Lifetime Caps Bill Introduced On Friday, February 13, 2009,
Anna G. Eshoo(D-CA) and Jim Langevin (D-RI), along with Senators Byron Dorgan(D-ND) and Olympia Snowe (R-ME) introduced the Health Insurance Coverage Protection Act (H.R. 1085; S442).
I was so excited about this UNTIL Mike said it was a bad idea to mandate something like this... He said that it would then cost employers more money for the premiums. I hadn't thought of that. I do wish there were no such thing as a lifetime cap. Mostly because when you run out, you can't buy more (as we found out) due to pre existing clauses. So, what are you to do???? The legislation, introduced in both houses in 2008, will set a $10 million minimum lifetime cap on health insurance, with future increases based on inflation.
The National Hemophilia Foundation (NHF)played a vital role in encouraging the legislation and assembling a coalition of more than 50 patient advocacy and health organizations currently working for its passage.
“However, nothing could happen without the critical leadership of the members of Congress who recognized this problem and decided to do something about it,” said ValBias, NHF CEO.
“We applaud these leaders for identifying this critically needed piece of healthcare reform and moving it forward.”
On Thursday, February 26, 2009, more than 350 people affected by bleeding and clotting disorders will gather on Capitol Hill for our annual Washington Days advocacy event.
We will express our support for this important legislation and discuss other key healthcare issues with members of Congress and their staff.
“Having an inadequate lifetime cap defeats the purpose of health insurance and forces those with disabilities and chronic illnesses into an impossible situation,” Dorgan said.
“Low caps also end up costing the taxpayer because once people with illnesses hit their cap, they often turn to government programs for their care.
This legislation will raise lifetime insurance caps and allow those with illnesses to focus on recovering—not worrying about how they are going to pay for their treatment.”
“This bill addresses a critical lack of coverage for those with disabilities or chronic illnesses,” said Eshoo.
“It’s a travesty to think that people are job-hopping in order to switch insurance plans or quitting their job all together to access Medicaid.
Increasing the minimum lifetime cap will result in a net savings for federal and state governments because individuals with high medical costs can maintain private health insurance.
As medical treatment costs continue to increase, the issue of lifetime insurance maximums will become even more important. This legislation will protect individuals who are struggling to pay for the expensive medical treatments that are a result of disability or chronic illness.” NHF applauds the efforts of the bill’s sponsors and co-sponsors.
Someone was having all kinds of doggy fun. *giggling* Look at that guilty face.
A Stanford sweatshirt Nurse Raji gave him. She cared for Matthew pretty much the entire time we were in the CVICU 4 yrs ago.
"Dwamma" spoiled Magoo w/an awesome Mr. Potato Head. He has TWO, yes, TWO ~ one for our house and one for her house. This child wants for nothing.
These are real fun to step on. Yup... nice. It can give ya a case of Tourette's.
Daddy and Magoo playing on his chaulk board. Matthew loves to have us draw him a Magic Bullet. Goofy kid.
Matthew suckered Daddy into taking him for a spin around the block. He is hard to resist.
Off they go! He loves this red wagon.... yes, "Dwamma" got it for him.
