Very long medical update.

Kerissa • May 2, 2018

Hey friends,

I’m sorry I haven’t posted in a while!  It’s been a pretty rough two months..

The last half of March, I started experiencing severe, cramping abdominal pain, terrible nausea, distention (I looked pregnant!)….and just felt really unwell.  The abdominal pain started happening every few days to every single day.  Pretty soon it hurt terribly to eat (much worse than the usual pain from gastroparesis) and drink water. Even pushing meds through my jejunostomy tube caused pain right away.  I lost weight and felt really weak.  Everything was getting worse and not better, so I finally told my GI dr.

He wanted me to get a work-up at the ER.  So on Tuesday, April 10, I went in.  I was dehydrated from not being able to drink much at all (my daily IV magnesium and nightly TPN wasn’t enough even).  So the doctors gave me more than 2 liters of IV fluids with dextrose.  That helped a lot.

They drew a ton of labs and also checked to see if I had a bladder infection.  Here’s where it gets kind of hard to understand…  There are different parts to a urinalysis—-the first part showed that I had trace white blood cells.  So the doctors weren’t sure if this was a borderline infection or what.  The second part (called a culture screen) came back positive for infection.  So I got admitted overnight, and they started treating me with antibiotics.  But the next morning, the actual culture test (where they wait to see what kind of bacteria grows) came back and said, “No significant growth.”  So it turns out that I didn’t have a bladder infection!  We don’t know why it showed white blood cells or why the culture screen was positive…

One blood test (called lipase) did come back pretty high..  Lipase is made by the pancreas and small intestine.  When I saw my GI doctor a couple of weeks later after this hospital stay, I explained everything that happened.  And here’s what he thinks caused the severe abdominal pain, nausea, etc.  He thinks I had a partial small intestinal obstruction. He explained that they can be VERY painful and cause all of the symptoms I was experiencing, including the elevated lipase.  The abdominal CT scan the ER ordered didn’t show an obstruction but he believes it’s because the scan wasn’t done in time and because I was at the tail-end of this (i.e., the obstruction was resolving which makes sense since I was starting to feel better later that day in the ER..).  You might wonder, “What caused you to have a partial bowel obstruction?”  The answer is—-adhesions.  Having a jejunostomy feeding tube surgically placed in my small intestine (done back in 2014) can cause adhesions.  I always thought adhesions were inside of the intestine, but he explained how adhesions are like webs outside/around the intestine.  And sometimes, the intestine can get kinked, caught, or twisted on an adhesion….which then causes a partial or full obstruction.  Hope all this makes sense.. :/  I asked him if this will happen again.  He said it could or it may be years from now before another one occurs.  I really hope it doesn’t because the abdominal pain was simply horrible!!

The day after my GI appointment, I had a follow-up with my urology surgeon.  And we both were on the same page regarding this major bladder surgery.  She (and I) feels like we need to put this surgery on the back burner for a little while because of all that has happened recently.  Doing this surgery would involve using a part of the small intestine which would then cause more adhesions to form. And because my GI system is not in the best shape in the first place, surgery would most likely cause complications.  She brought up the Hippocratic oath, and she doesn’t want to cause more harm than good.  Thankfully, my neurogenic bladder hasn’t gotten worse and has been stable for the most part, so I will be monitored and see her again in 6 months.

I’m more glad than sad about this decision because going into it, I just felt uneasy and didn’t feel ready for this major of a surgery.  Also, it got postponed twice so I kept wondering if that was the Lord telling me that now is not the right time to have this surgery.

Anyways, this update is getting super long!!   Tomorrow, I have a follow-up with my ENT (swallowing) specialist.  Next week I have a genetics appointment at OHSU to discuss whether I need to take “malignant hyperthermia” precautions and stay away from certain anesthetics because of a specific gene mutation I have.  And in two weeks, I see my orthopedic hip surgeon to get the ball rolling for hip surgery…. Still need to get another MRI to officially confirm that my right hip labrum is torn, but it most likely is because I had a diagnostic ultrasound-guided hip steroid injection (the needle was so huge!!)…I had immediate pain relief which tells my doctors that the problem is directly in my hip joint and not something like muscle pain..  You’re probably wondering why I have these hip problems….well, it’s because I have loose joints from Ehlers-Danlos Syndrome.  Too many things going on at the same time..

In addition, I officially weaned off one of my pain medications (with my pain doctor’s guidance), and it has not been easy at all.  My small fiber neuropathy has been so painful now. Every night, it’s been taking me hours to fall asleep due to the pain!  So hoping things soon improve because I’ve just been extremely exhausted every day..

