Fred has tried medications, platelet transfusions and surgery, but won’t let his condition keep him from the most important life experiences.
By Catherine Cooke
Fred was “living in la-la-land,” according to his wife Cynthia. He skied, hiked and enjoyed the outdoors as much as possible. Physical activities were a major part of what fueled his interactions with people and contributions to his community.
But one day, something changed.
Doctors can’t figure out why, but something triggered his immune system to mark his platelets as bad, which causes his own body to destroy them.
Fred can now bleed out very easily and can no longer do anything where he’ll get a bad bruise. Almost overnight, his once active and social life became much more isolated.
“I’m tied to my medical facilities right now. If something goes way down, I’m going to have to go in and get platelets... In the last year, it’s not quite so livable,” Fred reflects.
His rare disease, idiopathic thrombocytopenic purpura (ITP), has no cure, and the treatments that have shown success in some other patients — medication, platelet transfusions, and surgery for spleen removal — have sadly not helped Fred long-term. His doctor has jokingly, yet truthfully, deemed him his “problem child” because of the trouble they’ve had finding relief for Fred.
“I’m about out of options to be very honest with you,” Fred shares. “I keep looking and looking, and there’s nothing out there as far as another drug or treatment plan.”
He was hit hard when one medication led to two heart attacks. Often times with rare disease, doctors don’t know how patients will react to medications or even the proper amounts to give. Treatment can be very experimental when the options are so few, making Fred “feel like a guinea pig.”
Although he has come to a standstill in his medical treatment, Fred continues to dig for new options. His search led him to RDMD, a platform that makes it easy for patients and families to contribute to drug research from home to power faster, better drug development for rare diseases:
“RDMD is trying to open some doors that need to be opened. I’m still not defeated as far as throwing down the towel and saying ‘I quit. I give up.’ There’s things out there. There are promises out there.”
RDMD collects and de-identifies medical records, then works with researchers to design better clinical trials with faster outcomes and a higher chance of success. Fred was particularly intrigued with the prospect of gaining higher-level insights into his disease by aggregating ITP patient data:
“The more information you have, the more power you have...that’s what I’m trying to do— give [doctors] more information so that some place down the line they can link things together.”
Despite all the devastating challenges and setbacks Fred has had in his medical journey, he continues to count his blessings:
“Fortunately, I have a faith that keeps me going, and I have a wonderful wife that keeps me going. Life is precious. Handle with prayer. That’s kind of one of our thing around here.”
With no children of their own, Fred and Cynthia have been sponsoring four children in Peru through Compassion International, and they have a trip planned next spring to meet the children who have helped them “put life into perspective.”
It’s risky to take a trip like this, but Fred is determined to “not [give] up certain things in my life that mean more to me than taking a chance a little bit on going someplace and seeing something I desperately want to see and meet.”
Above all, Fred lives a life of “look[ing] for positive things out there. I can’t change the past. I can look forward and hopefully grow in the future.”
His wife Cynthia encourages everyone to, “Do it now! Do everything you can now while you’re healthy... Live every day to its fullest.”
If you are a patient, or family member of a patient, with ITP and are interested in contributing to research from home learn more at rdmd.com/itp.