Is there any natural treatment for Moyamoya?

Are there natural treatment(s) that may improve the quality of life of people with Moyamoya? Here you can see if there is any natural remedy and/or treatment that can help people with Moyamoya

Natural treatment of Moyamoya
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Natural treatment of Moyamoya

Moyamoya life expectancy

What is the life expectancy of someone with Moyamoya?

3 answers
Is Moyamoya contagious?

Is Moyamoya contagious?

Celebrities with Moyamoya

Celebrities with Moyamoya

Is Moyamoya hereditary?

Is Moyamoya hereditary?

ICD9 and ICD10 codes of Moyamoya

ICD10 code of Moyamoya and ICD9 code

Living with Moyamoya

Living with Moyamoya. How to live with Moyamoya?

3 answers
Moyamoya symptoms

Which are the symptoms of Moyamoya?

6 answers
History of Moyamoya

What is the history of Moyamoya?

World map of Moyamoya

Find people with Moyamoya through the map. Connect with them and share experiences. Join the Moyamoya community.

Stories of Moyamoya

Moyamoya stories
  Hi I am Jenna's Mom, Kristina and I run this page. I am so excited to be able to get Moyamoya Disease listed on Disease Maps. Please read Jenna's Story and contact me with any questions or to talk. Our Facebook page is listed at the bottom.   ...
Moyamoya stories
I have 3 children born with mm  my oldest was misdiagnosed for so long that it wasn't until my 2nd child was born and began having strokes at age 2 months,  multiple tests multiple procedures and acquisitions of shaking baby syndrome  did we find ...
Moyamoya stories
My son is 2 years old and between  August 2015 and October 2015 he has had 3 strokes, he was dignosed with moyamoya, he has had surgey in the right side of the brain and we  are waiting to get second surgey in early 2016, as I no how hard and shock...
Moyamoya stories
I have had heavy headaches for as long as I can remember. I was diagnosed to have migrane when I was 12 years old. In year 2011 I started to work in a big company as a payroll accountant, it was at the end of the year. It was a really hectit time sin...
Moyamoya stories
My sons name is jayden and he's two years old he was diagnosed with mws almost 8 months ago if he could talk this is what he would tell u about this syndrome and himself. I am have mws but mws does not have me doctors said i never crawl but I'm scout...

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