Bahamas Breast Cancer Initiative Foundation

Bahamas Breast Cancer Initiative Foundation Dedicated to improving and saving lives of individuals affected by breast cancer in The Bahamas. The Susan G.

It was through the efforts of Former US Ambassador to The Bahamas, Ned L. Siegel, his wife, Stephanie and BBCIF that Sunshine Insurance secured the Komen Race series for the Sunshine Insurance Race Weekend. During Ambassador Siegel’s tenure, his wife, Stephanie was diagnosed with breast cancer. While being treated, she was alarmed at the number of Bahamian women, particularly young women, being di

agnosed with breast cancer and decided to take action. The Siegel's founded the Bahamas Breast Cancer Initiative Foundation (BBCIF) in 2008. BBCIF was dedicated to genetic testing in order to ascertain why such a high percentage of Bahamian women were diagnosed with the disease. The Sunshine Insurance SGK Bahamas Race for the Cure® series officially debuted in January 2011, however, a SGKRFTC on Island began with the US embassy and the Siegel's in 2008. Today, it remains an important event on many people’s calendars – locally and internationally. Bahamas Race for the Cure® provides funding to local non-governmental organizations (NGOs) – BBCIF, the Cancer Society of The Bahamas, the Cancer Association of Grand Bahama, the Princess Margaret Hospital Foundation and the Sister Sister Breast Cancer Support Group. Komen Race for the Cure® Series is the world’s largest and most successful education and fundraising event for breast cancer ever created. OUR MISSION

The mission of the Bahamas Breast Cancer Initiative Foundation is to facilitate the collaboration of multiple partners to improve breast cancer care in The Bahamas. To provide the women of The Bahamas with a comprehensive breast cancer program to include education, early detection and care. To conduct and support clinical research and trials in The Bahamas translating the results into effective breast cancer treatment. BACKGROUND

The Bahamas Breast Cancer Initiative Foundation (BBCIF) is a public-private partnership that was formed in Nassau, The Bahamas, in April 2008.The Bahamas Breast Cancer Initiative sprung from the observations, commitment and dedication of The US Embassy, a group of Bahamian, American and Canadian, professionals, medical oncologists, radiologists, and survivors, united in their determination to improve breast cancer care in The Bahamas. THE ALARMING FACTS

Research has shown:

*48% of the women diagnosed with breast cancer in The Bahamas are under the age of 50.

* 20% of the women diagnosed with breast cancer in The Bahamas are under the age of 40.

*42 is the average age of the women diagnosed with breast cancer in The Bahamas.


*44% of the women diagnosed with breast cancer in the Bahamas present with late Stage 3 or late stage 4 breast cancer.

*43% of the women in The Bahamas who die from breast cancer , die under the age of 50.


*23% of the women in The Bahamas diagnosed with breast cancer carry the BRCA1 gene mutation - the highest known population in the world studied to date to carry this mutation. RESEARCH PROGRAM

The BBCIF program offered genetic testing and counseling to all newly diagnosed women with breast cancer and ovarian cancer in The Bahamas. In addition, testing was offered to unaffected relatives of women who are found to carry a mutation in the BRCA1 or BRCA2 gene. Ongoing studies are designed to determine the risk
of hereditary breast cancer in women in the Bahamian population. WHAT CAN BE DONE

Increase awareness about breast cancer and early detection through continuous public education and programs encouraging good diet, exercise and a healthy lifestyle. Promote early detection of breast cancer by advocating mammograms, clinical breast examinations and monthly breast self-exams. Establishing national guidelines for breast cancer screening in The Bahamas recommended by the Ministry of Health. Create a Patient Navigation Program tailored to the needs of The Bahamian women which will assist them in receiving proper treatment and care. Conduct medical research and translate results into breast cancer treatment and protection for the benefit of all Bahamian women.

16/02/2026

She survived ovarian cancer in 2003. Then breast cancer in 2012. And after a double mastectomy, she did something most celebrities avoid at all costs: she spoke—plainly, publicly, without varnish—about a chronic condition many patients live with but few ever hear named.

Her name is Kathy Bates, and long before illness entered the picture, she was already one of the most formidable forces in American film. By the early 1990s, Bates had secured her place in cinematic history with Misery—a performance so precise, controlled, and terrifying that it earned her the Academy Award for Best Actress. She became known not for glamour, but for gravity: women who were sharp-edged, intimidating, complex, and impossible to ignore.

Then, in 2003, ovarian cancer arrived—quietly, privately. Bates told almost no one. She went through treatment away from press cycles and inspirational headlines, recovered, and returned to work. For nearly a decade, the public didn’t know. Not because she was ashamed—but because she refused to let illness rewrite her identity or eclipse her craft. She didn’t want to become a story about survival instead of an actor doing the work.

For nine years, she succeeded.

Then came 2012. This time, it was breast cancer, and concealment wasn’t possible. The recommended treatment was a double mastectomy. The physical changes were irreversible, and the cultural expectations surrounding women’s bodies—especially older women in Hollywood—were unforgiving. At sixty-three, Kathy Bates made a choice that cut against industry instinct: she told the truth. She revealed not only the breast cancer, but also the ovarian cancer she’d survived in silence. Two diagnoses. Two recoveries. No dramatics. No performance of gratitude. Facts, stated plainly, and then—forward.

