Uncategorized

Shetland: Hemophilia at 60° North

admin May 20, 2018

The Shetland Islands are a wind-swept, treeless, group of islands belonging to Scotland, that are carpeted with lush green, rolling hills, rugged rocks and daring cliffs that overlook the crashing North or Atlantic Sea. They are enchanting and idyllic. Having the best of the modern world—airport, hospital, cable TV and internet—they preserve a way of life not seen often in modern society. Community is paramount; civility the glue that holds communities together. You immediately take a deep breath of fresh sea air, and slow down your pace to enjoy a land where the surrounding sea seems to buffer you from cares and woes elsewhere.

Their history is more about Nordic explorers than Scotland proper. The Viking invasion began around 800 AD, and Shetland over time became a strategic location for explorers, shippers and eventually maritime activities during the World Wars. The Norse dominated Shetland for 200 years until 1468, when James III of Scotland married Margaret, a Danish princess. As the Danish struggled to create a dowry for the princess, Shetland was mortgaged to Scotland and finally annexed in 1471. Despite that, about 60% of Shetland men stem from Norwegian (perhaps Viking?) heritage.

My trip to Shetland actually began many years ago, when a mother from Shetland contacted me about her son with hemophilia. To assist answering her questions, I shipped her a copy of Raising a Child with Hemophilia, and our children’s books, and some things for the children, at that time numbering six—all free of charge. And so began a sweet pen pal relationship. Jan Howard is a thoughtful sender of cards, notes and photos of the children. I also love to send things by mail, so we exchanged birthday cards (home made by the children), Christmas cards and regular greeting cards. Jan always suggested I come visit and I wanted to. I had read about the Shetland Islands since a child, because of the Shetland ponies. And Jan ensured I read more by sending me books, some of which have become my favorites!

The World Federation of Hemophilia Congress is being held in Glasgow, Scotland this week, and this decided it for me. I would take a side trip before the Congress and fly to Shetland to visit Jan and the kids.

To read about a place is one thing; to visit, a lifelong memory, an experience that embeds itself in your heart and soul. What is there not to like about Shetland? With a population of only 30,000, people are polite to one another consistently, the pace of life is moderate and steady. The air is fresh, the countryside, though devoid of anything tall, and barren of trees, is stunningly beautiful. Stone cottages and stone walls landmark the horizon. Blue sky meets green land, which borders the ever-moving ocean. I was warmly greeted at the airport by David and Sandra, Jan’s parents, and Abigail, Jan’s 16-year-old daughter, who has mild factor VIII deficiency. Two other daughters have low levels of VWF.

A short drive over winding roads in the open countryside and we arrived at Jan’s pretty home, perched not far from the ocean. First order of business was to walk the gorgeous border collie Eddie, who enjoyed a brisk romp on the nearby beach! I worried even whether the children would understand me as my accent is different, but the Shetland accent is not like what you think of as a typical Scottish accent. It sounds more neutral, with some Welsh accent mixed in. In short, it’s delightful to hear!

Laurie Kelley and Jan Howard at Sumburgh Lighthouse

I come from a big family myself, so to be surrounded by the loving and delightful chaos of laundry, snacks, board games, homework, happy dog, beady-eyed hamster, and chatty children were a throwback to my childhood. I lost 10 games of UNO with seven-year-old Talia. Abi and I belly-laughed recalling hw much we enjoyed the movie Deadpool. Hillel and Talia peppered me with questions about what’s on the American dollar bill.

We had a lovely visit to the Sumburgh lighthouse, an incredible feat of engineering. Lighthouses are vital to Shetland and Scotland’s safety and made a great contribution to saving thousands of lives through the years. Jan sent me The Lighthouse Stevensons, about how the lighthouses were designed and built by the family of Robert Louis Stevenson, one of my favorite childhood authors. Excellent book! We visited a croft house, representative of the way inhabitants lived centuries ago. We spotted puffins and guillemots on the cliffs in Sumburgh, with the birds nestled into their small coves like people in a high-rise condo.

