Hayden's Hope

Thursday, October 2, 2025

Life after Hayden

 I had lunch today with Michelle Davis, who is the  Executive Director of the IFOPA. She is just an amazing person and has led the IFOPA from a grassroots family led organization to one the that has staff and an ongoing mission to find a cure for FOP.   

The IFOPA supports multiple drug trials through out the world.  Hayden participated in one of the first drugs trials that ended up being passed by the FDA. It was such an exciting moment. Hayden and I had long conversations about what it would be like to be able to have a surgery to remove all of the bone in his body and replace it with graphed muscle.  He told me he really wanted to do this but wanted to wait until he finished with college.

Yesterday marked another mile stone in research.  Regeneron announced that its Optima drug trial with Garetosmab prevents greater than 99% of abnormal bone formation.  Its so exciting now to have yet another option.  

https://investor.regeneron.com/news-releases/news-release-details/regeneron-announces-positive-phase-3-trial-adults-ultra-rare

The IFOPA is supporting 8 active drug trails which are looking at different ways to target/stop the extra FOP bone from growing.

Saturday, September 28, 2024

Epilogue

Hayden Pheif 5.15.2000 - 8.6.24

Hayden Pheif was born on May 15, 2000. In September 2002, he was diagnosed with an ultra rare genetic condition called Fibrodysplasia Ossificans Progressiva, or FOP. He was one of 900 people in the world who had itFOP causes bone to grow where it shouldn’t so Hayden had to be very careful not to fall or get injured as that would trigger the bone to grow.  He never wanted this condition to define him and he tried to live his life as full as possible.  He played in Little League, he was on the soccer team, he skied and loved to play with friends.   

In March of 2011, Hayden got pneumonia and ended up in the PICU for 4-1/2 months. He came home with a trach and on a ventilator. He still never let FOP define him. Hayden loved sports and enjoyed going to watch his friends play soccer or baseball.  He also was a big Giants and Warriors fan.  He loved going to games and even went to Giants spring training last April.  If you needed sports stats, Hayden was the guy to go to. He knew it all. 

Hayden was an avid gamer. He went twice up to Seattle to watch The International (DODA). He was an amazing multitasker. Gaming on one screen, homework on another, a Giants game on the TV, and Reddit or YouTube on another screen.

Hayden always had a love of art. His grandfather was an architect, Don Olsen of Sausalito, and his father is an engineer, so it must have been genetic. He started taking private art lessons in 2017. And his skill of drawing was honed weekly starting with charcoal, then watercolor and finally oils. 

As an avid movie fan, he watched 1,857 movies — yes, he kept track — he initially thought about being an artist to design for green screen backgrounds in movies.  However, he finally found his calling in architecture and decided he wanted to go to Berkeley. This past year he had at Berkeley was his most independent. His assistants were never allowed in his classes with him and weren’t allowed in crits either. He did as much as possible on his own. He was very excited to go to the launch party for the Student AIA Trace magazine and made his dad wait in the car for him for 3 hours.

Most of all, Hayden loved hanging out with his friends, whether watching sports on TV or grabbing a beer in the city.

Hayden passed away on August 6, 2024 from complications of pneumonia and sepsis.  His entire family was by his side.

You can donate in Hayden's memory at www.ifopa.org/hayden. Your generosity will ensure that his legacy to support research, patient support and family outreach will continue for those that remain.

Hayden leaves behind his mom, Megan, his dad, John, his stepmom, Jen, his younger sister, Elsa, and his dog, Bailey.


Hayden at Elsa's High School graduation.

Hayden in 1st Grade Art Class.

Hayden and Elsa visiting their grandmother in July 2024.


Monday, August 12, 2024

Hayden 5.15.2000 - 8.6.2024




This guy just takes my breath away. So much love. Hayden lived his life with courage, determination, stubbornness against a disease he didn’t ask for, and mostly a beautiful heart.

Yesterday he peacefully left us surrounded by family. I was holding his hand during it all and know that he was so thankful for all of his amazing friends and the life that he was able to live to its fullest with them. He did things I never thought he would be able to do and that is a testament to the power of friendship and his will to be independent.

We will be planning Hayden’s after party - “Haydenfest” - to happen later this year. In the meantime hold your memories of him near and dear to your heart. 