And then she did something even rarer.

She talked about lymphedema.

Lymphedema is a chronic condition that can occur when lymph nodes are damaged or removed during cancer treatment. The lymphatic system can’t drain fluid properly, leading to painful, often permanent swelling—most commonly in the arms. It can limit mobility, cause fatigue, increase infection risk, and require lifelong management. It is common. It is life-altering. And it is almost never discussed.

After surgery, Bates developed lymphedema in both arms. Compression sleeves became part of her daily life. So did physical therapy, constant monitoring, and planning around pain and swelling. Ordinary tasks required new calculations. Many survivors aren’t warned about it in advance; many don’t learn the word until they’re already living the reality.

So Kathy Bates said it out loud.

She became a national spokesperson for the Lymphatic Education & Research Network, using the visibility most celebrities guard to draw attention to something deeply unglamorous. She appeared publicly wearing compression sleeves. She explained what lymphedema is, how it happens, how it feels—and why silence harms patients. She didn’t sugarcoat survivorship. She spoke about what comes after cancer: the permanent changes, the chronic conditions, the truths that don’t fit into celebratory narratives.

And she did all of this while continuing to work.

In 2013, she joined American Horror Story, delivering performances so commanding they earned her multiple Emmy Awards—work that arrived in her mid-sixties, post-mastectomy, while managing chronic lymphedema. The awards mattered not as trophies, but as evidence: losing parts of your body does not mean losing authority; chronic illness does not cancel power; survival does not require disappearance.

Bates also spoke candidly about body image after mastectomy—the grief, the adjustment, the time it took to recognize herself again. She never claimed acceptance was immediate. She never pretended it was easy. She simply refused to vanish. She acted. She advocated. She lived.

Her humor became part of her honesty—not deflection, but ownership. Joking about compression sleeves wasn’t denial; it was control. “Survivor” wasn’t a marketing label to her—it was a fact earned through endurance. Her advocacy has had real impact: more patients are warned about lymphedema, more research is funded, and more survivors feel less alone knowing an Oscar-winning actress manages the same daily pain and limits they do.

Now in her mid-seventies, Kathy Bates is still working. Still speaking. Still insisting that what comes after cancer matters just as much as beating it.

She survived ovarian cancer.
Then breast cancer.
Then she refused silence.

She didn’t let illness end her story.
She let it give her purpose—and made room for millions of others to tell theirs too.

13/01/2026

Breast implant calcification is one of those slow-burn, cellular soap operas where your immune system plays both detective and demolition crew. It is not the implant “turning to stone.” It is your body quietly wallpapering it with minerals.

When any foreign object is placed in the body, including silicone or saline implants, the immune system immediately builds a fibrous capsule around it. Think of this as biological shrink-wrap made of collagen and fibroblasts. That capsule is alive, vascularized, and constantly remodeled.

Over years, especially decades, that capsule can undergo chronic low-grade inflammation. Macrophages keep bumping into the implant surface. Fibroblasts keep laying down collagen. Tiny areas of cell death appear in the capsule. And wherever dead or stressed tissue exists, calcium loves to show up.

That process is called dystrophic calcification.

It is the same thing that makes old scars, damaged heart valves, atherosclerotic plaques, or long-healed TB lesions turn chalky. The blood calcium level is normal. The tissue is what is abnormal.

The implant itself does not calcify. The scar capsule around it does.

Three main forces drive this.

#1 Time.

Calcification is rare in the first decade and increasingly common after 15 to 30 years. Many studies find visible calcium in more than half of implants over 20 years old.

#2 Mechanical irritation.

Implants move with every breath, every arm swing, every workout. That constant micro-friction irritates the capsule. Textured implants, in particular, create more micro-trauma and inflammation than smooth ones.

#3 Leakage and biofilm.

Even “intact” silicone implants slowly bleed microscopic silicone molecules. This is called gel bleed. The immune system reacts to it. Bacteria can also form thin biofilms on implant surfaces that never cause infection but keep the immune system switched on.

Chronic inflammation plus dying cells plus calcium in blood equals mineral deposition.

The calcium deposits start as dust. Over years they become gritty, then chalky, then sometimes rigid plates. On mammograms they can look like cancer, which is why very old implants complicate breast imaging.

Importantly, this is not rare, not mysterious, and not dangerous by itself. It is simply the biology of foreign materials living inside mammals for decades.

23/12/2025

There’s Still Time to Schedule Your $60 Mammogram! 💓

Doctors Hospital Health System remains committed to women’s health and the power of early detection. We’re offering $60 mammograms until December 31, so there’s still time to book your screening and prioritize your well-being.

Research shows that Bahamian women have the highest prevalence of inherited BRCA gene mutations in the world—over 25% of women with breast cancer carry this predisposition. Early identification can lead to preventative strategies and life-saving interventions.

