Uncategorized

Check the Pulse in Illinois!

L to R: Zoraida, Michelle, Laurie, Kelly, Elizabeth
Chicago, Illinois was the location of
our first Pulse on the Road in 2015. The
Bleeding Disorders Alliance Illinois
was our gracious host for this
day-long event, attended by 70 families.
Laurie with Audrey Taylor, 2002
It was a joyous day to be alive and together
after two tragedies had just struck: Illinois suffered about 14 tornadoes the
day before, which leveled the town of Fairdale, causing two deaths. The
community also lost the beloved Audrey Taylor, a sassy and compassionate nurse
at Rush University Hospital, one of the main hemophilia treatment centers.
Audrey was a great colleague who I always loved seeing and her death at age 51
is just devastating for all.
Our guest speakers included: the
fabulous Michelle Rice, vice president, Public Policy and Stakeholder
Relations, National Hemophilia Foundation; Kelly
Gonzalez
, a Nevada woman with von Willebrand disease, teacher, and now
advocate; Elizabeth Stoltz, senior manager, Market Access, Baxter Healthcare; and Laurie Kelley, yours truly!
Mona and Bob of BDAI, with Laurie Kelley
Executive director Bob Robinson welcome
everyone and introduced POTR, and me. I presented “Where We Were, Where We Are
and How We Got Here” to explain why the Affordable Care Act (ACA) come into
being, and how hemophilia fits in. With a few stats, I showed that skyrocketing
medical costs, particularly in specialty drugs (which factor is), was straining
state budgets; it was only a matter of time before private insurers caught on.
Looking to cut costs, insurers turned to increasing prior authorizations,
formularies, decreasing choice of factor provider, and more. As payers scramble
to cut costs and states try to cut their bloated budgets, the bleeding
disorders community is facing more and more restriction to access to medical
care and factor.
Michelle Rice, VP at NHF
Laurie and Zoraida with the DePaz Family
Enter Michelle, who explained in much greater depth how
this was happening, and gave great examples of where this was happening in our
country. After lunch, Kelly gave a lively and impassioned chronology how she became an advocate, to get access to medical care and the right factor brand for her
daughter Jacey, who accompanied her to this meeting. It was an incredible story that took 30
minutes, and left the audience in tears! But Kelly triumphed, and became a role
model for other parents fighting for access to care for their families.
Genny Moore earned $20 with our Q&A!
We tried
something new! Role playing! With Michelle acting as an insurance rep, we had
two volunteers come to the stage and act as patients, calling their insurer to
find out about 1) whether factor was covered, and 2) if their HTC was covered
under the plan. Theresa and Chrystal did a great job asking questions and not
accepting Michelle’s runaround answers. The audience got to weigh in an offer
what they thought the ladies did well and what they might have done
differently.
Finally, Community Forum, where our panel of experts field questions from the audience
on any subject, from their personal healthcare situation to state issues to
national affairs in insurance. We had some great questions and responses.
Amigas!
Thanks Zoraida Rosado, who planned our
trip so well, set up displays, tables and handouts, and dissembled everything;
to Michelle and Kelly for sharing their expertise and their weekend; and to Bob
and his BDAI team, to the Spanish translators, and to Baxter Healthcare, for providing the funding for all
the Pulse on the Roads, now in our 7th year!
Please
check www.kelleycom.com by December to see where we will be in 2015!
Good
Book I Just Read
Metallica:
Justice for All
[Kindle]
Joel
McIver
Metallica
is one of the best selling bands in history, and is often said to have defined “thrash”
metal. This is a look at their origins, spectacular rise, wayward path, and an in-depth look
at every song and every album. Probably a book for fans only, and not the best
book on rock I’ve ever read. The book gets terribly bogged down in detail, as
though it’s a ledger, schedule or chronology. Is it essential to know every city the band visited on every single tour? (It’s exhausting to
read! How did they travel so much and so often?) Much of the information is
gleaned from interviews appearing in magazines, and then pulled together to
weave some kind of story. There are layers of information missing, such as the
drug and alcohol binges throughout the band’s career, which McIver seems to
gloss over. Incredible detail on every song, how it compares to others in each album, with
McIver voicing his opinion on each song. Some of this is interesting, but you
lose the focus of the book and get sidetracked. I’m a huge fan of Metallica,
but found this book a bit tough to get through. Choppy writing, too much detail
here, not enough there. Three/five stars.

