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(单词翻译:双击或拖选)
For patients with sickle1 cell disease, fertility care is about reproductive justice
Teonna Woolford has always said that when it came time to build a family, her ideal would be to have six kids.
Why six?
"I don't know where that number came from. I just felt like four wasn't enough," says Woolford, a Baltimore resident. "Six is a good number."
Woolford, 31, was born with sickle cell disease. The genetic3 disorder4 affects patients' blood cells. They become misshapen, which makes it harder for the blood to carry oxygen and flow throughout the body. This can cause strokes, organ damage and frequent bouts5 of excruciating pain.
Sickle cell disease affects an estimated 100,000 people in the U.S. and the vast majority of them are Black. Federal and charitable dollars dedicated6 to sickle cell pale in comparison to other less common diseases that affect a majority white patients.
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This story was produced in partnership7 with Kaiser Health News.
Physicians and researchers say the disease is a stark9 example of the health inequities which pervade10 the U.S. health system. A poignant11 expression of this, patient advocates say, is the silence around the impact on fertility, and lack of reproductive and sexual health care for the young people living with this complex disease.
Crushing hopes for fertility
Woolford has lived through the entire gamut12 of sickle cell complications. By 15, her hip8 joints13 had become so damaged that she had to have both hips14 replaced. She was dependent on frequent blood transfusions15 to reduce pain episodes and vascular16 damage, and her liver was failing.
"So many complications, infections, hospitalizations, and so by the time I graduated high school, I just felt defeated [and] depressed," says Woolford, who first spoke17 with an NPR reporter from a hospital bed in Baltimore, Maryland. She'd experienced a sickle cell pain crisis a few days earlier, and was still receiving pain medication and intravenous fluids.
In her late teens Woolford sought out a bone marrow18 transplant: a treatment that enables sickled19 cells in the patient's body to be replaced with healthy cells from a stem cell donor20. The procedure comes with risks, and not everyone is eligible21. It also relies on finding a compatible donor match. But if it works, it can free a person from sickle cell disease forever.
Woolford couldn't find a perfect match, so she enrolled22 in a clinical trial where doctors could use even a half-matched donor.
As part of the bone marrow transplant, patients are first exposed to chemotherapy, which can impair23 or eliminate fertility.
Woolford hesitated. After all, her ideal family included six children.
When she told her doctor about her worry, his response crushed her. "This doctor, he looked at me and he was like, 'Well, I'll be honest, with all the complications you've already had from sickle cell, I don't know why you're even worried about this process making you infertile24 because you're probably already infertile.'"
Even without a transplant, sickle cell disease can damage patients' bodies in ways that can affect their ability to have children, according to Dr. Leena Nahata, a pediatric endocrinologist at Nationwide Children's Hospital in Ohio.
For women, chronic25 inflammation and sickling26 of blood cells in the ovaries can make it harder to get pregnant. For men, sickled blood can jam inside the blood vessels27 of the penis, and that can cause painful, unwanted erections which last for hours. This condition, called priapism, can damage sexual function and decrease sperm28 count.
And it's not just the disease. Researchers are evaluating how some widely-used treatments may affect fertility — for example by decreasing sperm count.
"It remains29 unclear how that translates directly to fertility outcomes, but at least raises the concern that this may be an issue," Nahata says.
Even more concerning to Nahata were the results of a small study she co-authored that showed some patients are unaware30 of the many fertility risks related to sickle cell disease.
Would hope for a cure mean giving up on fertility?
Woolford was only 19 when her doctor shocked her by telling her she was probably already infertile. But no one could be sure, so she held out hope that she might still undergo a procedure to preserve her fertility, before undergoing the chemotherapy required for the bone marrow transplant.
After extensive research, she learned egg freezing could cost more than $10,000, her insurance wouldn't cover it, and she couldn't afford that on her own.
Woolford wondered if maybe she could find another way to pay for egg freezing. "So I started looking into financial resources. And I saw all these foundations [that] give away grants. But you had to have a diagnosis31 of cancer," she says.
"So long story short, I went through with a [bone marrow] transplant, kind of feeling like if I was going to be cured from sickle cell, it'd be a fair tradeoff to give up my dream of biological children."