Anywho, that’s all for now.. Thank you so much for continuing to pray for me!!  You are all a blessing.❤

P.S. In April, I participated in the famous 30 Days of Bible Lettering challenge on Instagram.  If you use IG, you can see all my lettering posts (like this one above). My IG handle is @kerissa_kreative!

By Kerissa Lee June 17, 2026
Hello, friends, I just wanted to share a blog update and thank you all so much for your prayers these last several weeks. ❤️ They help me to persevere! I previously posted that the interventional radiology team said my old port needs to be removed because of the site being too exposed from skin breakdown. Well, on May 19th, I had a virtual appointment with the IR nurse practitioner. To my great disappointment, she didn’t want me to get a new port and said I need a central line instead. I tried explaining to her that all my previous central lines always got infected and caused sepsis, but she still wouldn’t budge. 😞 I left that appointment and cried. I kept reciting Romans 8:28 (“And we know that for those who love God all things work together for good, for those who are called according to his purpose”). I knew that God was in control, but I was still so sad.. The next day was my port removal surgery and central line placement. Many of you already know this from FB/IG, but I wanted to re-share the following here on my blog as well! When I met the attending physician who was going to do the surgery, I told him my whole story and asked if he could please consider placing a new port instead of a central line. And do you want to hear something soo amazing?! He nonchalantly said, “I can place a port!” I was so shocked! 🥹 I immediately felt God’s mercy and kindness in sovereignly arranging this specific doctor to be the one to care for me. Both surgeries were back to back, and everything was much more difficult than he was expecting! In his chart notes, he stated that it took “more than twice the usual time, an unusually large amount of materials, and required a very high level of technical expertise and skill.” It was a great challenge removing my old port because of scar tissue and because it was so embedded to my chest wall. 😥 He had to yank, pull, and manipulate a ton—all of that caused a huge bruise to form over my chest. When he used fluoroscopy (moving x-ray), he also saw on x-ray that there’s a 7 mm cylindrical foreign body in my chest (pictured below). He assumes it’s a retained port fragment from an old port surgery that happened years ago. We’re just going to leave it there.. 😟 I was awake the whole time because none of the sedation meds worked! I’ve unfortunately had more than 20+ surgeries/procedures, so my body has become immune to certain sedation meds. The team recommends that I have much stronger anesthesia next time.. So thankful that the Lord helped me through this painful process! In other news, I finally get to have this temporary, bulky j-tube replaced with a low-profile one on the 23rd! My GI surgeon was hoping that the temporary tube would give the site a break and help heal all the inflammation (which was caused by buried bumper syndrome when the balloon got stuck in the abdominal wall 2 months ago). And I think that did the trick because the site is no longer leaking a ton! 🥲 Praying that switching back to the low-profile tube doesn’t cause an uptick in pain/leaking.. Last week, I had a bit of a scare when blood started coming out of the j-tube stoma (hole) for several days. We don’t exactly know what caused the bleeding, but thankfully, it stopped! If it does happen again, the GI nurse practitioner ordered an abdominal ultrasound.. If you made it this far, I’d so appreciate continued prayers for my sleep. Still experiencing bad insomnia as a side effect from an important medication that I need. It’s so hard when I can’t fall asleep until after 5:30-6:30 AM every single day. 😔 I don’t know what else to do except take each day as it comes and lean on the Lord for endurance. 💚 Aside from this, still so grateful to God that I’m doing really well mitochondrial-wise! For those who may not remember, my naturopathic doctor at the OHSU pain center started me on 2 very strong antioxidants last year: liposomal glutathione and n-acetyl cysteine. When I started taking both regularly for several months, the neck weakness resolved and the overall muscle fatigue improved a lot. By God’s grace, I’ve physically been very stable which is a huge answer to prayer!! 🥹 P.S. It’s taken me a while to share this, but a few months ago, I added 11 new card designs to my shop. Here are some of my faves. ☺️ I’ve sadly run into another unfortunate predicament with the e-commerce site I sell on, but I’ll try to share that story another time.. 😕 
By Kerissa Lee May 15, 2026
