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Hospital time again...


beaterjeep
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So, can anyone guess where I am? Yep, I had to come into the hospital for complications due to my C.F.. I had a sinus infection that led it's way into my lungs, now I'm sitting in here for a week or so, then back home on I.V.s for anouther few weeks afterwards. My laptop hasn't been working too well for a while now, but I had brought it with anyways, only to find out that I forgot my wireless card at home. :wall: I'm currently using the computer in my room, as they got the place on almost lockdown due to the H1N1 virus risks. Thankfully it lets me on here at least, but I can't access much else, which really sucks. Anyways, just thought I'd drop by and give everyone an update.

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God speed for a speedy recovery.

My girlfriends cousin has C.F. and I have an idea what's going on.

 

Gah, hospital food is terrible. Was there for a week a few year back when I was diagnosed as a Diabetic. I wanted nothing more than a Taco Bell burrito!

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Keep your chin up, I have a good friend and coworker who had CF. Watched what it did to him, not fun!!

 

I work in a hospital, we filter everything!! But CC comes thru our filters loud and clear!! WOOHOO, GOOD JOB PETE!!!

 

As for hospital food.. how do you think I lost all that weight!! :rotf: :rotf: :rotf:

 

Now you get better!!

 

CW

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Thanks to all, really does mean a lot to me. Yes, it is Cystic Fibrosis, and I can relate to the diabetic content as well, as because of my CF, I too am diabetic, which brings on an ultimate suck. I've always said that this is something that I would never wish upon a most hated enemy, but at the same time, I'm glad I have it, as it's made me who I am today.

 

Pat (Jeepco), thanks man, definitely appreciate that. I did get my linux disc for my desktop, before I came in here, so once I'm back home, I'll be working on that.

 

Darren, no worries man, I don't plan on leaving this world any time soon, got too much to be here for.

 

87Warrior, wish her luck for me, I feel her pain, and yes hospital food SUCKS!

 

CW, wish him luck from me as well, and I agree on CC coming through loud and clear, as well as the thanks to Pete; and LOL to hospital food being 'to blame' for your weight loss.

 

Pat (pingpong), I'm still wishing you the best of luck as well. Once I get back home and get my desktop back up and running, I'll look for a viable online chess game for us to play.

 

Eagle, thank you, although 'complete' recovery isn't possible with this. It's a genetic mutation, so only option to live a normal life again is a cure, which is many years away yet.

 

dakal, I appreciate it, and I'll be stopping in everyday I can.

 

freakjeep, thank you as well.

 

jpnjim, I should be home this weekend if all goes well.

 

WBBKrazy, will do, and I'm sorry to hear that. I too have lost friends due to this disease, and it never gets any easier. I was actually told when I was 6 years old that I wouldn't make it to see 18; I am now 28, so theres always hope, just have to keep your chin up as you said.

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87Warrior, wish her luck for me, I feel her pain, and yes hospital food SUCKS!

I will certainly pass on your kind words 8) She actually seems to do pretty well for a high school senior, maintaining high hopes and dreams. Recently she worked on raising a bunch of money to bring in a motivational speaker to her school to speak.

 

Here is a short news clip of the ordeal: http://www.wibw.com/localnews/headlines/70074052.html

 

Hope you can get out of the hospital soon and get some real food :thumbsup:

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Just anouther update. Sorry I haven't been updating in a couple days, I had a minor surgery on Tuesday to put in a permanent I.V. system. I'm still not quite completely with it from the drugs I was given, but I am alright though. Again, thanks to all for the well wishes, I can't express how much it means to me to know people I've never met care so much for the health of a fellow member. jamminz.gif Because of the placement of my new I.V., I can't do my PFTs (lung function tests) until the pain subsides and I can take a full breath without risking damage. This in turn means I'll be in here longer than I had anticipated. The new I.V. is called a port, which is placed under the skin in my abdomen, has a line that also runs under my skin up to my neck. They had to make 3 incisions to do this; one right under my ribs on my right side, one to the right of my right nipple, and one just above my collar bone. It hurts like none other, but in the long run will be better for me, as whenever I come back in here, they only have to insert a needle, instead of having to place a regular I.V. for a couple days at a time, until I would get a P.I.C.C. line (Peripherally Inserted Central Catheter).

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Will they let you bring your 'manche bedside so you can wrench on it? :yes:

Seriously, though, you are an encouragement to all of us. You are going through this with what appears to be a good attitude, and we who do not have such problems can complain about a headache! Thanks for your being a good example to the rest of us! And, my prayer is as we approach Christmas that what Jesus birth, life, death, and resurrection means for you and all of us will be of great comfort.

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hope you get to feeling better every day Joe :cheers:

 

I can't comment on hospital food, as my wife is a clinical dietitian, and works in a hospital. All the patients keep blaming her for the bad food....but she has nothing to do with the preparation. Drives her insane, 'cause she knows they're right...... :shake:

 

Jeff

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