With extended hours and Saturday appointments now available, we’re making it easier than ever for women to access high-quality, affordable imaging services.

📞 Call 302-4662 to schedule your mammogram.

23/12/2025

Doctors Hospital Health System (DHHS) announces that Dr. Charles Diggiss will transition from his role as Chief Executive Officer effective February 1, 2026, while continuing to serve as President. His tenure as President & CEO has been defined by transformational growth, clinical excellence, and a steadfast commitment to accessible, high-quality healthcare.

“It has been an honor and a privilege to lead this extraordinary institution as President & CEO” said Dr. Diggiss. “Doctors Hospital Health System is widely respected for its clinical standards, patient-centered care, and dedication to developing the next generation of healthcare professionals.”

Dr. Charles Diggiss began his medical career as a general surgeon and developed laparoscopy in general surgery at Doctors Hospital in the mid-1990s. Dr. Diggiss also developed the contracted Emergency Room physician services. Under his leadership, Doctors Hospital Health System (DHHS) evolved into one of the region’s leading private tertiary healthcare systems, earning international accreditation for safety and quality. The organization achieved six consecutive Joint Commission International (JCI) accreditations and became the first hospital in the region to receive this distinction.

During his tenure, Doctors Hospital Health System expanded to include two hospitals and 13 primary and specialty care clinics, launched the LAMP affordable care program, and established a NAECOB-registered allied health training institution. His commitment to philanthropy, strengthening patient care and employee programs, became a defining hallmark of his leadership. Today, the health system employs more than 800 team members and affiliated physicians.

“Serving Doctors Hospital Health System has been the privilege of my lifetime,” Dr. Diggiss said. “From my early days moonlighting at Doctors Hospital to cover nighttime patient needs in the early 1980s, to assuming the role of President and CEO in 2021, I have been inspired by our mission to provide exceptional care to every patient. I have a deep sense of gratitude for the confidence and trust that so many patients placed in me over the years. I am deeply grateful to our Board of Directors, leadership team, physicians, and associates, whose dedication made our success possible. I look forward to participating in this new role as Doctors Hospital Health System continues to advance healthcare delivery and improve lives.”

The Board of Directors will announce Dr. Diggiss’ successor as CEO imminently.

“Dr. Diggiss’ vision and leadership have been instrumental in shaping Doctors Hospital Health System into the trusted institution it is today,” said Felix Stubbs, Chairman of the Board of Directors. “We thank him for his extraordinary service.”

22/12/2025

🩵Why Compression Garments Can Cause Pain (and What It Means)🩵

Compression is often recommended for lymphedema—but for some people, it causes pain, burning, numbness, or makes swelling worse. That doesn’t mean compression is wrong. It usually means something important is being missed.

Common reasons compression can hurt:🦋

1. Wrong type of compression
Not all compression is made for lymphedema. Many people are given elastic/round-knit socks meant for venous disease. These can constrict, trap fluid, and increase pain in lymphedema. Flat-knit or short-stretch compression is often more appropriate.🦋

2. Poor or generic fit
Compression that is too tight, uneven, or not custom-measured can create pressure points, cut off circulation, or push fluid into the foot, ankle, or knee—causing pain and swelling.🦋

3. Advanced or fibrotic swelling
When swelling becomes hard or fibrotic, strong compression applied too quickly can be painful. These limbs often need gradual, professionally guided compression after softening the tissue first.🦋

4. Mixed conditions
Many people have both lymphedema and vascular disease, nerve issues, or lipedema. Compression that helps one condition can aggravate another if not carefully selected.🦋

5. Nerve sensitivity and inflammation
Lymphedema can irritate nerves. Compression may cause burning, tingling, or stabbing pain if nerve involvement isn’t addressed.
🦋
6. Skin and pressure intolerance
Fragile skin, infections, or inflammation can make compression feel unbearable—even when the garment “fits.”🦋



Important Truth🦋

Compression should never be unbearable or cause severe pain. Pain is a signal—not a failure.

Proper lymphedema care involves:
✔ Correct garment type
✔ Accurate measurements
✔ Gradual compression when needed
✔ Professional guidance
✔ Ongoing adjustments as the limb changes🦋

If compression hurts, it doesn’t mean “push through.”
It means pause, reassess, and get the right help.🩵🦋

22/12/2025

LE&RN is proud to be part of a growing global community advancing lymphatic research through collaboration and shared purpose.

This year took us from the inaugural launch of Australia’s first Centre of Research Excellence in Lymphoedema and Lymphatic Regeneration to the 6th International Lymphology Conference in Vienna, where leaders from around the world came together to move the field forward.

As Dr. John Tzou reminded us: “Act with purpose, lead with your heart, make a positive impact on the world.”

Together, we’re building a worldwide movement—one partnership, one discovery, and one step forward at a time. 💚

17/11/2025

Your lymph nodes do more than fight infection; they can also reveal if breast cancer has spread.

🔬Learn how lymph nodes are checked, why it matters and how it impacts treatment in our latest Know More blog: https://bit.ly/3LTsADI

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