PA, Pennsylvania
Gender: female
Re: Polymiocitis and MM
Reply #1 - May 1st, 2005 at 11:46pm
 
Hi... I am not sure about polymiocitis and Moyamoya, but I would not be surprised, at all, if you found out the two were related.

My daughter also has a number of "rare" problems that seem to be moyamoya related.  First, she has a heart defect called coarctation of the aorta, where the aortic arch of her heart was thickened/narrowed (she's had surgery).  She also had a rare form of epilepsy, called infantile spasms, which probably was a result of the decreased blood flow to the brain.  She also has some unusual eye findings that we think might be moyamoya related.

I've seen research on moyamoya being an autoimmune disease, which could go along with the muscle inflamation.  Also, my daughter's doctors are investigating her elastin gene... mutations of this gene can cause a number of problems throughout the body.  So, whatever the pathology of your moyamoya... it could be the same pathology of your other health issues.

Jenny
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alamo7300
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San Antonio, USA, TX, Texas
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Re: Polymiocitis and MM
Reply #2 - May 2nd, 2005 at 8:59pm
 
Thanks for the info Jenny, I will run this by my Dr's. My prayers are with your  daughter and you.

Chuck
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alamo73_99  
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Mayhem
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diagnosed 1996

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Rochester, USA, NY, New_York
Gender: male
Re: Polymiocitis and MM
Reply #3 - Jun 14th, 2008 at 3:29pm
 
This thread was created by my brother three years ago. He has since had a massive stroke and has been in a vegetative state for eight months.
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« Last Edit: Jun 14th, 2008 at 3:30pm by Mayhem »  
 
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gotchlorine
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Our daughter, Tara, lives
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San Jose, USA, usa, 24, 158, CA, California
Gender: female
Re: Polymiocitis and MM
Reply #4 - Jun 14th, 2008 at 3:46pm
 
I am so sorry to hear this about your brother, Mayhem.  Had he had surgery/ies for his moyamoya?  Have the doctors given a prognosis?

My thoughts and prayers are with Chuck and your whole family.

Smiley Jill
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sca4gold2002  
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Mayhem
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diagnosed 1996

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Rochester, USA, NY, New_York
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Re: Polymiocitis and MM
Reply #5 - Jun 28th, 2008 at 3:53pm
 
gotchlorine wrote on Jun 14th, 2008 at 3:46pm:
I am so sorry to hear this about your brother, Mayhem.  Had he had surgery/ies for his moyamoya?  Have the doctors given a prognosis?

My thoughts and prayers are with Chuck and your whole family.

Smiley Jill
He had the same surgeries I had seven years ago, the EDAS I think, sorry my memory is bad, and his surgeon was Dr Ogilvy at Mass General. Prognosis isn't good, as far as ever regaining higher functions.
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