May 2017: Updates from Washington

The Latest in Washington: Healthcare & Budget News

There's a lot of policy activity happening in Washington with the potential to have a big impact on children with cancer. We're monitoring these issues closely - notably, the American Health Care Act and the president's budget proposal - and working with allied coalitions to express the needs and priorities of children with complex medical conditions like pediatric cancer.

The American Health Care Act, as passed by the House of Representatives earlier this month, would roll back the pre-existing condition protections that families have come to rely on since the enactment of the Affordable Care Act. This bill would bring the return of costly, limited high-risk pools and lifetime caps on coverage. The legislation also includes significant cuts to Medicaid, which insures approximately one-third of children with cancer in this country. Read more on our blog.

We are sharing testimonials on social media from families who are anxious about what AHCA could mean for their child battling cancer, with the hashtags #LetMeGrowUp and #ProtectOurCare. Find out how to take part in several ongoing social media campaigns here.

In other news, President Trump recently submitted his budget proposal to Congress, which calls for big cuts to medical research and health insurance for low-income children. Of particular concern are the threats to Medicaid and the Children's Health Insurance Program (CHIP). Together, Medicaid and CHIP cover nearly half of children age 6-and-under, including thousands of children with cancer.

The president's budget also calls for $6 billion in cuts to the NIH, including $1 billion from the National Cancer Institute. It is critical to note that Congress, not the president, controls the federal budget -- and medical research continues to receive bipartisan support in Congress. In fact, Congress just added $2 billion to the NIH budget for the remainder of this fiscal year (ending September 30). Read more on our blog.


200 Attend Childhood Cancer Action Days

Approximately 200 childhood cancer advocates took to Capitol Hill for this year's Alliance for Childhood Cancer Action Days at the beginning of May. Attendees spent a full day receiving issues and advocacy training, followed by a busy day of meetings with Members of Congress and their staffs. Advocates focused on three key issues this year: the STAR ActNIH funding, and the RACE Act

We were proud to be part of this annual event and thank all the attendees for their dedicated advocacy efforts, including those who joined in virtually by writing, tweeting or calling their Members of Congress.

- News coverage: 8-Year-Old Cancer Survivor Fighting for More Childhood Cancer Research

Next week, we'll be taking part in the One Voice Against Cancer lobby day -- follow along on FacebookTwitter or Instagram!


Financial Impact of a Childhood Cancer Diagnosis

On our latest advocacy webinar, we delved into the topic of treatment-related financial hardships facing families with a childhood cancer diagnosis. Among the key points we learned from research experts Kira Bona (MD, MPH), Anne Kirchhoff (PhD, MPH) and Elyse Park (PhD):

- 1 in 5 children diagnosed with cancer were already living in poverty. Among the families who were not poor at the time of diagnosis, 10-15% became poor during treatment for their child's cancer.

- Childhood cancer survivors are more likely to be covered by Medicaid than their siblings, more likely to have a history of being denied health insurance because of their cancer treatment, and they spend a greater percent of their income on medical expenses. Over half of adult survivors in one study reported skipping recommended medical care in the past year.

- Young adult survivors - especially uninsured survivors - lack needed familiarity with the Affordable Care Act and other available insurance protections.

A more detailed summary and the webinar recording are available here.


Research News Round-Up

Precision Medicine Breakthrough: Keytruda Approved by FDA

In a groundbreaking research development this month, the Food and Drug Administration approved Keytruda, the first ever cancer therapy based on a patients' specific genetic traits, rather than cancer type. This approval includes children with the identified genetic trait whose cancer has progressed and who have no alternative treatment options. This is a huge leap forward for the field of precision medicine, which uses a patient's genetic makeup to deliver immuno-targeted therapy.

Find additional recent research developments on our blog.

Jessica Kean
April 2017: Three Big Things

Still Time to Register for Friday Webinar!

