Happy Passover

I was unable to host Passover this year. I was terribly depressed about not celebrating. But painful shingles on three fingers of my left hand meant I was unable to make the numerous courses required for this meaningful tradition.

The universe has stepped in and allowed me to still connect with my heritage. I reread the Passover story. Each day I made one of my holiday dishes. Yesterday, I purchased some wonderful macaroons and today I came across this lovely blog with terrific upbeat Passover tributes.

Thank you universe for lifting my sadness.

“One of the most life-changing realizations you can have is “I don’t have to believe my thoughts… they are just thoughts!”

Tara Brach, “A True Taste of Peace”

More/Less List

I’m feeling more like myself lately, which means I’ve been reading more blogs. For some reason, I cannot reply to blogs on my IPhone. It says I must get Jetpack in order to reply. I don’t know about the good or bad of effect of doing that. So for now, I am tied to my computer. It too, has been giving me difficulty replying to blogs. I refuse to take this as a sign that I am not meant to interact with this wonderful community. So, I shall do my best to venture forward.

One of things the universe has sent to me is the idea of a more/less list. I read about this list in four different places. Of course, that meant I needed to look up the idea. I heard a voice in my head that said this would be good for me. From what I found, Julia Rothman has been drawing a more/less list for years.

Then I read Cheryl Loreglia ‘s  post about No Buy February, which I had never heard of. I wondered if the universe was talking to me again. I read Pete’s comment and it struck a chord with me. I do NOT drink alcohol at any time, so dry January will never be a part of my life. I did some research on No buy February. Just as Pete mentioned that he only buys what they need, I feel that February could definitely be a good month for that. I found this quote in my search, It seems like just the right thought process for me to follow.  “It’s not about punishing yourself ― it’s about making intentional choices with your money.”  

I found an article on More/Less lists from 2020. you can check it out if you’s like to see what some office workers wrote. It talks about making lists instead of resolutions. The current thoughts in my brain are telling me to create a monthly More/Less List. That way, as things change, I can go with the flow and generate modifications.

More List 
Rejoicing about being NED
Blogging
Reading time
Exercise
Making new recipes
Scrapbooking
Listening to music
Connections to others
Experiences

Less List
Feeling hopeless
Involved with drama I have no control over
Wishing without action
Spending on unnecessary items
Toxic energy
Limiting beliefs

“To live is the rarest thing in the world. Most people just exist.” — Oscar Wilde

 

 

 

It’s Too Late To Still Be Awake

It’s 4AM and I am sadly,still awake. My spouse returned to teaching high school after winter break. Unfortunately, he ended up with an awful flu bug. I did my best to take care of him, but stay away.

It took me all week to fully recover from my lung biopsy. His car was in the shop, so he was able to just use my car without having to get a rental. On Saturday, his car was ready and we drove the hour to retrieve it. Unfortunately, Saturday night the flu bug hit me with a vengeance. Because of my immunocompromised body, my lungs are always a worry.

I checked all my cold/flu medications and every one of them were expired. I masked up and went to the store to get treatment supplies, as well as OJ , and some other necessities. I knew I was in a fog because when I got home I realized I bought a bag of cat food, not dog food. Silly me. I wasn’t up to returning the bag, so it will need to be returned later.

I slept almost the entire day Sunday and much of Monday. Sadly, that meant I couldn’t sleep at night. The coughing has been terrible. I try not to take too much medicine because almost all of them are dangerous for my body. The oral chemo pills are already effecting my liver and kidneys. It is a slippery slope between reducing symptoms and not harming my body,

I’ve been binge watching Netflix to pass the time. When I have my coughing fits, they are accompanied by nausea and vomiting. I’ve been pretty miserable for 3+days now.

I had to cancel my allergy testing I was scheduled for on Wednesday. They told me the tests would be inaccurate because of the virus. I rescheduled for two weeks from now. I am hoping I am better by a week from tomorrow. They obviously won’t let me come to a cancer hospital if I am sick.

Other than my wonderful Annie cuddles, I’ve not found much joy. Luckily, after feeding Annie in the morning, I can sleep as much as I want. I finally succumbed to taking some cough medicine. With any luck, I will get an hour or two of rest before needing to feed Annie.

Good thoughts and healthy vibes are most welcome right now.

The Great News and The Terrible News

First and foremost, the great news. My doctor called about an hour ago with terrific news. She informed me that the biopsy showed no cancer cells. Her voice was clearly indicating joy for me, but an underlying sadness could be heard. I questioned why I am feeling more exhausted today, than yesterday. She let me know that it is not a concern. The pneumothorax that occurred, added extra time to my recovery. I am doing pretty well, unless I cough or sneeze. Then sharp pains occur in my chest.

She asked about my status with the fires going on. I informed her that we were warned last night that we might lose power because of the high winds. The electric company now turns off electricity in areas where the winds get too strong and might ignite a fire. Her family is safe because she lives by the beach in an unaffected area. She has graciously taken in friends who were evacuated from their homes. The entire KECK medical facility in Pasadena has been shut down because of the fires. It’s quite scary out there.

