June 16, 2017
August of 2016, Reid was diagnosed with X-Linked Myotublar Myopathy (MTM1). Learning that our baby boy was diagnosed with such a rare and terminal genetic disorder was tough to swallow, but the Ward family has been one of our biggest blessings. Their son was the severe marker for the disorder before Reid was given that title. This family continues to make a difference in our small medical community by organizing the MTM-CNM Family Conference every other year. This year, conference takes place in Nashville, TN and we need YOUR help! The support and resoures our family will gain by attending conference are priceless, but everything else that conference provides adds up quickly. By donating today, you provide families like ours a place they can feel hopeful and connect with others just like them. To learn more, please visit www.mtm-cnm.org. Thank you for your generosity and participation in making this event a reality!