Yesterday, our day started early. I began by having a chest x-ray at the diagnostic center. We then proceeded to the oncologist office for lab work.
Met with the oncologist to go over results. My platelet count was back up so I could get chemo. The chest x-ray showed fluid again on my left lung and a little on my right. That certainly wasn't a surprise to me because I definitely was having trouble breathing all week. I would be scheduled to have that drained after chemo.
Chemo went well. I use that time to think. I haven't read a page from a book or more than a few pages from a magazine in quite some time. I rested with my eyes closed for a little while.
We left chemo and headed to the hospital for the thorocentesis. I had a different team this time...new radiologist and new doctor. First the injection to numb the area. They compare it to a bee sting. Next the insertion of the needle to drain the fluid. Bad news...only 20 ml. of fluid was draining. They said that they don't have to do this often but they could insert a wire into the tube and work it around to break up any strands and scar tissue that was causing the fluid to not drain. I gave the go ahead...after all, my road is never the straight one. The wire procedure wasn't making a difference because fluid would still not drain. That meant another decision. Did I want them to reinsert the needle into a new area and try again. Road is more curvy but because I was systematic and having trouble breathing, I knew that I had to get as much fluid off as possible while I was there. Gave the go ahead to begin the procedure all over again. Second bee swarmed in for another sting, new needle inserted in between rib bones. I gave a cheer, well more like a command. "Come on fluid....drain". They got 320 ml. out total. That's all that would come out. From using the wire, they actually showed me the "strands" that were in the fluid. The doctor that watched the radiologist do the procedure was wonderful. He held his hand on my shoulder the entire time as he told me each and every step. I actually raised my head from the pillow during the procedures and told him how much I appreciated him. His hand on my shoulder gave me such comfort. My two thorocentesis for the price of one and the wire blue light special was over. Off to get an x-ray.
I wasn't able to go home for a couple of hours because the lung had air that had accumulated in the bottom. I had to stay in recovery to make sure that the lung didn't collapse. Off for another chest x-ray. Things looked the same so I could go home. It was again stressed that if I had any difficulty breathing as a result of the lung collapsing, to call 911 right away. Homeward bound!
Got home, threw up and settled in for a nice siesta!
7 comments:
Hang in there braveheart! We are all praying for you.
Hang in there our Special Grasshopper. All your friends have their arms around you and your family praying each and every day. We're so glad to hear that you had such a wonderful doctor beside you. Stay strong and listen to your body. We're all with you and your wonderful fmaily...
Sweet Sharon,
Sending you a BIG but gentle hug. Also, thanking the Lord for placing that kind Doctor in your room throughout the procedure.
Rest peacefully,
Darla
Dear Sharon,
Sending hugs (gentle) and prayers (bountiful) your way today and always. Your Faith is an inspiration to everyone. Stay strong. We all miss you!!
Judy
Sharon-continue to think about you often. Stay strong, miss you. Patti (I finally figured out how to leave a comment on this)
Hi Sharon!
I feel as though I have deserted you because I haven't left a comment for a little while. Well, first of all I would NEVER desert you dear friend..NEVER, EVER. Secondly, even though you haven't heard from me does NOT mean I haven't been continuing to pray for you...on the contrary--only each and every day!
With that being said, as I read your blog I found myself in memory lane. You are experiencing many of the things my sister has too--especially the fluid on the lungs. She too had some unpleasant experiences but she was always so glad to have that 'stuff' out of there! Unfortanately, it's not a perk...but instead a very bumpy, uncomfortable road. Don't lose heart..keep putting one foot in fron of the other...the pace can remain slow...or slower if necessary. Rest as much as you need...throw up what you need...but NEVER, EVER lose faith. When your Dr. laid his hand on your shoulder..he wasn't the only one..God did too...that's why it was so comforting dear lady. He knows what you need and when you need it most.
While you rest your eyes remember to listen to that small quiet voice... HE will speak to you and give you stregth as HE pours out HIS mercy over you. And from time to time you may even be able to sense that someone is lifting you in prayer...it's happening Sharon....REALLY happening. We love you, that you know for sure, but there are thousands of folks who are lovingly calling on God to restore you. Listen....He IS there with you...while we all wish we could be...
special love and tons of hugs,
KB
Sharon,
Kathy said it better than I ever could. I pray that you are indeed able to feel God's presence in your journey through all the twists and turns and detours. He is there with you, as are we.
Missing you tons...
Rosemary
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