It’s actually kind of amazing….


Chatting with Katie tonight as she’s doing an English paper how we found Dr N and Mito disfunction came up. 

Click here to start reading the story.

Continuing the story

The last piece of it…

Amazing, if you think about what we know now. 

Now we know that mito isn’t the primary condition. In our case it is secondary to a genetic condition not previously associated with mitochondrial disfunction. That everything is a symptom of a genetic condition that we are working on identifying. 

With us it’s most likely the kif1a gene, as Hugh and I carry similar recessive mutations on chromosome 2. 

So amazing how far we’ve come within Dannys lifetime. 

I can’t wait to see how much farther science goes.  

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