Online Liver Transplant Group Offers Support Regardless Of Health, Schedule Or Distance
Main Category: Transplants / Organ DonationsAlso Included In: Liver Disease / Hepatitis
Article Date: 30 May 2006 - 0:00 PDT
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Lori Dunn, who received a transplanted liver on July 24, 2005, attends weekly support group meetings at Cedars-Sinai Medical Center as often as possible to share her experiences and offer encouragement to other patients. But because distance and schedules don't always cooperate, she often turns to an online offshoot of the group, which enables everyone to participate, no matter how far away they live or what their physical limitations may be from week to week.
The idea of the online support group came to John Pappas, licensed clinical social worker in the Liver Transplant Program, because only a few patients are able to come to the face-to-face meetings; attendance ranges from about seven to 17 patients each week. About 70 have signed up for the online group so far.
"We have quite a few patients who are really sick and unable to attend, and we have patients who are working. The support group meets every Wednesday at noon, and it's hard for some people to attend a mid-day group," Pappas says, adding that many of the online patients participate from the Inland Empire and Ventura and Orange counties.
In fact, with patients on Cedars-Sinai's liver transplant waiting list scattered throughout Southern California and in several other states, the Internet seemed an ideal vehicle to keep communication flowing. For its innovative use of technology, Cedars-Sinai has been named one of the "most wired" hospitals in the United States by Hospitals and Health Networks, a journal of the American Hospital Association.
Lori Dunn received her transplant just six months after being diagnosed with liver disease. She was sick enough to rise to the top of the donor organ waiting list and fortunate enough to have a compatible liver become available at the right time. But she knows other patients who have not been so "lucky" - people she met through the Wednesday support group. Now, when she can't meet with them in person, she catches up electronically.
"I try to check in daily with the online group, especially for those individuals who are pre-liver recipients. A lot of them have been on the waiting list for quite some time," Lori writes in an e-mail. "I started going to the (actual) group in September, two weeks after my release from the hospital. I've watched some of them decline in health since I've been attending. … It breaks my heart. They become like family. We share something so personal with each other."
Lori developed cirrhosis of the liver even though she did not drink heavily, use drugs or have hepatitis C - "the things I thought would cause liver problems." She did take quite a bit of acetaminophen over the years and wonders if that may have led to her liver damage. Whatever the cause, her health deteriorated rapidly, her thought process became clouded, and the Chatsworth resident was afraid she would not live to see her 50th birthday, which came and went last September.
"She said she is afraid to have the transplant," Lori writes. "I told her I was afraid, too. But I was tired of feeling sick and weak. That gave me the incentive to be strong and accept the fact the surgery is going to make me feel better. She stated that she was tired. I told her the surgery will give her the energy she once had. I was also tired, but now I'm a ball of energy. I explained to her that you have to be a fighter when dealing with liver disease because of the confusing state of mind you're in. The ammonia levels give you 'the crazies' and hallucinations."
Another pre-transplant patient, Leslie Bohn, 51, of Los Angeles, has a couple of candidates willing to provide a partial liver donation. Because of the liver's regenerative capacity, a friend or relative can sometimes donate part of his or her liver, with the organ growing back to its original size within a few months.
In 2002, after becoming increasingly aware of tingling and pain in her feet, Leslie underwent a series of tests to rule out diabetes, multiple sclerosis and other conditions that could precipitate these symptoms. In 2003, a liver biopsy performed at Cedars-Sinai found she had liver disease. Now waiting for testing and paperwork to be completed on the potential donors, the mother of a 19-year-old son and four stepchildren says her medical condition has declined, and she dreams of someday resuming a normal lifestyle, free of the dietary restrictions liver disease imposes.
"I am still in pain and my feet are really worse so that I often need a wheelchair. My stomach retains fluid and I have to limit my sodium like a hawk, as well as watch my intake of fluids. A transplant couldn't come (soon enough) for my liking. I would just love to have an artichoke with a piece of baguette and a sliver of quality parmesan," she writes. "I used to go to the (support) groups every week until I became too debilitated with my feet, etc., but I do check in on a regular basis (online) and think that John came up with a great idea."
The virtual support group, in existence for about five months, is completely confidential and restricted to those on the liver transplant waiting list at Cedars-Sinai. Lori and Leslie agreed to allow their names and situations to be made public.
"It is basically an e-mail distribution list," says Pappas, noting that the online group is currently exclusive to the Liver Transplant Program. "When a member sends an e-mail to the Cedars-Sinai Liver Transplant group, it goes to everyone in the group. And when someone in the group receives that message, they can either respond to the individual who wrote the e-mail or to the whole group."
Although all of the specialty areas in Cedars-Sinai's Comprehensive Transplant Program - heart, lung, liver and kidney/pancreas - provide support and educational groups, not all transplant centers do.
"It's great that we have a high level of interest and are able to extend support to the online community," Pappas says. "This is just another avenue for our patients to get more support and stay connected to the transplant program here at Cedars-Sinai."
