Guest guest Posted March 28, 2005 Report Share Posted March 28, 2005 Kris, I am so glad to hear you are doing some better. I hope the procedure gives you some relief! Don't over do it! Take it easy for a few days! Angie in SC " The happiest of people don't necessarily have the best of everything; they just make the best of everything that comes along their way. " Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2005 Report Share Posted March 28, 2005 Just wanted to say hi to everyone here. I am feeling much better since my release from the hospital. As most of you know I had an ERCP last monday and was kept in the hospital for 5 days after because of pain and a flare from the procedure. After my office consult with Dr. Lehman , we decided to do an ERCP with a couple of stents in the pancreatic duct that would last approximately 1 year. But once he got in there, he said that the pressure was up in the panc duct again so he decided to do a deeper cut on the panc duct and extend the bile duct side too. He then put a temorary stent in the panc duct. I woke up and felt fine for about 1 hour and then the pain hit. They had a real hard time getting my pain under control. After I got up to my room they tried me on Dilaudid, anyway, I kept having bad muscle spasms on the left side of my body for about 15 -20 seconds after the injection. So we decided that I was possibly having some sort of an allergic reaction so I went back to demerol. The next morning I found out that they were only giving me 25g of demerol in the ERCP recovery room and that's why my pain wasn't under control. I told the nurse that I take 50mg 2x a day on a good day at home. So the floor doctor upped my meds to 50mg demerol every 3-4 hours. Well, that worked for about 24 hours and then my pain was bad again. Finally they upped my meds to 100mg demerol every 3-4 hours and bingo! I was having some pain-free hours! Then I find out that I could only be on demerol for 3 days (because of the risk of seizures), and that I would have to switch medications again. I chose morphine. It makes me itch but relieves the pain. So I believe I started the morphine on Wednesday pm and then I tried to eat some jello and it caused more bad pain. Back to IV fluids only and my favorite (ice chips). Then Thursday my floor nurse comes into my room to say that Dr. Lehman's nurse scheduled me for a PICC line. I told her to call the nurse back and ask why I needed that! So the nurse comes back in alittle while and tells me that the nurse practitioner would meet me downstairs (where I would have the procedure) and she would explain everything. So I agreed and then my hubby and kids show up. Now, my hubby (and me) were both under the assumption that I was possibly going home on friday, and he about freaked out. When we got downstairs, the nurse practitioner explained to me that I needed the PICC line if I was going to need continued IV pain meds. My veins were not good and they had a hard time with my IV. I just requested that my IV be changed because my present IV was EXTREMELY painful. Come to find out that my first IV had gotten infected, so I am on anti-biotics for that too. So I told the nurse practitioner that I would try to use my own pain meds (pills) through the night and if I could do fine then I could go home the next day and avoid that PICC line. Everything went well (luckily) through the night and I didn't require any further IV pain meds. Yipee! So friday I had a CT scan and then I was discharged in the afternoon. I stayed overnight in the hotel (friday) and then my hubby drove us home saturday. So I guess that is my summary of my hospital stay. I came home with alittle more that I expected, an infection in my right arm (from the IV), and a rash on my stomach. BUT, I am feeling much better every day. I just started to eat some solid foods and I'm doing ok. I still am very nauseous and very tired. I also wanted to say (sorry for the long post), that it was VERY nice to meet Karyn! I am sooo glad that she stopped by, and visited with me and my family. She is a wonderful person! She brought me some gifts and that was a total surprise!! THANK YOU KARYN! I also wanted to thank for the phone call. It was a nice surprise too! -when I talked to you, you sounded just like my sister-in-law. She is also an Aussie. Thanks for cheering me up. Thank you everyone who posted good thoughts and concerns for me. It is nice to be home!! Kris in TN Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 28, 2005 Report Share Posted March 28, 2005 Kris; I am so so glad that you are home and getting better. I was very worried about you. had called me and I had your number but had to stay off the phone. Could'nt even play online like I like. I am so desperate (housewife...LOL) to go back to work and dont want to miss a call. then my two oldest kids have homework online, how about that and they are usually on until 9pm and I thought it was too late to call you. Cant remember where the time change is. anyway I am very glad you are home now, I am sure your family is as well. What an ordeal you had. Are the stents the type that pass on their own? It sounded that way from your post. If so, you may be achey until they pass, usally around 2 weeks give or take. I had one in for 10 weeks and it had to be pulled. I think that caused a lot of damage, but there is really no way to know for sure. Did they schedule you for a x-ray in a few weeks to see if they have passed? Lucky you not having to get a picc line. I remembe somebody had mentioned one to me years ago and I ignored it. I really didn't want to get one even with the bad veins I had back then (dehydration). Gosh it was bad enough getting the g-j tube. I couldn't talk them out of that no matter what tricks I pulled. Actually there is a kind of funny story associated with that, but I will save that for another time. do you have to go back to Indy to see Dr. L anytime soon, a follow up or something or is your local GI going to take care of that part. Well try to rest, I have heard for every day in the hospital it take tiwice that many to get over it and every day in the ICU (or dependancy unit as Fliss calls it) is a weeks recovery. So give yourself time to recover. The stents should really help and I will hope and pray for you that it does. Feel better, but dont do too much too soon. You had quite an ordeal and you will need to give yourself time to get over it all. I know when we get home we fall very easily back into our " super woman " role and try to do all the things that have fell by the wayside while we were gone and not feeling so hot. Well the world wont come to an end if those towels are folded just yet. Shoot sug, they will just end up on the bathroom floor anyway, unless your husband is like mine and leaves the wet towell on the foot of the bed (grouds for divorce in my book...LOL). Let me know if there is anything I can do. Warmly, Chrissy Quote Link to comment Share on other sites More sharing options...
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