Healthcare Forum Video Now Available

Whole Washington and Our Revolution Teamed Up for a  Healthcare Forum

11/5 was a great evening to talk health care and the way we’ll achieve Universal Healthcare. Speakers include:

  • Stephanie Kang, Health Policy Advisor for Congresswoman Pramila Jayapal
  • Melinda St. Louis, Director at Public Citizen
  • Elaine Waller-Rose, Mental Health Professional
  • Sean Cavanaugh, Campaign Director for Whole Washington

Check out the recording here: https://youtu.be/Oj8nI8rpCgA

Town Hall Recording

An Open Letter: Fixing Health Care Is Not Just a Good idea

Check out this insider perspective from a healthcare reform advocate in California. Thank you, Keith McCallin.

The biggest takeaway? We have to do this ourselves. We must use the power of the initiative process to force change.

On the issue of health care, there is no health care debate happening, the election is
irrelevant, and there is no health care reform coming.

Open Letter

How What County You Live in Could Affect Your Healthcare Coverage – A Healthcare Story from Benton County WA

In 2010 I suffered a hemorrhagic stroke at the age of 40, due to an incredibly rare type of benign brain tumor that the neurosurgeon said had probably been there since birth (they could tell it had been there a very long time because of the way blood vessels had grown around it). I was incredibly fortunate that when this completely unexpected major health emergency occurred, I was covered by my then-husband’s health insurance through PSEW (Puget Sound Electrical Workers).

Unfortunately, the marriage was not destined to last, and we separated. However, I asked my now-ex if he would be willing to technically stay married until I hit the lifetime maximum on his work insurance policy that had covered my 11-week hospitalization. Many, many people during that time assumed that because Obama was president and had enacted the ACA, that lifetime maximums had been eliminated, but that was not the case. The policy I was under had a $1 million lifetime maximum (it may be that some companies were able to get grandfather clauses allowing them to keep lifetime maximums).

As Explanation of Benefits (EOB) statements began arriving in bundles in the mail, we started referring to me as “Million Dollar Baby.” The amount that is shown as what was paid for any service or provider on an EOB statement is the highest amount a provider could receive. However, the insurance companies always negotiate that price down. So what shows on an EOB statement is not usually what the insurance company actually paid. Most likely, they paid less, but the health consumer is not privy to that information! The only information we had were the numbers showing on the EOBs, and I was inching my way up to that $1 million. At that point I had weekly check-in calls with the woman who was the insurance case manager, to ask how close to the cap I was.

My then-husband did agree to technically stay married so I could keep that insurance coverage until I hit the million dollar limit. However, being an electrician is feast or famine, and he got laid off with no new work – a routine we had sadly become incredibly familiar with. He needs a certain number of work hours accumulated to keep his benefits instated, and with no work, he lost his benefits. The last time I checked in with the insurance case manager, I was up in the $600 thousands somewhere.

I was then forced to find a private health insurance policy until I qualified for Medicare. Anyone under 65 who becomes disabled has a two year waiting period before eligibility for Medicare kicks in. During that interim two year period, after my husband’s benefits ended, I was lucky to find a non-profit org that helped me navigate the process of finding a private policy without getting booted to the high-risk pool, which would have been insanely expensive. They helped me answer questions truthfully on applications. I believe that organization was called the Washington Health Foundation. At the time in 2011, they actually had an office space (somewhere in Seattle I think – no idea exactly where) and like three employees. I don’t think they exist anymore, but with their help, I secured a policy with Assurant until I finally got Medicare in 2012. I also learned that the key is to never have a lag period in which you are not covered. If you do, THAT is when insurance companies can pounce and charge you outrageous premium prices.

Disability does not make you rich (cue bitter laughter), and after getting divorced I was forced to do a short sale of my house because of the housing crash. I moved my young daughter and myself into an apartment in Bothell, WA. Rent prices skyrocketed, and I was then forced to move to a more affordable area. I chose the Tri-Cities (West Richland) because I have family and friends here and it is close enough to the west side that my daughter can see her father and his family on a regular basis.

When we lived in Snohomish County I had a Medicare Advantage plan (part C) for my supplemental policy. What Medicare does and does not cover can be lengthy and convoluted. However, as a general rule of thumb, Medicare part A covers hospital stays (although people need to be sure their stay qualifies – there are minute details that are best read in an article I’ll post at the bottom, if you’re interested), and Medicare Part B is the part that covers outpatient services. However, Medicare only covers 80% of outpatient visits. So most people pay for a private, supplemental policy, in addition to their Medicare coverage (which each person also pays for). Medicare Part C refers to Medicare Advantage plans, which are supplemental policies offered by private insurance companies. While we lived in Snohomish County, I had a Medicare Advantage plan (Part C) through Regence.

When we moved to West Richland, which is in Benton County, I just assumed I would be able to stay on my Medicare Advantage plan since we were moving within the same state. I assumed it all went by state; but it does not. It goes by county. After the move was complete and my daughter had already started 4th grade, I discovered that I was NOT eligible to stay on the Regence plan.

