Fast and Furious!

Barry the Biker is at it again…. riding clear across America to raise money for and public awareness of hemophilia!

Barry Haarde is a 47-year-old with the stamina and ambition of a 20-year-old athlete and the soul of an ancient sage. He also has hemophilia and HIV, and lost a brother with hemophilia to AIDS. He conceived the idea to ride across America two years ago, and completed one trans-American trip last summer, covering over 3,600 miles in 7 weeks. You can read about that exciting journey in a previous blog.  http://blog.kelleycom.com/search/label/Barry%20Haarde

Last year, Barry became the first person with hemophilia/HIV to complete a trans-American bike trip.

WFTW2013MapThis year, he does it again, but in only 30 days! Starting from Costa Mesa, California, Barry will ride an average of 110 miles a day,  through the southwest and plains, to arrive after 3,456 miles in Amesbury, Massachusetts on May 23. This is also the day of our annual Spring Gala for Save One Life, the beneficiary of Barry’s fundraising. Barry plans to attend, as soon as he hops off his carbon-framed steed. 

Each day of his trip, as he did last year, Barry devotes to someone with hemophilia who died of HIV. He posts daily on Facebook. If you are friends with Barry on Facebook, you will be reminded of each beautiful man who died. What a tribute! Does anyone anymore put this kind of thoughtfulness into action?

Last year Barry raised about $50,000 for Save One Life, the child sponsorship program for children with hemophilia in developing countries that I founded. This year he hopes to raise $35,000. Please consider sponsoring Barry in any amount. Thanks to Baxter Healthcare, our Gold sponsor!

Yes! I want to support Barry’s ride across America to support Save One Life!

Please make a donation by using Paypal, your credit card (Master, Visa, Discover, American Express) 
 

Donate by the Mile (3,456 miles):

– Donate 5 cents a mile – $185
– Donate 10 cents a mile – $370 
 

Donate by the State (15 states):

– Donate $10 a state – $150
– Donate $25 a state – $375 
 

Donate Now 

Great Book I Just Read

Freddie Mercury: The Definitive Biography [Kindle] by Lesley-Ann Jones
I’m on a Queen kick since I witnesses the amazing performance of Gary Mullen and the Works as the Queen tribute band a few weeks ago. I always liked Queen but now love them and appreciate them even more. This is an in-depth look at one of Rock’s most intriguing and talented front men, Freddie Mercury, who is often cited as the greatest vocalist in Rock history. Certainly no one could match his range. This book is a great first look into his life, from a childhood on Zanzibar (I actually saw the house there he grew up in) to his life at boarding school, the roots of his neediness for praise and adoration, the strange duality of his nature–and not just his bisexuality. He was complex, talented and self-destructive. And a showman all the way. His personal charisma, charm and intelligence are clear. This is also about Queen, probably one of the most educated of all Rock bands. Life on the road, Freddie’s affect on the band, how they grew in influence and hit the heights. Those of you who watched Live Aid will recall how Queen stole the show. Their live music far surpasses their recorded. Freddie adored opera and even produced “Barcelona,” an album with his favorite opera diva. You’ll learn about the history of the band, and Freddie’s sad demise to AIDS in 1991. Great read. Four/five stars (but then I am biased)

Pulse on the Road in Alabama!