Donations to the IFOPA can be made in his memory IFOPA.org/hayden

Hayden Pheif 5.15.2000 - 8.6.2024







Thursday, February 29, 2024

Rare Disease Day 2024

  rare/re(ə)r/ Adjective

1.) marked by unusual quality, merit or appeal, distinctive
2.) seldom occurring or found uncommonly

Typically when we think of something as rare, 
we think of something special, 
unique or hard to come by.

Something spectacular such as the Hope Diamond,

 or discovering long, lost ancient ruins


or even a fossilized sand dollar 
such as the one I found recently on the beach.


Rarely, no pun intended, do we like to associate 
the word "rare" with an illness. 
However there is nothing spectacular about 
receiving a diagnosis of a rare disease. 
It is, in a word, devastating.
FOP is a rare disease.

Less than 5% of rare diseases have 
any therapies or treatments.
And 70% of genetic rare diseases 
like FOP start in childhood

There are over 6,000 identified rare diseases with no cures.

300 million people have a rare disease.  
That is more than all those with 
Cancer and AIDS combined.

FOP affects 1 in a million people, 
so its not just rare,
it's ultra-rare.

Finding funding for research, advocacy 
and community outreach 
for these orphan diseases, 
as they are called, is beyond challenging.

However within this rare community of people,  
there is something special about a rare disease, 
the people.

These special people are… 

...the scientists who study it,
Researchers in the FOP lab at University of Pennsylvania.
Meiqi Xu, Drs Frederick Kapkab and Eileen Shore

...pharma companies who pursue the discovery of 
treatments and drug trials
There are currently 9 ongoing drug trials for FOP treatments.  

...the patients and families who live with it
Hayden Pheif, skiing in 2008, at the Far West
Disabled Sports Center in Alpine Meadows, CA

...the amazing people who have only yet learned of FOP and
 will go to "great lengths" to fundraise for research
which will help to find a cure
Team "Girls with Grit" ran the Napa Valley Ragnar
(36 hour - 206 Mile) Relay in September to as a fundraiser
for Hayden's Hope
.


...Jeannie Peeper, who stood up to FOP by starting the  
International FOP Association 25 years ago. 
Her goal was and is to raise awareness, 
provide outreach to families and those effected with FOP 
as well as to create a 501c to support fundraisers for research.  


Jeannie Peeper with Dr. Frederick Kaplan,
head of FOP research at U of Penn, at the 25th
anniversary IFOPA celebration.

These people are rare in a very special way.
They give us hope.

Even though the people afflicted with rare diseases 
create a very large community, 
their conditions remain largely unknown 
to the vast majority of the world population.  

Today, February 28th, 
is 
Global Rare Disease Day.

This day was created in the United States 
by the National Organization for Rare Diseases (NORD) 
to raise awareness and 
increase advocacy for these special diseases,
as well as to provide hope to the 
patients and families afflicted by them.



Tuesday, August 15, 2023

In Pursuit of a Cure 2023

 




Hayden's life was permanently altered when he was diagnosed 
with FOP in 2002 at the tender age of 2-1/2.  

FOP is one of the rarest, most disabling genetic conditions known 
to medicine.  It occurs in approximately 1 in 1 million 
people world wide.

It causes bone to form in muscles, tendons, ligaments and other 
connective tissues rendering the person immobile.  
Essentially frozen within a second skeleton.

In 2006, the FOP gene was discovered by the 
FOP Lab at U of Penn.  Since then, the IFOPA has been working 
towards finding multiple therapies for those with FOP.

Please help us, Hayden and the FOP community on our 
relentless mission to find a therapy and a cure for FOP 
by donating to the In Pursuit of a Cure Fundraiser. 



Please join us at an exclusive LIVE research webinar on August 30th. 
There will be three time options available so you can hear updates on 
gene therapy research and learn about research priorities.  
This is an exciting opportunity to learn how your donation is 
making an impact.  



WE ARE RELENTLESS!




Sunday, September 18, 2022

In Pursuit of a Cure

In Sept 2002, Hayden was diagnosed with FOP, a rare debilitating bone condition that will eventually leave him frozen in his own body unless a cure is found.  At the time there was no cure or therapies available.  In 2006, the gene mutation which causes FOP was discovered and since then the race has been on to find a treatment and a cure.  While there are several drug trials going on right now which, if FDA approved, will provide a treatment for FOP.  It is gene therapy that will ultimately be the cure for Hayden and the rest of the FOP community.