Pfizer’s Soozie Courter Scholarship Program Turns 18!

I am honored to say I knew Soozie Courter: she was a “neighbor,” just living in the next town, and we one time shared a ride to the airport. A lovely, committed and intelligent woman, taken too soon. Below is a special annoucement by Pfizer, to benefit the community in the name of this wonderful woman. — Laurie

Pfizer Hemophilia is excited to
announce the 18th year of the Soozie Courter Scholarship program.
Named to honor a valued and respected friend of the hemophilia community, the
Soozie Courter scholarship is a tuition assistance program sponsored by Pfizer that
aims to help students advance their academic goals.
Scholarships are awarded to applicants
who present the best combination of a creative and persuasive essay, excellent
recommendations and superior academic standing. For the 2015-2016 academic year, Pfizer will
award:
·       Five $4,000 graduate scholarships
·       Ten $2,500 college scholarships, including vocational
schools
William
Bowles, 2014 Soozie Courter scholarship winner, is using the scholarship funds
he was awarded to help him obtain a Master of Public Affairs degree at Columbia
University in NYC and plans to eventually pursue a PhD in Business Policy. He
ultimately hopes to work with local state governments on policies to help
improve business development in the rural south. According to William, “coping with a genetic
disorder does not mean sacrificing commitments, dreams, or career aspirations.”
To be eligible for the scholarship,
students must have either hemophilia A or hemophilia B and be a high school
senior, have a high school diploma or general education development (GED)
credential, or be currently enrolled in an accredited junior college, college
(as an undergraduate or graduate student), or vocational school. All completed
applications must be postmarked or sent via e-mail no later than
May 20, 2015. To download an application, please visit here. To learn about the
inspiring stories of past winners, check out the Pfizer Facebook Page, Our Hemophilia Community.

The 18th
anniversary of the Soozie Courter scholarship illustrates the long standing
pledge by Pfizer to help patients with hemophilia further their education. To
learn more about other ways Pfizer is supporting the hemophilia community,
visit Hemophilia Village. From diagnosis to
dating, the newly refreshed site provides tips, resources, and words of wisdom
to help you navigate through the various challenges that arise throughout the
years.

This is a paid announcement by Pfizer.

March’s Child

I remember the Boston Globe column called “Sunday’s Child,” which profiled a beautiful child every Sunday in the Boston area in need of a foster home, in the hopes it would end in adoption. Let’s call this week’s blog post “March’s Child.” We have children with hemophilia in need of sponsorship!

It’s March, Hemophilia Awareness Month, and yet there are children in developing countries who lie at the fringe of our community, unaware that it’s “their” month, poor, suffering, waiting for help. We do our best to provide factor to these children through Project SHARE. But did you know you can sponsor one of these children through our sponsorship program Save One Life?

Helping us promote our cause is the amazing Chris Bombardier, who just spent 3 weeks in the wilderness, summiting Carstenz Pyramid in Indonesia. Yup, he flew all the way there, and suffered up that enormous mountain (the highest in Oceana–a stand-in for continent Australia) and #5 on his Seven Summits Quest) to raise awareness for hemophilia in March and for Save One Life in particular. How is that for sacrifice and dedication?

