Showing posts with label hospital. Show all posts
Showing posts with label hospital. Show all posts

Tuesday, 23 July 2024

We're still alive!

I've written of ADLs, activities of daily living. It is the difference between a senior successfully managing life at home, or not. I was proud of myself. We NEVER put out garbage out the night before garbage day. I had to. I couldn't face the stress of doing that Monday morning with my fatigue and coughing. Out it went in the secure can. You just can't put kitchen garbage out with bears, raccoons, and coyotes. I had to this once.

All was well. No mess. WHEW!

 

It is wonderful being outside, at least. 

The wild Oregano is full of insects. If I had more energy (I was up coughing twice last night) I'd figure out this first one. The second is obvious.


Look what Merlin told me was out back: a Black-billed Cuckoo! 

COVID UPDATE: Sunday night I actually slept through the night. JB not so much. It is interesting that it attacks my weakest part, my lungs. Joe's is his nose, and his faucet continues to leak. It seems to me that COVID is attacking us in our weak spots. I have always gotten bronchitis when I had a bad cold. Joe's nasal passages, hay fever and such, is his weak point.

Monday was the last day for my Paxlovid pills. Also the last day of Joe's Lyme Disease meds, Doxycycline. I'm drinking a ton of water. It really helps. He was supposed to be checked by the doctor this morning, but that ain't happening.

Poor JB is having two naps a day. Monday, after dinner, I could not stop the coughing. Hawking up cloudy phlegm over the back deck railing – so as not to freak out Joe. I'd clear it, then sit back down. Three times. At this point I figured I best be seen by someone. Is this bronchitis or what? 

I dialled 9-1-1. The dispatcher was kind and demonstrated caring.


The female paramedic, an experienced one, was wonderful and took a full history, as well as the meds I was on. In hindsight that spared them in the ER. They were slammed. She handed in my health card, and all I had to do at that point was wait.

In the ambulance my paramedic explained the Paxlovid doesn't cure COVID, it ameliorates symptoms.  The ambulance crew set me up in the hallway. Both in masks – as I am Typhoid Mary. Hospital staff had to clear a room for me. By 9 p.m. I had a room, away from the old with oxygen masks, a poor screaming preschooler, and other vulnerable people. What a job.

The irony is that this is the room I was in for 6 hours when I had chest pains after Joe's cancer surgery. I had driven myself in as I didn't think it was a heart attack. I read a book that time. It was high blood pressure from stress. 


Anyway, back to Monday night. The one nurse wanted to know what I wanted from them. To be able to breathe? At this point, the terrible coughing spells stopped. This whackadoodle old white woman just wanted someone to listen to her lungs to rule all this out. I know they were busy. I know COVID is old hat now, but I felt diminished. 

I'd brought a book, and when I passed another couple of people on beds in the hallway, they were reading. 

Eventually I could feel an anxiety attack coming on. I'd phoned Joe twice, first letting him know I had a chest Xray. The woman that took me to that was cheerful, sweet, and kind. No one else was checking in on me. 

I'd phoned Joe at 9:15, 10:00 and 11. First to tell him I was in a room and the ambulance team had left, total professionals. Next I phoned to say I'd had the X-ray. He said he was still awake. He might still be up when I was done, but I could take a taxi. Panic. I don't know if we have taxis in Perth at 11 p.m! 

By then the anxiety kicked in. By 11:00, I opened my cell door, and most of the other patients were gone. I couldn't take it any more. I asked him to pick me up outside the ER entrance. ANXIETY was rearing its head. Worried about Joe looking after his COVID bout, and letting him get rest. This morning, we had coffee, and he went back to bed for a nap.

I called to another nurse to tell her I had to leave. I'm sure the doctors were finishing up paperwork and all, but I was falling asleep. Joe, pretty ill, needed to get to bed. A neighbour offered any help, but you can't call people to take a COVID patient home.

We arrived home at 23:24 hours. Joe went right to bed. I lay down to read more of my book (an excellent  Canadian thriller, by the way), but thought I should try sleep. In 10 minutes I was coughing. I got up, coughed up what I could, had some water, and went back to bed. I was up twice in the night coughing, but got back to sleep. 


 

I've an appointment with my GP this morning at 11. He'll interpret the X-ray for me. I am deeply suspicious that nothing else can be done for me. I loathe going into the office with COVID. I just don't know what else to do.