We just
wrapped up a great weekend in Montgomery, Alabama, after a terrible week in
Boston. Zoraida and I were lucky to have no problems at the airport, given the
tight security, and arrived in sunny Montgomery Friday afternoon. We were
greeted by a wonderful display at the Renaissance Hotel: streamers of green and
purple, big Mardi Gras-style mask, and the warm hospitality of the Hemophilia
and Bleeding Disorders of Alabama staff. The theme: Unveiled… Our Future Revealed, a theme the HBDA will use all year long as they
raise public awareness of this rare and mysterious thing called hemophilia.
And
we were surprised by a lovely and patriotic display of fireworks right outside
our hotel window that night!
Michelle Rice presents NHF’s Toolkit
On
Saturday morning, while the kids were organized to be bussed to the local zoo,
we adults visited another kind of zoo—the world of health care reform! Our
session kicked off with a full audience of about 100 people with hemophilia and
their families. “Pulse on the Road” is a three-hour insurance symposium that
brings our newsletter Pulse to life.
This year we will visit six states; we’ve already been to New York for Albany
Days and Colorado for the annual meeting.
Our
guest speakers were Michelle Rice, public policy director at NHF, of course,
and Marvin Poole, a senior reimbursement manage with Baxter Healthcare, sponsor
of this symposium.
Laurie Kelley with Vicky Jackson
Marvin
opened with a review of the Affordable Care Act (ACA) which led to an explosion
of questions. The audience, attentive and curious, was hungry was answers. I
jotted down questions as they came:
1.    
Will your employer be able to deny you
due to hemophilia?
a.     Marvin replied no. Under the ACA, no
pre-existing condition exclusions are allowed. This is one of the beauties of
the legislation!
2.    
Will the “navigators” (the helpers who
will guide us using the new exchanges, now called marketplace, websites where
we can buy insurance) be neutral? Or will they work with the payers? Whose side
are they on?
a.     Michelle noted that they are not on
anyone’s side. They are trained to be neutral, and are there to help us
evaluate the cost versus the benefits of any given plan, to help us decide
which is best for us.
3.    
What are the essential health benefits?
a.     Michelle noted that certain packages
called essential health benefits (EHB) must be included in all insurance plans.
These are basic services that must be covered. But… the definition of what these things are may differ! For
example, ER coverage when there is an emergency. What’s the definition of an
emergency? For Michelle it might be an ear infection as she travels a lot. But
for a payer, it might be loss of life or limb!
Laurie Kelley and Michelle Rice
4.    
Are payers going to cap insurance for
premiums? I’m paying $900 a month!
a.     Marvin answered that there will be a cap
on copays, but premiums will be expected to rise.
5.    
Explain what the marketplace is.
a.     Michelle replied that these are web
portals (websites) created by the states that allow people to “shop” on line
for insurance plans. You can plug in your requirements and needs, and the
system will bring up various plans for you to compare. These plans will be
denoted by a cost-sharing scheme: Bronze, Silver, Gold, and Platinum. You can
choose one of these plans based on how much you are willing to pay. For
example, a Bronze plan might be 60/40; you pay 40%, with lower monthly
premiums. A Platinum might be 90/10, with high premiums but lower out of pocket
costs after that.
Attendees work on the toolkit
But Michelle noted that the maximum out-of-pocket
(OOP) costs to us, consumers, for health insurance through the marketplace
regardless of the plan are $6,200 for an individual and $12,000 for a family.
What counts toward it? Copays, coinsurance, deductibles related to EHB.
6.    
What about tiers? If you have a Platinum
with 90/10 cost sharing, even 10% of the cost of factor is outrageous.
a.     Michelle replied that our understanding
is that your OOP, even with tiers, goes toward that OOP max in the marketplace.
7.    
If you have private insurance, can you
still use the marketplace?
a.     Not if you have a large employer. As of
now, no.
With friend Kelly Champagne
8.    
What about Medicaid? What changes will
happen there?
Brian Ward, president of the
HBDA answered this one: Alabama is not currently managed Medicaid, but might be
soon. Almost certain of it. Managed Medicaid is when it is managed by a payer
like Blue Cross Blue Shield (BCBS) or Aetna, for example. It may have a PDL or
formulary which lists the drugs covered by your plan (know this one, for factor!).
Michelle said it is very much like a Medicaid HMO: it uses a Primary Care Physician
(PCP), and in network hospitals and physicians. Coverage will be the same for
services but the networks will be different.
9.    
Can payers reject prophy on Medicaid
managed care?
a.     Michelle: NHF hasn’t seen formularies yet
or restricted prophy. They will restrict factor provider (meaning specialty
pharmacy). They seem to “get” prophy for kids, not so much for adults and may
argue that coverage.
Laurie with Tricia, a mom with
a child with hemophilia
b.     Michelle also replied that most changes
in Medicaid are not related to ACA. Managed care has been with us for years,
and now Medicaid is trying to use it for more groups like hemophilia. Sometimes
managed care is better for us all, but the biggest problem for us all is
coverage for factor.
One
mom lamented, “My son uses $30,000 a month and he’s only 2 year old. I can’t
have caps!” Brian then stressed: tell us your stories, your struggles, because
we will then tell Michelle at NHF and NHF will can set policy.
After
this lively session, I then spoke for 20 minutes about the importance of being
able to choose your health care plan, followed by Michelle Rice’s excellent
hands-on seminar about NHF’s toolkit, which has attendees crunch through numbers
to calculate the different between two plans for “John Doe,” who must choose
between two plans. Wow, the numbers were flying, and attendees quickly
calculated the costs. This is a great exercise for families who feel
intimidated by insurance policies and questioning charges.
Hemophilia Unveiled!

