June 2018: A busy month of policy progress
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Authorization to Appropriation: Next Steps for STAR Act

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Earlier this month, President Donald Trump signed the Childhood Cancer STAR Act into law, authorizing $30 million annually from 2019-2023 for programs and research to combat childhood cancer through the National Institutes of Health (NIH) and the Centers for Disease Control and Prevention (CDC). 

Passage of the bipartisan STAR Act - the most comprehensive childhood cancer legislation ever introduced - was the result of many years of hard work from our Congressional champions, our community at large, grassroots advocates from all over the country, and this organization. Its provisions are grounded in solid data, smart analysis, and a robust roundtable process that achieved community consensus on top policy priorities. 

Now, we work to get the STAR Act fully funded -- and all indications suggest this process is off to a good start! On Thursday, the Senate Appropriations Committee approved a fiscal year 2019 spending bill that includes funding for implementation of STAR, including survivorship research, biospecimen research, pediatric and adolescent surveillance, and additional funding for state cancer registries that track cancer in children, teens and young adults.

We thank Senate appropriations leaders for moving this bill quickly through Committee and invite you to join us in asking other Members of Congress to support full funding of the TAR Act: Take Action.


Appropriations Committee Calls for GAO Review of Barriers to Care for Childhood Cancer Survivors

The House Committee on Appropriations included a formal request that the General Accounting Office (GAO) study the "existing barriers to obtaining and paying for adequate medical care for survivors of childhood cancer" and submit recommendations to Congress based on their findings. 

The Children's Cause has been working to achieve this milestone for the past several months, after similar language was removed from the Childhood Cancer STAR Act. We express gratitude to the Appropriations Committee for recognizing that this is an important first step toward improving the long-term care of childhood cancer survivors, a cohort expected to reach 500,000 by 2020. 

Specifically, the GAO will be tasked with identifying barriers to coordinated survivorship care and making recommendations to "provide improved access and payment plans for childhood cancer survivorship programs and palliative care, including psychosocial services."


Hope Portal Resource Database Launches Nationally

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CCCA Communications Director Jess Kean (left) was recognized at the Coalition Against Childhood Cancer Summit in Seattle this month for her contributions as a member of the Hope Portal Launch Team.

Earlier this month, we shared a new way for families to find the resources offered by Children's Cause for Cancer Advocacy – and hundreds of other childhood cancer nonprofits! We join the Coalition Against Childhood Cancer in inviting you to visit the Hope Portal, a first-of-its-kind community directory of curated childhood cancer family support organizations.

At hope-portal.org, you can navigate a wealth of resources according to your family’s specific needs, diagnosis and geographic location. Whether you're looking for help paying the bills, a care package or wish granting, a nearby camp, or just someone to talk to, the Hope Portal brings vetted information to families in an easy-to-navigate format, and we’re thrilled to be part of its national launch.


June Advocacy Webinar Highlights Local, State Progress

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If you were unable to join us on Wednesday for our webinar on local and state-level advocacy around childhood cancer policy issues, the recording is now available on our website

We thank these terrific advocates for sharing their time and expertise with us: 
- Lynn Schaeber, author of Peyton's Law
- Christopher Winters, Founder of National Children's Cancer Consortium
- Joyce Reinecke, JD, Executive Director of Alliance for Fertility Preservation

In discussing advocacy tactics that have worked in communities around the country, several common themes emerged around the importance of: sharing patient stories; working within coalitions; tapping into local experts; and building relationships with a wide range of stakeholders. "You've just got to keep going until you find someone that listens," said parent advocate Lynn Schaeber.

Save the date for our next webinar on the topic of new pediatric oncology therapies, scheduled for September 26th. We will let you know when registration is open!


PFDD Workshop on Chemo-Induced Hearing Loss

Registration is now open for the September 13th Patient-Focused Drug Development workshop on chemotherapy-induced hearing loss in pediatrics. If you or someone you know is interested in childhood cancer hearing loss, we hope you'll join us this fall in Hyattsville, MD, just outside of DC.

The half-day meeting follows the FDA model for PFDD meetings and will feature a series of facilitated panel and audience discussions, focused on providing the FDA and other stakeholders with patient views on key issues related to burden of the condition, potential treatments, risk-benefit analysis and clinical trials.

