Skip to main content

Inspector Gadget Parts. Malfunction.



I tend to joke I'm an Xmen (since I have mutated DNA) and that my weird medical devices are my inspector gadget parts. Go-go-gadget automatic IV Line. Convenient? I'd say so.The next day I have off from work that I don't have school I am going to make my appointments for that day. I just hope it is within the next few weeks.


You may remember me blogging a couple weeks ago about some problems I have been having with my mediport (automatic IV line that is in my chest) and my g-tube (my stomach feeding tube). Well I need to have a surgeon look at the G-tube to see what size I need to put in. Dr.B thinks the one I have may not be the right size.  Which, I'm not looking forward to changing it again, BUT I get the new style tube (the mini) which is smaller and thinner, so it is easier to hide under a bandaid. I'm looking forward to not taping gauze around my G-tube anymore. Its really hard to hide that sometime and it is impossible in swimsuits. Plus, scraping off tape marks everyday doesn't equal fun.

I know I shouldn't be, but I am a little self-concious about it. But I know how much I need it, since I can tell a difference in energy on nights that I do my feeding and nights I don't. So I keep it in. It's just smarter for me. But now I will be able to hide it and no more GAUZE! YAY! Excited!

And my mediport has been hard to flush, so I need to have them put TPA through my mediport. I have never had this done before, I'm a lil nervous, since I'm allergic to so much. But if i have an allergic reaction I have faith in the staff. I have to go to an outpatient lab at St. Alexis (first time ever at that hospital, kinda of excited to see what it looks like). However, I've had my mediport since 1996. Most ports are lucky to last even 6-8 years. I've had mine for 12. I tend to baby it. I don't use it for blood draws, only long term IVs that I have to do at home (mediports are great for hiding needles). I can go to class, perform in musicals, do anything with them (well except swim) :-).

But this means my mediport doesn't do "blood returns" well. I'm okay with that. That is why I have arms and I don't mind nurses not getting mine on the first stick ( I know my veins are tiny). My arms are great learning tools  :-) However, fingers are crossed the TPA works, so I don't have to have surgery to replace my mediport.

Not gonna lie, haven't had a surgery since 2003 and I don't want to pick up the "habbit" again. Plus, anesthesia and I don't mix well. Since I'm a new hospital I have to hope I get a surgeon as talented and sweet as Dr. Vagunta. He placed my mediport perfectly (nobody even knows its there) AND all my scars all smooth thanks to him.

So next day off I have in the next 3 weeks, I'm driving up to Chicago and getting everything figured out! Ready to have it all fixed! Can't wait!

Comments

  1. Well, I can vouch for the not knowing all this stuff was there. I didn't notice any of it at all. I honestly thought (before reading your blogs) that your enzymes and stuff were just syringes like diabetes. This is John btw. Strange it doesn't let me comment as a Facebook user.

    ReplyDelete
  2. You are such an inspiring lady. You take CF lightly and you grace well with life. The advent of such medical device is extremely beneficial.

    ReplyDelete
  3. John, thanks. Yeah, I try to conceal it for the most part (so people don't give me weird looks). but if I'm open to sharing about it for sure. I'm not ashamed I have a feeding tube or mediport, just I don't know what others think.

    Heidi, Thank you. All the new medical devices are extremely helpful. Cf makes life interesting, there is never a dull moment. I don't mind it and besides if I can do well, then maybe I can help others who are younger learn to do well too.

    ReplyDelete

Post a Comment

Popular posts from this blog

Today's BIG Appointment

 I discussed last week about my recent struggles & goals. I have been dealing with a lot all at once! Family planning (update on that in 2 weeks), my Grandma's funeral, lower lung function. Through it all I have remained very compliant with my meds! My health is VERY important to me. So this last weekend I took my vest machine, wabi sterilizer system , and packs of ensure to my parent's for the weekend. I wanted to make sure I did everything. While it was a sad occasion, it was still pleasant seeing almost all of the family together again. Actually 27 out of 29 of the cousins made it to the funeral. Grandpa is in the middle of the picture (can you find me?) LOL   On top of my medications I have been doing some dancing & walking, but no jogging or anything. I'm still counting calories on my fitbit (hitting over 3000) a day (& 40 grams of protein, 50 grams of fat at least). I knew I was feeling a bit better than before, but wasn't sure what to expec...

Sunny Days!

Since my last Cystic Fibrosis clinic, which you may have read about on my Facebook page , I have been working on a couple goals... both medical and personal. And boy do I love this summer weather! Summer weather combines one medical and one personal goal!! EXERCISE + MORE FAMILY TIME! I'm not one to enjoy extreme heat (90+), but have really LOVED the nice days outside with the family this summer! Sun (+sunblock LOL), freezie pops, flip flops, YES PLEASE! We have even spent some time at the lake this summer! Our kiddo(s) LOVE(S) the water and so does Andrew! I don't enjoy being IN the water as much as I like being ON the water. We have spent a dozen days this summer at our two favorite park/splashpads as well! Even days spent at home are usually in the kiddie pool. We are enjoying this weather and getting some exercise too! WALK! I try to talk advantage and do some walking when its nice out and I feel good. My Physical Therapist at clinic said it needs to be 15 mins of full acti...

Holding Down the Fort

My husband, Andrew, is currently at Wartburg Theological Seminary and is starting his first week of his second year there. Every year he lives on campus for one week. He enjoys starting each semester on campus where he can build friendships with other students and professors. It's the only time he is on campus. Usually he does long-distance learning, online, from home. It was the only way we could manage him doing a four year Master degree program while working. This week is the hardest for us. However, we have something on Thursday and Friday this week, so Andrew will only be gone 3 days instead of the typical full five. So that will make this week a bit easier than the other semesters. It's hard for Andrew to be away, although I know he is having a blast. We send random pictures back and forth like a book he may be reading or a game I may be playing with our kiddo. It is hard for the kid(s) to not see Andrew every day. We are foster parents and stability is a BIG issue for ...