I gave a talk on hemophilia and our charity work to the medical staff at the Gilbert Bain hospital in Lerwick, where Jan works as a pediatric nurse.

And we visit Yoel, 19, who has hemophilia, in Scalloway. What is it like having hemophilia and living on an island? There’s a hospital in nearby Lerwick; Yoel does receive excellent factor products, all paid for by the National Health System. One look at this over 6 ft lad is to see that he has received excellent medical care. His joints are in good shape. He is charming and fit. We walked about Scalloway, a quaint seaside community, and scaled the stone steps of Scalloway castle. While Yoel gets good medical treatment, he would still be reliant on an emergency helicopter ride to the mainland if needed. And the ambulance service in Shetland is… well, slow. There is a lack of community in hemophilia; there is only one other known family with hemophilia. I met the mother, Joanne, at the hospital, and gave her my book. It would be hard to start a chapter there, as there are only the two families.

But the families search the internet to get info and make contacts, have a great relationship with their hospital team, know the Haemophilia Society in Scotland, and Jan is attending the WFH Congress this week, for the first time. In fact, it’s her first time ever attending anything in hemophilia!

We flew down together yesterday, and she was excited. While the five children (Yoel lives independently; Hannah is away at school) stayed with Sandra and David, the grandparents, Jan took a week off to be with her other “family,” hemophilia.

Did I mention she is a single mom? Single, nurse, mother of seven (three of whom have bleeding disorders), living on a remote island. She also, incredibly, sponsors two children in Nepal with Save One Life. If she doesn’t get Mother of the Year, I don’t know who would. I’m so incredibly happy to have visited her special community and to be in her country. I’m honored to have been with her family, and proud she is part of our bleeding disorder family.

You can read more about Jan next May, in PEN’s special issue on Island Life and Hemophilia.

On the Horizon: HFA Part 1

Laurie Kelley April 30, 2018

Last week the bleeding disorders community met in Cleveland, Ohio at Hemophilia Federation of America‘s annual meeting. It was a fabulous time to meet with friends and colleagues, and to learn about new treatments in inhibitors, new drugs in the pipeline and about psychosocial issues. One of the best attended sessions was the one on gene therapy. Entitled “On the Horizon,” the session was a 90-minute review of new products coming our way, and an overview of gene therapy, how it works and who is working on it.

Dr. Sanjay Ahuja, medical director of Rainbow Children’s Hospital, first spoke about “New and Emerging Therapies.” Expression Therapeutics is working on “ET3i,” a recombinant
factor VIII (rFVIII), that should give a higher yield, with the focus on lower cost per unit.

Another interesting therapy is called “transgenic.” Pharming Group has found a way to derive transgenic rFVIII from the milk of rabbits. Ahuja explained that scientists have learned how to take a human gene that makes factor VIII, put in rabbits, and have factor expressed through their milk. This is called “lacto-recombinant factor.”

This generated laughs from the audience, and one man gestured like he was milking a cow. And while Ahuja joked that we could get our kids to drink more milk finally, the actual drug would not be in milk to drink, but commercially available as an infusion. It would be cheaper to produce, with a high yield, making factor much more affordable.

“New things and better things coming,” Ahuja said.

Many people in the audience already knew about the innovative therapy called emicizumab (commercial name: Hemlibra), a bispecific monoclonal antibody that mimics factor VIII by bringing together activated FIX and FX together, replacing the function of FVIIIa. It’s not a factor product! There was a brief discussion about the deaths associated with its use [see our upcoming article in PEN for a detailed discussion on these]. Bioverativ and Shire are also working on bispecific monoclonal antibody and Shire’s is actually a bi/trispecific. These drugs are called “FVIII-Mimetic.”

Another innovation for FIX is from Salk Institute/Arcturus Therapeutics, currently in pre-clinical studies. It’s not gene therapy, though it involves taking RNA to the liver to
make factor.

