IgAN Journey is dedicated to those affected by IgA Nephropathy (IgAN) and, in this episode, we have the pleasure of hearing from Texas Senator Kelly Hancock whose positive outlook has helped him live his best life despite his diagnosis with IgAN over 30 years ago. 

His diagnosis came at a time when much less was known about the disease, and there was so much uncertainty. Senator Hancock and his family kept his diagnosis private for many years, but after publicly sharing his story and talking about the importance of having access to resources and support early on, he found the IgA Nephropathy Foundation.

Senator Hancock talks about his IgAN journey and recent transplant and shares his advice for others affected by the disease: staying positive, learning from it, and keeping up with the things that bring you joy. He also talks about his efforts to educate others about organ donation and support legislation to protect living donors. About 1 in 3 people with IgAN will eventually need dialysis or a kidney transplant at some point – organ donation can be lifesaving

The Senator also shares what it was like to:

• Receive a live-saving kidney transplant from his son-in-law

• Changes since his transplant 

• Healthy habits he’s maintained throughout his life

“Do what you can do for as long as you can do it.” – Senator Kelly Hancock

Senator Hancock is proof that people with IgAN can live a full life. Yes, it’s uncertain, unpredictable, and difficult, but with the support of family and the right approach to life, it’s possible.

The IgA Nephropathy Foundation

Connect with Senator Kelly Hancock:

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Relevant Links:

Article: TX Sen. Kelly Hancock Recovers After Receiving a Kidney from His Son-in-Law by NBCDFW

Article: My son-in-law’s gift may have saved my life by Dallas News