Skip to main content

One week til my surgery (all the details).

One more week!

I've had many surgeries throughout my life ( 14 ish I believe). Most due to intestinal twisting and complications. I've had a couple mediports ( a disc, that is an automatic IV Line in my chest), stomach tube, etc. Not a big deal, right? Just another surgery. Here is an article about the surgery they are doing on me too: Read It Here! - Double Inguinal Hernia Repair.

Not a big deal, Right... totally.

I have an amazing surgeon, who is VERY talented and really cares about the patients.. unlike the last guy I went to see about this problem. I knew I needed a new mesh put in, I could tell the hernia (both sides of my groan) repairs both needed to be fixed.  The last surgeon, said I was too much of a "risk" and thought I should just "take it easy, stop dancing, etc" .... HA HA HA. no way. That's ridiculous. I blogged about him and his "amazing" bed side manner in This Blog!

I'm sooo thankful to have this new surgeon! I can't wait to just get this over with, I have been putting it off for almost 2 years, working on getting my health up more. I'm almost back to the health I was at in 2003 when I had my last surgery.

2003! Isn't that crazy! I had sooo many surgeries as a child, yet, I haven't had one in 10 years. I think that might be why I'm a lil nervous. In 2003 I had a major medical emergency/ surgery and it was bad. You know its not good, when friends who never visit the hospital come up to see you.

So that is my last memory of a surgery. I remember having complications with the anesthesia, etc. However, It was a major surgery and it was a horrific night. I wrote about that emergency/ambulance trip, etc and the surgery in This Blog Here!

Bottom Line: The surgey is not a major surgery, its not an emergency, I'm really healthy right now, and I have spring break to heal. It should all work out perfectly. I think my dad, mom, and boyfriend are all going to be there.  I just wanted to keep everyone posted on what the surgery was for and why I may be a lil nervous, which I think is irrational of me. But, that's okay.

I'm just glad I got all my pre-surgical testing done today!

And best news of the day, a Cyster (CF online friend) got her new lungs a couple days ago and she is off the vent and breathing on her own now! <3

found this on pinterest the other day and thought of her and all the fibros and cysters waiting for lungs and fighting to keep their lungs!!




Comments

  1. Sorry about the bed side on that last surgeon. i'm glad you moved on and found one who is passionate about his patients!
    Best wishes <3

    ReplyDelete

Post a Comment

Popular posts from this blog

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 ...

Oh the Joys of a Colonoscopy!

Colonoscopy, Fun: As you may remember from reading my October Posts (  Oct Post #1   &  2nd Oct Post ) that I was admitted a second time that month for Gastrointestinal issues. I was having stomach cramps and what was believed to be Antibiotic Associated Diarrhea. However, CT scan revealed my colon and intestines were inflammed.  After having a rough 2 months of GI issues, and cuting out most food (diary, meat, grease, carbonated beverages, and sugar). I finally am getting a Colonoscopy to see what in the world is going on! I'm been taking Probiotics, was on meds for both C. diff and AAD. I even added driking Kefir to add to the probiotics and good bacteria.  Only now am I seeing any changes, less stomach aches, etc. I add a 1/2 cup pf the Kefir to my smoothie, its not bad -yum! I really reccommend it and Probiotics (so talk to your doctor about it), it could really help you out! Read about Colonoscopies here! So I'm glad to be g...

What Else Should I Do?

Need Some Feedback.       May has almost come to an end. I love May, nice weather, summer starts, AND its Cystic Fibrosis Awareness Month! A lot of the CF walks are in may and its a great time to raise funds and awareness for CF! However, I'm also excited that it will be June soon! June 28th is the Princeton Cystic Fibrosis Walk. I've helped organize other events in the past. Whether for school or other non-profits I've volunteered at, but this CF Walk is a little different. It is the first time, I've put together a City event. Or put together an event that is so near and dear to my heart. I'm so thankful that I had so many people sign up so quickly. Pretty much everyone family member I have on my mom's side signed up the first day. And I've have had some family and friends help me (giving me ideas, helping me recruit, etc). But, Its the first time I didn't have a committee or team behind me to help execute the ideas and actually plan the event. I lo...