Stay Hydrated

I am typing here to you with some burnt fingers and a 3:00 AM knowledge that I should be sleeping. But When the doctor prescribed at big steroid boost, it is hard to stay asleep, unless that sleep gets read weird.

Therefore after attempting to follow one of the first commandments of palliative – get rest – I am attempting another: stay hydrated. Apparently i am not so good at it because I just dropped and cracked a glass tea travel mug. Burnt some fingers too. The even would have happened regardless of the time of day. I poured myself a second cup. The idea here is that I stay hydrated BUT don’t over water myself, as I has been done a lot tonight. Loads of ice chips and cold drinks. Mostly water, also some clever juice and fizz combos. Attempting to slow this down, i am trying to tea and type. So far the tea is working – i have not touched it – but the type is keeping me awake.

Yesterday, or rather Tuesday now, came two separate visits from a nurse and a chemo home doctor later. While I am gracious for both, they are way more harsh than Dr Canada ever was. Though maybe all this will change as we get to know one another. Anyhow, it was tooooo much and truly draining. Hopefully this set up bit goes steadily, and I don’t fully lose my mind.

There are good, smile moments too…floating in the pool, dancing again with Zsolt, and even eating eggs. Just here is a challenge. We will work through it all… even the broken tea travel glass mug current sitting in my sink.

Good morning.

P.S.

Good evening. Following this rough night where only a hot shower was the cure, we had a lovely day. Friends took us for ice cream, Z&I picked up medications, I bought a cane, we rolled in my rental chair around the grocery store, and went to get pizza. Tonight upcoming be what it may, today was actually fun. πŸ™‚

Catherine

 

try to keep living until you feel alive again

Which is what I will try to do.

It’s official, I’m being moved to pallative care. Zsolt and I visited with Dr Canada who, and he officially bowed out. There is nothing more that he can offer in the form of treatment. Now I move into a different circle of suppourt that involves home visits, wheel chairs, IV for hydration and more. It is very hard to accept. But I will do as the saying goes – try to keep living until I feel alive again.

In the meanwhile, I’ve just today discovered that I enjoy filtered apple juice.

This is all I can manage to type. It’s a sad day for us.

This and That

Chances are that if i spend much time editing or worrying over this post it will never get written. We went to see the doc last week. Turns out the hard mass is the result of the cancer, but is fluid, not a mass. At least now I imagine the stuff being drained, drained away.

The more challenging news is he doesn’t want to put me back on treatment until I am stronger. Right now I am desperately weak. So, it could mean I will try again, and it could mean there is no more trying. I feel conflict between these realities. I want to be strong, treatment could do that, but also treatment makes me weak. I really want to feel good and healed, but i am really tired of swallowing pills on which I choke

However, very good things happened this weekend. It was my wedding anniversary! 8 years married. 12 years together. I like those numbers. πŸ™‚

To celebrate, we stayed at a resort called The Opinicon. It was wonderful! The cabins are all so beautifully redone. It has a classic vibe mixed into modern taste and highly clean rooms. There is a fresh feeling in staying there – fresh air, fresh paint, fresh sheets, fresh mind. Our cabin, Juniper, faced the lake. And even though it was close to the golf cart maintenance road the cabin was perfect in all ways. Because it is close, the cabinΒ  is accessible via wheelchair. The grounds held an ice cream parlour, there was a beautiful main lodge, a kitchen garden and in time there will be a pool, hot tub, and very long dock.It is located somewhere between Kingston and Ottawa, next to Chavey’s Locke.

Unfortunately, I find myself knocked out and unable to write more.

nap NAP nap nap nap.

That is all.

PS. I’m test driving a wheelchair – weird