My only choice in Benton County, as a person on Medicare who is under 65, is a Medicare Supplement Plan F, offered by Premera. If I was 65 or older, I would have plenty of different Medicare Advantage plans to choose from in Benton County. However, because I am under 65, it is either the Supplement F plan or nothing. I assume this is because Benton County is much less populated than Snohomish, and there may be too few people under 65 to make it worth the insurance companies’ while to offer Medicare Advantage plans to the disabled here. Apparently I am lucky that there is a supplemental plan available to me at all in Benton County!

Trust me, I have thought many times about risking it and going without the supplemental. My monthly premium doubled, compared to what I had been paying for the Advantage plan, but I now have zero copays. So instead of paying $175 a month, which was what I paid for the supplemental in Snohomish County (Part C), I now pay $356 a month for the Supplement F plan, which covers the 20% gap that Medicare Part B does not – but I never have a copay.

I also pay approximately $130 per month for Medicare (it is deducted from my SSDI before it hits my account, which is why I am never exactly sure how much it costs me). I have also opted to pay for Medicare Part D, which is the prescription drug coverage. That also comes out of the SSDI before it hits my account, so I am not exactly sure how much I pay on that each month.

After the dust had settled and I figured out my only supplemental plan option in Benton County, I begrudgingly purchased the Supplement F plan. I then decided I would have to MAKE it worth it. As mentioned, I had only paid $175 per month for the supplemental on the west side, but over there I had co-pays. As a stroke survivor, PT and OT are now part of my regular routine. Since both PTs and OTs are considered specialists (as opposed to someone like a primary care provider), there was a $45 copay for each appointment. As rent prices increased on the west side, I was only able to go to PT and OT once a month each. I used to go to a place in Seattle one Saturday per month. If I had both PT and OT that day, the combined copays were $90. Factoring in gas to get me there and back, I started referring to those Saturdays as my “hundred dollar days.” Eventually, I stopped going to PT and OT altogether because I had to make rent. However, now that I don’t have copays (although double the monthly premium), I have been going to PT and OT regularly here on the east side.

Finally, Medicare does not cover vision or dental, so I have two separate policies for each of those, as well. All told, I have six insurance policies (Medicare A, Medicare B, Medicare D, the supplement F Premera plan, VSP for vision and Cigna for dental) for a total of approximately $520 a month, just for me. My daughter is currently covered by her father’s health insurance through PSEW, however, there have been times throughout the past 10 years when she had to be transitioned to Apple Health (WA state Medicaid) because my ex lost his benefits. Because of the current shutdown, he has been laid off again. So I do not know how long his benefits will cover him and our daughter. She will just go back to Apple Health, if necessary.

Does your brain hurt yet??? Is it complicated enough? Sometimes I envision how someone from a different country would react to this tale. I’m sure it would blow people’s minds, and I know that it is only ONE story. There are millions of similarly messed up narratives out there!

This is a website that spells out the details of what Medicare covers for hospital stays (Medicare Part A): https://www.healthline.com/health/what-medicare-covers

This one talks about what Medicare Part B covers (outpatient): https://www.healthline.com/health/what-medicare-covers

LET’S STOP THIS MADNESS!!!!! Go Whole Washington!!!!

-Kim H., Benton County WA

How COVID-19 has affected my life, Vicki Rhoades, ND

Hello.  My life is affected in so many ways.  Here are a few.
1.  As a PCP in private practice, the clinic where I rent has been open to one provider at a time, with patients scheduled such that there is no waiting in the waiting area.  This has vastly reduced the number of patients I see with a corresponding reduction in income.  I also introduced telemedicine, and may also introduce house calls shortly.  These are cash visits, but I really don’t make much money from them.  Still a vast reduction in income.  I do these things to reduce risk, both to myself and my patients.
2.  As someone very close to the “increased risk” age range, I have vastly reduced my social conversations in real life.  While I tend to be an introvert, this definitely changes my ability to see friends.  Zoom is good, phone calls are okay, but the true face to face conversations have a depth to them that virtual reality does not convey.  Still, I do these things too.
3.  Perhaps the most disturbing to me is the inability to visit my mother, who is in her late 80s.  I call her twice daily to “check in.”  She asks me repeatedly, “how much longer will this go on.”  I answer repeatedly, “I don’t know, mom.”  Because, really, I do NOT know how much longer.  It depends on so many things, both known and unknown: will people behave as I do?  will the government rules change yet again?  how does this virus behave, REALLY?  (etc etc)In the face of uncertainty, and a desire to continue to serve all while still protecting myself and others, I carry on.  I have no idea of how much longer this is practical.  Still.

Sincerely, and thanks to Whole Washington for asking.
Vicki Rhoades, ND
Tracey’s Parents Bob and Bano

Whole WA Volunteer Tracey’s COVID-19 Story

My parents told me they had fevers on March 18th.  Until then they had continued acting like the world was normal.  They live in Florida and COVID was in Washington State, not Florida, they thought.  My brother convinced them to go to get tested and on March 25 they gave in and did.  By then they both had pneumonia.  They texted my brother and I to let us know they were going in to the ER to get tested.  That was at 12:15 EST.  14 minutes later they told me they were being admitted into the hospital.
At around 6:30 EST the hospital called me on my Dad’s cell phone to let me know that my mom had been intubated and taken up to the ER and my dad insisted they call me before sedating and intubating him so he knew we knew what was happening.  I didn’t get to talk to him because he didn’t have enough breath.
Tracey's Parents

Tracey’s Parents Bob and Bano

I called my family to let them all know what was going on and that is when I found out that there might be an insurance problem.  Dad wasn’t technically admitted into the hospital yet.  He was still in the ER waiting for an ICU bed.  If he wasn’t sent up to the ICU then Medicare would not cover the ER visit according to my aunt.  She insisted I call the hospital and make sure he was in the ICU before midnight.

