A rough start to the new year.

Kerissa • January 9, 2016

All last week, I wasn’t feeling my normal and just felt “off.”  I kept losing my balance and had nystagmus/dizziness.  This past Saturday, I was feeling so bad with horrible body aches, headache, and nausea, so I ended up going to the ER to make sure I didn’t have a central line infection.

The ER docs followed my mitochondrial specialist’s ER protocol letter, so I received through my central line a dose of IV carnitine and more than 3 liters of continuous D10 with sodium chloride and potassium.  I also had a ton of labs drawn.  It turns out I was nearing a metabolic alkalosis state (opposite of metabolic acidosis), and I was diagnosed with hypomagnesemia (lower-than-normal levels of magnesium which is an electrolyte).  This happened even though I still receive daily IV fluids with extra magnesium for 2 hours…!

I just had labs drawn with home health 3 days before Saturday which showed some abnormal things, but my magnesium level was fine.  So it dropped quickly.  Hypomagnesemia can be very serious and cause seizures and even cardiac arrest, so my GI dr. is glad I went to the ER to get checked out.

I got admitted to the ER observation unit for 2 nights and received 3 different IV pain medications because the pain was so bad.  I also had to be placed on a continuous cardiac monitor to watch my heart rhythm and high heart rate.  Though short, it was a rough hospital stay—all the IV fluids overwhelmed my neurogenic bladder (and when I’m in a mito crash, body system functions don’t work well)…I had to be cathed because I had over 1 liter in my bladder which I couldn’t empty.🙁  TMI, but mito is no fun.🙁

To correct the low magnesium, the doctors gave me 4 grams of IV magnesium.  That brought the levels back up, but they soon dropped again.  So I had another magnesium infusion early Monday morning before I got discharged.

My GI dr. thinks the prescription zinc I was taking 3x a day for Wilson’s disease caused my body to get depleted of magnesium.  But, if my MG levels start dropping again while off of zinc, then he said something else is going on..  I had weekly labs drawn yesterday.

This coming Tuesday, I have a monthly follow-up with my GI dr.  Wednesday, I finally see the hepatologist (liver specialist) after waiting 2 long months.  And Thursday, I have an appointment with my neuro-urologist.  It’s gonna be busy! :/

I wasn’t expecting a hospital stay right at the beginning of the new year, but the bright side is, I went without an ER visit for almost 11 months which is a record!😉  I’m thankful to the Lord for His protection this past weekend.  My condition could have been a lot worse if my very low MG wasn’t corrected!

By Kerissa Lee January 21, 2025
Hi, friends, First off, the piece of art above was hand lettered by me last year before all “this” happened. I’m sad to say that I only have 3 or 4 pieces left to share until I run out.. 😢 I went to see my neuromuscular neurologist in Seattle on January 8th. My neck weakness continues to progress which has been so scary. He said I need to get a neck MRI and some specific blood tests to check for polymyositis. If it is normal, though, his opinion is that this is mitochondrial disease progression. 😔 I haven’t seen my mitochondrial specialist in San Diego in more than 3 years (I started seeing him in 2014!), so I’m sadly no longer considered his patient. The neurologist sent a new referral to him, but I’m not sure if it will be accepted.. He’s almost 80 years old (one of the pioneers of “mitochondrial medicine”). And I don’t know if he’s cutting back on “new” patients.. Even if he did accept my case again, I’m currently not physically well enough to fly down from Oregon.. 😞 My quality of life continues to worsen ever since this unusual neck weakness started this past October. I know I’ve said this before, but I truly miss doing all of my favorite things (like hand lettering art) or even simple tasks (setting up my own IV infusions, vacuuming, washing hair, etc.). 🥺 Before October, I was even starting to drive to physical therapy or the grocery store. Yes, I’m 32 and still don’t have my driver’s license due to being preoccupied fighting mitochondrial disease for almost 15 years now. I never shared the exciting news that I was able to get my driver’s permit over 2 years ago, and it was so fun to drive myself to appointments close to home. Now, I can’t do any of the above which has been difficult to process. I shed tears every now and then just thinking about all that has changed. 😢 I’m having to go to bed around 6:30 PM to lie down and rest my neck. But I’m so uncomfortable from the pain, and I don’t fall asleep until after 3 AM every night. So my pain dr. referred me to palliative care. 😢I know it’s not hospice, but I’m still sad we’re at the point where I even need palliative care. Unfortunately, they’re most likely going to deny the referral (if they haven’t already) because we were told they only see cancer or heart transplant patients. I even checked if there’s palliative outside of OHSU, but they, too, see only oncology. It’s so hard that cancer gets a lot of funding, research, and support, and those with rare diseases are left “on their own.” It’s isolating and lonely. 🥺 I saw my PCP again, and he is just the best and full of compassion. ❤️ He placed the neck MRI as urgent and also ordered more labs to keep pursuing answers since all this is such an atypical picture if it was mito progression.. In case palliative turns my case down, my dr. told me that the internal medicine clinic has a complex and chronic pain management clinic (different from the pain center that I’ve been going to since 2011). He referred me to them to try and help me get more comfortable. I have a wonderful team of doctors and an amazing naturopath, but I’m even going to see a functional medicine doctor for the first time on the 23rd. Praying he could maybe have some additional insight on everything and will offer some fresh ideas for treatment as well.. I also have an appointment with the metabolic geneticist on the 28th.. I’ve read through the Bible more than once, but it’s amazing how the Lord points us to specific verses at just the right time. I don’t know about you, but sometimes I think, “I don’t remember reading this before!” Paul David Tripp’s newest devotional Everyday Gospel has been so very encouraging. He shared 2 verses from the book of Genesis where Jacob said that God “answers me in the day of my distress and has been with me wherever I have gone” (35:3). Several chapters later, Jacob also said that God “has been my shepherd all my life long to this day” (48:15). When I read that, I felt such peace. God spoke to my heart to remind me that He is with me and for me….in every circumstance no matter how hard. ❤️ Could you please pray that I can have the MRI completed this month and not have to wait many weeks? Pray that all of my doctors will have wisdom as my case is so complex. Lastly, could you pray that I will persevere and keep walking by faith? I feel so weary, not only physically but also mentally and spiritually. 😥 Thank you so much for praying for me all these years. ❤️
By Kerissa Lee December 13, 2024
"He alone is my rock and my salvation, my fortress; I shall not be greatly shaken." Psalm 62:2
By Kerissa Lee November 9, 2024
“Be still, and know that I am God.” -Psalm 46:10 
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