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Monthly Archives: December 2019

Thought for Today

12 Thursday Dec 2019

Posted by Tim Hughes Living with CML in diet

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Bell Ringer, Christmas, diet, Salvation Army

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Cat’s do the strangest things sometimes.

Happy Holiday’s everyone!!  Or, as I like to say, Merry Christmas!!

The past few days have been pretty busy and according to my calendar, it’s only going to get worse.  When I worked, I always disliked the holidays because I never had enough time to do what I wanted to do. With my job being what it was, I always had to be there.  If there was a threat of snow, I had to make sure I brought clothes with me to stay however long I was needed.  I always felt that I couldn’t spend enough time with my family.  Now that I’m retired, it seems that it still holds true.  For now anyway.  Both my girls have come home for Christmas but one is leaving tomorrow to go to Texas with her boyfriend to spend some time with them over the holidays.  When she returns home she’ll spend a couple of days here then back off to college.

This year it’s going to be different for my wife’s side of the family.  She lost her mother a few months back and her good for nothing brother and his family are trying to steal the family’s inheritance.  We’ve had one court date but that got put on hold until further notice.  I never really liked that family anyway.

A quick note about my diet.  I’m back on it.  I’ve been on it for a couple of days now.  So far, so good.  If I can just get my wife on board.  I keep telling her not to fix me stuff that I can’t eat but she continues to do it.  She fixed french-fries tonight and I just left them there.  Of course, she got offended that I wouldn’t eat the food that she had prepared.  It’s a constant battle.

I went to Wal-Mart today and I saw what most everyone sees this time of the year.  A Salvation Army Bell Ringer.  This one was different. He played the trumpet and played Christmas music. What a wonderful experience.  He was drawing in the dough.  I could listen to him all day long.  I wished that all Bell Ringers had some sort of talent.  I’m sure their donations would double.

 

Do Over Again

03 Tuesday Dec 2019

Posted by Tim Hughes Living with CML in Weight Loss

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Tags

Dieting, Weightloss, Will Power

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I was doing so well and then just like a car hitting a stone wall, it stopped.  It’s really laughable.  This has happened so many times in my life that it really didn’t come as a surprise.  I’m upset and then again I’m not because I knew this was going to happen.  In the past several months I have forked out about $100 on diet plans and a gym membership.  I was following both when I got sick and had to be put in the hospital.  Of course, when I got out I was so weak that I didn’t feel like doing anything, including eating right.  I saw myself sliding down but I just didn’t feel like doing anything about it.  I thought about Thanksgiving coming up and that didn’t help any with all that food around so I decided to wait until the first of December.  Starting on the first of the month always seems easier for me for some reason.  Well here it is the 3rd of December and I’m already sliding a bit. It’s been too cold to get out and do any walking or hiking.  I’ve got a membership at a local church gym but I have always had an excuse as to why not to go.  It’s will power, or should I say, the lack of it, is the main reason I’m not doing well.

Since I know what the problem is you would think I would know how to fix it.  Well, I don’t.  I eat the wrong things, I snack too much, I don’t exercise enough.  I come up with a plan to exercise and I always find an excuse why not to exercise.  I’m doomed.  I’m by myself during the day and I have no one to push me out of this recliner.  I have no one to hold me accountable but me and I’m not doing a very good job.  This cold weather is killing me because it’s too cold for me to get out and do any type of walking.  I don’t want to even get out to get to my truck to drive to the church where I’m sure the gym is heated.

I’ve lost 50 pounds before and I know I can do it again but I was working then.  I had to get up and get out of the house by a certain time.  I walked at least 15,000 steps a day then, now, I’m good to get around 4,000 steps.  I had my meals at the same time every day because everything was structured.  Now, not so much.  I have my wife get me up at 6:30 every morning so that I can take some of my daily meds.  I have to wait an hour before I can finish my meds and eat breakfast.  Then it’s a six-hour wait until lunch. I do this because of my cancer med can’t be taken within six hours of one of my morning meds.

Tomorrow is a new day.  Let’s hope I do better than the past two.

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