Hope for Inclusion Body Myositis?

Recently we discharged to home care a patient with neuropathy and weakness secondary to Inclusion Body Myositis, an inflammatory muscle disease with sensory and strength changes (weakness). As far as I am aware, there is no known cure.

In no way am I suggesting curative care was achieved. But this patient was 20% better in just five weeks, and this is after 2-3 years of standard interventions. The most striking gain though was in proximal lower extremity muscle strength gains, which objectively improved substantially off base-line measurements.

We modified our ND Protocols to include enhanced anti-inflammatory activity by boosting glutathione levels (a master detoxification system in the human body) and increasing EPA (the most anti-inflammatory Omega 3 EFA) levels, monitoring vitamin D levels, and a few other tweaks.

The best thing about our work is to see patients like this respond, and that gives us both hope, and reason to explore how we can help more people with similar illnesses.

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