Visit www.childhoodcancerpfdd.org to register today. We'll keep you posted as details are finalized, including hotel block information, speakers and the full agenda.


In other policy news...

  • Senate Rejects Rescissions Package: By a 48-50 vote, the Senate rejected the White House's plan to claw back $15 billion in previously-approved funds, including $7 billion for the Children's Health Insurance Program. (The Washington Post,6.20.18)
  • NIH Poised to Receive Funding Increase: House and Senate appropriations committees have approved FY2019 spending bills that would provide $38.3 billion in NIH funding increases of between $1.25 billion (House bill) to $2 billion (Senate bill) over FY2018's budget. (Science, 6.26.18)
  • Pre-Existing Condition Protections at Risk: The Children's Cause is proud to join with 45 cancer advocacy & professional organizations in a campaign to oppose efforts to get rid of pre-existing condition protections. We ask The Justice Department to stand up for millions of Americans with pre-existing conditions, including childhood cancer survivors:
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Thank you ... 

... to everyone who attended or supported our Jazz in June event last week! We had a terrific night with good friends enjoying great music, and we thank everyone who helped to make it a success. We give special thanks to everyone who donated or purchased a silent auction item and to the Eric Boyd Trio for sharing their talent with us.

Finally, please join us in thanking the evening's generous sponsors, including:

  • Presenting Sponsors: Genentech, Rusty and Lori Ring, and Novartis
  • Gold Sponsors: Amgen, Association for Accessible Medicine, Susan L. Weiner, Agios Pharmaceuticals, Jazz Pharmaceuticals

To see photos from the event, visit our blog or Facebook page.

Jessica Kean
May 2018: STAR Act Passes Congress; College Scholars Announced
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Congress Passes the Childhood Cancer STAR Act

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Last week, the House of Representatives passed the most comprehensive childhood cancer legislation ever introduced. The Childhood Cancer STAR Act is expected to be signed into law by President Trump this week.

We thank our champions on Capitol Hill for leading the way toward this huge milestone for our community, especially the original sponsors of theChildhood Cancer STAR Act: Senators Jack Reed (RI), Shelley Moore Capito (WV), Chris Van Hollen (MD) and Johnny Isakson (GA) and Representatives Michael McCaul (TX), Jackie Speier (CA), Mike Kelly (PA) and G.K. Butterfield (NC).

We also thank each and every one of you who've reached out to your Members of Congress over the past few months -- and years! Every email, tweet, phone call and meeting from the tireless advocates in our community played a part in this monumental victory for our kids. This has been a true collaborative effort with many organizations working together to get us here. We give special recognition to the coalitions of the Alliance for Childhood Cancer and the Coalition Against Childhood Cancer for their leadership.

The bipartisan STAR Act is designed to advance pediatric cancer research and child-focused cancer treatments, while also improving childhood cancer surveillance and providing enhanced resources for survivors. This legislation is the result of many years of hard work from our Congressional champions, our community at large, and this organization. Its proposals are grounded in solid data, smart analysis, and a robust roundtable process that achieved community consensus on top policy priorities.

What's next? At the Children's Cause, we have already turned our attention to funding, and work is underway to ensure the STAR Act receives the appropriations it needs for implementation. In the coming days and weeks, we'll be asking you to join in that effort. Please continue to follow us onFacebookTwitter and Instagram for updates and action steps.


Survivor Scholarship Recipients Announced

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We are excited to introduce the inaugural class of our College Scholars Program! We congratulate Malachi Thompson and Melissa Peace on their selection as our 2018 College Scholars, among a competitive field of applicants.

About the College Scholars Program: Children’s Cause offers an annual opportunity for two childhood cancer survivors to gain valuable cancer advocacy experience. College Scholars, who receive a $2,000 academic scholarship, agree to complete a project of their choosing related to childhood cancer advocacy.

About Malachi: At age 6, Malachi Thompson was diagnosed with Acute Myeloid Leukemia (AML). Just months after finishing a year and a half of intensive therapy, he relapsed and was successfully treated with an umbilical cord blood transplant from an unrelated donor. Today, Malachi is a high school graduate with plans to study Aerospace Engineering at the University of Alabama in Huntsville. Malachi has been cancer-free for the past ten years because a transplant saved his life. Now, he wants to give back and encourage others to become bone marrow donors. For his College Scholars project, Malachi will organize a bone marrow drive in his local community in Alabama.

