Making it Matter Podcast Ep. 11

Making it Matter Podcast Ep. 11 – This Past Week

Julia and I catch up with each other about the last week. I had an encounter with a security guard a concert over my pill case, Julia talks about her New York City Marathon training and then we both give our opinion on my blog post about Continue reading Making it Matter Podcast Ep. 11

5 things I learned from BreatheCon

BreatheCon, held this past weekend, was an online conference for CF patients from around the country to come together to be able to share life experiences, ideas, and give inspiration to each other in battling this disease.
I attended, and it was an incredible experience. Hearing from keynote speakers who have faced such adversity and have come out of it stronger and more motivated than before, was so uplifting to hear. I believe it created a lot of hope and courage for those that still have our toughest challenges to face.

I want to share the top 5 things that I now understand better about life with Cystic Fibrosis: Continue reading 5 things I learned from BreatheCon

Jerry Cahill, Boomer Esiason Foundation Ambassador, Celebrates 60th Birthday and Demonstrates that People with Cystic Fibrosis Can Live a Normal Life with Exercise and Medical Compliance

As part of his 60th year, Jerry has Activated a “Living List,” and will Complete 60 Events this Year — This is 60:60

New York, June 27, 2016 – The Boomer Esiason Foundation (BEF) today celebrates the 60th birthday of Jerry Cahill, a BEF cystic fibrosis (CF) Ambassador and double lung transplant survivor, who proves that age is truly just a number and that success is possible with a strong commitment to your health. Within the last Continue reading Jerry Cahill, Boomer Esiason Foundation Ambassador, Celebrates 60th Birthday and Demonstrates that People with Cystic Fibrosis Can Live a Normal Life with Exercise and Medical Compliance

Boomer Esiason Foundation’s Cystic Fibrosis Ambassador, Jerry Cahill, to Ride in 3rd Annual Bike to Breathe Event

The West Coast Bike Ride Aims to Raise Awareness for Cystic Fibrosis
and Promote the Importance of Exercise

New York and San Francisco, September 19, 2016 – The Boomer Esiason Foundation (BEF) today announced that its cystic fibrosis (CF) ambassador, Jerry Cahill, and Emily Schaller, a CF patient who started cycling, running and Continue reading Boomer Esiason Foundation’s Cystic Fibrosis Ambassador, Jerry Cahill, to Ride in 3rd Annual Bike to Breathe Event

Announcing BreatheCon, a space by and for CF adults

For the first time, over 50 percent of those of us living with CF are over the age of 18. Our community has a wealth of knowledge and a great desire to connect, but little ability to interact face-to-face.
Continue reading Announcing BreatheCon, a space by and for CF adults

BEF Presents Inspirational Documentary, Up For Air, About 60-year-old CF Ambassador

We are proud to support Up For Air, a documentary about BEF ambassador and 60-year-old pole-vaulting coach living with CF, Jerry Cahill.
https://www.youtube.com/watch?v=5FhWPmFHcr0

The film, directed and produced by Artem Agafonov, was shot over a period of Continue reading BEF Presents Inspirational Documentary, Up For Air, About 60-year-old CF Ambassador

Top 10 Lessons On Running A Disruptive Foundation — Guest Blog By Emily Kramer-Golinkoff

Originally posted on Emily’s Entourage, on July 21, 2016
http://www.emilysentourage.org/top-10-lessons-on-running-a-disruptive-foundation/

Today’s guest blog post was written by Emily and adapted from a speech delivered at the Global Genes and Penn Orphan Disease Center’s Rare Patient Advocacy Symposium.

Like so many of you, I’ve been thrust into this role of disruptor out of desperation.

I’m learning on the job every moment of everyday. It’s a 24/7 job. It is painstaking, relentless work; there are no breaks; and then there’s this fatal disease to manage on top of it.

It’s a crazy, dizzying reality.

And so while I’m certainly no expert, I’d like to share with you a few things I’ve picked up along the way.

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#1: Stories are powerful.

You don’t realize the power of your story until you start telling it. It might be uncomfortable, but it’s a means to an end, and nothing touches people’s hearts like stories. It’s that thread of humanity that binds us together, and it’s pretty spectacular to see how much people connect and care.

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#2: It’s all about relationships.

Everything that has happened for EE, every major development, every pivotal connection, every advance in research, it’s all been because of relationships. When the test tube says Emily and not some random digital code, it matters.

So go to the labs, talk to the scientists, SHOW UP. Make it painfully personal. There’s nothing in the world more motivating.

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#3: Nobody can be a better or more tireless advocate than you.

I’m participating in a study where I’m be the first and only person in the world to try the therapy. The idea? It came from me and my mom. We have no scientific background, just a huge vested interest in the outcome, some creativity, and logic.