Most of us don’t need to go to such an extreme, though Chris so kindly asked me to accompany him (I would have if I didn’t have so much hemophilia-related work going on right now). We can just sponsor a child at only $22 a month. We are trying to get a mere 31 children sponsored in March, one for each day. We’ve almost reached our goal! Just FIVE more! We even have their photos below. Please consider helping us reach our goals to help give them a better life! It’s Hemophilia Awareness Month: Thanks to those who have pledged sponsorship! We hope more blog readers will rally to help these deserving children; what better month to make a pledge than March?

You can read more about Chris’s amazing climb here!

Laurie Kelley, founder,
Save One Life



Add caption


Great Book I Just Read
Eiger Dreams: Ventures of Men and Mountains by Jon Krakauer

From the mountain-climbing author of Into Thin Air comes nine gripping and informative stories about historic mountain climbs and the intriguing people who climb them. He covers K2, Denali, Everest and the Nordwand (Eiger) interspersing modern day adventurists and alpinists with history of climbing for each mountain. Krakaeur is a great storyteller: no nonsense but infusing his stories with awe, respect and love of the mountains. He also includes his own struggles with each mountain while portraying others’ climbs. Four/five stars.

Summiting to Save Lives!

March is Hemophilia Awareness month! But you already knew that.
What you might not know is that a brave young Denver man with hemophilia is making

Chris climbing Denali (Mt. McKinley)
history.
Chris Bombardier is doing something no one with hemophilia has ever done before: summiting Carstensz Pyramid in Indonesia.
Why this mountain? After all, the man lives in Denver, a mile-high city. (Yes, he has that to his advantage; lots of extra red blood cells to help with altitude). Carstensz Pyramid will be Chris’s fifth mountain in his goal is to become the first person with hemophilia to climb the highest peak on each continent, aka The Seven Summits.
Mt. Kilimanjaro in Africa. Mt. Elbrus in Russia. Mt. Aconcagua in South America, and Mt. McKinley in the US: been there, done that for Chris.

This will be  his most technical climb yet–that means hard!  Carstensz Pyramid is the highest mountain in Oceania standing at 16,024 feet above sea level. The mountain is in a remote area of Papua, Indonesia and the climb will involve specialized skills such as rock climbing, rappelling, and a tyrolean traverse. Chris will end the climb with a 4-5 day trek through an isolated region of the Papua jungle.

And he asked me to come with him, mentioning there were a lot of leeches and snakes in those there “isolated regions.” I wanted to go, believe me. One day I will go with him (though we are now narrowed down to Antarctica and Mt. Everest. I have to remind him I am twice his age), if only to base camp.

Chris infusing on a mountain top!

Chris left Friday, March 6 and has just landed in Bali. He is psyched and raring to go!

You can follow him for the next three weeks on his blog: AdventuresOfAHemophiliac.com

Quick background: The Seven Summits Quest began when Chris traveled to Kenya on a work-related trip. While there, he witnessed the difficulties of those living with hemophilia in less developed regions of the world and decided he wanted to do anything he could to help. Chris declares, “Of course I look forward to standing on the summits of these incredible mountains and feeling the accomplishment of doing it with hemophilia. I want to show young people with hemophilia what’s possible. Our world is an amazing place, and I don’t want people with hemophilia to think they have to live in a bubble. I want them to get out and experience life to the fullest!” But, more importantly, Chris is committed to spreading the word about hemophilia and raising people’s awareness of the huge disparity in care that exists in the world.
And I add proudly that Chris is a board member of Save One Life, the nonprofit I founded in 2001 to help support the world’s poor with hemophilia. We have about 1,400 children and young adults

enrolled, who receive direct funding, scholarships, camp funding and microenterprise grants!

Deepak Das of India, whose leg was amputated last year due to an untreated bleed

And in March, Chris is going to dedicate each day to a child in need. Our goal is to get 35 more sponsored. They are waiting on our website: http://www.saveonelife.net

Chris is taking risks at great expense to highlight the need of those in impoverished countries, where factor is limited or nonexistent. Please help support his climb by sponsoring a child today!
http://www.prweb.com/releases/2015/03/prweb12565783.htm
HemaBlog Archives
Categories