It
was an engaging, excellent three hours, filled with inquisitive audience
members (every speaker’s dream!), and much information sharing. It is a lot to
absorb but family members came away with new tools, new ideas and more solidarity.
Thanks
to the Hemophilia and Bleeding Disorders of Alabama for inviting us, to Vicky
Jackson, executive director extraordinaire and her team, and Brian Ward,
president. And to Baxter Healthcare for sponsoring Pulse on the Road and to all
the companies who supported this wonderful weekend!
For
more information on insurance, download Pulse on the Road for free at http://www.kelleycom.com/newsletters.html.
Great Book I Just Read
Angela’s
Ashes
by Frank McCourt
 Poignant, page-turning and superbly written story, based on the author’s life, of growing up impoverished in Ireland during World War II. If you’re Irish, you will especially love the historical references, phrases and cultural mind-sets, things we all heard growing up. But mostly this is a book about how a child thinks and perceives his world when he is trying to survive harsh poverty, hunger, loss of siblings, alcoholism, an absentee father and the brutal reception he receives from most adults, including those of the Catholic church. Five/five stars. 

Pulse on the Road in Colorado!

The Colorado Chapter of the National Hemophilia Foundation is flourishing under the leadership of Amy Board, executive director and her team. We had an excellent turnout for our Pulse on the Road insurance symposium yesterday, presented at the Colorado Chapter’s Educational Dayz! 2013.

Friday night started with a fun ice-breaker, dinner and then a great presentation in joint care by my friend Jeff Kallberg, a physical therapist who has hemophilia. This was followed by a carnival in the ballroom. There were lots of children and their families attending, so the whole event was kid-friendly, of course!

On Saturday, I was joined by Michelle Rice, policy director of NHF and Frank Quintieri of Baxter Healthcare to present Pulse on the Road. Frank gave an overview of the Affordable Care Act (ACA). In a quick review he stated that the ACA, passed in 2010:

  • Lifts lifetime & annual caps
  • Dependents stay on parents’ plan till age 26
  • Eliminates pre-existing condition exclusions
  • Creates “marketplaces”
  • Allows states to expand Medicaid eligibility 

Frank explained each of these changes in detail, all of which was good news for people with chronic disorders. The audience had excellent questions in response to his talk, from how does the ACA affect the self-insured plans, to what happens when a child with hemophilia turns 26 and then doesn’t have insurance. We all agreed that this was one of our most inquisitive audiences to date!

I spoke after a break about the importance of choosing a healthcare plan: you need to know terms used by payers, where factor is charged on your plan (major medical or pharmacy?), and what are the costs versus the benefits of the plan? Beware of what is covered in–network versus out-of-network. And most of all, know when your open enrollment period is—the time when your employer chooses a new plan. We all had a great laugh when audience member Maryann called it open season; “Like deer hunting?” I replied.

