Sock-it 2 Hunter Syndrome

Sock-it 2 Hunter Syndrome

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Our mission is to raise awareness for Hunter Syndrome and aide researchers in securing funds necessary to bring clinical trials to fruition for a cure

02/11/2022

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10/01/2020

Amazing news from RegenxBio! They are expanding their gene therapy trial to boys with Hunter Syndrome ages 5-18! πŸ’œπŸ’œπŸ’œ

REGENXBIO Announces Continued Progress and Expansion of Clinical Development Program for RGX-121 for the Treatment of Mucopolysaccharidosis Type II (MPS II) | REGENXBIO Inc. - Ongoing Phase I/II trial to enroll up to 6 additional patients in Cohort 2 while planning for next steps in program; further trial updates expected by the end of 2020 - New IND for Phase I/II trial cleared by FDA to evaluate RGX-121 in patients with severe MPS II ages 5-18 years old and

05/03/2020

2 years and 27 days... that's how old Ethan was when he was diagnosed with MPS II Hunter Syndrome.

We are posting this to raise awareness for , , and the β€œsigns” that lead to diagnosis. Our first sign something was awry was when Ethan’s speech was delayed and he suffered from constant ear infections. Help us spread the word and , leading up to MPS Awareness Day on May 15, 2020!

Copy and paste this text with your own photo, signs, and age of diagnosis. Try and tag FIVE (or six 😁) more people and challenge them to do the same!

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