Unfortunately, the partial-match transplant did not work. Woolford's body rejected it.
"So, here I am. I am 30, still have sickle cell disease and I'm infertile," she says.
A grim thought still sometimes pops up in Woolford's mind: Maybe if she had cancer instead of sickle cell, her dreams of having biological children could still have come true.
How systemic racism32 affects access to care
The first description of sickle cell disease in medical literature was published over a century ago. Because the vast majority of sickle cell patients in the U.S. were Black, it quickly became labeled as a "Black disease," and with that came a legacy33 of systemic racism that still affects patients today.
Black patients tend to have less social capital and fewer resources, according to Dr. Lydia Pecker, a sickle cell disease researcher and assistant professor of medicine at Johns Hopkins University. Pecker has studied fertility in sickle cell disease, and says there's a stark contrast between resources available to cancer patients versus34 sickle cell patients, when it comes to fertility treatment.
"There are any number of foundations, large and small, that help support and pay for fertility preservation35 for people with cancer," Pecker says. "Those foundations actually work with fertility preservation centers to negotiate lower rates for affected36 people."
There are clear clinical guidelines stating children with cancer going through chemotherapy should be referred for fertility preservation.
Children with sickle cell disease going through transplants are exposed to chemotherapy too, "but we don't really have guidelines like that yet for people with sickle cell disease," Pecker says.
It's not a perfect comparison, she adds, because the kinds of chemotherapy drugs used in pediatric cancer are different from the chemotherapies used in sickle cell treatment. But fertility preservation can be crucial when there is any risk of treatment-associated fertility impairment. Without clear and widely adopted clinical guidelines, sickle cell patients may not get referred to appropriate care.
Pecker says current medical practice forces sickle-cell patients to make a difficult choice: "Like, you can have treatment or you can have fertility. But what we say in cancer care is you can have treatment and you can have fertility."
Expensive treatment and fighting for access
In the U.S., health insurance coverage37 for fertility preservation and treatment is not guaranteed and varies from state to state. Only eleven states have laws that mandate38 coverage for fertility preservation for patients who undergo treatments that could imperil their ability to have biological children – usually referred to as iatrogenic treatments – like chemotherapy or radiation.
But even those laws don't always help, says Dr. Irene Su, an OB-GYN at the University of California San Diego, who researches fertility preservation policies.
Su says these laws are usually very vague in terms of who qualifies: "If you give insurers room to interpret, it's possible that they can be very broad, or they can be very narrow."
This means that many sickle cell disease patients who don't have this coverage are forced to pay out of pocket.
Phillip Sanders of Arkansas was a sophomore39 in college when his sickle cell disease complications ramped40 up.
"By 2016, that whole year, I spent 60 percent of my life in the hospital," he says.
Not long after, he married his college sweetheart. They wanted to have children, but were unable to get pregnant. A doctor then told them their best bet was to undergo intrauterine insemination, a fertility treatment where the highest-quality sperm is selected and inserted directly into the uterus.
Sanders' wife got pregnant after four attempts, but none were covered by insurance.
"It's so expensive. You're talking about thousands of dollars each try," Sanders says. "I mean, we had to, of course, borrow money. Because, you know, at the same time, I was going through school, opening a business, and I was in the hospital, always. So it was extremely tough."
Like Woolford, Sanders enrolled in a clinical trial for a bone marrow transplant, and it was a success.
He is now 31, is sickle cell disease free and has a son, Phillip, Jr.
Teonna Woolford for her part, has had to focus on other goals. After her transplant failed, the ongoing41 toll42 of the disease on her body continued. She has had to come to terms with the impossibility of her ever having a biological child of her own.
Woolford launched a new nonprofit, The Sickle Cell Reproductive Health Education Directive, to raise awareness43 of fertility issues at medical conferences and among patients. A future goal for the organization is to provide financial grants to sickle cell patients struggling to pay for fertility preservation and treatments.
Most days, Woolford finds the work empowering. On other days, she admits it reminds her of the bleak44 personal reality that she will probably never conceive a child.
"It's really hard, because I don't think a lot of people realize that I'm fighting for something that I didn't have access to," she says.
