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There is hope for those suffering from genetic diseases & disorders.
Advocate for affordable & timely cures for those suffering from costly genetic diseases and help reduce healthcare expenses for everyone.
Like our Facebook page and help us advocate for affordable curative medicine.
Raise capital for the people who need help accessing affordable cures.
Collaborate with relevant stakeholders & groups in the medical, biotech, and pharmaceutical industries, as well as government, to advocate for safe, affordable, and timely cures for genetic diseases & disorders.
Spread the Cure® was founded in 2018 by a dad of two kids with hemophilia. Our initial goal was to raise awareness & capital for an affordable cure to Hemophilia Type A. This goal evolved into a vision to raise awareness about affordable cures for all people with genetic diseases & disorders with the hope of reducing long-term healthcare costs for all.
SpreadtheCure.org® is a nationwide 501(c)(3) organization that aims to create awareness, and raise capital, to overcome the numerous obstacles standing between those who suffer from genetic diseases and a real cure. My two boys have endured countless trips to the ER, extended hospitalizations, a lifetime of weekly IV treatments, regular episodes of internal bleeding, extensive external bruising, debilitating joint pain, arthritis, surgeries, and the list of costly and painful treatments continues until they’re cured. We don’t share our story often, but here is a link to public images of others suffering from hemophilia. The cure to this disease, and hopefully many others, will transform lives and save our healthcare system countless billions in medical expenses.
After battling the insurance companies, government programs, healthcare companies, and the seemingly endless bureaucracy standing between patients and a solution to this costly & deadly disease, we created Spread the Cure to find ways to remove the obstacles. We hope to create safe, affordable & timely access to a cure thanks to ethical & safe revelations through CRISPR technologies.
Prior to recent developments, it would cost a minimum of $270,000 annually to properly treat one person with hemophilia. The lifelong financial burdens leave most families in turmoil as they seek compassionate employers, adequate insurance and the medications necessary to live. Without adequate and timely treatment, many people with severe cases of hemophilia endure extreme physical suffering and die before reaching adulthood.
Prior to current medications, the average life expectancy was 13 years of age.
With your help, we hope to remove financial obstacles standing between patients & a cure. We view our organization as an opportunity to do our part to help fix a broken and unfair healthcare system, particularly for anyone born with genetic diseases caused by a single-gene being out of order.
The former and current healthcare system fails to address severe genetic diseases, driving many families into perpetual poverty as their only means to qualify for long-term, affordable healthcare. There are countless untold stories about the obstacles that those with hemophilia have encountered as they seek treatment. Very few companies, nor individual states, nor the federal government are willing to take on the costs associated with providing a permanent solution. The social stigma and the financial burdens leave many families in a difficult situation.
Through donations, corporate sponsorships, and fundraising events, we will be strong advocates on behalf of individuals & families affected by diseases caused by genetic disorders. We will work tirelessly to overcome obstacles that stand in the way of safe, affordable & timely access to a cure.
Thank you for taking the time to learn more about us. We hope you help 'Spread the Cure' by donating. We also ask that you 'Spread the Word' about our mission on Facebook, Instagram, and Twitter, so that one day our vision can reach around the world.