Hi, friends, Last week, I unfortunately caught norovirus from my parents who caught it most likely from a wedding. 😞 All the vomiting caused dehydration, and my heart rate was high (up to 150 bpm). Every 30 minutes, I kept getting a notification on my Apple Watch saying that my heart rate was too high. Thankful I didn’t have to get admitted and could infuse the rest of my IV bags here at home. My neck is showing signs of weakness like after the time I got sick in Hawaii. 🥺 Really praying the muscles are just trying to recover from the vomiting/dry-heaving.. On top of that, the skin at my port site has sadly been breaking down over time. My dr. ordered a PICC line for me to let the port site heal. But the IR (interventional radiology) team said I need to have my port surgically removed because the site is “too exposed.” Definitely wasn’t expecting that! 😥 The IR team wants me to get a central line instead of another port, but I tried explaining to them that I’ve had sepsis too many times from multiple central lines. Plus, my quality of life is so much better with a port because I can shower when the needle is de-accessed. That’s just one of the reasons.. If I had a central line, I’d have to cover it and put tape all over which is not fun. I have a virtual appointment with someone on the IR team this coming Tuesday. Could you please pray the radiologist will be understanding, compassionate, and willing for me to have another port placed? I know this is in God’s hands regardless of the outcome. 💚 Surgery to remove my port and place something new (whether it’s a port or central line) is this coming Wednesday.. We’ll know the time the day before.. I’ve been reading a memoir by a young mother named Amber Emily Smith who tragically lost her 3-year old son to drowning in their family’s pool. In her book, she shared the story of the poet Annie Johnson Flint who developed a severe arthritis that left her hands disfigured and also caused her unable to walk. It was in the midst of her suffering that she became a poet. I’m sure many of you have read this poem before, but it’s such an encouraging one, and I hope it fills your heart with hope. ❤️ “God hath not promised smooth roads and wise, Swift, easy travel, needing no guide; Never a mountain rocky and steep, Never a river turbid and deep. But God hath promised strength for the day, Rest for the labor, light for the way, Grace for the trials, help from above, Unfailing sympathy, undying love.”
By Kerissa Lee April 16, 2026
Hi, friends, I just wanted to write an update on what’s happened since my last post. Sadly, the 2 different tube changes haven’t helped, and there’s still so much leaking around the tube. 🙁 The abdominal pain was decreasing each day, but for some reason, it has ramped up again and has been steadily getting worse the last several days. The pain is sharp and throbbing—it also hurts to use my abdominal muscles. I saw my primary care dr. this past Friday, and he ordered an urgent CT scan. I had that done this past Monday, and the scan shows that the balloon on the tube is lodged in my abdominal wall (it’s called buried bumper syndrome). 😥 So painful, but I’m thankful for answers! I actually had this issue many years ago, and usually, changing the tube size helps. But we’ve already tried 2 different tube sizes in March which hasn’t helped. I don’t know if the tract got damaged or what.. My PCP messaged the surgery team twice now, but they’re not responding still. Ever since my general surgeon left OHSU 2ish years ago to practice in New Orleans, it hasn’t been a good transfer to a different team. 😢 In addition, the CT scan also revealed that I have ground glass opacities in my left lung, so I have to go through work-up for that as well to figure out the cause.. Aside from these latest issues, I’m praising God that my mitochondrial disease has been stable still!! So thankful for God’s grace and faithfulness. The day I got my CT results, I read this excerpt below from one of Joni Eareckson Tada’s daily devotionals, and it was like the Lord was speaking right to my heart. I hope it’s an encouragement to you. ❤️ “Present pain and afflictions tend to heighten future joy. When is peace the sweetest? Right after the conflict. When does a cold drink taste best? When you’ve become very thirsty. When do you appreciate rest the most? After hours of hard labor. When is joyful company most pleasant? After enduring long days of loneliness. The truth is, our recollection of past sufferings may one day enhance the bliss of heaven. Eternity with the Lord will be so much more heavenly to those of us whose faith has been tested, battered, and tried, time and again.” -Joni Eareckson Tada One more thing.. I’d really love prayers for my uncle (my dad’s older brother). He’s been very sick in the neuro ICU with serious issues. First pneumonia, then bacteria in his spine which later broke his back. He had a major spinal surgery but still can’t move his legs. 🥺 On top of that, his kidneys started failing, so he had to be placed on continuous dialysis. He also had to be put on a ventilator due to fluid in his lungs. Then, he still couldn’t breathe well, so he had to get a tracheostomy tube placed in his neck. 🥺 Despite all this, he and his family are so strong and trusting the Lord which is a huge testimony to all of us and to the ICU. Could you please pray for peace, strength, and healing over his body? I know he and his family would be so grateful for your prayers. 💙 P.S. I wish I could show you my foster nephew’s sweet face in this photo from Easter Sunday! He is now 9 months old—the most precious and adorable little boy!! Our lives are so much sweeter with him in it. 🥹