My Journey to Finding the Right Feeding Tube With Rare Disease

Meghan describes how she was able to come to a place of acceptance with using a G-J (gastrostomy-jejunostomy) feeding tube to help treat her pediatric onset stiff-person syndrome (pSPS).



Original post here: My Journey to Finding the Right Feeding Tube With Rare Disease

Original post here: My Journey to Finding the Right Feeding Tube With Rare Disease

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