For the third year in a row, our FOP community will come together for In Pursuit of a Cure- an annual global event that supports the IFOPA's first-ever gene therapy research program and helps support the advancement of clinical trial research.  Please join me in supporting this program by donating here.  


Monday, February 28, 2022

Rare Disease Day 2022

      rare/re(ə)r/ Adjective

1.) marked by unusual quality, merit or appeal, distinctive
2.) seldom occurring or found uncommonly

Typically when we think of something as rare, 
we think of something special, 
unique or hard to come by.

Something spectacular such as the Hope Diamond,

 or discovering long, lost ancient ruins


or even a fossilized sand dollar 
such as the one I found recently on the beach.


Rarely, no pun intended, do we like to associate 
the word "rare" with an illness. 
However there is nothing spectacular about 
receiving a diagnosis of a rare disease. 
It is, in a word, devastating.
FOP is a rare disease.

Less than 5% of rare diseases have 
any therapies or treatments.
And 70% of genetic rare diseases 
like FOP start in childhood

There are over 6,000 identified rare diseases with no cures.

300 million people have a rare disease.  
That is more than all those with 
Cancer and AIDS combined.

FOP affects 1 in a million people, 
so its not just rare,
it's ultra-rare.

Finding funding for research, advocacy 
and community outreach 
for these orphan diseases, 
as they are called, is beyond challenging.

However within this rare community of people,  
there is something special about a rare disease, 
the people.

These special people are… 

...the scientists who study it,
Researchers in the FOP lab at University of Pennsylvania.
Meiqi Xu, Drs Frederick Kapkab and Eileen Shore

...pharma companies who pursue the discovery of 
treatments and drug trials
There are currently 9 ongoing drug trials for FOP treatments.  

...the patients and families who live with it
Hayden Pheif, skiing in 2008, at the Far West
Disabled Sports Center in Alpine Meadows, CA

...the amazing people who have only yet learned of FOP and
 will go to "great lengths" to fundraise for research
which will help to find a cure
Team "Girls with Grit" ran the Napa Valley Ragnar
(36 hour - 206 Mile) Relay in September to as a fundraiser
for Hayden's Hope
.


...Jeannie Peeper, who stood up to FOP by starting the  
International FOP Association 25 years ago. 
Her goal was and is to raise awareness, 
provide outreach to families and those effected with FOP 
as well as to create a 501c to support fundraisers for research.  


Jeannie Peeper with Dr. Frederick Kaplan,
head of FOP research at U of Penn, at the 25th
anniversary IFOPA celebration.

These people are rare in a very special way.
They give us hope.

Even though the people afflicted with rare diseases 
create a very large community, 
their conditions remain largely unknown 
to the vast majority of the world population.  

Today, February 28th, 
is 
Global Rare Disease Day.

This day was created in the United States 
by the National Organization for Rare Diseases (NORD) 
to raise awareness and 
increase advocacy for these special diseases,
as well as to provide hope to the 
patients and families afflicted by them.



Saturday, June 8, 2019

T minus 24 hours - 2019 Haydens Hope Dipsea Race


In 24 hours, team Hayden's hope will be running the Dipsea Race in honor of Hayden and to raise awareness and funds for research.  Please consider donating by clicking here.




Monday, May 27, 2019

Hayden's Hope Dipsea Race




2019 TEAM Hayden's Hope
Liz Lawler - Carol Tagliaferri - Kelly Bates - Lora Anderson - Megan Olsen

Sunday June 9th, Team Hayden's Hope will be running the Dipsea Race in honor of Hayden and the Int’l FOP Association to raise awareness and funds research for a debilitating disease called Fibrodysplasia Ossificans Progressiva or FOP.

Hayden was diagnosed with FOP on Sept 11, 2002. This genetic disease affects 1 in 2million people. He is one of 800 people in the world with the condition.  Slowly his muscles are turning to bone, creating a second skeleton, rendering him immobile.

Since Hayden was diagnosed in 2002, the gene that causes this horrific condition was discovered in 2006, multiple pharmaceutical companies have started collaborating to find a therapy. Currently, there are three active and recruiting drug trials for a potential therapy.  This is an amazing accomplishment considering that most genetic conditions never find a therapy.  There are no genetic conditions that have a cure.

