Call for help, zebra strong, Wendy Strong.
Hi, my name is Aaron. I'm organizing this GoFundMe for my friend Wendy. In the six years I have known her, I've seen how this horrific disease has impacted her life and her families'. I encourage you to make your donations 100% available to her since the cost of this procedure is extremely high. Wendy, her family and I appreciate all your support, energy and prayers. If you would prefer to donate directly to Wendy through Zelle, call me or text me and I'll provide you with her number, my number is [phone redacted].

Read below to learn more about Wendy.

 

Wendy is One in a Million. She was officially diagnosed with Moersch-Woltman syndrome, aka. Stiff Person Syndrome (SPS) on Jan. 6, 2020. This  neurological Rare Disease only affects one or two people in a million, and it mainly happens to women. At the moment I'm writing this, she is undergoing her procedure, her last chance at this; an autologous stem process.. Unfortunately, a cure doesn't exist for this severe disease. Please watch the linked video to hear from John Hopkins' Dr. Scoot Newsome explain SPS.