To this day I do not know if this is true. He got his ICU bed at 9:45 EST.  But, that isn’t really the point.  I had to call the hospital concerned about money while really all I care about is my parent’s lives.  Because, whether they would be charged or not, someone in the same situation as them in America will be charged.  It should not have been part of what I was stressing about.

My mother passed on March 30th.  Dad is still fighting after 20 days on a ventilator.  I have never gotten the chance to speak to either of them again.  20 days for Dad so far in ICU and 5 for Mom.  Without their Medicare and Medicare Advantage he would come out of the hospital destitute. In that we are lucky but I think of the thousands of people in this country with no insurance during this pandemic and have just one more reason to cry.

Tracey C., Olympia WA, She/Her

“Power to Heal”

Our Healthcare System is Racist

What can we do to right these wrongs? We must acknowledge the abhorrent discrepancy, listen, learn, and work to fix it. How? First, we can dig into recent history. Whole Washington is offering ways to see and show Power to Heal, a movie which tells the riveting story of Medicare and the Civil Rights Revolution. (Longer description from the website below.)

“POWER TO HEAL is an hour-long public television documentary that tells a poignant chapter in the historic struggle to secure equal and adequate access to healthcare for all Americans. Central to the story is the tale of how a new national program, Medicare, was used to mount a dramatic, coordinated effort that desegregated thousands of hospitals across the country in a matter of months.

Before Medicare, disparities in access to hospital care were dramatic. Less than half the nation’s hospitals served black and white patients equally, and in the South, 1/3 of hospitals would not admit African-Americans even for emergencies.

Using the carrot of Medicare dollars, the federal government virtually ended the practice of racially segregating patients, doctors, medical staffs, blood supplies and linens. POWER TO HEAL illustrates how Movement leaders and grass-roots volunteers pressed and worked with the federal government to achieve justice and fairness for African-Americans.”

So here’s what we’re asking: Can you host a movie showing in your area between now and March? We’ll provide you with a script and all the supplies you need to make the showing a success.

  • If you want to attend a showing, click the link below to see events in your area. Don’t see any showings on the map yet? Check back often as volunteers like yourself will be posting them in the next few weeks.
  • If you want to host, click on the link, then the button in the lower right – Click to Host.

Power to Heal Showing

September’s Walkathons – A Recap

Fun pix below

The September Walkathons were a great way to up awareness for our initiative campaign and raise some funds too.

We raised over $4200, had over 30 walkers and almost 100 individual donors!

Another surprising benefit? Connecting with other activists. We found out about each other's passions and strengths and brainstormed ideas to get us to victory.

#ImTheKey Campaign Is On!

Our first fundraising campaign is underway, and thanks to you, we’re making genuine progress.  Hashtags are going out. Donations are coming in!

Huge thank you to our supporters. Add your face to the gallery and let’s keep it going.

Donate Today!

Historic Progress for Medicare for All!

The tide is turning

On Tuesday, April 30th, the Rules Committee of the U.S. House of Representatives held the first ever hearing on Medicare for All. That’s right. The first ever. And we can attest, it was incredibly powerful. Whole Washington Campaign Director Georgia Davenport and Communications Director Jen Nye traveled to Washington D.C. to join other activists and hear the landmark arguments in real time. Witnesses laid out damning accounts of our broken, for-profit system, and advocates demanded real change.

From an overflow room in the Cannon building, we sat transfixed watching monitors. We chatted with members of Public Citizen who are encouraging citizens to pass local resolutions in city councils, school boards and other community entities. (Proudly, Seattle City Council was the very first to do so!) Check out their toolkit and push for passage in YOUR community–what a great opportunity to recruit signature gatherers and volunteers for our campaign! We also met members of the Be A Hero group founded by Ady Barkan that urges politicians to do the right thing. The right thing in this case? Pass Medicare for All. We exchanged contacts and swapped t-shirts for berets, courtesy of the generous Red Berets for Medicare for All.

We also met legislators, like Congresswoman Ayanna Pressley from Massachusetts and Congressman Abdul El Sayed from Michigan that wanted to thank engaged voters.

 

Take some time to watch the hearing or read the transcripts. There is a lot to learn and know, including age-old tactics used by the opposition. For a deep well of inspiration, be sure to watch the testimony of Ady Barkan, an activist, lawyer, husband and father, dying of ALS. Due to the disease’s progression, he had to use a computer-assisted device to speak. He shattered our hearts but strengthened our resolve. There’s much work we must do!

Check out Things You Can Do Right Now to help move the needle.