May5Foundation

May5Foundation The May5foundation is a private family foundation dedicated to research, advocacy, awareness & outreach.

Please visit our website to learn more about our outreach and programs. https://www.Mays5foundation.com

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May5foundation
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🩸 Sickle Cell Awareness & AdvocacySickle Cell Disease is a genetic blood disorder that affects thousands of people, espe...
03/12/2026

🩸 Sickle Cell Awareness & Advocacy

Sickle Cell Disease is a genetic blood disorder that affects thousands of people, especially within the African American community. It changes the shape of red blood cells, which can cause severe pain, fatigue, and serious health complications. Yet every day, sickle cell warriors continue to show strength, resilience, and courage in the face of it all.

Today we had the opportunity to meet with local and state representatives at the Georgia Capitol to discuss the importance of Georgia House Bill 334 – The Sickle Cell Disease Protection Act. This legislation helps ensure that Medicaid patients living with sickle cell disease have access to the most effective and up-to-date medications and treatments through annual reviews and greater accountability.

Advocacy matters. Awareness matters. And together we can continue pushing for better care, resources, and support for the sickle cell community.

🩸 Support the fighters
🩸 Honor the warriors
🩸 Remember the angels

Please join us in wishing Warrior Kaden a very happy 15th birthday!
03/08/2026

Please join us in wishing Warrior Kaden a very happy 15th birthday!

03/07/2026
🚨 BREAKING: HB 334 PASSES THE GEORGIA HOUSE 🚨Today marks a powerful victory for Georgia’s sickle cell community.HB 334 —...
03/07/2026

🚨 BREAKING: HB 334 PASSES THE GEORGIA HOUSE 🚨

Today marks a powerful victory for Georgia’s sickle cell community.

HB 334 — The Sickle Cell Disease Protection Act — has officially passed the Georgia House of Representatives with an overwhelming amount of support (159 Yeas, 7 Nays).

This legislation will require annual Medicaid review of services and treatments for individuals living with sickle cell disease, helping ensure the care warriors depend on is meeting their real needs.

Today, thanks to the unwavering leadership of Representative Omari Crawford, that vision is moving forward — stronger than ever.

Representative Crawford has been a true champion for sickle cell warriors, and I am incredibly proud to stand alongside him in this fight for accountability, transparency, and better care.

But the journey is not over.

HB 334 now heads to the Georgia Senate.

Tonight we celebrate this progress — and tomorrow we continue the work to ensure Georgia’s sickle cell warriors receive the care they deserve.

A heartfelt thank you to everyone who called, emailed, advocated, and stood with us.

This victory belongs to our entire community.

As they shift from pediatric to adult care, young adults with sickle cell disease (SCD) appear to visit the emergency ro...
03/07/2026

As they shift from pediatric to adult care, young adults with sickle cell disease (SCD) appear to visit the emergency room more often and be prescribed less hydroxyurea, a preventive treatment approved to reduce the frequency of painful crises.

Data shows that patients ages 24 to 33 years were prescribed a significantly higher number of opioids — strong analgesics used during painful crises — than those ages 16 to 20 years. This trend was particularly pronounced among young adults with moderate to severe symptoms of anxiety.

As with any disease, this transition can be challenging. When adolescents change doctors as they move to adult care, many stop regular visits and rely on emergency services instead. This can break the continuity of their treatment and increase the risk of serious complications and even death.

To investigate whether transitioning to adult care influences SCD treatment outcomes, data was obtained from 1,581 adolescents and young adults with SCD living in the U.S. Most were female (68%) and Black or African American (59.5%).

Participants were divided into three age groups: before the transition (16-20), during the transition (21-25), and after the transition (26-33). The team also examined whether mental health — specifically anxiety and depression — had any impact on this transition.

The two older groups, representing patients during and after the care transition, were less frequently prescribed hydroxyurea, a therapy used to lower the frequency of SCD complications. Consistent with this finding, these two groups had significantly more emergency room visits, suggesting greater reliance on emergency services.

SCD aged 21-33 demonstrated utilizing emergency at higher rates, which can compromise the continuity of care when they are not connected and engaged with an [appropriate healthcare] provider,” the researchers wrote.

The two older groups were also more likely to experience moderate to severe symptoms of anxiety than the group of patients not yet transitioning to adult care.

[These findings suggest] a pattern of increased acute care use and decreased preventive treatment as patients with SCD transition to adult care. These higher rates can also be associated with increased disease burden, as people with SCD age, which requires greater intervention.

Further prescriptions and a less pronounced reduction in hydroxyurea prescriptions in patients ages 21-25. In contrast, more anxiety in those aged 26-33 was associated with an even lower number of hydroxyurea prescriptions.

Depression, but not anxiety, was linked to increased emergency use. Patients with more severe symptoms of depression were more likely than those with milder symptoms to visit the emergency room within 30 days (10% vs. 3%) and three months.

The research will continue with more outcomes to be obtained so we can learn more about the transition from pediatric to adult care.

Please keep our warrior Phillip in your thoughts and prayers as he has surgery today.
03/06/2026

Please keep our warrior Phillip in your thoughts and prayers as he has surgery today.

Ben registered as a stem cell donor in 2018 because he wanted to help someone. At the time, he did not know much about t...
03/05/2026

Ben registered as a stem cell donor in 2018 because he wanted to help someone. At the time, he did not know much about the process.

Last month, while at work, Ben received the call that he was a match. He was shocked, excited, and surrounded by support.

Preparing for donation included injections to increase stem cell production and a lot of prayer for the person who would receive them.

The donation process itself was straightforward and comfortable. Ben watched movies with his wife while the procedure took place, and recovery was easy. After resting the day of donation, he felt back to normal by the next day.

Ben knows his recipient is a 55 year old man, and his hope is simple. That this donation gives him more time with the people he loves.

After losing his own father to stomach cancer, being able to help someone else through a similar journey was deeply meaningful.

Ben would donate again without hesitation.

Thank you Ben :-)

Please keep Ka’mari in your prayers. He’s back in the hospital with a crisis after being released on Monday.
03/04/2026

Please keep Ka’mari in your prayers. He’s back in the hospital with a crisis after being released on Monday.

03/04/2026

This is life for many sickle cell warriors. Warriors only wish to be seen, heard and treated with respect by medical professionals.

We fight for the unseen and unheard daily

A 12-year-old girl is dead. Khimberly Zavaleta was struck in the head with a metal water bottle while trying to protect ...
03/04/2026

A 12-year-old girl is dead. Khimberly Zavaleta was struck in the head with a metal water bottle while trying to protect her sister from bullying at Reseda Charter High School, according to Khimberly’s family. Khimberly suffered a traumatic brain injury from the attack, dying several days after falling into a coma. The LAPD has launched a homicide investigation.

Students gathered in protest, demanding that Khimberly’s attacker be held responsible for the life taken. Her death is a devastating reminder that there should be zero tolerance for bullying and that it should be addressed immediately, before there are tragic consequences.

Full story link: https://linktr.ee/protectiveleague

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