She reminded me to stay indoors because the ash will cause my COPD to worsen. I was told that if I must go out, I need to wear a mask. I explained that I have an air purifier to help me during these times.  She liked that. I will follow her directions to the letter because the last thing I want is another exacerbated COPD event like I had a few months ago. I was unable to take a deep breath and I was existing with halted breathing for weeks.

For my emotional wellness, I don’t watch the news. When important things come up, I Google the facts to learn what I need to know. Obviously, I saw the ash and smoke in the air. I had no idea how bad it was, until a loved one informed me of her being evacuated. Reading about the deaths and destruction broke my heart. These fires grew fast and furiously because of the lack of rain for months and months, the high winds (up to 100 MPH), and the inability of the water trucks to quickly reload. I read that President Biden has informed California that the federal government will cover the costs of fighting the fires. Unfortunately, the homeowners will most likely be out of luck getting help. The orange one, tRump, is blaming our governor. Personally, I never knew the governor was capable of creating 100 mph winds or causing another drought situation in our desert.


You can read more about the  LA Fires here.

POST NOTE: As I was finishing my blog, an emergency alert came on my phone. It states that the LA County Fire Department has issued an evacuation warning. My spouse will be home from school momentarily. We will decide our next step. Please keep us and all of our fellow citizens in your thoughts.

 

 

 

My Out-Patient Hospital Visit

It’s 10:30 PM, my time. I just woke up from a nap. My phone alarm went off, telling me to take my chemo meds. I should have turned off the alarm, because I didn’t take my morning dose until 3:30 this afternoon. My oncologist told me to take the meds after recovery from my biopsy.

That was a “fun” experience today. We had to get up at 4:15 AM to drive to Los Angeles. My check in time was 5:30 AM. I was surprised with the abundance of cars on the road at that hour of the morning. We were among a throng of people checking in for “same day surgery,” The first check-in process was without any hiccups. I had asked yesterday if my spouse might be with me until time for the procedure. Gratefully, it was confirmed that he could be with me. The nurse on the phone last night emphasized that he could not be with me during the procedure. (Like I actually though he could be.)

In the pre-op ward, the nurse took all my vitals, checked my ID, made me answer tons of questions, and had me change into a hospital gown. They don’t use my port most of the time so I had to have an IV line put in my arm. Sadly, the nurse wasn’t the greatest at inserting the needle. It hurt way more than necessary. Trust me, I get loads and loads of needles put in me.  My spouse looked a little faint as she poked and prodded my arm.

By this time, I was on sensory overload with all the noises around me. I could hear the questions and answers through all the curtains between us, I could hear all the interpreters on cell phones asking the patients their check-in questions. I swear, sometimes I wish my superman hearing, wasn’t as efficient as it is. After all the patients on the ward, all 18 of us, had been checked in, the nurse came by to tell me that it was going to get very chaotic at 7:15.

Boy oh boy, was she right. A flood of people started arriving on the ward. Standing by most beds there were surgeons, doctors at all levels of training, nurses, and whomever the people were who pushed the gurneys from place to place. It was fairly easy to tell who was whom. The doctor underlings, walked with heads straight forward like ducklings following their mama. There were typically three or more of them for each surgeon. The nurses, in their orange scrubs, walked past everyone around as though they were in charge. Doctors were explaining to the newbies, exactly what they were going to be doing. It was sensory overload to the max.

At 7:15 the ward filled up with people and the floor space became more constricted.  I had to laugh out loud. I told my spouse I was thoroughly expecting the entire crowd to break out in a flash mob performance. Needless to say, he joined me in laughter. Within minutes, we counted gurney after gurney leave to their next destination. A nurse came to my bed and told me I would be on my way soon because I was scheduled as the first CT scan patient. After an hour went by and no one came to get me, my spouse went to the desk and asked when I would be leaving for my appointment. The nurse called radiology and no one answered. She told us she would go there herself to see what the delay was. Upon her return, she informed us that there had an emergency patient and that I would be leaving soon for my biopsy.

Finally a 3rd year doctor-student arrived to have me sign consent papers and explain the procedure. I told her that I was expecting a flash mob to break out when the floor was overrun with medical people. Without skipping a beat, she said that of course, they had been practicing for weeks. We both had a good laugh at her reply. Another long hour went by. My spouse and I were dozing off and on from fatigue. Finally, a resident and an orderly arrived to take me away. My spouse and I hugged and the resident doctor told him that if he left, he was going to lose his parking spot. My husband informed him that he was in fact, heading to the Starbucks in the building and wasn’t leaving.

As soon as we went to the CT room, I was asked for 15th time who I was and what my date of birth was. First they apologized for the delay and thanked me for being patient. (like I had any choice) They stated the time out loud (9:30) and named all the doctors present. Once my wrist band was scanned, they explained the procedure once again. This time it was a little different version that what I had previously been told. I was indeed, going to be in and out of the CT machine as they located the exact spot for the biopsy. The main difference was that I was going to be on my side with the IV arm almost above my head for easy access. They told me I would be under medium sedation. I was happy to hear this because I had no desire to be awake during the procedure. When I had my colonoscopy years ago, I was told it would be light sedation and I was totally knocked  out.

