Sen. Daines Issues Statement on Children's Health Insurance Program - Insurance News | InsuranceNewsNet

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January 20, 2018 Newswires
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Sen. Daines Issues Statement on Children’s Health Insurance Program

Targeted News Service

WASHINGTON, Jan. 19 -- Sen. Steve Daines, R-Montana, issued the following statement, which was published in the Congressional Record on Jan. 18, on the Children's Health Insurance Program:

Mr. President, access to healthcare is on the line today for 24,000 Montana children. The House of Representatives is working to pass legislation that will reauthorize a program called the Children's Health Insurance Program, better known as CHIP, for 6 years and will keep the government open. If passed, it will then come to us for a vote.

Why don't we take the opportunity before us to come together on issues we agree on instead of always fighting on what divides us? I think we can all agree on keeping Montana kids healthy.

Let me tell you a story about a family from Helena, MT, the A-Gee family.

Jaxon was a normal baby--a happy, healthy baby--until October of 2016, when he was just 8 months old. That is when he was first flown from Helena to Missoula's Community Medical Center's Pediatric Intensive Care Unit. He was deathly ill with a respiratory infection.

At that time, it was not clear why Jaxon had gotten so sick, but his parents soon learned that he had Leigh syndrome, a disease in which the body is not able to process energy properly, which leads to muscle weakness, swallowing problems, and severe illnesses with just a simple or a common cold. His parents quickly learned to manage his new feeding tube, to suction his mouth and his throat, and to put him on oxygen monitors at night.

Unfortunately, Jaxon has had five more serious infections. Each time, he has become ill. It has happened so quickly that he has had to be flown to Missoula even though he has a team of pediatricians, nurses, dietitians, speech therapists, and physical therapists who are trying to help keep him from getting ill.

As Jaxon's mom would say, when Jaxon gets ill, the only way to keep him from having to be flown to Missoula is to get him seen by his pediatrician as soon as possible so that if he does get sick, it is relatively minor.

I can tell you that this family in Montana is grateful for Healthy Montana Kids, which is Montana's CHIP program. They are thankful for its providing Jaxon's insurance and the copay for his care and his medical supplies. His mom says that the insurance is what makes it possible to manage Jaxon's condition and possible to afford well-baby checks instead of their just going to the doctor's on an emergency basis.

To add more background to the story, Jaxon's dad was disabled in a workplace accident, so he is home, caring for Jaxon and the family's other two children. Jaxon's mom works, and her employer has been phenomenal to her--those are her words--as they have faced Jaxon's hospitalizations, but the family of five couldn't afford Jaxon's care without Healthy Montana Kids. A helicopter bill for the ride from Helena to Missoula alone can be as much as $34,000, and Jaxon has taken that flight six times.

This family doesn't know what it will do if the funding for CHIP runs out, but the family is committed to caring for its son no matter what. That is why I support a 6-year reauthorization of CHIP.

Let me provide another reason.

This is Danielle. She is 9 years old, and she lives in Deer Lodge, MT. When she was just 18 months old, she suddenly lost the ability to walk.

Cindy and I are the parents of four children. I cannot imagine a more frightening moment as a parent if one has an 18-month-old child, and he suddenly loses his ability to walk.

Danielle was diagnosed with a form of juvenile arthritis. You don't think about arthritis affecting an 18-month-old child. This is a disease that causes pain, swelling, a stiffness of joints, as well as vision problems.

Thankfully, Danielle was started on a medication--a twice-a-month injection that controls the swelling and inflammation. Because of that, she can walk and even run again. Yet these injections are expensive. To pay outright for just 1 month, it costs over $6,000. Last summer, for 3 months, Danielle was unable to get the injections. She stopped walking, and she no longer could go to school. Her mom had to carry her through the house.

When Danielle was approved for Montana's CHIP program, she was able to go to the doctor's and get on another medication--an infusion this time. She is now back at school and running around--to quote Mom-- "like a kid who doesn't have any problems." Danielle loves to study math and science, and when she grows up, of all things, her dream is to be a doctor for kids. Without CHIP, Danielle's family would be unable to afford the medication she needs. Without CHIP, Danielle wouldn't be walking.

Danielle and Jaxon and the thousands of other Montana kids and their families need us to work for them. So I am saddened that partisan politics would get in the way of access to healthcare for these children. We have the opportunity today to reauthorize CHIP for 6 years and avert a government shutdown at the same time.

I urge my colleagues to do the right thing here, to do the right thing for the 24,000 Montana kids who use this important program. I urge them to support a 6-year reauthorization of CHIP and to keep the government open.

I yield the floor.

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