Wednesday, March 4, 2015

One year later

Today marks the one year anniversary of Mackenzie having her colon removed. It's been quite a journey. I have my daughter back! Feeling blessed.

A message from Mason:






It's hard to believe it's been a year since the first surgery.  In some ways it's gone fast, but there were definitely long periods of struggle.  So far I've only been a reader of this blog, and am glad I finally have a chance to contribute to the storyline.  Here's the story in my own words:

Pre Surgery
Leading up to the surgery, Mackenzie had gotten used to a reduced quality life.  Lialda (sp?) had lost it's effectiveness, and she was trialing different medications to see if anything would get her back into a stable remission.  After a few unsuccessful attempts, the doctors starting recommending biologics.  This was very scary to me as they had several serious side effects.  The most frightening part was that biologics were being pitched as a long term solution.  In other words, Mackenzie would be exposing her body to harm inducing drugs for the next 60 years.  After every appointment I would bother her with 50 questions because I was convinced there had to be another solution.  As it turns out, surgery was an option that could completely remove the infected area.  This was not a perfect solution as there were several risks during surgery and a high likelihood of a compromised digestive system long term.  But regardless of the risks, it all seemed completely worth it to me.  Would you rather live your whole life at 60% health or spend one year at 40% health and then be back to the real you?  

Her condition worsened slowly until surgery was no longer an option but the recommended remedy.  She had been taking a large dose of prednisone and it had started to effect her body and her mood.  I could tell that she was increasingly self conscious  because there were more and more "do I look OK in these jeans" moments (but she still looked great!).  There was significant weight gain, but a lot of it was in the riiiiight areas.  As her condition worsened, I was sad to see her health declining, but glad that definitive action was being taken.  When I got the news that surgery was to be scheduled I was thinking "Alright let's fix this!"

First Surgery
We had a ton of confidence in Claudia Hriesik and knew we were in great hands.  The surgery went great and I was really inspried by the Da Vinci robot.  If you haven't seen it check it out.  Amazing.  https://www.youtube.com/watch?v=VJ_3GJNz4fg  
After her first surgery Mackenzie was free.  The root cause of the problem (the colon) had been removed and was no longer acting as a parasite to her body.  She was worn out from the invasive surgery, but had a very positive outlook and her energy quickly came back.  I was proud and took every opportunity to say "Kenz whip out your bag and show these people!"  If you have an illeostomy bag, OWN IT!

Second Surgery
The second surgery was scheduled about as soon as it could have been, and honestly we were a little caught off gaurd by Mackenzie's recovery.  The surgery went great, but her energy didn't quickly come back.  Our leading theory is that she was no longer on prednisone and therefore had to recover naturally.  She had several episodes of severe stomach pain where she would be doubled over on the couch or walking around like a 97 year old hunchback.  She went to get herself checked out several times and we even spent a Saturday in the ER in Michigan to get some MRI's.  Nothing conclusive was ever found, which sometimes is worse because there is no closure.  Our leading theory here is that there was some sort of kink or irregular path of her upper intestine near the stoma that was making it painful to pass food.  Her diet was supposed to be relatively unrestricted but to try to manage the pain she stuck to easy to digest low residue foods.

Just a quick note in here to say during this phase we also got married!  We had been putting of the wedding for health reasons and finally decided to book it.  Kenz was ill for some of the wedding day and a some of the honeymoon but overall everything was awesome and we both have no regrets about inviting her illeostomy bag to the wedding.

Third Surgery
By this one we were excited to end the process.  Going to the hospital, sleeping by her side in the room, eating the snack basket from the Britt's, it all felt fairly routine.  Tony and Marissa brought the nintendo Wii up to play Mario Kart..we had this process down.  The recovery was smooth and now Kenz had a new medicine marvel to show to her family and friends...the hole!  

Back to Life
Within 1 month kenz was herself again.  For the first time in over 2 years it wasn't me saying let's stay out with freinds a little longer or go do this or that.  This very welcome role reversal meant that my wife was back!

Currently kenz is back to substitute teaching and is looking to get a full time teaching job next year.  We are very happy and very thankful for all the support of our family and friends.    Also thank you to modern medicine, God, Claudia, and most importantly the da vinci robot.  No colon and still rollin'!  Also, Mackenzie's farts are now much more pronounced and nearly rival mine!


Mason




A message from Kenz:


So today marks the one year anniversary of my 1st of the 3 j-pouch surgeries.  It has been a little over 3 months since my reversal surgery, and I thought it would be a good time to give everyone an update on how things have been going.  

I am beyond excited to say that I feel amazing!  I feel like myself again.  I'm back into the normal routine of life; work, exercise, cooking, hanging out with friends and family, and being a much more fun wife (and aunt).  Shout out to my husband who has been so amazing and supportive through all of this. As difficult as the last year has been, it was so worth it.  I would do it all over again if I had to.  I know that UC is a constant battle for so many.  My hope is to share a positive story of how surgery can give you your life back. It certainly has given me mine back.

Here are some more details about my everyday life after surgery (mainly to inform my fellow J-Pouchers) :)

My surgeon recommended that I take a daily probiotic for the rest of my life.  I have been doing so ever since my reversal 3 months ago, and I have not had any complications (I know that a daily probiotic can help reduce the chance of complications such as pouchitis).  Besides my daily probiotic, I am completely medication free!  I Have an average of 4-6 bowl movements per day, 1 being during the night.  I honestly have to say that this does not affect my daily life in any way.  There is no urgency and no pain.  The only time a BM gives me irritation is if I eat something spicy.  Speaking of food, I can eat whatever I want!! Also, I am slowly gaining my energy back, and can get through my days without needing a nap (this is awesome for me, as simple tasks used to tire me out quickly).  Like I said before, surgery has given me my life back, and for that I will be forever grateful.  