The first of eight hospitals in California whose nurses have been honored with the prestigious Magnet designation, Cedars-Sinai Medical Center is one of the largest nonprofit academic medical centers in the Western United States. For 18 consecutive years, it has been named Los Angeles' most preferred hospital for all health needs in an independent survey of area residents. Cedars-Sinai is internationally renowned for its diagnostic and treatment capabilities and its broad spectrum of programs and services, as well as breakthroughs in biomedical research and superlative medical education. It ranks among the top 10 non-university hospitals in the nation for its research activities and was recently fully accredited by the Association for the Accreditation of Human Research Protection Programs, Inc. (AAHRPP).
http://cedars-sinai.edu
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Visitor Opinions In Chronological Order (10)
Hep c
posted by Doreen Faber on 31 May 2006 at 1:44 pmI reside in NC, I was on the transplant list in MI. at Ann Arbor, then when I returned home to NC, I was again placed on the list at Duke.
Because my other half of twenty years walked out on me, I was taken off the list. I recieved tainted blood, from giving birth in 1973. I am stage 4 now after doing 18 months of just Interferon Alpha A, I am non-responsive. I am a home owner, and have paid taxes all my life, I ran for and was elected to serve a goverment position.where I served two terms, which is eight years.Why is it that I can be a tax payer, a productive citizen, but I have no right to live.
Non-alcholic cirrhosis
posted by Sue on 2 Sep 2010 at 7:44 pmHi Lori and all, I don't know what caused my cirrhosis but I think it could have been due to too many antibiotics. When I was in high school and beyond, the Dr gave me tetracycline for acne. I think I took it every day for about 3 or 4 years. After living in the AZ desert and getting upper resp infections, and the Drs all treated them with antibiotics. That went on about every 6-8 weeks for two years. Then we moved to NY and our whole family got Lyme disease.
Well, the only treatment was doxicycline in huge doses. I was infected and treated two times. That is a lot of antibiotics. I guess it doesn't matter anymore as I am on the liver transplant list at Mayo in Jacksonville and have lost a quality of life probably due to the over-use of antibiotics. No doctors will admit it is a possibility for obvious reasons but patients beware of mega doses of antibiotics. I think it can cause irreparable damage to the liver.
Thanks For Nothing...
posted by Roger P on 12 Oct 2010 at 11:41 pmWas glad to hear that SOMEONE is getting some help coping with this but, the title of the article led me to believe that there was an online support group open to everyone who wanted to join in for support, info, and etc. But, after reading the article, I find that it was of no help what so ever and that evidently the group is STILL only open to people having the transplant done at Cedars-Sinai and to nobody else or there would have been a link or address to the reader to follow up and see if the group could help. So...like I said, thanks, for nothing.
Thnak you
posted by Kip Kalvick on 21 Dec 2010 at 10:29 amI have had 3 liver transplants starting 15 years ago and would like the families of the donors to know how grateful I am to be alive everyday. It has not been an easy trip but was worth every minute.
Dee
posted by Denise Eden on 7 Mar 2011 at 4:35 pmI got a liver transplant on 2/17/2011 and I am doing well. I get scared of rejection and the meds make me crazy moody but it is all worth it. I have so many questions and I feel totally lost in all the info I have gotten. It is hard to filter it all out. I would love to hear from some of you about how to handle the emotional roller coaster I am on right now.
liver support in Cincinnati
posted by Darlene on 3 Aug 2011 at 11:02 amI am taking over the liver support group in Cincinnati. We only meet every other month and I am going to change that. I give my phone number to everyone who just wants to talk whether pre or post transplant. I had a liver transplant in 2008 and this is my best year yet, and yes, the drugs do get to you sometime but hey, you're here aren't you? I was very sick for nearly 20 years and waited 2 1/2 years for my liver. Life is great and I am so blessed to be here. Look for our website soon. At our meetings we talk about everything from moods to bm's, we've all been there and I learn new things at every meeting.
newbee - liver transplant candidate with concerns
posted by Robert Martin on 16 Sep 2011 at 11:50 amI am on a liver transplant list at Cedar-Sinai. I have a very difficult decision as to transplant yes or no. Very complicated and I am concerned that rejection drugs may greatly increase chances of cancer elewhere and I wonder what quality of life with a transplanted liver is?
I had three liver transplants
posted by Maisah Rashid on 8 Nov 2011 at 2:37 pmI had three liver transplants 17 years ago in 1994. The road has been rough, but I'm very grateful of another chance at life.
Newbie, should get transpplant.
posted by Maisah Rashid on 8 Nov 2011 at 3:00 pmI've had this last transplant for 17 years now. I got cancer from the drug Azathiaprin, 12 years after the transplant. Within 6 months I was cancer free. Three treatments of chemo, four of radiation. You should really think about a better quality of life as a result of a liver transplant. GOD BLESS YOU
liver transplant-no family support
posted by joesaphine on 19 Dec 2011 at 8:12 pmHi Sue,
Me too! Antibiotics to the extreme. Now I am fouth stage after Avelox and clyndomiacin. I need a transplant. The problem is they won't register me because I am not married/signifigant other or have family. I have always been so healthy and have lots of friends but they have kids and can't be primary caregivers. I have developed vericies and am really scared. Does anyone have any ideas?
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