01-19-2021. I survived Covid-19 pneumonia. I was in St John's hospital for 22 total days. I was exposed I believe, on 12/4/2020. My friend, Jackie Pearson, called me to say that the baby momma at the baby shower she hosted tested positive for Covid. I was experiencing fatigue. I would sit down and fall asleep. I fought this until 12/14 and called for an ambulance. I just was so fatigued I couldn't function. When they checked my blood oxygen level I believe I was at about 69%. The EMSA man said he could understand why I was fatigued. I was oxygen starved. I got into the ER/ICU and they began to treat me using a CPAP type of oxygen mask. Dr talked to me about being intubated if needed. I said if they need to do it to save my life then save my life. They never needed to put me on a ventilator. The different cannulas they had to use on me worked to get oxygen into me. I got a IV injections of dexomethosone steroid. After reading about side effects, one is trouble sleeping. That would be me. The 22 days I was there I only was able to do cat naps. Sleep an hour at a time. Between the BP checks every 4 hours, finger sticks for blood sugar checks followed shortly by 1 or 2 injections of insulin (long term and short term insulin). Or a blood draw or a daily steroid injection. The food was pretty good and the menu was not too bad, though I was there long enough to eat the same meals multiple times. The nurses were good. My favorite was Melinda. I don't know her name but she was my nurse on 8th floor. She was so compassionate and would give me a few moments of company to break up the very long days of isolation.
I was able to go home on 12/25/2020 but that was short lived. I came back three days later because I couldn't keep my blood oxygen in the 90's. Got the same dr when I returned to the ER from an ambulance. He confirmed it was a mistake to send me home. I needed to have the IV steroids for several more days. And I got to see a pulmonologist doctor. I see her (Dr Dolin) at 6 weeks out for followup. Dr Coggins actually read my hospital information and texted and called us with information on my care and test results. That was such a blessing.
I had great doctors who took time to answer my questions about my illness and treatment. The last three days of my stay I was without a cannula or oxygen therapy and was able to keep my oxygen level in low 90's range which is what I needed to be able to do to go home. When discharged on January 6, 2021 I had a oxygen machine at home and was directed by my dr to use it. Reducing my level of oxygen daily to wean off of it. Today I am at level 1.5 and oxygen level is 95%. I have reduced my Predinose pills down to 1/2 for the next couple of days. Then none. I have been doing some exercises and Jeff helped me stretch yesterday. My muscles wasted away while I laid in bed for those 22 days. I went from looking 66 and in good shape to looking 86 and wasted. No muscle tone at all. Pam has been doing daily circulation therapy using a body brush to stimulate the skin. I can now feel all parts of my feet and legs, shoulders, back and arms. Such a good feeling to "feel" again. I can feel my feet when I take a step. Thats so reassuring that I will fully recover. I have been testing my oxygen level when just on room air, not the oxygen machine. I drop a bit to the upper 87-89. Maybe when the steroids are out of my system maybe it will be better. I go to the staircase and go up and down one step using railing for stability. My legs are so weak. But Alana, my PT, said I will get it all back. I leaned hard on Jesus while I was in the hospital. I needed him to give my family peace and comfort. He was there for me. I give all praise to God for His great mercy and healing.