
25/09/2024
Hey ya'll!🤗😍
I just want to say thank you to all who supported, to all who wanted to support and couldn't.
This page is closing, but the MediMom Caregiver Planners will be produced as a free product through fundraising for You Can't See My MG for parents of children with newly diagnosed Myasthenia Gravis. Kaleeya and I will continue to host the Kids Support Group to continue connecting kids with MG.
We are delighted to say that we have made great connections and connected great people. Including a pediatric Neurologist and kid from the support group who is now participating in a trial with this wonderful doctor who happen to attend our group meeting. This sweet kiddo is now receiving a treatment that's working for her. ALL because we hosted a kids support group meeting.
We look forward to 2025! Special thank to Myasthenia Gravis Foundation of America, Inc. for holding a space for all of this to happen.
Follow us You Can't See My MG to continue to support!
Get our email updates for Pediatric Kids Support Group Meeting
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[email protected]
Our find the Pediatric Support Group link by clicking the link below.
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The largest, leading patient advocacy organization solely dedicated to finding a cure for the rare neuromuscular disease myasthenia gravis (MG) while improving the lives of those living with MG.