I want to thank my mom for all of her continued support and for making this blog happen! She truly is an amazing woman.


If you have more questions as you consider or go through this process, please do not hesitate to ask me!

Mackenzie

Some pics during the journey and some pics 1 year later.





Friday, November 28, 2014

One week after take down surgery

Well we have so much to be thankful for this Thanksgiving. Mackenzie has completed all three surgeries and is on her way to having this journey all behind her. She has married the love of her life and has given us the most amazing son in law anyone could ask for. We love you Mason! Also we have our grandson Dominic, who not only has brought joy to our lives, but has been a wonderful distraction throughout this journey of surgeries. He has always put a smile on Aunt Kenzie's face. 

We are also so very thankful for the many connections we have made through this blog. So many people out there that we haven't personally met, but have been there for us. 
We are also so thankful for the support of wonderful family and friends. You have gotten us through. ......thank you.

Kenz is doing really well one week past her take down surgery. She is experiencing all normal recovery feelings. Even though some things are uncomfortable, it is all to be expected after take down.  

We said good bye to Colleen (that is what she named her stoma) and officially hello to the jpouch. 

Woohoo.... God is good!

I will be slowing down the blog for now. I may post occasionally for updates for those of you wanting to know how things are progressing.

 If anyone would like to contact myself or Mackenzie please feel free to email us anytime.

Rhonda: rrtuch@gmail.com

Mackenzie: Mackenzie.tuchrelo@gmail.com

These pics were taken just before she went into each surgery. From "moon face" to getting her health back. WOW!






Tuesday, November 25, 2014

4th day after take down

Kenz is still on the limited bridge diet today.  Tomorrow she can start the low residue diet. She is extremely tired but I think once she can add some chicken into some of her meals she might have more energy.  She got out of the house twice today. But both times really tired her out. I see her improving every single day!!! 

She sure does love snuggling Boosh!


Monday, November 24, 2014

3rd day after take down surgery

Mackenzie came home from the hospital today. She took a shower and got settled in at home. She is doing great.  At about 8:00 tonight the dreaded butt burn set in. She is experiencing intense gas pain but does get some relief with the Gasx. She said the butt burn is so uncomfortable. We ordered special cream called Calmoseptine at the pharmacy. I hope it doesn't last too long. 

So glad she is home and done with surgeries! 



Sunday, November 23, 2014

2nd day after take down surgery

Kenz will get to go home tomorrow. She has been able to pass gas and has pooped in the potty!! Lol. Honestly it has been so funny how we are all so excited for the first poop, just like she was just learning to use the potty. Finding humor during this journey has been a saving grace. She said it looked like little rabbit poop!

She has been off her IV today and started the "bridge diet." This consists of cream based soup broth, scrambled eggs, apple sauce and pasta.  

The gas pain does really get intense and taking gas x and some pain meds are getting her through. She is able to get herself up and walk around. She showered and really only complains about how tired she is and the gas pains. Other than that, things are going smoothly.

I think tonight I'm going to post a picture of Kenz on her wedding day. She and Mason had to change their wedding date due to her surgeries. They still wanted to have the wedding in 2014 so they decided to get married after the jpouch construction surgery but before this take down. She had a very rough time during that time with some blockages dealing with extreme stomach pain nausea and vomiting. She was in rough shape even on her wedding day. However she pulled together everything she could to get through the day. This disease truly is a hidden disease. Everyone saying, "You don't look sick."  Well all you fellow UCers know how that is. Here is a picture of my beautiful daughter who looks amazing and pushed through a very rough day on her wedding day. I know I keep saying it but.....she is one determined strong young women walking down the isle with her bag under her dress feeling like shit. I love her to pieces!




Saturday, November 22, 2014

1st day after take down surgery

Nov. 22, 2014

Mackenzie slept well last night. Her blood pressure was pretty low during the night, but was higher in the morning when she got up to walk around. Today she started feeling the cramping they said she would get as the gas was passing through the intestine. It got pretty intense during the day. 

Last night she took one walking lap around the hospital wing, and today she took 5 more laps. Her surgeon came to visit her and told us how pleased she was with the surgery. Kenz has been sleepy all day. 

Finally at 8:30 tonight Kenz passed gas for the first time. Yippee we were all so excited!! This is one thing that has to happen in order for her to be discharged. The other thing of course, is to finally poop using the J pouch.  Just like when she first pooped in the potty, we will all be celebrating!!! 

Mason got here from Michigan at around 9:00 tonight. He has been in constant contact with us until he could get here.  He is now on overnight hospital duty.

 So I'm going to end this post with a picture of what her stoma site looks like now. They pack the hole with gauze, no stitches, it will heal from the inside out.

Goodnight, so very tired. 

Friday, November 21, 2014

Final surgery take down!

7:30 am

November 21, 2014 the take down, Mackenzie's last surgery. I can't believe it's finally here. What a long journey it has been. The recovery after her Second surgery in July has been one tough road. So glad we are at the point of take down!


8:55 am

The surgeon called to let us know her surgery was done and she felt it went perfectly.

10:00 am

I finally got to see her in the recovery room. She said her surgery site where the stoma was hurt very bad, but other than that she felt good. She is just groggy and nauseous.

11:00 am

Kenz got to her room and she is in the new wing again! 

Guess who came to visit Aunt Kenzie already!?!? He is a loyal visitor. He even brought the beautiful new Vera blanket.