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A Hidden Pain, Padma Lakshmi Tells her Story

Why a famous beauty like ‘Top Chef’ host Padma Lakshmi is talking about a very unglamorous disease like endometriosis.

For Padma Lakshmi, a former model, and host of Bravo’s “Top Chef,” the problem began when she was a teenager.

From Newsweek: A Hidden Pain
Newsweek: A Hidden Pain

“I’d always had very bad menstrual cramps, and they got progressively worse over the years,” Lakshmi says.

She tried every new pain medication that hit the market, but nothing helped much. Eventually, she found herself relying on the powerful painkiller Vicodin to get her through the worst days of each month.

“I can’t tell you how many jobs I had to cancel because I was completely bedridden,” she says. “Sometimes, I would spend four days in bed.” Her mother had suffered the same symptoms. “I thought this was my lot in life,” Lakshmi says.

Lakshmi Meets Dr. Tamer Seckin

It wasn’t until 2006 after she had to leave a photoshoot because the bleeding and pain overwhelmed her, that her physician sent her for a consult to Dr. Tamer Seckin, a New York laparoscopic surgeon who specializes in endometriosis. After taking her medical history and doing a physical exam, Seckin told Lakshmi that he was fairly sure her problem wasn’t bad cramps but severe endometriosis.

What causes endometriosis?

Doctors believe endometriosis occurs when bits of the uterus’ lining normally dispelled during menstrual periods end up in the abdominal cavity. Doctors think this may occur when some of this tissue inadvertently backs up through the fallopian tubes. Others suspect that some women are born with displaced tissue. In some women, these clumps of tissue are able to take root and grow outside the uterus. Like the uterine lining, this tissue is hormone-sensitive, so it expands and bleeds with a young woman’s monthly cycle. Over time, lesions, scar tissue, or adhesions may also form. They may cause damage to a woman’s abdominal, pelvic, and intestinal areas. They may also lead to high levels of pain, usually around the time of her period (but not always).

Because few women are familiar with its symptoms and there is no simple screen. It often takes 10 years before an accurate diagnosis is made. Even Lakshmi, who went to top-flight doctors in New York and Los Angeles, was age 36 before she got her diagnosis. In Lakshmi’s case, Seckin suggested laparoscopic excision surgery. He meticulously removed the tissue in a procedure that took four hours.

“And that was the first of four surgeries,” Lakshmi says.

But as more and more of the tissue was excised, Lakshmi started to feel better for the first time in decades.

“Now I’m a different person,” she says. “I hid a lot of my pain for a long time because I thought people would think I was exaggerating. I suspect that even some of the people who are nearest to me probably felt that way to some degree.”

Lakshm and Seckin found The Endometriosis Foundation of America

The better she felt, however, the more frustrated she became that she’d had to wait so long for effective treatment of such a common disorder.

“She posed the same question that many of my patients have raised: Why didn’t anyone figure this out about me decades ago? There’s so much misunderstanding and confusion. I encouraged her to talk about it, because if she doesn’t, who will?”

That thought inspired Seckin and Lakshmi to launch the Endometriosis Foundation of America. The New York-based group hopes to raise awareness, improve education, press Congress for more research money, and lobby medical schools to teach students more about the disorder. They want more women to become familiar with the symptoms.

Diagnosing endometriosis

Dr. Aaron Styer, a Harvard reproductive endocrinologist who specializes in endometriosis research and treatment, says patients whose pelvic pain is not responding to over-the-counter pain medications should not assume that they are simply dealing with regular menstrual cramps or PMS. Doctors can use vaginal ultrasound and a physical exam to narrow down which women with pelvic pain are most likely to have it. But the diagnosis cannot be confirmed until suspect tissue has been surgically excised and biopsied.

Drug treatments

Depending on the woman’s symptoms and age, some doctors initially treat the condition with a range of pain medications and hormone suppressants. GnRH agonists, the hormone suppressants commonly prescribed, effectively shrinks the tissue, reduces pain, and stops menstrual bleeding. It does so by shutting off ovarian production of estrogen and creating drug-induced and temporary menopause. The downside is that many women exchange one set of miserable symptoms for another, as they plunge into a sudden (and temporary) menopause. Common side effects include hot flashes, vaginal dryness, sleeplessness, headaches, and loss of bone density. Styer says there is also very little known about this treatment’s long-term safety, particularly for younger women who still want to start families. (Endometriosis stops being a problem once a woman reaches menopause and her periods stop.)

“The other problem with drug treatment” adds Dr. Harry Reich, one of the pioneers of laparoscopic surgery “is that it has never cured anyone”.

He says that while attempts to subdue the growth of these cells with lasers and other forms of electrical surgery have largely proved disappointing, laparoscopic excision done by a skilled and experienced surgeon can often prevent the condition from returning. Seckin adds that these clean-up surgeries can sometimes help women whose infertility is related to endometriosis get pregnant without in vitro fertilization.

“Ten years ago, endometriosis surgeries were looked at as a gimmick,” he says. “But now we’re getting respect and attention.”

Questions about surgery

But that doesn’t mean surgery is without downsides too. Styer says there are relatively few surgeons around the country who specialize in this procedure. Reich suggests many insurance companies still don’t have a diagnosis code for the surgery and may balk at paying.

“But women who have not gotten relief by other methods and are really persistent can sometimes get them to cover the surgery,” Reich says.

In the meantime, research continues.

“Studies indicate that up to 80-90% of all women eventually have some of this tissue displaced in their pelvic region”, Styer says. “But only a minority experience problematic proliferation. We still need to understand what it is about specific patients that allow this tissue to form in the pelvis, to recruit a blood supply, and maintain itself over years”.

While this area of gynecologic medicine has traditionally been underfunded, he says it’s getting more attention now. And some of the new stimulus money is being spent on it. Lakshmi says she hopes to tour college campuses for the foundation and encourage women in pain to seek help.

“I want to educate other women so they don’t have to go through what I went through,” she says. “If we could find this earlier, more women could have more productive lives. If you’re having bad cramps all the time, you need to go and get this checked out.”

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Disclaimer: The information offered on the website is intended to educate users on health care and medical issues related to endometriosis. Any information presented should not be considered or used as a substitute for, medical advice, diagnosis, or treatment. You should always talk to your health care provider for specific questions regarding personal health or medical conditions.

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