These posts are more for me than anything. I think it'll be neat to have a journal of sorts to keep track of things we go through in life. With that being said, here's some rambling about what's gone on since the last post.
It's been 3 weeks to the day since my surgery. I'm still amazed at how much smoother the recovery has gone this time around. I expected that with the same size incision (actually it's an inch longer at 10 inches this time) the recovery would be the same as in March. It's been leaps and bounds better! I'm getting around almost like normal. I got the drain, staples and sutures removed this past Wednesday. The difference after that alone was night and day. The area around the drain had become very red and irritated and was the main source of pain. Coughing was still rather painful because of the drain and the staples.
Since those have come out I'm virtually pain free. I have one spot that gives me a lot of trouble only when I cough in any other position besides sitting. So for now, anytime I need to cough, I try to hurry and sit down somewhere so it doesn't hurt. As long as I'm sitting, it doesn't hurt at all. It's very strange. The nurse and doc said I may have some pain from where the drain was, and the source of my pain now is exactly where the drain stopped under the skin. Besides that, I feel really good! Now the hard part is taking it easy.
I feel really good, so I will be more inclined to start doing a lot more and lifting more. The surgeon told me I can increase the amount of weight I lift by 5 pounds each week, starting at 10 pounds. Pain being my indicator as to when I'm going too far. My first feat will be to tackle the yard. My sister was kind enough to mow the front yard for me after I got out of the hospital, after 2 weeks of not being mowed. It's been another week and a half and we've had a lot of rain since the last mow. It's looking like a jungle again. The backyard hasn't been mowed for almost 4 weeks now. It really looks bad! They boys were out playing in the backyard today and Jace found some weeds that were up to his chest. No joke! His chest! It's gonna be a blast mowing that, lol. It'll be good exercise though. I do have a self-propel mower that I will take full advantage of as well. I have a CF clinic appointment Monday. I'll post the results of that. I'm anxious to see where my lung function is at.
Everything has been going good around the Parks' home! The family is happy and healthy! Life is great!
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Friday, August 22, 2014
Monday, August 18, 2014
If Time = Money, I'd be more Wealthy
I have a little over an hour of time added to my days now! How did I accomplish this you ask? I didn't switch to a different way of telling time where there are 25 hours in a day. I got a new nebulizer machine. Actually it's a compressor. I noticed that several of my fellow Cysters and Fibros had the same machine. I read several reviews on various CFer's blogs, did some research of my own on the internet and decided to purchase this specific compressor.
My treatments used to take me over 2 hours a day and I wasn't getting the full treatment. I often cut each treatment short so I wouldn't spend 2 1/2 hours sitting taking treatments. With my new compressor it takes about 30 minutes to complete my treatments on Cayston months and about 45 minutes on TOBI months. Each treatment runs until it is BONE-DRY! I'm getting my full treatments and have cut my treatment times by more than half! I couldn't be happier! In the CF world, this is HUGE! We spend so much time doing treatments and exercising, any way to cut down on that time, gives us a more normal life. This means more time to spend with my boys! More time to exercise! Less times that we as a family will have to show up late to family gatherings, etc. I'm ecstatic! So, if you're spending a long time taking treatments, I suggest taking a look at your nebulizer machine/compressor.
By now you're probably wondering what machine I purchased. Ok, I'll spill the beans. I bought an Invacare MOBILAIRE 50 psi compressor. To read more about it, click on the name.
Unfortunately, my insurance couldn't get me one. None of the companies my insurance gets equipment from carried the compressor. The Invacare website has it listed around $400. I was able to find one online for $275 with shipping included. I couldn't be happier with it! Worth every penny!
Just a little fyi for any CFers that read my blog. I love it, and feel obligated to share the knowledge. Hope it helps!
