Connections.

What an interesting two days I have had. Has me thinking about the matrix of talent that I live amongst.

I was chatting yesterday with Ben Miller, our orthopedic surgeon who handles all the limb surgeries that sarcoma patients need. We talked about a sarcoma symposium and how to bring more talented researchers to understand sarcoma and melanoma biology. It is in these small discussions that I find the thrill of discovery.

I am surrounded by talent.

Our cancer center exists in an academic university environment. Like a spider’s web, we are able to connect through interactions that focus on improving the lives of the patients afflicted with this illness. Wherever I turn, I find an opportunity to connect with someone.

So how does this web come to life? What are its components?

As I learn to write to you all and share my thoughts tonight I want to paint a picture of people who facilitate all the work that comes into a decision for a patient. It extends from helping my colleagues in Missouri understand angiosarcoma biology or keeping it closer to home to understand obesity and how it affects immunity.

It’s Wendee who fights harder than me to keep my ship afloat.

It’s Tina and Laura working hard to maintain a registry.

It’s Marian fixing and regulating my clinical trials.

It’s Melanie and Reggie coordinating and facilitating the research that keeps our fires burning.

Many meet “Mo” and he is just an interface to the matrix that lives behind him. Our multidisciplinary teams that focus on the clinical aspects of caring for patients, down to Erin and Juli who help schedule all the meetings and make this a reality.

I have connected with Scott Okuno at Mayo Clinic and Mark Agulnik at Northwestern in Chicago. And now I’m talking to you. I wonder how this all started? I simply asked to get to know them and found them so receptive to collaborate. It must be the midwest.

I am blessed to be amongst such dedication and commitment. I can see no boundaries.

From Terry and Jo ‘Riding It Out for Amber’; to the Bailey’s for the courage to stand up and bike; to the Yates for yelling “fore”; to Nancy’s promise; to Alissa and her amazing determination to never give up; to Hannah for making me part of her family… no boundaries.

Hence this small introduction to my team- anyone can join us. These are some of the many faces that help me fight. Many who have gotten to know me have asked me how I do it every day, facing this.. I tell them, “I married a psychiatrist” and they laugh. Well, Arwa, my wife, knows better. It is the people that surround me that I draw my inspiration to help those in need. Understanding our connectivity to each other and the willingness of so many to put their best food forward makes me proud to be  a part of all of this.

Mo

 

Check out these websites:

Ride It Out for Amber

Courage Ride

The Steve Yates Golf Tournament

The Jim White Foundation

 

 

Melanoma, Iowa and Our Story.

Melanoma has been a disease that has fascinated me. Unpredictable, dangerous and exceptionally intelligent. Its funny to talk about a disease this way.

I have been wondering how one actually starts blogging, thought about a start but perhaps I can talk to all of you this way.

Through the science that is attached to our work and our mission. Melanoma is a disease that is increasing in Iowa and across the world. 1 in 68 people in the United States will be diagnosed with this Melanoma in 2013. How can something so small on the skin have such a powerful impact on us as human beings?

Perhaps its origin might shed light on how and why it is unpredictable ; It originates in a group of cells called the “Neural Crest” , these are found very early when we are only embryos. Neural crest cells, stem cell biology, melanomagenesis (the cancer biology of melanoma), how these cells function normally are important in helping scientists elucidate the secrets of this disease.

Over the last few years, A dedicated team in Iowa and the midwest is slowly coming together to focus its efforts on melanoma research and understanding this disease. We have partnered through the Midwest Melanoma Partnership (MMP), http://www.midwestmelanoma.org, with 15 institutions to create a robust mechanism to share ideas and collaborate on many projects.

I will be writing regularly every wednesday night telling you our story and letting you meet the amazing people who have really made an impact to help patients get the best care. We value collaboration, creative ideas, universal sharing and innovation. Let this be a platform for us to communicate and for us to understand how to do this better.

Mo