Michael Schulz Schulz’s Journey with ALD

First post: Jan 12, 2021 Latest post: Apr 20, 2021
Thank you to everyone who has given in prayer, love, support, and donations. We created this page for those who are interested in following our journey through ALD. Most of our boys have the x-linked genetic mutation, and we are navigating how this disease will affect them too. For now, we are focusing on Michael and all of his treatment needs. Thank you 💛

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