Location
New York,
NY
I am president of a print and digital media business specializing in writing and producing a web-based training and E-learning programs for health care, education and social service organizations.
My company (www.campbelldevelopmentgroup.com) also operates an e-learning site for 3-7 year old children called "Can Do" Street."(www.candostreet.com)
During my career, I've worked as a writer, author, former director and executive director for several nonprofit organizations.
I am a 2x breast cancer survivor and former director of the American Cancer Society Patient Navigator Programs in 14 NYC hospitals.
After my second cancer, I launched (www.noboobsaboutit.com) a blog that stresses getting through treatment and on with life after breast cancer. A sister site blog ( www.onyourcancerjourney.com) offers support and resources to Chinese speakers with breast or gynecological cancers.
way to be well created 10.21.10
Why Did You Wait So Long?
Doctors in the breast health centers, where I navigated, would often refer a new patient to me immediately following informing her, or in rare cases him, of a breast cancer diagnosis.
Those patients presenting with a visibly obvious tumor or one easily felt in a breast self exam often were asked by the examining physician, "Why did you wait so long to see a doctor"? Many times when they reached me, crying and badly shaken, they would spontaneously share why they waited so long to get help.
Many of the patients were new immigrants with language barriers who had little knowledge of breast cancer, breast screenings and the need for regular check ups. Most came from countries where health care was a luxury and women sought medical attention when pregnant, in severe pain or seriously ill. Preventative medicine and early detection practices were foreign to them.
Some said they could not afford to take time from work without losing a day's pay. A few women shared that they could not get to the doctor since there was no one to take care of their young children during they day. Young women, with a new baby, said they thought the lump was something to do with nursing. Some had even checked it out with a doctors in neighborhood clinics who told them that they were too young for breast cancer and that it was probably a blocked milk duct.
Still others gave cultural or religious reasons for not seeking care until the tumor was obvious to the touch or could be seen. Some stated that they were not allowed to touch themselves and therefore didn't check their breasts. Others shared they were not permitted to be examined by a male doctor and did not know where a female doctor would be available to examine them. Some shared that their husbands decided when they could get medical care and until they were convinced the lump was growing, they did not give permission.
Others shared their fears about treatment; loss of hair, loss of a breast. What would their spouses or significant others do?
After every visit, I was left to wonder what it was going to take to reach women in communities that live apart from mainstream society and have them take advantage of free, accessible, breast health care while their cancers were still small enough for a more favorable outcome.
Many organizations provide literature in a variety of languages and do outreach in these communities, but more needs to be done. Any ideas?
A very powerful piece, obviously with no simple answer. As you've identified, the reasons for women not seeking earlier treatment are multi-faceted. For the woman whose culture dictates the husband decides when they get help, accessibility is relative to the larger issue of her realities being a barrier to seeking medical attention.
As to the question we might naturally think of (Why did you wait so long), one hopes it is asked with the same goal you had in listening to their spontaneous sharing: to identify ways for preventing delays for others to get help. I can certainly envision it producing feelings of guilt on top of an already traumatizing experience.
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