The Living For Raysen Memorial Fund has been established by the parents and big brother of Raysen Glenn Frech to help children and families affected by cardiovascular disease.

Raysen Glenn Frech went home to be with the Lord on Sunday, April 27, 2014 at the age of 3 months and 28 days after giving everything he had to a congenital heart defect known as Hypo Plastic Left Heart Syndrome. Though young in age, Raysen’s journey touched thousands of lives. He never spoke a single word, yet his life ministered to countless people around the world.

Raysen’s family has managed to walk this terrifying journey with the love and support of extended family and friends. Their hope is that the establishment and growth of this fund will help other heart babies and families Live For Raysen as his family is determined to do everyday.

If you would like to read more of Raysen’s story or find out more about fundraising events please visit our Team Frech Facebook Page or visit Or