About Melissa: Melissa Peace was diagnosed with Non-Hodgkin's Lymphoma her freshman year at Colgate University. Today, Melissa is a medical student at George Washington University's School of Medicine with plans to become a pediatric oncologist. "I want to participate in the College Scholars Program so that I can be an advocate for children with cancer and work to better the field of pediatric oncology research from a legislative perspective," Melissa wrote in her application. As a CCCA College Scholar, Melissa will work to build an advocacy interest group at her medical school, creating a new cohort of informed, engaged voices speaking up to lawmakers about research and healthcare issues that impact children with cancer and survivors.

Find out more about Malachi and Melissa and the projects they'll be taking on this summer and fall : Meet Our 2018 College Scholars.


Registration Now Open for June Advocacy Webinar

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Register now for our June 27th webinar "Advocacy Tools and Tactics: How to be the Voice of Change," designed for childhood cancer advocates who want to learn more about effective advocacy practices. We'll hear from several advocates around the country who've been achieving progress around childhood cancer policy issues. This webinar, part of our 2018 Webinar Series, aims to arm you with creative new ideas and impactful tools to take to your own local legislators or statehouse in pursuit of a brighter future for children with cancer.

This webinar is being exclusively offered to members of our Kids Action Network, an active and engaged cohort of childhood cancer advocates. Byregistering to participate, you'll automatically become a KAN member. You can opt out of KAN at any time by notifying us at info@childrenscause.org.


PFDD Workshop on Chemo-Induced Hearing Loss

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Registration is now open for the September 13th Patient-Focused Drug Development workshop on chemotherapy-induced hearing loss in pediatrics. If you or someone you know is interested in childhood cancer hearing loss, we hope you'll join us this fall in Hyattsville, MD, just outside of DC.

The half-day meeting follows the FDA model for PFDD meetings and will feature a series of facilitated panel and audience discussions, focused on providing the FDA and other stakeholders with patient views on key issues related to burden of the condition, potential treatments, risk-benefit analysis and clinical trials.

Visit www.childhoodcancerpfdd.org to register today. We'll keep you posted as details are finalized, including hotel block information, speakers and the full agenda.


Quick Links | Recommended Reading

  • "All of Us" Enrollment Expands: The National Institutes of Health opened national enrollment of the All of Us Research Program this month, holding launch events in diverse communities around the country. (NIH, 5.1.18)
  • Advances in Medulloblastoma Screening: Researchers have identifed six gene variations that predispose carriers to developing medulloblastoma, paving the way for new genetic counseling and screening guidelines. (The Lancet, 5.9.18)
  • Childhood Leukemia & Germs: A controversial new study suggests that a lack of exposure to germs in infancy may contribute to the development of childhood acute lymphoblastic leukemia. Experts are emphasizing that this is early research, genetics are also a factor, and there is currently no magic formula to preventing ALL. (Nature Reviews Cancer, 5/21/18)
  • Good News and Bad News in Childhood Cancer Trends: In its annual report to the nation on cancer statistics, the National Cancer Institute reveals that cancer diagnoses are increasing among American children at a rate of 0.8% annually but survivorship rates are continuing to improve. Between 2010-2014, childhood cancer mortality decreased about 1.5% each year. (NCI, 5.22.18)

Join us for Jazz in June! Tickets are now on sale.

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Join us in Washington, DC on June 18th for a reception featuring jazz music from the Eric Byrd Trio! Our Jazz in June event will bring together new and seasoned childhood cancer advocates from 6:30 - 9:00pm at the Hamilton Loft near Metro Center. Tickets are now available, including complimentary admission for childhood cancer survivors.

Jessica Kean
April 2018: Action Day Brings 200+ Advocates to DC
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200 Advocates Ask Congress to Pass STAR Act at Action Days

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Group Photo Credit: St. Baldrick's Foundation
Right: Susan L. Weiner, PhD, presents at Advocate Training session


Over 200 advocates from 37 states joined together last week for Childhood Cancer Action Days, hosted by the Alliance for Childhood Cancer.