Of course we vetted it with tons of scientists and did all of our homework, but the original idea was all ours — ordinary, everyday Emily and Liza’s. Don’t underestimate your voice, your brain, your creativity, and your ideas.

#4: Be relentless.

When there’s a roadblock, find a creative way around and keep at it. Push and push and push and don’t accept no for an answer if you believe in what you’re fighting for.

#5: People really care, but you have to ask for them to step up and help.

If you don’t ask, the answer is always no. I’m naturally a very private person, a total introvert who hates asking for things. The only thing that has kept me sharing such personal details of my life and medical journey is the outpouring of love and support that results–and seeing how people rise.

After our inaugural event in NYC, I can’t tell you how many people came up to me and THANKED ME for the opportunity to get involved.

People want to be part of something bigger. They want to do good things. They want to make impact. It’s up to us to give them the opportunities. And it takes guts.

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#6: You need a scientist champion and a respected Scientific Advisory Board.

When we first started making phone calls to labs and biotechs, people wouldn’t even answer the phone (or they promptly hung up!).

A scientist champion is your key into the scientific world and a respected Scientific Advisory Board is essential for vetting research projects and securing major gifts and grants. People need to know their money is going to reputable work.

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#7: Build a nest of trusted advisors.

It truly takes a village.

We were thrust into this role of running a foundation. We still have no idea what we’re doing, we just know what we want and that we are willing to do whatever it takes to get there.

By building a nest of advisors, we draw on the expertise of so many different, brilliant people and pull them onboard.

We’ve had the privilege of meeting some of the most remarkable individuals. We call them our guardian angels and our progress is a testament to — and totally dependent on — them

#8: Don’t underestimate the value of YOUR creativity and ideas.

Sometimes the greatest innovation comes from outside of the biomedical institution.

Nobody has a bigger vested interest in your future. Desperation spurs creativity and innovation. You don’t need a PhD to have great ideas. Believe in them and tenaciously pursue them.

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#9: Digital technology is your best friend.

Technology is democratizing; content is king. Use technology to spread your content far and wide. The world is at your fingertips and they’re eager to hear your story. Make it concise. Make it compelling. Make it easily sharable.

#10: Know what you want.

You need a clearly defined research goal to raise money and effectively mobilize a community. Do your homework, identify the leading researchers, labs, biotechs, pharma and all the key stakeholders, and bring them together. It’s essential to draw on their expertise to clearly articulate your research strategy.

People want to fund good work, but they need to know the targets. And so do you! Otherwise, your wheels will be spinning, and let’s be honest, we don’t have time or energy to waste.

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Emily’s Entourage is a work in progress. We are learning as we go. We constantly have to realign, refocus on our end goal, and troubleshoot — and it is HARD.

I think about EE every second of the day, with every breath I take. Literally.

What’s next? How do we grow? How do we make the research go faster? How do we add more revenue streams? How do we make the organization sustainable? How do I balance running EE and managing my health?

So many questions. So much to do. So little time — with a disease that rages on and robs me of my life, my energy, my breath.

I feel the crunch of time, the terror of disease progression, ALL the time. And that is the propeller.

At Emily’s Entourage, we pledge to keep at this, with this same vigor until there is a cure for EVERYONE with CF. And then, we pledge to take these lessons learned and apply them to another disease, to help another disease community get to the finish line. That is our greatest wish. That would be our dream come true.

Continue reading Top 10 Lessons On Running A Disruptive Foundation — Guest Blog By Emily Kramer-Golinkoff

Last Chance to Run the 2016 NYC Marathon with Team Boomer

Join the fight against CF today!

SIGN UP FOR THE
NYC MARATHON

By competing for Team Boomer, you will receive:
• An official Under Armour Team Boomer uniform, Team Boomer wristband, and Team Boomer string bag Continue reading Last Chance to Run the 2016 NYC Marathon with Team Boomer

US Adult CF Association Scholarship Application Due November 30, 2016 for Spring 2017

The United States Adult Cystic Fibrosis Association (USACFA) is excited to offer the Lauren Melissa Kelly Scholarship award for the Spring semester 2017. The scholarship will range from $1500 to $2500 and be awarded to adults with cystic fibrosis who are pursuing associate’s or bachelor’s degrees. Read on to learn Continue reading US Adult CF Association Scholarship Application Due November 30, 2016 for Spring 2017

Deadline for article submissions for CF Roundtable is September 15th, 2016

The CF Roundtable thrives on articles written by our columnists, directors and you! If you would like to share your story or an experience of dealing with life and CF, we would welcome it. Articles can be any length, generally 750 to 1500 words and can be on any topic that appeals to you. Continue reading Deadline for article submissions for CF Roundtable is September 15th, 2016