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Author Topic: As U.S. Patients Await Organ Transplants, Potential Donors Struggle for Visas  (Read 1344 times)
okarol
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« on: January 20, 2011, 11:51:56 PM »

January 20, 2011
As U.S. Patients Await Organ Transplants, Potential Donors Struggle for Visas
By JACQUELINE BAYLON
The clock is ticking for Dr. Gabriel Danovitch’s patient. Dr. Danovitch, a transplant surgeon at the David Geffen School of Medicine at the University of California, Los Angeles, is treating an immigrant from Mexico in his 40s whose kidneys have failed. The patient is a good candidate for a transplant and has a donor, his brother.

But there is a big problem: His brother is a Mexican citizen whose application for a visa to come to the United States was not granted.

Physicians who perform transplants say patients who need organ donations from a family member or other close match outside the United States face hurdles that are often hard to surmount. Difficulties in obtaining visas leave many potential donors frustrated and force their sick relatives in the United States to wait months or even years on a list for organs like a liver or kidney.

In other cases, poor families cannot afford to pay for the donors to travel to the United States and undergo organ-removal operations that can require hospital stays of up to three weeks. In some states, Medicaid does not cover any of a donor’s expenses, and private insurance policies vary greatly in how much they will cover.

Getting organ donations is always difficult, but medical authorities say the problems have gotten worse for immigrants with the tightening of visa policies after the terrorist attacks in 2001. And with the slowdown in the economy, some states have been cutting back financial aid to transplant patients and donors.

“If there is someone living and willing and compatible, it’s concerning that, because of so much protection, they end up not being able to help a desperate person in need,” said Bryan Stewart, a spokesman for One Legacy, a nonprofit organization that deals with organ and tissue donations in the seven-county greater Los Angeles area.

Dr. Giselle Guerra, medical director of the Living Kidney Donor Program at the University of Miami Miller School of Medicine, has similar concerns. “I wish I could get rid of all the bureaucratic red tape, and it would be nice for every donor to fit the criteria so we can stop adding to the waiting list,” she said.

More than 110,000 people were waiting for an organ as of Wednesday, according to the United Network for Organ Sharing, a private nonprofit organization that manages the nation’s organ transplant system under contract with the federal government.

Over 60,000 of those on the list are black, Hispanic, Asian, American Indian, Pacific Islander or describe themselves as multiracial, according to the organ sharing network. Of those, 6,229 are resident aliens in the United States, compared with close to 1,900 resident aliens in 2000. Illegal immigrants are prohibited from the list.

“When patients need a transplant, most of the time, the first people they turn to is their families,” said Dr. Juan Carlos Caicedo, a transplant surgeon and director of the Hispanic Transplant Program at Northwestern Memorial Hospital in Chicago. “It becomes complicated when their families are not in the U.S., which in a lot of instances, that is the case.”

The State Department does not have a medical visa category, and people traveling to the United States have to qualify for the B-1/B-2 visa, more commonly known as the tourist visa.

“Our embassies and consulates around the world do their best to assist visa applicants who are dealing with life or death situations in order to expedite their cases,” a department official wrote in an e-mail.

An individual applying for a visa for a medical reason can fill out a form requesting that the application be expedited.

But some doctors say that they have contacted State Department officials on behalf of patients and even that has not sped up the process.

“When I call the consulates or embassies, they’re not very cooperative,” Dr. Guerra said. “We try to be as concise as possible, but also explaining the urgency in the letters that we write, but it just continues to be a waiting game.”

Dr. Linda Chen, a transplant surgeon at the Miller School of Medicine, said that for about the last five years, the State Department has required foreign donor candidates to get preliminary testing done in their home country.

Blood-collection tubes are mailed to the candidates, and the filled tubes are mailed back for testing. If the donor has the same blood type, there is a possibility that he or she could be a match with the patient, and the State Department will take that into consideration, Dr. Chen said.

“But even with blood work,” Dr. Chen said, “they don’t give people visas sometimes.”

Dr. Chen said she writes letters on a monthly basis. But she cannot do that for patients whose donor relatives are in Cuba.

“Since the U.S. does not have a relationship with Cuba, we cannot help them by writing a letter or sending tests over,” Dr. Chen said.

If patients cannot get a donor into the United States, their names go on the organ network’s list to receive an organ from someone who has died. Waiting times for patients vary, and among the factors is a person’s state of residence. Patients in New York, for example, wait an average of seven to nine years, while people in Florida wait three to five years.

The No. 1 transplanted organ is the kidney. When one is needed but not readily available, patients must go through dialysis. Medicare spent $9.2 billion in 2009 on dialysis patients, according to an annual Medicare Payment Advisory Commission report due to Congress in March. Martha Escamilla-Arias, a social worker at Northwestern Memorial Hospital, said that in most cases dialysis cost the State of Illinois more than a kidney transplant in the long run.

“In Illinois, two and a half years of dialysis pays for one kidney transplant,” Ms. Escamilla-Arias said. “Some people are in dialysis for five to seven years, and if things were easier for foreign donors, it would help.”

Jean Viera, 34, a Cuban immigrant on the organ network’s list, has been going through dialysis for six years.

His left arm is disfigured with two purplish raised scars where he is connected to a dialysis machine.

