Wednesday, December 14, 2011

The First of MANY Colonoscopies for My Kiddos

Today, each of my kiddos had his/her first colonoscopy.  The prep was easy...lots of clear liquids yesterday and an enema this morning.  I actually started working on cleaning their systems out starting this past weekend...lots of fiber, including prunes & Plum-Smart juice.  They were not thrilled with the prospect of having an enema, but there are certainly worse things than having that done...like getting colon cancer.

Because of their ages, it had to be done at the hospital instead of as an outpatient at the doctor's endoscopy center.  All 3 of us survived the experience.  The staff was nice enough to put them next to each other so I didn't have to run back & forth checking on them.  I do not want to be the solo parent for their next scope...not at all.


Cae had 4 or 5 minuscule polyps. Dr Brown wasn’t even comfortable calling them polyps. He said they looked more like hyperplastic (fake) polyps. He biopsied and removed all 5 and suggested that the scope be repeated in a year.

Cas had 15-20 real, full-blown polyps. He biopsied 12 of them...not sure if he only removed those 12 or if he also removed the others.  We go back in 4 weeks for a follow up and will talk about “what’s next” for her. I think Dr Brown is inclined to repeat the scope on her in a year, too. I’m not sure that I’m comfortable doing that but am willing to listen to what he has to say.

Tuesday, November 29, 2011

FOUR YEAR WHIPPLE-VERSARY!


Today, I am BLESSED to be a 4-year Whipple survivor! I will NEVER forget this day in 2007...what a journey it has been! God has tested me, stretched me and grown me beyond what anything I ever thought was possible...all the while, He was holding me in the palm of His hand.  Life is precious for sure and will definitely never be the same again. (If you don't know what a Whipple procedure is, you should google it because it is definitely a “no-joke” surgery.)  Today, I am so thankful to be alive, to have avoided cancer, to have the privilege of living, and eating, and doing the things that God created me to do.

I owe all that I am today to God who has given me the strength I needed to endure…especially when times were tough beyond what words can ever describe.  He is the One who got me though this HUGE medical challenge. What was really amazing was how He enabled me to let go and entrust my kids to my brothers- and sisters-in-Christ whom I barely knew.  Really…who would have expected me to be in the hospital for a month?!  I am so thankful for the Goodings who watched them on a few occasions leading up to the surgery, for my mother-in-love who flew in to stay with them for a week while the surgery & initial recover took place, for Art and Amy Nagy and their kids who took them in after my MIL had to go back home, and then for the Ruperts who took over when the Nagy family had to go out-of-town for Christmas. It was just such a blessing to know that my kids were taken care of because I had no time or energy to even think about them.

I am also thankful for my parents and the comfort and answered prayers that God provided them as my Daddy was going through chemo for colon cancer at the same time that I had my Whipple procedure done. Praise the Lord for taking care of and comforting us all!

Most importantly, I am blessed and honored to have been chosen to take this tough journey so that I can be a source of encouragement and support to others who are either post-Whipple procedure or living life with FAP.  Those of us who have been disemboweled AND Whippled need to especially stick together to encourage and support one another as we continue to be FAP survivors and guinea pigs!  It’s one of those things that you definitely have to live in order to truly understand what it's like to live with FAP. I am thankful that we can be proactive about it and remove organs before malignancy occurs, but sadly, regardless of how many organs are removed (so far, for me, it's 6+ in whole or in part), there is no cure. We will continue living with this disease, with altered digestive/bowel systems, and with a 100% chance of an adenoma turning malignant. I pray for the day when a cure can be found!!

ONE FINAL NOTE:  It's "funny" how we use milestone markers in life like before/after high school, before/after college, before/after marriage, before/after kids, etc. I also have before/after colon surgery, before/after j-pouch surgery, and before/after Whipple Procedure. Those last 3 befores/afters, were each big adjustments; however, I must admit that the Whipple procedure was the most dramatic adjustment ever. So, for those of you reading this who are on a Whipple journey, whether your procedure was just yesterday or years and years ago, you are each Whipple Survivors...CONGRATS for surviving another day along with me!

Sunday, November 27, 2011

A Post Just Because It's One of "Those" Days


Living with FAP is definitely unusual. Most people who in the j-pouch groups on FB have pouches because of UC or Crohns so they went from having bad potty issues to better potty issues. The same thing with Whipple survivors...most had pancreatic cancer or other issues where those organs weren’t working so the Whipple improved things for them. When you have FAP, you go from no problems to lots of problems. Don’t get me wrong...I am thankful for the opportunity to be proactive and avoid cancer, but it’s a much harder transition when you go from normal to abnormal with the snap of the fingers (aka surgery) with no downward spiral.

I have definitely been de-gutted (several times) and Whippled (once) and think that while the Whipple was the easiest surgical recover (incision, etc), it was definitely the longest recovery (internal, emotional, etc). I cannot even imagine having to go thru chemo after this surgery...there is no way I’d have survived. Anyway, this Tuesday will be 4yrs since my Whipple and things are still adjusting. We homeschooled until after I had my Whipple.  After that, I was barely able to focus on getting myself through the day so my hubby made the decision to put them in base school. That has been a blessing although I miss having them home with me and using every moment as a teachable moment.

Fatigue is definitely an issue. I go for Venofer infusions every 8wks. I was on oral iron capsules, but my body just wasn’t absorbing it so my gastro told me to stop taking it. I also have issues with delayed gastric emptying (DGE or gastroparesis) which is really strange since I no longer have a pyloric valve due to an adenomatous polyp in the duodenum right by the pyloric valve which caused the surgeon to remove that portion (5%) of my stomach.  You would think that things would flow straight through, causing me to battle with gastric dumping, but it’s just the opposite...especially as the day goes along.

We had our kids (boy 12 and girl 10) DNA tested and found out that they both carry the gene which makes them the 4th generation in my family to have FAP.  I’m 3rd generation and got it from my dad.  He has 2 siblings with FAP and 1 without it.  He inherited FAP from his mom who died of colon cancer. Our family’s history probably goes back even further than that in the generation count, but since medical technology wasn’t great in the early 1900s and before and since information like that wasn’t discussed in families back then, we don’t know who else died from colon cancer that would have been associated with FAP. Anyway, they’re both scheduled for their 1st scope on 12/15. I will be surprised if my oldest has no polyps and am even thinking that maybe my youngest will have them already. My hubby is a Marine and we’re due for orders next summer. I told him that the next house will have to have FOUR bathrooms if he ever expects to use a toilet without waiting in line!