On the horizon for inhibitors are products in the FVII market. HEMA Biologics/LFB, are working on an activated FVII. rEVO Biologics/LFB are working on FVIIa in transgenic rabbits.

Even a long acting, subcutaneous FVIIa is being made by Catalyst Biosciences and OPKP Health.

Perhaps the biggest surprise of all is rFVIII being made in lettuce at the University of Pennsylvania, and this you do eat!

Dr. Stacey Croteau, medical director Boston Children’s Hospital, and Associate Director of the Boston Hemophilia Center next spoke about gene therapy. She gave a brilliant overview, too detailed for here, but if you look at the slides, you’ll get a sense of just how much activity is underway. And all through the four-day conference, I kept hearing chapter leaders talking about not “if” gene therapy occurs, but “when.” More and more, it is becoming a reality.

Dr. Croteau first explained that there are three basic types of gene therapy:

1) Direct therapy (injection into the patient)

2) Cell based (in which you take cells out, alter the genes, then reintroduce the altered cells to the individual, called ex vivo)

3) gene editing (going directly into a defective gene to make it work)

Branded Content

There was a good discussion of how adeno-associated viruses (AAV) are mostly used as the vehicles (vectors) to introduce the altered genes into the patient. Why a virus? They are good at replicating—viruses need to quickly replicate to infect the host and survive. But Dr. Croteau stressed that the AAV8 is stripped down and rendered harmless, so just the FIX gene is left. It’s then introduced back into the patient and goes to the liver (AAV vectors love the liver!), embeds into hepatocytes (liver cells), degrades and becomes part of that cell and starts to express normal coagulation factors into the bloodstream.

Dr. Croteau explained how difficult gene therapy is. You must get the gene delivered to the right cell type in sufficient quantities; then it must switch the gene on, all the time avoiding body’s natural immune response.

In 2011 there was the first successful AAV gene therapy for hemophilia B. With high doses, the patients in the clinical study had their factor levels go from severe to moderate and even to the mild range.

Not all gene therapy research is using AAV; there are all types of AAV vector subtypes. Looking at the slides, why so many? Not everyone will be eligible to use a particular vector. Just like with factor, one gene therapy won’t fit all. Dr. Croteau concluded that it’s good we have several options for gene therapy, and many look very promising!

To learn more about gene therapy trials, you can look at Clinicaltrials.gov

And very honorably, the speakers reminded us that those patients who have volunteered and are volunteering for new therapies and gene therapy make it possible for the rest of us to enjoy a higher quality of life. Indeed, they are our heroes.

This was a great session to attend; thanks to Drs. Ahuja and Croteau for their presentations! Please read HemaBlog next Sunday when I’ll give an overview of the entire HFA meeting… which was fantastic!

Living as a Refugee

Laurie Kelley April 22, 2018

World Hemophilia Day was celebrated last week around the world. While everyone was wearing red, to symbolize the blood and treatment we have in common, I wore white, to symbolize those without treatment. After all, the logo of the World Federation of Hemophilia is a red figure with their arms around a white figure. The haves and the have-nots.

We ship donated factor to the tune of over $7 million per year to developing countries. Once in a while we get an unusual request, such as this one, from a refugee.

“I am a Syrian refugee whose son is in dire need of a particular medicine which is not consistently available here in Jordan and is extremely expensive. I am a Syrian national, born in 1974, married with four children. I was forced to leave my country after the war broke out in my hometown Darayya in Western Gouta of Damascus, when the regime forces broke into the town. Then, the local people were forced to leave due to the bad shelling by the regime.

“My house was damaged after being hit by many shells and was not able to live elsewhere for a long time because I was subject to detention by the regime’s checkpoints. Therefore, I was forced to leave my job as a teacher and became jobless. Then, I had no other choice but move to Jordan.