My treatments used to take me over 2 hours a day and I wasn't getting the full treatment. I often cut each treatment short so I wouldn't spend 2 1/2 hours sitting taking treatments. With my new compressor it takes about 30 minutes to complete my treatments on Cayston months and about 45 minutes on TOBI months. Each treatment runs until it is BONE-DRY! I'm getting my full treatments and have cut my treatment times by more than half! I couldn't be happier! In the CF world, this is HUGE! We spend so much time doing treatments and exercising, any way to cut down on that time, gives us a more normal life. This means more time to spend with my boys! More time to exercise! Less times that we as a family will have to show up late to family gatherings, etc. I'm ecstatic! So, if you're spending a long time taking treatments, I suggest taking a look at your nebulizer machine/compressor.
By now you're probably wondering what machine I purchased. Ok, I'll spill the beans. I bought an Invacare MOBILAIRE 50 psi compressor. To read more about it, click on the name.
Unfortunately, my insurance couldn't get me one. None of the companies my insurance gets equipment from carried the compressor. The Invacare website has it listed around $400. I was able to find one online for $275 with shipping included. I couldn't be happier with it! Worth every penny!
Just a little fyi for any CFers that read my blog. I love it, and feel obligated to share the knowledge. Hope it helps!
Labels:
CF,
Cystic Fibrosis,
equipment,
nebulizer,
treatments
Saturday, August 16, 2014
Surgery #2 of 2014
March 2014 surgery incision |
Fast forward to a couple months ago and I noticed a bulge in the center of my stomach near my belly button. I knew instantly it was a hernia. I could just tell. On the plus side, it didn't hurt. I had no feeling left in that area of my stomach from all the surgeries. After a couple weeks, it kept growing, sticking out more and more. I called and had an appointment to have it looked at. Fast forward 6 weeks, a CT scan and two more doctor visits and I had a surgery scheduled to fix it. I had my appointment with the hernia doc on a Wednesday afternoon. The only opening they had was for that Friday (two days from then). I'd have to wait another month or so before having it fixed if I waited. I scurried to make all the arrangements with work, etc. and went in Friday, August 1st to have it fixed.
I'm just over 2 weeks out from surgery. This time has been much, much better! So much less painful than in March. So far the toughest part has been not being able to hold my two precious boys. It's a 6 week recovery again and I can't lift anything over 10 pounds. They didn't leave any part of the incision open this time, thankfully. However, I do have a drain in place. It honestly hasn't been that big of a deal. I expected it to be much worse. I have to empty it once a day and that's about it. The past few days it has been causing me a lot of pain. I think mostly because my body is trying to heal itself, but can't because there's a suture and large tube in the way. It's very red and irritated. It keeps forming scabs that get torn off (which is causing most of the pain) from the dressings and from moving around. The skin around the drain is extremely tender. My incision on the other hand is doing great! It looks awesome so far! The surgeon did an excellent job of putting me back together. He used a biologic mesh to hold my guts in and reinforce the area. The scar will look phenomenal compared to the two I had prior. It looks like someone drew a line down my stomach with an ink pen. It's put together so well and I think it'll leave a very nice, neat looking scar. It's hard to tell from the pictures, but it's much better than the one in March I promise.
Thankfully, my lungs have remained healthy through all of this. I give all the credit to God! I've stayed faithful to my treatments and kept myself busy, up and moving around to help keep my lungs healthy. I haven't had PFT's post-op yet, but I know they'll be much better than the last go around. My FEV1 dropped to 47% after the surgery in March, which was pretty scary. Even though I knew it was because I was still in a lot of pain and couldn't give a maximal effort, seeing that 47% was scary. I know I'm doing much better than 47% this time and for that I'm extremely grateful.
I get the drain and all 29 staples and 7 sutures out this coming Wednesday! I couldn't be more excited! I'm anxious to get on with my recovery. I feel like I never fully recovered from the surgery in March. I got the hernia so soon, I never got to get back into running and working out. I'm extremely motivated! I've been down and out for almost 7 months when it's all said and done. I'm ready to get back at it! I should be back to tip top fighting shape after this surgery and am looking forward to getting myself back into the best shape of my life!
I'll keep you all posted on how things continue to progress! Thanks for reading!!
Labels:
CF,
Cystic Fibrosis,
hernia,
motivation,
surgery
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