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I’ve been in the hospital for 14 days now. It has been a bag of mixed tricks up to this point.

I got some good news this morning. They are going to leave me on the antibiotics until Monday and do the surgery on Monday. So I will not have to go home and come back. That is great news to me. Going home sounds wonderful but coming back again for the surgery did not. At least now I am settled in.

The procedure itself should be pretty minor and fast. A camera is inserted into my penis and run up to my bladder. They will then use a laser to break up the stone and suction the pieces out. The journey then continues up into my left kidney. They will “pulverize” the 7 stones there and suction out the pieces. A stent will be put in for two weeks making sure everything is clear.

When I get home Palliative Home care will be working with me reduce pain an get my life back to normal! ๐Ÿ˜

After that, my life can hopefully get back to normal!

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My youngest daughter came down to visit me this weekend. I asked her to bring her guitar so we could sing. I love music. We sang a lot and she played and sang many songs for me. I could not have asked for better medicine!

My wife and two daughters hold my heart in their hands.

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I have been transferred to the VA Hospital in W. Roxbury, MA. One of the odd things is that I am right back in the Ward I started out in 20 years ago. Strange being here. Made the full circle I guess. Several things going on. UTI, Sepsis, prostate cancer, kidney stones and bladder stones. Looks like they are saying next phase is surgery to get rid of the stones. The are “probably ” harboring the Super Bug! ๐Ÿœ I’m still very tired but hanging in there. I just do what I’m told. Will update here when I can.

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This post will be pretty brief and to the point. With the cancer thing dragging me down, my immune system thought a UTI would be nice. But not just any UTI, one that turned into Sepsis. I got very sick the same day we got 24 inches of snow. Great. Wendy dragged me to the ER Wednesday morning. They checked things out and sent me home. I made it home and Wendy called 911. Fever of 104 was enough for her. And I’m still in the hospital but hopefully on the mend. Fever is down and the morphine is controlling the pain. So I came in at ๐Ÿ˜ก and currently at ๐Ÿ˜ . Wednesday night I made MY decision to be put on Hospice. By Thursday night Wendy decided that I had decided wrong. So…I’m still here. Yay me! For any further updates please annoy, I mean call Wendy.

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My diseased prostate

A cancer I do not need

Extinction for you

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Lupron Shot

I had my last Lupron Shot on Tuesday. Out of the many side effects I would say I have fatigue, swelling of legs and feet, overall weakness, and mood changes.

This Shot is good for three months. I still take me bicalutomide every day. Nine radiation treatments to go.

My numbers look good according to my blood work.

My moods are the scary part. We all have good or bad moods. But as adults we know when to control them. As for me right now I just need to avoid people and all will be good! I’m so tired that all of my filters are gone. So I apologize in advance for what may come out of my mouth.

I’m normally a pleasant person…really!

๐Ÿ˜‚๐Ÿ˜ฌ๐Ÿ˜ ๐Ÿคช๐Ÿคจ๐Ÿ˜‡๐Ÿ˜ก๐Ÿคฌ

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Here at Dana-Farber for my three month hormone injection.

Eleven radiation treatments to go.

Do I feel like blogging?

No. So this is all there is to say.

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