Mucosal Melanoma Survivor
Speaking about Mucosal Melanoma……
Do you have a Conference, Symposium, or Summit coming up and need to book a Keynote/Motivational/Inspirational Speaker?Make your Event memorable with a One of A kind Experience from Chris White as he shares about his diagnosed Mucosal Melanoma. With all odds against him to live, he defied the odds of all probability, and not only survive, but thrived through terminal cancer by way of clinical trial and TIL Therapy. From Clinical trials, Rare disease, Rare cancer, Patient Engagement, Patient Experience, Patients as Partners, Cell Therapy, Immunotherapy, Melanoma,
Merchandise Coming Soon!
Some of my favorite sayings, some of my favorite quotes. Original artwork all design by yours truly. Come shop at my online store from Hats, shirts, socks, and beanies. Coffee Cups to blankets to cushion straps for your seat belts to protect your Port. SHOPIFY Purchased and site in development
METS to the brain Strike 3 I’m out? I don’t think so
At the 11th hour at the bottom of the ninth I hit a home run that got me back in the game and saved my life Mucosal Melanoma Speaker/Advocate cancer blog Mucosal Melanoma Survivor. More about this can be found on Chapter 18 of my Blog “TILs from the Chris”
Juice Plus Affiliate
My mother introduced me to Juice Plus in 2017. In 2018 I tripled up to bridge the gap and prime my system nutritionally. As a Mucosal Melanoma Survivor, I continue to promote and share Juice Plus and healthy living but now as an affiliate.
Tower Garden
to get the most out of your nutrition, you should be eating 10 to 12 servings of fruits and vegetables a day. That can be extremely expensive and also time consuming going to the store regularly. Why not grow your own? The benefit pays for itself over and over again both nutritionally and monetarily
You only miss 100% of the shots of those you don’t take
There’s no better time than the present
There's much to see out there and you never know unless you look. Figure out what you don’t want to do, and don’t do that But the only way to know is to try new things and then try some more.
It’s not the years it’s the mileage, let’s take a walk
Let's Get Acquainted
This blog came about from a form of therapy for myself. I started writing about my story as a way to summarize my journey. The more I researched my specific story the more I come to find that I am one of the only one of my kind.
There is very little to nothing out there about anybody that had as much medical decline and metastasis and was able to bounce back as I did. Being that there was nothing to really compare me too, I wanted to start to and make a record so that way the next person would have something to compare them to. I was stage IV + Metastatic Malignant Anorectal Mucosal Melanoma and I had metastasis to the lungs, liver, kidneys, lymph nodes, and eventually the occipital lobe on my brain. My strong attitude and power of will kept me alive long enough until I got the TIL
The TILs treatment I got is not just revolutionary for people with my type of cancer but for other rare cancers as well. My hope is TILs will one day be used as a first line of defense instead of a last and that my story will inspire others to continue the fight and share their stories. Mucosal Melanoma Speaker/Advocate Mucosal Melanoma Survivor cancer blog
You only miss 100% of the shots that you don’t take!
Constantly evolving and putting out new content so more people understand that mucosal melanoma is not skin cancer. Please follow and subscribe like and share so we can spread awareness so that nobody has to go through the experience that I did. Hopefully we can make enough noise to make a difference.
About Me
Making Important change on a High Level
The month of May is known as Melanoma Awareness Month, but for the state of Texas, it’s now full on OFFICIAL
Advocacy 2023
If I’m going out I’m going out swinging
2023 In Patient Forum in Washington D.C.with the MRA
Advocacy Days March 5-7 in Washington D.C.
I don’t know how to describe it but I believe that I survived Metastatic Mucosal Melanoma so I could share with others Who are fighting the same battle that I did and encourage everyone to keep moving forward.
Mucosal Melanoma is a very rare cancer and it does not fight by any known rules. I took a very unique approach to how I had to beat this disease.
Advocacy Days March 5-7 in Washington D.C.
2023 In Patient Forum in Washington D.C.with the MRA
Advocacy Days March 5-7 in Washington D.C.
I’m headed to Washington DC to spend my birthday meeting with lawmakers on Capitol Hill. I have meetings with representatives from the district that I live in from from North Texas including Keith Self along with meetings With representatives from Senator John Cornyn from my great state of Texas from where I live.
When I was diagnosed in 2018 I didn’t know anybody in my area that had currently been fighting Mucosal Melanoma. I currently now know at least 2 to 3 people within 20 to 30 minutes from where I live that are fighting this. There’s gotta be something that can be done and more than I can do.
2023 In Patient Forum in Washington D.C.with the MRA
2023 In Patient Forum in Washington D.C.with the MRA
2023 In Patient Forum in Washington D.C.with the MRA
Immediately following Advocacy Days with the MRF, I will be attending meetings with the Melanoma Research Alliance on March 8
Community Oncology Alliance-Hill Day 2023
Community Oncology Alliance-Hill Day 2023
2023 In Patient Forum in Washington D.C.with the MRA
travel to Washington DC to meet Wes legislator about PBM reform. I was able to share my story. Discuss about the change that’s needed.
Melanoma Charity Pickleball Fest
Community Oncology Alliance-Hill Day 2023
Melanoma Research Foundation-Webinar
Courts Of McKinney Sat June 24, 2023 Click link to register and more info
Melanoma Research Foundation-Webinar
Community Oncology Alliance-Hill Day 2023
Melanoma Research Foundation-Webinar
MRF Ask the Expert-Early Detection of Mucosal Melanoma Through routine Health Exams.
Just Giving Page for Melanoma Charity Pickleball Fest-Donations for Melanoma Research Foundation
Just Giving Page for Melanoma Charity Pickleball Fest-Donations for Melanoma Research Foundation
Just Giving Page for Melanoma Charity Pickleball Fest-Donations for Melanoma Research Foundation
June 24, 2023 Dallas TX
Melanoma research leads the field for resear cancers
RARE Across America 2023
Just Giving Page for Melanoma Charity Pickleball Fest-Donations for Melanoma Research Foundation
Just Giving Page for Melanoma Charity Pickleball Fest-Donations for Melanoma Research Foundation
Volunteering my voice and sharing my story with the RDLA for Virtual Hill Day
MRF 2023 NYC Gala Courage Award
Just Giving Page for Melanoma Charity Pickleball Fest-Donations for Melanoma Research Foundation
MRF 2023 NYC Gala Courage Award
I am so happy to announce that on October 26, 2023 I will be given the courage award by the MRF as the first ever for Mucosal Melanoma. This year marks my five year anniversary from my diagnosis and in my world that means I beat what little odds there are.
more details to come soon. Thank you everybody for your support and God bless
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MRF 2023 NYC Gala Courage Award
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