Hunter appointed to Illinois Commission to End Hunger

CHICAGO – To help ensure every Illinois family has access to fresh, healthy food, State Senator Mattie Hunter (D-Chicago) has been appointed to the Illinois Commission to End Hunger.

“My career in public service has been dedicated to helping families lead safer and healthier lives, which is why I’m honored to join the Illinois Commission to End Hunger,” Hunter said. “I look forward to working with my colleagues on the commission to identify and execute solutions to address the systemic factors that give rise to poverty and child hunger.”

Launched in 2010, the Illinois Commission to End Hunger is a public-private partnership comprised of stakeholders from across the state tasked with developing a continuing plan of action to eradicate food insecurity.

Overall, 10.7% of Illinoisans experience food insecurity, including more than 15 percent of all children in the state.

The commission is set to release the Illinois Roadmap to End Hunger later this year, which will outline recommendations for both short-term recovery and long-term solutions.

The commission is currently holding regional listening sessions to gather input from local leaders, advocates, and families around the state. The remaining listening sessions are:

• Northern Illinois – Wednesday, July 15, 12:00 p.m.-1:00 p.m.
• Southern Illinois – Thursday, July 16, 1:00 p.m.-2:00 p.m.

Registration for the listening sessions is available here.

New Hunter law expands access to health care for low-income communities

CHICAGO – State Senator Mattie Hunter’s (D-Chicago) legislation aimed at improving access to health care in communities across Illinois that have been disproportionately affected by the COVID-19 pandemic was signed into law yesterday by Governor JB Pritzker.

“In Illinois, you deserve access to high-quality health care and treatment, no matter your economic status, your ZIP code or what you look like,” Hunter said. “This law extends that promise to many of our neighbors who have been left out, often due to long-standing racial health and economic disparities.”

Senate Bill 1864, known as the Health Care Affordability Act, eliminates or loosens requirements on who can access Medicaid by:

•  Providing HFS with the authority to accept an applicant’s or recipient’s attestation of income, incurred medical expenses, residency and insured status when electronic verification is not available;
• Eliminating resource tests for some eligibility determinations;
• Suspending redeterminations;
• Suspending changes that would adversely affect an applicant’s or recipient’s eligibility;
• Allowing phone or verbal approval by an applicant to submit an application in lieu of applicant signature;
• Allowing adult presumptive eligibility;
• Allowing presumptive eligibility for children, pregnant women and adults as often as twice per calendar year; and
• Suspending premium and co-payment requirements.

The law recognizes that families have experienced unique challenges as a result of the pandemic and helps them enroll and maintain coverage through the Children’s Health Insurance Program and the ALL KIDS Act.

The new law also supports medical research and patient health by requiring Medicaid to cover routine care costs for members who participate in clinical trials to treat cancer and other serious diseases. In addition, it helps expand access to affordable home health care and mental and behavioral health care.

“We know that African-Americans are significantly underrepresented among those who participate in clinical trials, meaning we lose out on life-saving opportunities. Unanswered questions then remain on the effectiveness of these medications for Blacks,” Hunter said. “Because Medicaid recipients are much more diverse, this law will help reduce that disparity for Black patients and for low-income white residents, while advancing the overall fight against cancer and other life-threatening diseases.”

The law allows individuals who are not otherwise eligible for Medicaid to qualify for medical assistance for the duration of any federal or State declared emergency due to COVID-19. However, these services are limited to testing and treatment related to COVID-19.

SB 1864 takes effect immediately.

Hunter appointed co-chair of Kidney Disease Task Force

Commits to meaningful investments to close racial disparities in kidney health

CHICAGO – State Senator Mattie Hunter (D-Chicago) has been appointed co-chair of the Kidney Disease Prevention and Education Task Force, a new panel charged with raising public awareness and presenting solutions to reduce the prevalence of kidney disease and racial disparities in diagnoses and outcomes.

“Especially in the African-American community, a largely preventable disease is claiming the lives of our neighbors simply due to lack of awareness and access to treatment,” Hunter said. “I look forward to working with my colleagues and the leading professionals on the task force to reduce the burden of kidney disease and eradicate the racial inequities in kidney health. It’s time for meaningful investments in outreach, research, and health coverage to close this disparity.”

The task force will work with leading educational institutions in Illinois to create health education programs to increase awareness of and examine chronic kidney disease, early detection, transplants and kidney donations, and the greater rates of diagnosis in minority groups. This will include a public outreach campaign consisting of health education workshops, seminars, preventative screening events, and social media, TV, and radio outreach.

African-Americans are four times as likely to develop kidney failure as Caucasians, while Hispanics are twice as likely. Almost half of the people waiting for a kidney in Illinois identify as African American, but, in 2017, less than 10% of them received a kidney.

Hunter is a long-time advocate against racial health inequality. In recent months, Hunter has bolstered her calls for accelerated investments and policy solutions following the COVID-19 pandemic’s disproportionate impact on minority communities.

“Closing the vast health disparities can no longer be an afterthought. It must be an urgent and primary priority for leaders at every level,” Hunter said.

Kidney disease is the ninth leading cause of death in the United States. If chronic kidney disease is detected early and managed correctly, swift treatment can slow and even stop kidney deterioration.

Diabetes is the leading cause of kidney disease. Roughly one in four adults with diabetes has kidney disease. An estimated 31 million Americans, including 1.12 million Illinois residents, are living with chronic kidney disease.

The task force will consist of legislators, doctors, non-profit leaders, and officials from the Department of Public Health and the Department of Healthcare and Family Services. It is required to submit a report to the General Assembly on or before December 31, 2020, and then be dissolved.

Hunter calls on African-American blood donors to help address shortage

CHICAGO – State Senator Mattie Hunter (D-Chicago) is calling on healthy, eligible African-Americans in Illinois to help replenish the state’s blood supply, which is declining rapidly due to blood drive cancellations at businesses, churches and schools in response to the COVID-19 pandemic.

African-American blood donors are particularly needed to help patients battling sickle cell disease amid the COVID-19 pandemic. Sickle cell patients are at high risk of serious complications from coronavirus infection.

“For the black community, this is another layer to our public health emergency. Sickle cell disease tends to affect African-American communities, which are disproportionately suffering from COVID-19 and already lack equal access to preventative health care and treatment,” Hunter said. “Even one donation could save the life of someone in our community.”

Red Cross blood centers have seen donations by African-Americans drop by more than 50% since the novel coronavirus outbreak began in March.

Patients with sickle cell disease depend on transfusions from donors with closely matched blood – beyond the A, B, O and AB types – to reduce the risk of complications.

According to the American Red Cross, each donation center is required to follow the highest standards of safety and infection control, and additional precautions – including social distancing and face coverings for donors and staff – have been implemented to ensure the health of all those in attendance.

“This is a matter of life or death for patients with sickle cell disease and those who rely on transfusions to make it through surgery,” Hunter said. “Now is the time to support our neighbors. I strongly encourage all healthy, able Chicagoans to step up and help fill this void.”

Many blood centers throughout the state have extended their operating hours to meet the critical need for donations.

To make an appointment to donate blood with the Red Cross, residents can visit RedCrossBlood.org or call 800-733-2767.