Please consider donating to the IFOPA in honor of Hayden’s Hope.  Click here to donate on line. Or if you wish to send a check, please make the check out to the International FOP Association and send to Hayden’s Hope / IFOPA c/o Megan Olsen 164 Tamalpais Avenue, Mill Valley, CA. 94941.

The International FOP Association is a 501c3 and has received a gold rating for transparency from GuideStar.

Monday, February 4, 2019

FOP National Organizations

Although FOP is a rare disease, affecting only approximately 2500 world wide, the work of the International FOP Association is supported and complemented by national organizations across the globe. Organizations are listed below, along with website, social media pages and email contact, if available. While these organizations are not formally affiliated with IFOPA, we are deeply grateful for the work they do outside of the USA to serve the FOP community and connect individuals and families with resources and other FOP patients on a regional and national level.



Wednesday, November 14, 2018

27th Annual Research Report on FOP

The 27th Annual Report is Now Available!

Each year, the Center for Research in FOP and Related Disorders at the University of Pennsylvania issues its annual collaborative report on FOP research. The 27th Annual Report written by Drs. Fred Kaplan, Eileen Shore and Mona Al Mukaddam is now available. 

Download the report for the best interactive reading experience. The arrows at the top allow you to flip through the document; the link in the middle at the top of each page returns you to the Table of Contents.

If you would like a print copy of the report, please contact Kamlesh (Kay) Rai at kamlesh.rai@uphs.upenn.edu

Thank you to Fred, Eileen and Mona for writing the report and to the entire FOP research community for all that you are doing to understand more about FOP and develop treatments and, one day, a cure.

Friday, September 28, 2018

Dr. Hsaio's Research Lab

Hsiao Lab at the University of California, San Francisco

The Hsiao Lab at UCSF has a variety of ongoing clinical studies related to the genetics and disease progression in FOP. 

Hormone and Genetic Regulation in Human Disease
Musculoskeletal disorders affecting the bones and joints are a growing health problem. Skeletal birth defects and dysplasias often cause significant physical stigmata and medical complications. In adults, osteoporosis, chronic joint symptoms, arthritis, and fractures lead to significant morbidity. Unfortunately, our ability to effectively prevent or treat any of these skeletal diseases is still very rudimentary. 
Our lab uses the skeletal system as a basis for understanding how hormonal and genetic factors affect human development and disease. By using a wide spectrum of approaches, we hope to develop a broader understanding of the biology underlying skeletal development, develop new models for studying disease pathology, and devise novel therapeutic approaches for treating human skeletal disorders and bone injuries.
Learn about what we do in 46 seconds!
See Ed Hsiao's elevator pitch from the 2013 CIRM Grantee's conference: Edward Hsiao - 2013 CIRM Grantee Elevator Pitch

Wednesday, May 30, 2018

Hayden's Hope 2018 Fundraiser

grit
/ɡrit/

noun
noun: grit
  1. 1.
    small, loose particles of stone or sand.

    "She had a bit of grit in her trail shoe after running the Dipsea Race."


  2. 2.
    courage and resolve; strength of character.

    "Hayden displays the true grit in the face of a rare debilitating disease."

-->
2018 TEAM Girls with Grit
Megan Olsen - Lora Anderson - Liz Lawler - Monika Kaplan - Mimi Hahn - Carol Tagliaferri

Sunday June 10th, the Girls with Grit will be running the Dipsea Race in honor of Hayden's Hope and the Int’l FOP Association to raise awareness and funds research for a debilitating disease called Fibrodysplasia Ossificans Progressiva or FOP.

Hayden was diagnosed with FOP on Sept 11, 2002. This genetic disease affects 1 in 2million people. He is one of 800 people in the world with the condition.  Slowly his muscles are turning to bone, creating a second skeleton, rendering him immobile.

Since Hayden was diagnosed in 2002, the gene that causes this horrific condition was discovered in 2006, multiple pharmaceutical companies have started collaborating to find a therapy. Currently, there are three active and recruiting drug trials for a potential therapy.  This is an amazing accomplishment considering that most genetic conditions never find a therapy.  There are no genetic conditions that have a cure.

Please consider donating to the IFOPA in honor of Hayden’s Hope.  Click here to donate on line. Or if you wish to send a check, please make the check out to the International FOP Association and send to Hayden’s Hope / IFOPA c/o Megan Olsen 164 Tamalpais Avenue, Mill Valley, CA. 94941.

The International FOP Association is a 501c3 and has received a gold rating for transparency from GuideStar.