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

CF isn't all tears and saddness. Get a Full Picture.

  CF and Laughing Cystic Fibrosis can bring sad times and times of tears (like losing a close friend with CF, etc) BUT, it can bring so much joy and love. I've noticed most people love to talk about the people they meet while traveling. This is usually, because they have learned something from the person. Or the person is considered unique to them. I can do the same thanks to my Cystic Fibrosis. I may not have traveled much in my life thus far, but I have learned mountains of lessons from my CF. [Picture right:  Me ready for surgery in 2nd grade!] Forgive my shoutouts (but I must recognize a few amazing people) I have met some of the most amazing doctors: Chatrath, Dr. B Nurses: Sara & Marie (from Clinic), Lizzard, Melody (best IV stick ever), Deb, and Kris (you know a nurse is amazing if you love her after putting tubes down your nose!) Respitory Therapists: Jeannette, Lanell, and Don (you da Man) And Cookie Marrow (Musical Therapist- She would sing to me a...

Video Blog: Life in the hospital (as a child)

The daily life in the hospital! Most people cringe at the idea of a hospital. However, when I was little I never minded going into the hospital. I usually would have at least one other friend with Cystic Fibrosis to hang out with there (before we knew about the "CF Bugs"). I didn't love being sick, but I loved my CF friends that I would hang out with. Also the hospital, nurses, and my parent's tried to make it a "normal" environment. I got up and put on cute clothes, "walked to school", flirted with a couple CF boys, did homework, came "home" (back to my room), my friends would ask my parent if I could go play with them. We'd hang out in the play room or go on a walk with one of my parents! My dad loved taking me on walks and I LOVED going on our walks! Here is a video blog of the route we took and bit of information on what is was like growing up (for a chunks at a time) in the hospital! (it is posted via youtube, let is dow...

How Fostering and CF impact my work

I haven't been on my blog much.... I think that is because most of my blogging is currently been done on Health Union's Cystic-Fibrosis.com (here is link to all my posts on their site: https://cystic-fibrosis.com/members/cherizkunkel/ ). I decided last fall to step away from real estate after 3 years in the business. It was tough to say good-bye, especially since I had tripled my volume and business in the last year. However, I didn't have time to add any new clients; I kept saying, maybe next week, next month I can fit more work into my schedule. The truth is fostering takes a lot of time. We have between 5-8 monthly visits at the agency, 1 court ate a month, 2 home visits from the caseworker a month, plus e have 2-3 doctors/specialist appointments for our current kiddo. We have lots of paperwork we fill out, gas mile logs, receipts to add, and more! Our kiddo also participates in gymnastics and dance two nights a week. We go to a fosterparent support group with our kid ...