Michelle Rice presented NHF’s excellent Insurance Toolkit, designed to walk you through a hypothetical patient who wants to compare two plans. It’s detailed, challenging and incredibly useful. If you can do this Toolkit, you are ready to compare plans under the ACA through the marketplaces. The audience dug right in and got to work, using the calculators we supplied. And right away people caught on that there was a trick question when it came to plugging factor costs in! Impressive!
In summary, we reiterated that:

  • Everyone must have health care coverage in 2014
  • You may need to select your coverage in a marketplace
  • You must read your insurance policy annually

Hats off to Amy and her team for an excellent weekend, and for being such gracious hosts for us. We’re excited to see Colorado flourishing!


No book review this time. Colorado patient Chris Bombardier, who summited Mt. Aconcagua in Argentina in February (first person with hemophilia ever to do this!) and girlfriend Jessica Carter kindly spent the day with me Sunday to take me hiking and caving. The original plan was to hike 14,000 ft Pike’s Peak but conditions were very bad—high winds and lots of snow. But we had a great day hiking the Gardens of the Gods, and later visiting the Cave of the Winds. Beautiful rock formations under ground, a mile of stunning beauty including stalactites, stalagmites, columns, cave popcorn, cave bacon and soda straws. Colorado has tremendous natural beauty: go see it if you can!

Lest We Forget: Ryan White

This morning my friend, Barry Haarde, and many of those on Facebook reminded me what a special day it is. The anniversary of the passing of one of the heroes of the HIV/hemophilia community, Ryan White.

I recently met someone my age who had never heard of him. It seems hard to believe, given that he was a pioneer in advocacy for the rights of those with HIV, at such a tender age. And HIV in the 1980s was paramount to the plague, the Black Death, sweeping the country and causing people to react with fear, superstition and discrimination towards those who contracted HIV.

Ryan was born December 6,1971, to Jeanne White, in Kokomo, Indiana, who learned three days later that her baby had hemophilia. Treatment then consisted of factor concentrate injections which were not pasteurized or treated to remove viruses. Shortly after surgery on his left lung in 1984, doctors informed Jeanne that Ryan had contracted HIV. At age 13, Ryan was given six months to live.

What we didn’t know then and what we know now staggers the imagination. No one could have made up a sci-fi story as incredible as a microscopic virus infecting the entire nation’s blood supply and leading to the deaths of 10,000 with hemophilia. Ryan was one of them, and one of the most famous. Why?

His fame stemmed from how he handled discrimination in the Indiana school system, which would not allow him to attend classes. Ignorance about the disease caused mass panic and hate crimes. Ryan was shunned, harassed; one night a bullet was even fired into his home.

Ryan and his mother took the school discrimination case to court. Eventually, Ryan won. He was allowed to come back to school. But, people’s minds didn’t change so quickly or with the court decree. Ryan continued to face harassment by schoolmates, and parents pulled their children out of school. Ryan faced it all with characteristic grace, dignity and acceptance.

Ryan eventually found a school that welcomed him in Cicero, Indiana: 
Hamilton Heights High School. He thrived there.

His story of courage found its way to the media, and Ryan became a celebrity. A made-for-TV, a biography, many television spots…. and even friendships with Elton John and Michael Jackson. Ryan was hemophilia’s earliest advocate: on March 3,
1988, Ryan spoke before the national commission on AIDS, about hemophilia, HIV, discrimination. It’s fair to say this child–a suffering child–changed the way everyone viewed HIV. He was a pioneer, a role model, and transformational leader.

He died on April 8, 1990, Palm Sunday, surrounded by Jeanne, his sister Andrea, his grandparents and his friend,
Elton John. Jeanne remains fairly active in the hemophilia community and attends various events to remind us all of the importance of advocacy. Ryan’s impact goes far beyond his short time on earth, and he will eternally be remembered as a compassionate child who suffered, transformed his suffering into a mission for a greater cause, and left a lasting legacy so that others could avoid the discrimination he endured. His life is a blueprint of hope and courage in the face of alienation and pain, like so many others in our very special community.

ADVERTISEMENT