At this point, she said, it's no longer a medical justice fight. It's a reproductive justice one.
1 sickle | |
n.镰刀 | |
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2 transcript | |
n.抄本,誊本,副本,肄业证书 | |
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3 genetic | |
adj.遗传的,遗传学的 | |
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4 disorder | |
n.紊乱,混乱;骚动,骚乱;疾病,失调 | |
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5 bouts | |
n.拳击(或摔跤)比赛( bout的名词复数 );一段(工作);(尤指坏事的)一通;(疾病的)发作 | |
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6 dedicated | |
adj.一心一意的;献身的;热诚的 | |
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7 partnership | |
n.合作关系,伙伴关系 | |
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8 hip | |
n.臀部,髋;屋脊 | |
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9 stark | |
adj.荒凉的;严酷的;完全的;adv.完全地 | |
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10 pervade | |
v.弥漫,遍及,充满,渗透,漫延 | |
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11 poignant | |
adj.令人痛苦的,辛酸的,惨痛的 | |
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12 gamut | |
n.全音阶,(一领域的)全部知识 | |
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13 joints | |
接头( joint的名词复数 ); 关节; 公共场所(尤指价格低廉的饮食和娱乐场所) (非正式); 一块烤肉 (英式英语) | |
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14 hips | |
abbr.high impact polystyrene 高冲击强度聚苯乙烯,耐冲性聚苯乙烯n.臀部( hip的名词复数 );[建筑学]屋脊;臀围(尺寸);臀部…的 | |
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15 transfusions | |
n.输血( transfusion的名词复数 );输液;倾注;渗透 | |
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16 vascular | |
adj.血管的,脉管的 | |
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17 spoke | |
n.(车轮的)辐条;轮辐;破坏某人的计划;阻挠某人的行动 v.讲,谈(speak的过去式);说;演说;从某种观点来说 | |
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18 marrow | |
n.骨髓;精华;活力 | |
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19 sickled | |
vt.用镰刀割…(sickle的过去式与过去分词形式) | |
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20 donor | |
n.捐献者;赠送人;(组织、器官等的)供体 | |
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21 eligible | |
adj.有条件被选中的;(尤指婚姻等)合适(意)的 | |
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22 enrolled | |
adj.入学登记了的v.[亦作enrol]( enroll的过去式和过去分词 );登记,招收,使入伍(或入会、入学等),参加,成为成员;记入名册;卷起,包起 | |
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23 impair | |
v.损害,损伤;削弱,减少 | |
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24 infertile | |
adj.不孕的;不肥沃的,贫瘠的 | |
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25 chronic | |
adj.(疾病)长期未愈的,慢性的;极坏的 | |
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26 sickling | |
镰状化,镰状形成 | |
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27 vessels | |
n.血管( vessel的名词复数 );船;容器;(具有特殊品质或接受特殊品质的)人 | |
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28 sperm | |
n.精子,精液 | |
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29 remains | |
n.剩余物,残留物;遗体,遗迹 | |
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30 unaware | |
a.不知道的,未意识到的 | |
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31 diagnosis | |
n.诊断,诊断结果,调查分析,判断 | |
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32 racism | |
n.民族主义;种族歧视(意识) | |
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33 legacy | |
n.遗产,遗赠;先人(或过去)留下的东西 | |
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34 versus | |
prep.以…为对手,对;与…相比之下 | |
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35 preservation | |
n.保护,维护,保存,保留,保持 | |
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36 affected | |
adj.不自然的,假装的 | |
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37 coverage | |
n.报导,保险范围,保险额,范围,覆盖 | |
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38 mandate | |
n.托管地;命令,指示 | |
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39 sophomore | |
n.大学二年级生;adj.第二年的 | |
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40 ramped | |
土堤斜坡( ramp的过去式和过去分词 ); 斜道; 斜路; (装车或上下飞机的)活动梯 | |
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41 ongoing | |
adj.进行中的,前进的 | |
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42 toll | |
n.过路(桥)费;损失,伤亡人数;v.敲(钟) | |
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43 awareness | |
n.意识,觉悟,懂事,明智 | |
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44 bleak | |
adj.(天气)阴冷的;凄凉的;暗淡的 | |
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