We've got two immediate opportunities for you to engage around the issue of financial toxicity as a side effect of a cancer diagnosis. If you're interested in learning more about the financial barriers that impact access to care and quality of life for families impacted by childhood cancer, here's how you can help us tackle this issue right now

Join us TOMORROW - April 28th - as we start to explore what we as policy advocates can do to work toward effective solutions to lessen the financial burden of cancer care on families in our community.

Academic researchers Anne Kirchoff, PhD, MPH, and Kira Bona, MD, MPH, will lead a discussion about challenges and opportunities facing childhood cancer advocates in our efforts to decrease financial barriers and expand access to affordable cancer care for families with a child battling cancer. CLICK TO REGISTER.

Also: Survey of Caregivers, Patients and Survivors

The Children's Cause, in collaboration with the Patient Advocate Foundation, is conducting a survey of childhood cancer families, patients and survivors. Your participation is completely voluntary and your individual responses will be kept confidential.

As an incentive for participating, you'll be entered into a weekly $100 Amazon gift card drawing! CLICK TO LAUNCH THE SURVEY.


Childhood Cancer Action Days: Participate Virtually

Join us from home on Monday, May 1st and Tuesday, May 2nd

We are just days away from the 2017 Childhood Cancer Action Days and we are anticipating another terrific year of storming Capitol Hill with the Alliance for Childhood Cancer.

If you are not able to join us in Washington, rest assured that you can still play an important role from home by amplifying the message of our advocates on the ground (follow hashtag #CCAD2017).

Watch your email on Monday morning for messages to share on social media and with your legislators about these key issues: the STAR Act,NIH funding, and the RACE Act.

Follow us on Facebook and Twitter all day Monday and Tuesdayfor updates and easy-to-share messages.


The Latest on Capitol Hill: Amended GOP Healthcare Bill & Efforts to Avoid a Shutdown

Revised American Health Care Act

We are closely following updates on the new healthcare proposal announced on Tuesday, and we hope to have more information and action steps for you next week. Our top concern is the impact the legislation would have on people with pre-existing conditions, including childhood cancer survivors. The amended bill would allow states to opt out of protections for people with pre-existing conditions, essentially reviving expensive high-risk pools.

Three Things You Should Know About the GOP's Latest Healthcare Plan (Time Money, 4/26/17)

House Freedom Caucus Leaders Back New Healthcare Plan (Washington Post, 4/25/17)

- Here's where we stood on the original American Health Care Act, which failed to progress in March: What Would It Mean for Children with Cancer?

Congress Seeks to Avoid Government Shutdown

Congress has been facing a deadline of midnight Friday to pass a new spending bill to fund the federal government through September butreports from late Wednesday indicate that Congress may opt to extend that deadline for one week, buying them some extra time to avoid a government shutdown.

A major stumbling block has been funding subsidies for low-income people enrolled in the insurance marketplace through the Affordable Care Act. It appears that the Administration has dropped its opposition to those subsidies (known as Cost Sharing Reductions), which greatly improves the odds of avoiding a shutdown.

We will keep you posted as negotiations continue.

Jessica Kean
March 2017: HIGH ALERT for Cancer Research Funding

HIGH ALERT: Cancer Research Funding at Risk

White House Asks Congress to Slash NIH Funding for Remainder of FY2017 and Beyond

FY2017: A new White House proposal calls for $1.2 billion in cuts from the current fiscal year budget of the National Institutes of Health (NIH). Mid-year cuts on this scale would have a devastating and immediate effect on research grants across the nation with the potential to impact all disease areas, including childhood cancer. 

Current government spending will expire at the end of April, when Congress must pass a new spending bill for the reminder of the fiscal year (ending September 30, 2017). We're asking all advocates to contact their Members of Congress immediately and ask them to stand with us in defense of childhood cancer research at this critical moment.

