Life Today

This Shark, Swallow you whole

 
 
This photo was from my 40th birthday- six months after we lost Samantha.
 
A friend quoted it perfectly, “And then Heather opened her mouth, took all of her friends and swallowed them whole.”
 
And I would have.
 
Because I was so empty.
 
Oh yes dear friends, swallowed you whole. Anaconda ain’t got none…
 
But that was 8 years ago. Eight years ago when Missy Moo left us. Eight years ago today.

I still pose with an open mouth

 
 
 

 

 
 
 
 
Even in the final photo…..in front of hundreds of people accepting a great big check…
 
Mouth
 
Wide
 
Open
 
Eight years later, would I still swallow you whole? Nah, I think you might be a tad chewy. Dare I say too spicy?
 
But more importantly, I don’t need to anymore. The hunger to replace a famine in my soul has subsided, the want, desire, the miss, it is no longer so gut wrenching and desperate. Eight years later.
 
You all have helped me to fill that void and for that I am forever grateful.
 
So despite the perpetual open mouth, I no longer need to devour you.
 
Perhaps a nibble.


Life Today

Hope is Being Able to See that there is Light- Despite all of the Darkness- Desmond Tutu

A mitochondrial diagnosis is dark. And lonely.

Here is where your donation will go to provide some hope and light.

Every 15 minutes a child is diagnosed with a mitochondrial deviation that will manifest by age ten. Since mitochondria generate energy within muscle and organ cells, clinical problems such as seizures, heart and liver issues, vision and hearing loss, muscle weakness, migraines, and developmental delays are prevalent.

Because of the complexity of the disease and the difficulty in getting an accurate diagnosis, mitochondrial disease is considered rare and is grossly underfunded. In 2012, our clinic at the hospital was at risk of closing its doors. The funds raised by our team enabled the clinic to remain open and continue to employ its researchers.

It is because of this team and their amazing efforts that we have a research presence in Colorado.

–  2013 we purchased a diagnostic piece of equipment for the lab called an Oxygraph. The Oxygraph measures oxygen exchange from one cell to another and can analyze where the breakdown in energy exchange happens.


2014 we contributed funds so that our neurologist could input needed data to make Children’s a part of NAMDEC – the North American Mitochondrial Disease Consortium.

–  This contribution made it possible for Dr. Austin Larson to come to Children’s through a  NAMDEC grant. He joined us as a fellow and is staying on as an Attendee focused on Mitochondrial research, treatment and clinical testing. Dr. Larson spoke and met with families this year at the UMDF conference- we are very excited to have him on board.

–  2015: We continue to support the clinic and bring on another research assistant

  2016: We sponsor a grant between Dr. Larson and Dr. Green to fund a research project looking at the link between mitochondrial deviations and type one diabetes.

–  2017: We have a protocol approved by Children’s Hospital to study mitochondrial disorders specifically in Colorado

   Stealth Biopharmaceuticals announces that Children’s Colorado will be a trial site for a new mitochondrial drug Elamepretide.  This trial was only granted because of our ability to show sustainable, financial support to the clinic- all through Summits for Samantha. 33 sites were chosen internationally


And in 2018…. Children’s Colorado became part of the Mitochondrial Network of Care; one of 23 national sites.

  Our researcher was awarded an NIH grant to advance her work. The Oxygraph we purchased was instrumental to her research.

   We will see our first clinical trial patients in July

  We continue to provide supplements, support and family grants to our mitochondrial community


What will next year bring????

All because of you.