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Eds & Mitochindrial Issues


jjb

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Hi all. I brought Ava to see a mito specialist last week who said it sounds as though we both could have mito disease.

We also have EDS.

I had mentioned to her that a cocktail of supps similar to the mito cocktail is also used for EDS and we started talking about a possible relationship between the two conditions.

In the past I know I have read EDS effects the mitochondria, but now I cannot find any info.

Does anyone have any info connecting the two? Does anyone here have both mito disease and EDS?

Thanks

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Jen,

Go to google scholar and type both conditions in the search engine. A multitude of hits will come up. Peruse and see if anything fits Ava. I searched already & there's a lot of stuff to wade through.

Let us know what you find out. I hope you're on the road to getting her some much needed help.

Hugs-

Julie

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I don't have any info connecting the two, I can tell you I'm waiting test results from Dr Shoffner on my mito testing. Who did you go to for testing? Did you have fresh or frozen tissue testing? I hope you get some answers that help your feel better

We saw Dr Sims. So far just had blood work done.

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Julie, yes a lot come up but none are really about the two conditions or whether or not mito is effected in EDS.

And of couse those are only the articles I was able to wade through as many of those articles on GS requires payment.

:/

Jen,

Go to google scholar and type both conditions in the search engine. A multitude of hits will come up. Peruse and see if anything fits Ava. I searched already & there's a lot of stuff to wade through.

Let us know what you find out. I hope you're on the road to getting her some much needed help.

Hugs-

Julie

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