National Feeding Tube Awareness Week
Long time no see! Thought I would do a quick post in honor of it being National Feeding Tube Awareness Week! I've had a feeding tube (on and off) for around 4.5 years now and I can without a doubt say that it has saved my life. Sometimes you have to be patient and try different types. Before I was diagnosed with positional Superior Mesenteric Artery Syndrome, I was given an NG tube. It was pure hell. I went from throwing up all day to throwing up all day AND all night. It was horrible. Despite still believing that I was having a "brain to gut" response and that there was nothing structurally wrong with me, my doctors eventually switched me to an NJ tube which bypassed my stomach altogether. The tube was on my face but it was okay because in a way it validated all that I was going through. I was diagnosed with SMAS in a clever way that helped change the way that doctors test SMAS now, but that's a whole other topic. BUT when we discovered that I had SMAS, it explained