posted
i live in massachusetts and want to have a workup for mitochondria disorders and damage. can anyone direct me to a good mito doc in my area? i was thinking boston was the place, but there is at least five docs to choose from
Posts: 723 | From boston,ma | Registered: Jan 2011
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Your LLMD should be able to help guide you. However, since lyme CAUSES mitochondria problems, that is where to begin. Mostly,
* address infection(s) that target mitochondria
* support the mithochondria with key nutrients.
You can search the web for organizations to learn more about mitochondria but they will not usually be lyme literate.
A muscle biopsy is a key diagnositic tool but, really, may be unnecessary - quite frankly, IMO, if one has lyme, they have mitochondrial dysfunction / damage.
Most LLMDs can very quickly determine if a patient needs mitochondrial support (we all do) so that we can achieve REPAIR as the infection(s) are treated.
MYHILL's information here discusses testing, etc. And there are many support links here, too:
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