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[This is Part 3 of my No Longer Starving series, a belated editorial for Feeding Tube Awareness Week. As I noted before, life got in the way during the actual awareness week so I’m raising awareness on my own schedule.]

Today’s blog is brought to you by the Letter “W.” Yep, we’re going to talk about the Who, What, Where, When, and ever-important Why involved in the use feeding tubes. There are tons of types tubes and even more reasons why an individual might get one. So I’m going to give you and general overview of the primary classes of tubes. I know everyone who has a tube, or “tubie,” has gotten those looks and questions. Truth is: most people don’t see tubes everyday; they may be curious, weirded out, or even afraid of them. When I first got my GJ tube, my nephew – the sweetest, most empathetic kid you’ll meet – was so incredibly gentle with me. I think he thought he was going to break me by giving me a hug. It took him a while to warm up to it and we talked a ton about it, but I’ve got those bear hugs back.

Tubes aren’t something to be scared of. Tubes don’t necessarily equate to loss of freedom and worsening of disease. In fact, feeding tubes prevent the progression of disease! And I have more freedom with my feeds and infusions than I have had in years. There are very few people that I know with tubies who don’t feel the same.

So let’s get rid of all the stigmas attached to tubes and take a journey with some of my incredible friends who just happen to also have tubes…

I want to issue the same warning I did yesterday: there are some pictures in this post of medical interventions; if this makes you uncomfortable, I advise you not to read on! 🙂

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[This is Part 2 of my No Longer Starving series, a belated editorial for Feeding Tube Awareness Week. As I noted before, life got in the way during the actual awareness week so I’m raising awareness on my own schedule.]

I thought I’d leave a window open and allow you all a peak inside life with a tubie – complete with pictures and the extensive vocabulary one acquires with this life. Due to the expanse of this vocabulary, I know I’m going to miss something. If I’ve missed something you feel important, I encourage you to add on in the comments section.  I also want to issue a warning that there are some pictures in this post of medical interventions; if this makes you uncomfortable, I advise you not to read on! 🙂

I’m going to start with the most important word of all:
Tubie – Although some use this word to describe a person with a tube, I prefer to use “tubie” to describe the tube itself. It can refer to an ng-tube, an nj-tube, a g-tube, a j-tube, a gj-tube, or even a central line used for TPN or other nutrition. All of these will be addressed further in my next post on the types of tubes, what they do, and who might have one. I want to note that I realize it’s commonplace for some to refer to tubie-users as “tubies” themselves; as a personal preference, I choose not to define someone based on the adaptive equipment they use, but rather on who they are despite that adaptive equipment.

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[This is Part 1 of my No Longer Starving series, a belated editorial for Feeding Tube Awareness Week.]

Today I went to see my tummy doc for the second time since I got out of the hospital in January. In honor of that visit, I’m going to start off what I intended to be my series on Feeding Tubes for Feeding Tube Awareness Week back in February. As one of the newest inductees in the tubie world, I want to take you on a journey. A journey through feeding tubes, why they’re necessary, and who may have one. But I’ll start it off with a bit on today’s visit and an update on our progress and my current state.

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