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Isn't Katie Ledecky amazing!

I know what you mean about the drama. Sometimes I think that I will ignore something serious with my DS because everything gets so blown up.

LIz, what will DS do in Portland, ME? No more restaurant work, correct?

Last night I cobbled a weekly dose together from my left overs. If my math was correct, I got a little extra dose this week. I didn't go as berserk as I could have. I still had an extra 20 units of 10mg/ml concentration left (basically 2 mg) that I chose not to use.

So, here's an example of "Fat Brain" or eating disorder thinking/behavior. I am not hungry this morning and am still working on my Venti dark roast from the Starbuck's next door. Yet......the hotel serves an included breakfast. I could smell it in the hall when I took Molly out. My nose told me eggs and breakfast meats were available. Of course, I went to check it out. I put some scrambled eggs and two sausage patties on a plate and made a waffle. Rationale? I can heat the eggs and sausage for lunch in the microwave for lunch. The waffle? Absolutely no clue. It was there and fun. Did I eat it? 1/4 of it with sugar free syrup. IF there was no sugar free syrup I would not have eaten any of it. So, my "free" breakfast sits on the table. I still fascinate myself with my well honed and ingrained dysfunctional eating behaviors.

Weather here is cooler than I've experienced in the midwest - upper 60s and cloudy. Rain is likely this afternoon. Molly has not peed since yesterday morning. UGH.... She's usually so good. She started this morning, but changed her mind. No clue what's up.

I am loving getting to see how the landscape changes as I travel. Grand Rapids, MN is pretty far north in MN. It's closer to the Canadian border than to Minneapolis. The woods and wildflowers are gorgeous. I've taken some pics I can share on TT.

Tomorrow it's on to North Dakota!

Weight 123.2. And just like that it is August already. Shot day this morning. I dropped down to 5 mg last week and I really felt much, much hungrier yesterday. I was reading some FB support group comments where people were saying that most people don't feel the effects until 7.5 mg or higher. I wonder if some of the reason is because of people's size, though it isn't dosed based on that. I have also been reading articles and comments on maintenance doses. The theme has been to try lower doses and/or try less frequent injections. No real parameters have been developed.

I somewhat chuckled at the discussion about crappy patients. My son is really skilled at being sick. When he was a toddler he caught everything under the sun and had ear infections constantly. So much that we took him to an immunologist at age 3 who said some kids are just like that and once his immune system strengthened he would stop getting so sick. Of course he was right. But man, when DS has even a mild cold you would think he had the plague!

Speaking of DS, we were just talking about the fact that a week from now we will be packing his stuff and he will spend his last night here as a household member. He is getting his second launch (he was in California, then a different part of Massachusetts after college). He has been living here for 5-6 years, first to help with his Dad, then COVID hit and he lost his job and retrained. So it is time for him to be on his own again. But bittersweet that I won't see him very often after he moves to Portland, ME. Sort of like an empty nest feeling again, though I look forward to not having his clutter around all the time.

Last night DS cooked a pork loin and my SIL and niece came to dinner. We had a really nice visit with the niece (different one than the ones we visited with the night before). She went through breast cancer last year and is now trying to enjoy the summer and the freedom of not being in active treatment.

Today Justice is getting his little chihuahua teeth cleaned. Poor little guy but we need to keep them in good shape to keep him healthy. DH and I are going to the beach after my PT.

I hope you all have a thriving Thursday!

I haven't been able to watch much of the Olympics yet this year. I do enjoy them. Will have to watch some reruns I guess.

He needs something! Claudia said she is forcing him to talk to his doctor tomorrow morning. So hopefully she can get through his thick skull to seek help. He's sliding backwards having felt pretty good over the weekend, but felt awful today. He's exhausted and super sore in his ribs. And still coughing up a lot of sputum though he says it's white, not yellow or green (TMI, sorry). My concern is pneumonia especially as he gets more tired and can't get it all out.