Advocates asked their Representatives to pass the Childhood Cancer STAR Act, which the Senate unanimously passed last month. The Childhood Cancer Survivorship, Treatment, Access and Research (STAR) Act is the most comprehensive childhood cancer legislation ever taken up by Congress.

You can still take action from home to back up the impact these advocates had on the Hill. Find out how.

Our task now is to get the bill to committee and onto the House floor for a vote, so we can get it signed into law as quickly as possible. Please join in this effort while we have momentum from Action Days!

Be sure you're following Children's Cause on FacebookTwitter and Instagram for the latest on the STAR Act. Thank you for helping us get this bill signed into law. 


Securing a Strong Federal Budget for Medical Research

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Fiscal Year 2018
The National Institutes of Health received a $3 billion funding increase as part of a $1.3 trillion appropriations deal passed by Congress last month. This $37 billion budget for NIH represents an 8.8% increase, the biggest percentage increase seen by the NIH in the past 15 years. President Trump signed the FY2018 omnibus into law – but has reportedly been considering a rescission package. Rescission is a process by which the president formally requests (within 45 days of a spending bill’s passage) that Congress backtrack and cut out some of what has already been signed into law.

A large and united community of public health and medical advocates spoke up to ensure strong funding for the National Institutes of Health – and now we speak up once again to protect that funding. We’re asking advocates to call, email or tweet their Senators and Representative today and urge them to defend the budget and rebuff any attempt at rescission that would put life-saving research funding at risk. Our action alert makes it quick and easy.

Fiscal Year 2019
President Trump sent his FY2019 budget request to the Hill just days after the FY2018 omnibus passed and - because of the timing - didn't include any of the funding agreements reached in the 2018 budget. Instead, the Administration's budget includes cuts to most of the health programs that children with cancer and their families rely upon.

Despite the bipartisan deal by Congress to boost domestic spending to $597 billion, the Trump budget includes only $540 billion in such funding, which puts a squeeze on NIH and NCI. In terms of Medicaid, the budget proposes various policy changes that will negatively impact the health and well-being of children and families who rely on this program. On our blog, we share a sampling of what's at stake for our community. 


Chemotherapy-Induced Hearing Loss to be Explored in PFDD Workshop

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Chemotherapy-induced hearing loss in pediatrics will be the focus of an upcoming Patient Focused Drug Development (PFDD) workshop in Washington, D.C. The Children's Cause, in partnership with other childhood cancer organizations including Mattie Miracle Cancer Foundation and the Children's Brain Tumor Foundation, will host an FDA-approved PFDD meeting on September 13th.

The half-day meeting will feature panel presentations by survivors, parents, and medical specialists with an opportunity for public comment and input. This will be a chance for those affected by chemo-induced hearing loss to give the FDA the benefit of their experience. If you're interested in this meeting, please fill out the interest form so we can keep you posted on details and registration.


Quick Links | Recommended Reading

  • Larotrectinib proves 93% effective in kids: A new phase 1 clinical trial finds a new cancer drug, larotrectinib, to have a "nearly universal response rate" in treating pediatric patients with a fused gene called TRK, which is found in several types of solid tumors. (The Lancet, 3.29.18)
  • Genetic screening for leukemia improves: Researchers at St. Jude have discovered a fourth gene (IKZF1) that can predispose carriers to B-cell acute lymphoblastic leukemia. (Cancer Cell, 4.19.18)

Upcoming Events

  • Children and Cancer Forum, May 22: The Atlantic will host its second annual childhood cancer forum at the Newseum on May 22nd from 8-11am. This event brings together physicians, policymakers, activists and health care leaders to examine the state of pediatric cancer care and look towards innovations in the future. Learn more.
  • CAC2 Annual Summit, June 12-14: The Coalition Against Childhood Cancer (CAC2) is hosting its annual Summit and membership meeting from June 12-14th in Seattle, Washington. Learn more.
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Join us for Jazz in June! Tickets are now on sale.
Join us in Washington, DC on June 18th for a reception featuring jazz music from the Eric Byrd Trio! Our Jazz in June event will bring together new and seasoned childhood cancer advocates from 6:30 - 9:00pm at the Hamilton Loft near Metro Center. Tickets are now available, including complimentary admission for childhood cancer survivors.

Jessica Kean