![Chuck Burton Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, holds some of the drugs and medical equipment he uses near his home in Greensboro, N.C., Wednesday, June 12, 2024. (AP Photo/Chuck Burton)](https://mapi.associatedpress.com/v2/items/9a5741fdb2e94b95a22411771aecbc94/preview/preview.jpg?s=680x)
Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, holds some of the drugs and medical equipment he uses near his home in Greensboro, N.C., Wednesday, June 12, 2024. (AP Photo/Chuck Burton)
![Chuck Burton Robin Alderman, right, looks up to her son, Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, as they pose for a portrait near their home in Greensboro, N.C., Wednesday, June 12, 2024. (AP Photo/Chuck Burton)](https://mapi.associatedpress.com/v2/items/79df3664ecc946e2883336f73f4f0e05/preview/preview.jpg?s=680x)
Robin Alderman, right, looks up to her son, Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, as they pose for a portrait near their home in Greensboro, N.C., Wednesday, June 12, 2024. (AP Photo/Chuck Burton)
![Chuck Burton Robin Alderman, right, and her son, Camden Alderman, 21, pose for a portrait near their home in Greensboro, N.C., Wednesday, June 12, 2024. Camden, 21, was diagnosed as a baby with a rare disease called Wiskott-Aldrich syndrome, which is caused by a mutated gene on the X chromosome. It primarily affects boys – up to 10 out of every million — and can cause frequent infections, eczema and excessive bleeding. (AP Photo/Chuck Burton)](https://mapi.associatedpress.com/v2/items/dc031a7608be4663bd758c9f3e3b9a09/preview/preview.jpg?s=680x)
Robin Alderman, right, and her son, Camden Alderman, 21, pose for a portrait near their home in Greensboro, N.C., Wednesday, June 12, 2024. Camden, 21, was diagnosed as a baby with a rare disease called Wiskott-Aldrich syndrome, which is caused by a mutated gene on the X chromosome. It primarily affects boys – up to 10 out of every million — and can cause frequent infections, eczema and excessive bleeding. (AP Photo/Chuck Burton)
![Chuck Burton Robin Alderman, right, and her son, Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, pose for a portrait near their home in Greensboro, N.C., Wednesday, June 12, 2024. (AP Photo/Chuck Burton)](https://mapi.associatedpress.com/v2/items/7d9055eab9c348929e1a9bccb43b4dd9/preview/preview.jpg?s=680x)
Robin Alderman, right, and her son, Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, pose for a portrait near their home in Greensboro, N.C., Wednesday, June 12, 2024. (AP Photo/Chuck Burton)
![Chuck Burton Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, holds with an infusion pump he uses near his home in Greensboro, N.C., Wednesday, June 12, 2024. When he was a toddler, doctors removed his spleen because of uncontrolled bleeding. As a young boy, he wound up in the hospital many times and was told he couldn’t play baseball. (AP Photo/Chuck Burton)](https://mapi.associatedpress.com/v2/items/efe93efdf8e34cb6a33e2a60f23f33fa/preview/preview.jpg?s=680x)
Camden Alderman, 21, who has a rare disease called Wiskott-Aldrich syndrome, holds with an infusion pump he uses near his home in Greensboro, N.C., Wednesday, June 12, 2024. When he was a toddler, doctors removed his spleen because of uncontrolled bleeding. As a young boy, he wound up in the hospital many times and was told he couldn’t play baseball. (AP Photo/Chuck Burton)