Still at the health club

March 30, 2008 at 9:26 pm | In Challenges, Cystic Fibrosis, Cystic Fibrosis Related Diabetes, Tune-up | 3 Comments
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I’m still in the hospital tonight. Just thought I would make a quick post before heading off to bed.

It is quite a surprise to be back on IVs so soon. Usually I only do them once a year, but this is my second time in three months. I am a little disappointed as I have stepped up my care at home, yet I end up worse off than I started. Apparently it is common, I guess it is because I started stirring stuff up in my lungs, pissed it off, and now it is retaliating.

The food sucks, I miss the time I was admitted on the Research wing with the personal chef and unlimited kitchen. Ahhh the good ol’ days. :) I asked for a low/no dairy diet since it plugs me up in all directions, but the hospital nutritionist told me to drink some warm water and I will feel better. What a laugh! I wanted to kick her. I have been trying my best to choose items that are dairy free, which is hard given the few choices I am given.

My nurses have all been super awesome always checking in to make sure I am comfortable and am doing ok.

The entire reason I chose to come into the hospital was to get four respiratory therapy treatments a day, done by professionals. Well, I have yet to experience that. So far I received one treatment the first day and slowly have worked up to three treatments today. Apparently the respiratory staff here is too busy to help me. And YES, I have raised holy hell about it. Wish me luck in getting four treatments tomorrow.

Over all, I think I turned a corner today. I got a lot of crud out of my lungs with my afternoon treatment using an IPV (I’ll post about that soon). I am feeling a bit clearer, although I am still quite short of breath when I walk around my room, even on 2 liters of oxygen. My oxygen stats are up a little, from 88% (room air) when I first came in to 96% tonight (but on oxygen). My weight is stable, but I was hoping I could gain a few pounds.

The doc is changing up my antibiotics in hopes to really kick these lung bugs in the butt. Right now I am on three, tobramyacin, aztreonam, and cephtaz. Doc is going to look at which drug caused my penicillin allergy and may switch one of those for merrem.

My blood glucose levels were really high when I first came in. Doc increased my 24-hour insulin dose and it seemed to work well since this morning I had a fasting level of 104, which is in a normal range. I am really happy about that.

Guess that is all for tonight… hope everyone is doing well!

CFRD Fact #12

March 28, 2008 at 7:01 am | In CFRD Facts, Cystic Fibrosis, Cystic Fibrosis Related Diabetes | Leave a Comment
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How might early diabetes cause CF clinical decline? It is currently unknown, but here are some theories:

  • Insulin Deficiency
    • Insulin is an anabolic hormone which promotes conservation of body protein, fat and carbohydrate stores.
  • Malnutrition and protein catabolism are clearly associated with death in CF.

Couldn’t resist…

March 26, 2008 at 8:19 pm | In Life in General, Music | Leave a Comment
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I found another awesome YouTube video, this one is of Johnny playing my favorite song of his… Enjoy!

It’s that time again…

March 26, 2008 at 7:20 pm | In Challenges, Cystic Fibrosis, Tune-up | 2 Comments
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Had a CF clinic visit today. I have been feeling a little cruddy and tired recently. My cough has become more of a nag and more productive, so I wasn’t surprised when the Doc suggested I do another round of IV antibiotics. Usually I only have to do this once a year, but I just did my last round in December. A bit frustrating, but this is life with CF.

For the past, oh say, 10 years I have done my once-a-year “tune-up” of IVs at home, doing my own treatments and having a nurse check on me every few days. This time I have decided to go in to the hospital for the first several days so I can take it easy, have food made for me and have someone beat me four times a day. I hope the rigorous treatment will knock the bugs in my lungs on their arse!

Wonder if the hospital has a wireless internet connection. If not, it is going to be a really boring weekend! Sad I am going to miss the Railbenders headline their first gig at the Bluebird in Denver…. can someone video record it for me?!! :D hehehe Oh well, good thing I saw Jim and Johnny play last weekend, so maybe I won’t go into withdrawal. ;)

Here’s a video of the boys playing a cover of Sundown with Roger Clyne. It’s a little noisy, but the crowd is having so much fun!! (yep! One of those screaming was me!!) I just looove Jim’s voice! Hugs to ya Johnny! Can’t wait to see you again!

Gotta run, I need to pack my bags for my “vacation”!

CFRD Fact #11

March 26, 2008 at 7:23 am | In CFRD Facts, Cystic Fibrosis, Cystic Fibrosis Related Diabetes, diabetes | Leave a Comment
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The American Diabetes Association (ADA) classifies CFRD under “other specific types of diabetes” involving diseases of the exocrine pancreas. CFRD shares some features of type 1 and type 2 diabetes but has important clinical distinctions that make its medical treatment and medical nutritional therapy (MNT) unique.

CFRD Fact #10

March 24, 2008 at 6:16 am | In CFRD Facts, Cystic Fibrosis, Cystic Fibrosis Related Diabetes | Leave a Comment
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Weight loss and decline in pulmonary function began 4-6 years before the onset of diabetes.

After two years of insulin therapy,weight returned to levels seen six years earlier and the decline in pulmonary function stabilized.

This suggests a cause and effect relationship between clinical decline and the pre-diabetic state.

Lanng, Diabetic mellitus in Cystic Fibrosis: effect of insulin therapy on lung function and infections.

Lanng, Influence of the development of diabetes mellitus on clinical status in patients with Cystic Fibrosis.

Helpful carbohydrate data

March 22, 2008 at 9:06 am | In Cystic Fibrosis Related Diabetes, Nutrition, diabetes | Leave a Comment
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As the day of chocolate easter bunnies and jelly beans is upon us I thought it would be a good time to share one of my favorite diabetes secrets!

Counting carbs is the most frustrating thing about diabetes. I can deal with the shots, I can figure out how much insulin I need (usually), but counting how many carbohydrates in the food I am about to consume is a challenge if there isn’t one of those handy nutrition labels stuck to the side.

Here is one of my secrets…

CalorieKingCalorieKing, is a great website to look up carb, calorie and fat contents of a whole variety of foods, even some restaurants! They also have a mobile website you can pull up on your cellphone, but I can’t seem to get it to work.

Calorie King BookIf I don’t have access to the internet I keep this little book handy, The Calorie, Fat and Carbohydrate Counter. It too has restaurants in it, which is oh so convenient! Since I am already carrying my meter, needles, insulin, enzymes, along with the normal girly stuff, my purse is now the size of small luggage, so one little book fits easily in there! (now if I could only get someone to carry it for me!) :D

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