“I wish I did not have to go through this,” Mr. Viera said. “This is just not the best way to live.”

http://www.nytimes.com/2011/01/21/us/21transplants.html?_r=1&scp=2&sq=dialysis&st=cse
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Admin for IHateDialysis 2008 - 2014, retired.
Jenna is our daughter, bad bladder damaged her kidneys.
Was on in-center hemodialysis 2003-2007.
7 yr transplant lost due to rejection.
She did PD Sept. 2013 - July 2017
Found a swap living donor using social media, friends, family.
New kidney in a paired donation swap July 26, 2017.
Her story ---> https://www.facebook.com/WantedKidneyDonor
Please watch her video: http://youtu.be/D9ZuVJ_s80Y
Living Donors Rock! http://www.livingdonorsonline.org -
News video: http://www.youtube.com/watch?v=J-7KvgQDWpU
DrMoskowitz
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« Reply #1 on: January 22, 2011, 07:41:20 AM »

The US has become totally unwelcoming to foreigners. It's obvious when you land at an airport from overseas. I'm embarrassed for what 9/11 has turned the US into.

But on a more practical note, there wouldn't be a waiting list for transplants if there were 90% fewer transplant patients. I published how to prevent diabetic and hypertensive kidney failure back in 2002 (1). News of my paper has been completely suppressed since then (http://tinyurl.com/healthcrime).

Reference
1:  Moskowitz DW. From pharmacogenomics to improved patient outcomes: angiotensin I-converting enzyme as an example. Diabetes Technol Ther. 2002;4(4):519-32.
PMID: 12396747. (http://www.genomed.com/pdf/diabetes.technology.therapeutics.pdf).
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David W. Moskowitz, MD, MA(Oxon.), FACP
Chairman, CEO & Chief Medical Officer
GenoMed, Inc.
"The public health company(TM)"
 
9666 Olive Blvd., Suite 310
St. Louis, MO 63132
website: www.genomed.com

Cell phone 314-378-7864
Office phone 314-983-9938
FAX 314-754-9772
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RichardMEL
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« Reply #2 on: January 22, 2011, 09:00:24 PM »

Comment: It's not just the US (though yes, INS and DHS do not make the US a very welcoming place, but that's a whole other issue in my book - still can't wait to land at SFO or SEA and have my picture taken and fingerprints taken, because that means I'm BACK!!!  :rofl;). Anyhoo back to the topic at hand - there's a paitient in my (er, my ex) dialysis unit who is English, but originally from Ghana. He's actually a doctor himself, and has been trying to get his uncle a visa to come for a live donation. Apparently they were stuck in the visa process for over a year (I am not certain what the hold up was). I just talked to him yesterday and he told me FINALLY the visa was granted, which is obviously a big first step to getting his uncle over and getting that transplant. So, it's not just the US of A. It's Australia too. I hate to say this, but I am sure there is more than a little bit of profiling going on in this respect - if the guy was from say Germany or Canada I doubt he would have the same level of problems as he would being from Africa - in a similar vein to the Mexican issue in the US. Authorities are terribly afraid that folks will get visas, often with the best of stated intention, and then disappear into the community.

On a personal note on my very first visit to the United States in 1994 I was treated exactly this way! I entered at Honolulu (having just endured 8 hours flying from Auckland being squished into my seat by a H U G E moari rugby player next to me - and I was NOT going to complain to him!!) and it's 5am HNL time, hot and sticky and basically the INS guy who processed me was immediately suspect about me. Why? I had a brand new, blank passport, I was visiting friends I kenw from the Internet (remember, this is 1994... it wasn't very common back then) who I had not met before just emailed with. I had all their names and addresses typed up though (thank God!) so could show him, I had my paper ticket proving I was flying to London in like 10 days time, but he still was basically treating me like he thought I was going to fly into Denver that afternoon and go illegal (from Australia? Really?  :rofl;). I know they were just doing their job, but it wasn't the best welcome.

Of course since them I've entered the US maybe 20-30 times, and in general they treat me well. I guess my record of coming and going is sufficient that they're not worried that I pose a risk to them. What little do they know!!! bwahahahahaha.... :rofl;
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3/1993: Diagnosed with Kidney Failure (FSGS)
25/7/2006: Started hemo 3x/week 5 hour sessions :(
27/11/2010: Cadaveric kidney transplant from my wonderful donor!!! "Danny" currently settling in and working better every day!!! :)

BE POSITIVE * BE INFORMED * BE PROACTIVE * BE IN CONTROL * LIVE LIFE!
DrMoskowitz
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« Reply #3 on: January 23, 2011, 07:48:38 AM »

I'm working with a scientist now from Ghana who's friends with the Minister of Health. Only problem is, the cabinet just got reshuffled, and his friend no longer handles health. So after 4 months of planning, we're back to square 1. We're trying to get the new Minister of Health's attention. The goal is to make Ghana dialysis-free in 5 years.

Australia, although I visited there in 1998, had no interest in preventing 90% of dialysis. It could be because I was only talking to nephrologists on that trip, and not ESRD patients and their relatives (i.e. potential future patients).

I also have a contact in Turkey, at the Ministry of Health, and Pakistan. My guess is that many countries will become dialysis-free before the US even hears that it's possible.
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**********************************************
David W. Moskowitz, MD, MA(Oxon.), FACP
Chairman, CEO & Chief Medical Officer
GenoMed, Inc.
"The public health company(TM)"
 
9666 Olive Blvd., Suite 310
St. Louis, MO 63132
website: www.genomed.com

Cell phone 314-378-7864
Office phone 314-983-9938
FAX 314-754-9772
email: dwmoskowitz@genomed.com
**************************************
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