“The problem is that I have a 13-year-old son who suffers from hemophilia B, which is a blood clotting disorder, so that when my son gets injured or hit, he bleeds to death unless he is given factor IX medicine. The bleeding specific to his condition is generally internal, inside the joints. For this reason, I was forced to leave Syria because the internal bleeding could likely be fatal, especially due to the difficulty in reaching hospitals in Syrian wartime conditions.

“I have been a refugee in Jordan since March 31, 2013. Although therapy expenses are incurred by the UNHCR, the medicine sometimes is missing all over Jordan and not sold in pharmacies there. This medicine is very expensive so that individuals cannot afford it. The alternative medicine is plasma. Yet, it is very dangerous if patients take large doses of it.

“When my son gets sick, he must go to the children’s ward because it is not possible for Syrians to be treated in the hemophilia B ward in the Jordanian hospitals. This means that my son must stay with his mother in hospital for one day at least each time he is sick.

“The only hospital that has the medicine is way far from our residence, which disunites my family. I do not know where to leave my other kids when their mother is absent; the youngest kid is only 3 years old. This prevents me sometimes from taking my son to hospital when his bleeding is not heavy. This leads to harming his joints when bleeding continues and makes them stiffen and therefore, he will lose his ability to move especially that his left knee’s joint is greatly damaged due to continuous bleeding. It is known that it is unnecessary for the patients who suffer from hemophilia B to stay in hospital because they only take the medicine and return back home.

“Sometimes my son might bleed outside regular operating hours. This means that we might not get the medicine on time. This causes a handicap to my son’s joints and paralyzes his movement as doctors has warned from such results many times.

“I extend my sincere thanks to you for your selfless humanitarian effort to help the refugees of our country. I would like to thank all those, governments, individuals and non-governmental organizations, cooperating to support the vulnerable Syrian people.”

This is a gripping account of pain, love and survival. Fortunately, we were able to send a donation of factor, and will continue to help this family, and hundreds more, through Project SHARE. We are grateful to our supporters, and to those who donate factor to us each day.

Learn about Project SHARE here. Call us at 978-821-6197 or email us at share@kelleycom.com if you have factor to donate. Thank you for caring and sharing!

Angels Among Us: Steven Riedle and His Gift to China

Laurie Kelley April 15, 2018

Chinese boy with hemophilia before his accident

Tuesday is World Hemophilia Day, and we celebrate by sharing stories from patients in developing countries, and the angels among us who help them. Here is another story by Steven Riedle, who has been helping children with hemophilia in China quietly for years. Thank you, Steve!

———————————————————————————

My brother Jack got the call for his liver transplant in October 2016. [This
would cure his hemophilia eventually] On that same day, he received his last regular
ship of factor VIII. I was hoping for that, so I could donate his factor to the
island of Hainan, in China. I waited a few months because I really didn’t believe
the transplant would cure his hemophilia. It did! The product was shipped.

The next year while playing with my neighbors in the backyard on
the day of the eclipse, in August 2017, I got a message asking if the medical team in China
should use the factor we donated to try to save a young boy’s life. He was only
four years old, and had fallen and hit his head. Of course, I said yes, try it!
I knew a mom there, Xiaohua Liu, who has a son with hemophilia and she handles
shots and factor needs on the island. A few years ago, I even bought her a new
moped so she could get around better to help the other hemophilia families. This
is China: she risked jail, while gathering the hemophilia community at the
island, and then petitioning the government for more factor for the patients.
Instead of going to jail, she won the petition and got nine boxes of 200 IU of
factor a month! This was a success but hardly enough. My brother’s factor came
in much larger assay sizes: 4,000 IU every other day. The little boy needed
bigger shots for physicians to even attempt the surgery. They had to take a piece
of his skull off to relieve pressure on his brain. I know he would have surely
died without this gift of factor VIII. Mostly, I thought I would just be
keeping children from having to be wheelchair-bound. Saving a life wasn’t
really in my mind when I sent the box.