FY2018: This alarming news follows the White House release of a budget blueprint (PDF) earlier this month that proposes steep cuts to research agencies, eliminating $6 billion (20 percent) of the NIH budget. The National Cancer Institute's share of those cuts - an estimated $1 billion - would severely impact already-underfunded childhood cancer research.

It's important to emphasize that Congress - not the Executive Branch - controls the federal budget. But the President's blueprint traditionally presents the starting point for budget deliberations on Capitol Hill.

Cancer research has always had bipartisan support, and we are optimistic that we will be able to soften the blow of these cuts through the appropriations process -- but we will need all-hands-on-deck! Progress in childhood cancer research is almost entirely dependent on federal funding. Please speak up with us to advance new treatments and find cures. Take action here.


Register for Childhood Cancer Action Days: May 1-2

You're invited to join the Alliance for Childhood Cancer in Washington on May 1st and 2nd for this year's Childhood Cancer Action Days. A strong showing of advocates at Action Days 2017 is more crucial than ever. We will be at a critical point in the legislative process on several key issues for children with cancer. Sharing your story in Washington this spring will ensure the voice of children with cancer is heard loud and clear!

The 6th Annual Action Days event will consist of a full day of issues and advocacy training, followed by a day of pre-arranged meetings with Members of Congress and their staff on Capitol Hill. Learn more.

The deadline to apply for a scholarship to off-set your travel expenses and/or the $50 family registration fee is today, March 31st. The deadline to secure a room at the Renaissance Hotel in the Alliance room block is April 2nd. 

Register now.


CCCA's Founder to Receive ASCO Award

Partners in Progress Recipient: Susan L. Weiner, PhD

We offer congratulations to our founder Susan L. Weiner, PhD, for her recognition by the American Society of Clinical Oncology (ASCO) as the recipient of this year's Partners in Progress Award.

The Partners in Progress Award recognizes a person involved in patient advocacy activities that impact public awareness about cancer and supports legislative efforts around research, treatment, prevention or care. Dr. Weiner will be presented with the award at the June 2-6ASCO Annual Meeting in Chicago.

Learn more about Susan here, and see the full list of ASCO Awardeeshere.


STAR Act Supported by 130+ Members of Congress!

The bipartisan STAR Act is life-saving legislation designed to advance pediatric cancer research and child-focused cancer treatments, while also improving childhood cancer surveillance and providing enhanced resources for survivors.

Members of the Alliance for Childhood Cancer, including our CEO George Dahlman, held a "mini lobby day" earlier this month on Capitol Hill, a prelude to the larger Action Day taking place May 1-2. To date, this bill has 131 sponsors and cosponsors in the House and 6 in the Senate.

We must continue to build momentum for this bill's passage, and you can help get us there:

1. Check the cosponsor map to see if your Senators and Representative have signed on.

2. Use our Write Congress form to quickly and easily send a letter to your Members of Congress to thank them for their support or ask them to add their name. We are hoping to quickly gain as many cosponsors as possible to get momentum for this bill's passage.

3. Share this ask with your friends and neighbors. 


Quick Links: Highlights from March

CCCA Formally Endorses Psychosocial Standards of CareChildren's Cause has given our endorsement to the evidence-based psychosocial standards that define a minimum level of care that all children with cancer and their families should receive. We thank the Mattie Miracle Cancer Foundation for spearheading these groundbreaking standards.

Eighty-Seven Organizations Call on Congress to Protect Medicaid: Children's Cause joined with leading patient advocacy organizations to denounce the American Health Care Act and its threat to Medicaid. Although the AHCA effort was defeated, there is much more work to be done to ensure the protection and stability of Medicaid for the one-third of childhood patients who depend on it for their care.

College Scholarships for SurvivorsBristol-Myers Squibb is giving away fifty (50!) scholarships of $10,000 each to childhood cancer or young adult survivors who plan to attend college or vocational school in the fall. The application deadline is today, March31!

In the News: 

Jessica Kean