Well, this time I was awake and heard much of their conversations. I was warned about the burning pain from the numbing needles. I assured them that I had had these needles often for my tailbone pain. I could handle the numerous needles. Once the area on my back was numb, the only thing I felt was the medicine being pushed through the IV. Every time they added something, I felt it. Gratefully, I had no pain whatsoever. Being sideways on a hard gurney is not very comfortable. If I moved a tiny bit at all, they told me to hold perfectly still. I listened to their conversations. Either some things were in code, or I was unable to quite understand everything that was going on. Once they informed me that they were finished, they said they were taking me to post-op.

As soon as we got into the elevator, I started feeling chest pain. By the time we traveled the three floors to post-op, the pain had increased from a 3 to a 5. I was in a lot of pain. The post-op nurse called the doctor and said she needed to get there STAT. He kept telling me I was going to be OK and that they would take good care of me. After checking my wrist band and my telling him my name and date of birth, yet again, my pain was at a 7. My breathing was labored, and I was starting to get worried. The nurse kept calling out to the nurse’s desk that it was an “emergen…t” situation. He repeatedly said this and never spoke the actual word emergency.

The doctor arrived and ordered an immediate EKG. She ordered a pain med to be inserted immediately into my IV. Thank G-d, the EKG showed that I did not have a heart attack. Typically, for this procedure you have a chest X-ray about an hour after the biopsy and then again 3 hours later. The doctor wanted the chest X-ray as soon as they finished the EKG. They did find a pneumothorax, which the doctor had cautioned me that in about 40% of patients this occurred. Air had escaped outside the lungs. My pain reduced from a 7 to a 5. I was grateful for some relief. I repeatedly asked if I could have a sip of water. The nurse kept declining my offer. I asked if the reason was because I might need to go back into the surgery room. He nodded but did not speak his answer. After a few more minutes he questioned me about my pain level and other symptoms. I let him know I still had difficulty taking in a deep breath and my pain level was still a 5. He responded by calling the doctor on her private phone number, which she had given him. She ordered another pain med. When he returned with the medicine, he stated me that he ordered a pill for two reasons. First, that he didn’t need to access the IV and second because… I cut him off mid-sentence. I said it was because he was being kind and the pill meant I could have a sip of water. He smiled and asked if I was a retired nurse. I told him no, but I could tell empathy from a mile away. I was grateful for his kindness. I asked for more water, but he declined stating I had to wait for the second chest X-ray. He was smart and left the cup of water on the far side of the computer table where I could not reach it. The pain med did its job and my pain level decreased to a 3. Breathing became easier. I was told I could finally change my position in the bed. After the chest X-ray, the doctor wanted me to only lay on my left side where the biopsy was done.

For the next three hours, I drifted in and out of sleep. I was exhausted from my early morning wake up, my procedure, my “emergent situation,” and my nerves. My nurse kept checking on me and adding stats to my file on the computer. I was continuously awakened by the blood pressure cuff going off or because I started snoring. When it was nearly time for the second chest X-ray, my nurse asked about my pain level. I informed him that I was no longer in pain. He told me he had spoken to the doctor and she felt my heart was not involved at all. She felt that I was under such little sedation, that by the time I got to the elevator, I felt all the pain from the procedure. That’s what put my body into such immediate high levels of pain.

I was grateful when they moved my gurney to the pre-op ward where I was able to get dressed and wait for my spouse. The new nurse went through all the discharge directions. I had to laugh when he said if I turn blue or gray, I should call 911 immediately. I was finally offered a beverage. I asked for ginger ale because I needed to take my chemo meds as soon as I got to the car. My oncologist told me to take my meds once I was released. We had no idea it would be so late.

Part of the discharge directions were to eat something light as soon as I felt OK doing so. My typical, post procedure meal is pancakes. I am a snob about yummy pancakes. We tried two different pancake/breakfast restaurants. Both were closed by the time we arrived. My spouse remembered that I like Norms’ pancakes. By this time, it was 3:30 PM and I hadn’t eaten since 6:30 the night before. I was starved. The pancakes tasted like a little bit of heaven. I added two eggs to my meal to get some protein in my system.

We didn’t get home until 5:00. We were right on time to give Annie her dinner. She is not used to being left home all day by herself. She was overjoyed that we were home. After feeding Annie and giving her lots of cuddles, we both took a nap. My spouse slept for about 45 minutes and I slept for over two hours. My alarm to take my meds, woke me up. I’m grateful that I did wake up because otherwise I would have slept until the middle of the night and I wouldn’t have been able to go back to sleep.

I need to wait until right before going to bed for the evening before taking my chemo meds. Then tomorrow I will get back on schedule. I’m not sure how long it will take to get the results of the biopsy. The fact that my PET scan in November did not light up, makes me hopeful. I am grateful that the procedure is done. I am grateful for the great care I was shown at the hospital. I am grateful for the members of my tribe who love me.