Guest guest Posted August 16, 2002 Report Share Posted August 16, 2002 From: " rekadaub " <http://groups.yahoo.com/group/pancreatitis/post?protectID=1940562112372480\ 31130171203245147187078145139218183041rekadaub@...> Date: Thu Aug 15, 2002 3:06 pm >>>I am a new member and just want to say hello to everyone. I was diagnosed with acute Pancreatitis on April 20, 2001. I have been e mailing a few members and just wanted to let you all know what a great help this site has become for me. Thank you. Becky<<<< Hi Becky, We are glad you are here. Please share your story with us, where you live, etc. I am glad that this site has been helpful to you. Have you been diagnosed with Chronic Pancreatitis since you had Acute Pancreatitis? Karyn , RN Founder / President http://www.pancassociation.org KarynWms@.../ Pancreatitis Association International Many People, Many Faces, One Voice Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2002 Report Share Posted August 17, 2002 I live in North Central Pennsylvania. I am single and live alone. I have not been diagnosed with chronic, but I have been having problems the last several months. I went to my GP and had tests run and a CT scan done. The results came back and my pancreas and spleen are enlarged, especially the tail of my pancreas. My experience began on January 31, 2001, I was very ill with nausea and vomiting, I went to the ER and was told I had GERD, I was given meds for that. Well on February 14, 2001, I began vomiting about every 20 - 25 minutes for about 30- 36 hours. I called my GP and he told me I had a touch of the bug and gave me a script for the vomiting. Several days later I began to feel better. But on March 14, 2001, it all began again, but the vomiting was about 15 - 20 minutes apart for almost 40 hours. Once again I called my GP and he told me that it was the bug and refilled my script, and told me if it happens again they will get me in. A few days later I began to feel better. But I was still not feeling like myself the entire time. On Thursday April 19, 2001 around 2:00 in the afternoon it began again, and my boss sent me home. I called my GP right away and he set an appt for the next morning, too busy to get me in that day. Well, as the evening progressed I continued to get worse, the vomiting was about every 5 minutes. Around 12:30 am I began to get double vision, and just associated it with dehydration, around 1:00 am I began to breath so fast that I was panting. I called 911. The medics came and hooked up all kinds of machines. My heart rate was 300, they shot me 3 times with eppy trying to get it to slow down, to no avail. My BP was so low that it wouldn't register. They finally had me stable enough for transport. I don't remember to much about what happened in the ER. My brother had recently changed his phone # and I couldn't remember his new number. The next thing I remember was being wheeled into the ICU unit around 8:00 am. My nurse, Mark, informed me that they were going to put me on life support, which I told him no. I was addicted to Trauma, LIfe in the ER on TLC, and saw what happened to people they put on life support. He told me that I could do it now or when I crash and if I crash I will not survive. After signing the papers myself, I blurted out my brother's phone number. It took them 3 hours to reach my brother. He was online and they broke through 3 times before he just gave up trying to download. Well the next call was the dreaded call. I was on life support for 7 days and in a medically induced coma for 10 days. I had 13 IV lines, 50 lbs of IV fluid, and 2 blood transfusions. Sometime after they removed the ventilator but while still in a coma, I climbed over the side rail of the bed and fell to the floor, the nurses found me several minutes later laying on the floor. When this happened I injured my right leg, so now I have a disability. My right leg does not work from the knee down. I ended up spending a month in the hospital. I would have been home much quicker, but I had to go through rehab, I had to learn how to walk again. I was dealing with pancreatitis, being newly diabetic and now being handicapped. I had to learn how to walk all over again. I was wheelchair dependant, I had a metal brace to my knee built into a shoe just so I could walk. I was dependant on a walker for several weeks, and then to a cane. I was also homebound because I could not walk, let alone drive. I lived with my brace for 11 months. I now am free of that but still am considered handicapped. My right leg still doesn't work properly. I had a CT scan done on July 17, 2001, and my surgeon discovered a pseudocyst had formed on my pancreas. It was about the size of a football. Surgery was set for Aug 28, 2001. I