It's been a crazy, busy weekend, so I haven't gotten around to posting about my bronchoscopy/doc appt last Thursday. Since I had to go see the doctor that day in clinic after he did my bronch, I got to Duke early to get my blood work, chest xray and pulmonary function tests (pfts) done. I had just done all of this 3 weeks earlier, and that's when they determined that I needed to be bronched because my numbers on my pfts were very low for me. I was very tired last Thursday, because I had only gotten about 2 hours of sleep and then I had a 2 hour drive to Duke, so I just knew my numbers weren't going to look good. I was wrong!!! Here is the improvement on my lung function in just 3 weeks.....
8/7/08 FEV1 67% (my normal is 75% or higher) FEF25-75% 47%
Wednesday, September 3, 2008
Bronchoscopy and such!
8/28/08 FEV1 79% FEF25-75% 71%
All of the other numbers were higher too, but these are 2 of the most important. If your FEF25-75 is low, then that might be an indication of chronic rejection. My pulmonologist was amazed at these results. He said that he can never figure me out anyway. :)
He went ahead with the bronch even though my numbers were up, so that he could go ahead and "clear" me for kidney transplant. I had no infection or rejection!
We discussed my insomnia... it seems to be one of those problems we are always discussing now. He gave me a new med that didn't work, so I got ANOTHER new med yesterday, and had my first good night's sleep last night, so hopefully this is the one.
My weight is down to 97 again. I was up to 102 at one point, but now I just think that was fluid instead of mass.. unfortunately. I see my nephrologist next week on the 16th to discuss whether or not I want to have dialysis before transplant. I also see the surgeon at Duke on Sept 22nd. She will be the one performing my transplant. I am not sure if a date will be scheduled then or not. If I decide to do dialysis first, then it probably won't be scheduled yet. I'll keep you posted on that.
Other than that, I enjoyed this weekend with Casey so much. We ran around and shopped and played for 2 days (and I probably overdid it) and then we hung out at home (mostly b/c of my pain) for 2 days. I didn't feel like getting online much, plus I like to save my blogging when Casey is sleeping, at her dad's, or in school. I hate taking time away from her.
I was just bragging last week to a friend of mine how my fibromyalgia might be going into remission like it did last year, but this weekend told me... "NOT YET". Unfortunately, I was in a lot of pain all weekend. I will be seeing the rheumatologist in November.
I have so much to do around the house, but I will definitely be pacing myself the next few days, hoping that the fibro pain starts to lessen.
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6 comments:
This is awesome Christy! God is working:)
yes you are a complicated pt! no one can ever figure us living lobes sisters out:) i know one thing and that is God is still working on u and you literally have your breathing #s to prove it! i am so excited for you! tomorrow i find out the plan with me...they are on top of it and i am a topic at there weekely meeting in the morning. i will post what they come up with...have a good night! I love you:)
I'm glad you were able to get a good nights sleep and that your numbers were better. It sounds like you had a great time with Cassie. It is all about building good memories for our kids. I am sure she is learning a lot from you about the Lord as she watches how you deal with every day life. Keep looking to the Lord. Thanks for your great attitude. I am sure it gets hard at times but keep looking to our Lord.
Hey Christy,
I'm glad your nunmbers were up. What a nice surprise!
I just discovered the link to your blog today from your Caringbridge site. I like it!
Take care,
laura/catboogie
Wow those are some good numbers!!! I think anyway...I have no idea about numbers post tx :)
Hope this med works for you and you get some much needed sleep!
<3
Nice increase on the numbers!!
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