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
Comments
Post a Comment