After head injury: 70% die soon after getting in this condition

Here’s the thing: my brother Frank died when he was 19. I was 17
years old then. Back in 1982, they didn’t even try to give him a proper dose of
factor, as I remember. Maybe they didn’t have the surgery option ether. I
really don’t know. All I know is about 15 hours later he was dead. Saving this
boy’s life— and I don’t even know his name— in a way helped heal me. That event
back in 1982 broke me. It would be years later before I cared about my future
or school again. Helping to save this boy’s life was a great thing for me, and for
the boy and his family. Those few times I found some factor in my luggage or
stuffed in the back of the cabinet where I keep all the hemophilia stuff
certainly can save a life. Even just helping to relieve the pain of an
untreated bleed for a person living in a country where factor is rare.

Tweezers holding piece of his skull,
taken out to relieve the pressure

The boy lived, and here he is in this video. There are children in
need of factor all over the world. Donate factor here. Save a life there.

Steve Riedle has
hemophilia, and is the inventor of Noseebudd, a therapeutic device to help stop
nosebleed. You can purchase a Nosebudd at nosebudd.com

Recovery

Boy with his baby sister at
birthday party

How Blood Brothers Support One Another

Laurie Kelley April 8, 2018

Untitled Document

We just finished Hemophilia Awareness Month, and now are heading towards World Hemophilia Day, April 17. I’d like to focus on a few stories of people with hemophilia who live in developing countries. If you know me at all, you know this is where my greatest passion lies—to help those in need who have little to no access to factor. When you read that a child has died from a tooth extraction, or a bloody nose, or that a promising young man has died riding his motorbike in the congested cities in developing countries, it breaks your heart. Our children in America strive to play sports, and live with no bleeds. The other 75% in the world just want to live… here is one story from the Philippines. We just finished Hemophilia Awareness Month, and now are heading towards World Hemophilia Day, April 17. I’d like to focus on a few stories of people with hemophilia who live in developing countries. If you know me at all, you know this is where my greatest passion lies—to help those in need who have little to no access to factor. When you read that a child has died from a tooth extraction, or a bloody nose, or that a promising young man has died riding his motorbike in the congested cities in developing countries, it breaks your heart. Our children in America strive to play sports, and live with no bleeds. The other 75% in the world just want to live… here is one story from the Philippines.

In 1990 my twin brother Luigi, age one, had a swollen left knee. Our parents had him tested, and he was diagnosed with severe hemophilia A. Because we are twins, I was tested too, and also diagnosed. It was very tough living with hemophilia, especially without access to factor VIII. We just took pain medication when we were in pain. My worst, most painful bleed was in 2008. I was coughing hard for days, and then I felt a small pain in my lower abdomen. Ignoring it, I went to school. There I felt the pain worsen, and I had trouble urinating. It seemed that something was blocked inside me, and my lower abdomen was swelling. I went to the hospital and was confined for seven days. The doctors did an ultrasound and inserted a catheter so I could urinate.

I was told it was good that we rushed to the hospital, as the internal bleeding was worsening and might have been fatal. I was infused with factor VIII for five days. This cost a lot, and we had no money then, so my parents went fully into debt. A year later, Blood Brothers Aid was established by a group of men with hemophilia in Manila. My brother and I were among the first board members!

I was able to finish college, with the assistance of Blood Brothers and Father Don Kill, who volunteers to help people with hemophilia in the Philippines. Now I’m employed, and I’m still a member of Blood Brothers Aid after nine years. I participate in their activities, including Christmas parties and summer camp. I’ve learned from my past bleeding; the pain I experience now is less severe, and my joint bleeding episodes are fewer. I’m getting infused with factor VIII that is donated to Blood Brothers from Project SHARE, but I take it only when the bleeding and pain are not tolerable. Without Blood Brothers, I would not be able to work. I’m very thankful to Blood Brothers, Father Donald Kill, and Project SHARE!

Leeroy Atanacio
The Philippines

Uncategorized

Shetland: Hemophilia at 60° North

On the Horizon: HFA Part 1

Living as a Refugee

HemaBlog Archives

Categories