Tiffany Fitzsimmons

I am starting this YouTube channel to encourage other parents with children who have hypertonia. I will also have updates on Tucker and give recipes for feeding tubes.


Hello my name is Tiffany Fitzsimmons. I am married and we have three wonderful boys. Our youngest was born in November 2018. He was born with Pierre Robin Syndrome. We spent 32 days in the NICU. He had to undergo a major jaw surgery at just 7 months old. At 8 months old we found out that he had a muscle condition hypertonia. With the combination of Pierre Robin Syndrome and hypertonia. Tucker had a G-tube inserted at two weeks old. He still relies 100% on a G-tube to his nutrition.


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