I am processing all this. I am very emotional, crying at the drop of a hat, and feeling guilty for taking up healthcare system time. In hindsight, I deserve it, as much as anyone. I am putting it all into perspective. 

In foresight, the news cycle has changed. With Kamala Harris' nomination, the continent, if not the world seems lighter and brighter. We had rain, and now the sun is out.

Sunday, 18 February 2018

Process of Cancer Treatment PART LVI: Injection #3

Thankfully, someone reminded somebody that he needed to pick up his needle of Lupron from the pharmacy on Wednesday, while she was about to cook ❤️dinner. Whoopsie. Fortunately, they had one for us. We buy it at our local pharmacy, then take it into the appointment in the hospital. They cost $1100 or so each, but since he is a senior, he gets a senior's discount and pays $4.11. (Treatment is free with OHIP.) We have drug subsidies in Ontario for: seniors, people on disability (ODSP),  youngsters, those living in long-term care, or those enrolled in the Trillium Drug Program.

Thursday, Feb. 15, 2018

Back to the city for another injection, every three months. It appears that the injections are doing their work, keeping the PSA down. It's been 0.08 for 3 months, surgery was in 2014 so it should be zero.

10:00 we departed

It's a heckuva drive (~90 km one way) and 90 minutes long, without heavy traffic.
The weather didn't look good. We had to travel from the dark green (rain) to the pink (ice rain).
 

It was wet and foggy. Pretty miserable. A long drive through swamps, North Gower, Manotick, fog, and speed sensors. Nearer to home, it was 3˚, as we approached the city, it went down to 2, 1, then 0˚.


This speed monitor is a hoot! If you are in the green, it shows a happy face! It's on River Rd., near Manotick.


I wore my snappy boots, with the ice picks on the bottom. Our sidewalk, and the parking lot was still icy.

11:52 Our Meal was Ordered

The trick with going into the city, is planning meals around our trips. We schedule them early afternoon, driving in early for lunch, and straight home afterwards, avoiding any rush hour traffic.
This is our Go To place. The guys with whom JB volunteers said they thought the city a great opportunity to visit different restaurants, but we go back to this one, as we know their menu, we know the speed of their service, and we can depend on them.


It being the day after Valentine's Day, the flowers were amazing!

Someone had a birthday. This was on the floor!

Ottawa Hospital Parking Lot 12:53 p.m.

It was packed! People were driving around in circles looking for parking. Finding parking can be tricky. There was an attendant (which was unusual), and he told me where to park. Right on the end, on top of no-parking lines!

Our appointment was for 1:10, and we were ushered into the room at 1:00 p.m.. Our Dr. popped in, we chatted, and talked about next steps.

The research is very interesting. JB falls into the middle of the two study groups. One research project compared those who received intermittent injections, have a course of therapy, then stopping, or having it continuously. There was no difference mortality rates between the two groups.

 His symptoms are minimal, so we'll keep on with this treatment. The whole course of treatment should buy us 10 years. ENJOY EACH DAY!

Eventually, the cancer cells (in his lymph nodes, determined from imaging) will be able to resist the anti-androgens, and we'll deal with that. The next step is a bone density test, to determine a baseline. (Often, prostate cancer spreads to the bones.)
We won't repeat any other imaging until the PSA begins to rise again. (He's had: Bone Scans–4, MRIs–2, CT Scans–6, Ultrasounds–3.)
We are also participating in a research study on the efficacy of this treatment, including lifestyle and activities. A researcher came in with the questionnaire. He's working hard on his nutrition, and exercise.

The nurse poked him in the left hip. (They alternate sides.)


As we waited for paperwork, and another appointment, I took some photos of the grounds. We've seen this scene in all seasons, lo these several years (beginning in 2013). I even grabbed a photo of the building being built.

Despite the crowded parking lot...


There was a line-up to get into the hospital parking lot when we were leaving at 2 p.m. It appeared to be getting worse.

We stopped for more washer fluid.


We also stopped in Manotick, to see the birds on the river. I'd spotted them on the way in.


There are lots of snow machine trails, including stop signs at people's driveways. (I wonder if there have been collisions?!) I saw one guy out on his machine, even in this less than ideal weather!


Through Marlborough Forest.


You know you are familiar with the roads when you recognize a new stop sign! This one at Dwyer Hill Rd.


At home, it was up to 10˚ C. Hooper decided to talk a walk on the deck. They were happy we were home by 4 p.m. He was watching deer and turkeys.