basically had the cut of a whipple proc, but they resectioned my small intestine to accept the end of the cyst for drainage. While I was open he took my gall bladder and my appendix. They weighed me before and afer the surgery, I lost 13 lbs. I have had several episodes of attacks of pain and nausea. Just recently called my new doc for help. Needless to say my original GP has been replaced by a new doc that is very understanding of what I went and am going through. So I am just trying to make it through each day. I still work and have a new job. My new boss had never heard of this disease, so I took in some info so she is aware of what might be going on if I suddenly get sick. This site has been very helpful and I have meet a lot of great people here. Thank you all. Becky Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2002 Report Share Posted August 18, 2002 Becky, wow, you have been through the mill haven't you. I certainly hope your new doctor is a lot better dealing with your medical conditions. My story is on the http://www.pancassociation site. Unfortunately, living with chronic pancreatitis and all the complications it can cause is on a day by day basis. Some days are good, some days are bad. I'm still able to work, but have daily pain now as I'm end-stage chronic pancreatitis. I've got it because of a birth defect called a pancreatic divisum. Basically, my pancreas has been autodigesting itself since I was born. I'm 32 now. I have an acute attack about once a year. Plus I have multiple other health problems, some related to the CP, some not. I also have a genetic blood clotting disorder I didn't know I had until I had a heart attack and single heart bypass. Nice introduction, huh? Well, just wanted to say hi and that I sympathize with all you have gone through. Kimber -- Kimber Vallejo, CA hominid2@... Southwest Representative Pancreatitis Association, International Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2002 Report Share Posted August 18, 2002 Becky, wow, you have been through the mill haven't you. I certainly hope your new doctor is a lot better dealing with your medical conditions. My story is on the http://www.pancassociation site. Unfortunately, living with chronic pancreatitis and all the complications it can cause is on a day by day basis. Some days are good, some days are bad. I'm still able to work, but have daily pain now as I'm end-stage chronic pancreatitis. I've got it because of a birth defect called a pancreatic divisum. Basically, my pancreas has been autodigesting itself since I was born. I'm 32 now. I have an acute attack about once a year. Plus I have multiple other health problems, some related to the CP, some not. I also have a genetic blood clotting disorder I didn't know I had until I had a heart attack and single heart bypass. Nice introduction, huh? Well, just wanted to say hi and that I sympathize with all you have gone through. Kimber -- Kimber Vallejo, CA hominid2@... Southwest Representative Pancreatitis Association, International Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2002 Report Share Posted August 18, 2002 Becky, That is a horrible experience that I am so sorry that you had to go through with the ER. GERD? Are they crazy -- there's no vomiting with GERD -- usually you feel like you're having a heart attack and the first thing they do is give you an EEG -- these people had worked too long on their shifts. I have a hiatal hernia(which is a breakdown on the muscles in the esophagus) and GERD and the first time it really got very bad (up to then it was just indigestion), I was in Puerto Rico working and they immediately hooked me up to an EEG and put me in coronary care -- but then moved me when they found out what it was by doing an upper GI. I hope your new doctors and surgeons are not affiliated with that " old hospital " . Hope you're doing better and are having a pain free day. Kathie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 18, 2002 Report Share Posted August 18, 2002 Hi Becky, WOW! What a story. I am glad you made it and I hope you are having a good day today. Best wishes, Poncho - GA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 20, 2002 Report Share Posted August 20, 2002 Becky, Thank you for sharing your story with us. I am so sorry you had to go through all of that alone. And that you ended up with your disability. I am glad that things are going ok for you right now... I hope and pray they continue to. I am glad we got the chance to chat and hope to get to again sometime soon! Take care and Keep in touch! {{{HUGZ}}} --------------------------------- Quote Link to comment Share on other sites More sharing options...
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