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Prevention article



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jphilpo
Posts: 169
Joined: Mar 2010
March 28, 2011 - 9:13am

Hi all,

I just read an interview with Robin Roberts from Good Morning America, In Prevention magazine.
It was really good. She addressed "post chemo" depression and the fact that no one really tells you about this. Just reading these boards can testify to that! She also mentioned that tamoxifen doesn't work for her, but didn't say why. I am going to e-mail her and thank her for the article and to ask about the tamoxifen.

Post breast cancer depression is real. I hope one day it will be included in the "whole" breast cancer teatment, from initial diagnosis and beyond.

Just thought you all would like to read the article.

Jean

MAJW
Posts: 2030
Joined: May 2009
March 28, 2011 - 9:16am

Robin is triple negative...as am I...Tomoxifen is for bc that is estrogen positive...

jphilpo
Posts: 169
Joined: Mar 2010
March 28, 2011 - 9:37am

Oh, Thanks for the info! I will just thank her for the depression info.

Mitzi333's picture
Mitzi333
Posts: 483
Joined: Feb 2011
March 28, 2011 - 9:59am

For the information. Which month and year is Robin's article posted in Prevention. I'd love to read it.

Have a Wonderful Day~
Mitzi ;0)

jphilpo
Posts: 169
Joined: Mar 2010
March 28, 2011 - 10:11am

Hi Mitzi,

It was March,2011.

You have a wonderful day,too!

Jean

jphilpo
Posts: 169
Joined: Mar 2010
March 28, 2011 - 10:10am

Hi Mitzi,

It was March,2011.

You have a wonderful day,too!

Jean

Mitzi333's picture
Mitzi333
Posts: 483
Joined: Feb 2011
March 28, 2011 - 6:33pm

Jean... I'm going to get that Prevention magazine. ;0)

CypressCynthia's picture
CypressCynthia
Posts: 2359
Joined: Oct 2009
March 28, 2011 - 10:11am

I agree completely. There is a movement afoot nationally to include palliative care (see below) of cancer patients from the time of initial diagnosis. Research is beginning to show a trend of increased cancer survival in patients who have received palliative care from initial diagnosis. Of course, to me, the big question is why do we need these studies when it is commonsense...sigh. Seriously though, without the studies there would be no possible future reimbursement for palliative care, so I really am grateful to the scientists doing them. My center does not yet do this, but I am hoping....

"Palliative care is comfort care given to a patient who has a serious or life-threatening disease, such as cancer, from the time of diagnosis and throughout the course of illness. It is usually provided by a specialist who works with a team of other health care professionals, such as doctors, nurses, registered dieticians, pharmacists, and social workers.
Palliative care is different from hospice care. Although they share the same principles of comfort and support, palliative care begins at diagnosis and continues during cancer treatment and beyond.
Hospitals, cancer centers, and long-term care facilities provide palliative care. Patients may also receive it at home. Physicians and local hospitals can provide the names of palliative care or symptom management specialists.
Palliative care addresses the emotional, physical, practical, and spiritual issues of cancer. Family members may also receive palliative care.
Research shows that palliative care improves the quality of life of patients and family members, as well as the physical and emotional symptoms of cancer and its treatment."

Link from the NCI:
Palliative Care in Cancer

Link from the AMA:

Early palliative care lengthens survival for lung cancer patients

Lynn Smith
Posts: 804
Joined: Mar 2011
March 28, 2011 - 10:54am

Thank You for the answer about Tamoxifin.I take it and I was told it was a estrogen blocker.

The thing I see on this board is something my doctors never talked to me.Just said take tamoxifin, a estrogen blocker.Also I was never give other statistics like some I read about.

Here is what I got.DCIS non invasive, no nodes and tumor 1/2 centimeter. What is grade??? Do you see it here with my diagnosis. Is it tumor size??? I see so many more things I know nothing about.

Lynn Smith

CypressCynthia's picture
CypressCynthia
Posts: 2359
Joined: Oct 2009
March 28, 2011 - 11:53am

There is a lot to learn, but don't stress, because you will learn it with time.

Tumors are graded from 1 to 3. They are graded by:
•How much the cancer cells look like normal cells
•How many of the cancer cells are in the process of dividing
Thus, a tumor whose cells look abnormal and are fast-growing will most often be classified as Grade 3 (poorly-differentiated). Grade 1 is the most like a normal cell (a good thing). Grade 2 is in between.

Katmy
Posts: 93
Joined: Mar 2011
March 28, 2011 - 12:00pm

I want to thank you for the informative comments you post. I have tried in the past to email individuals and cannot figure out how to do it. Yet, again here, you provide resourceful information with compassion. Rather than think "thank you" quietly, I'll say it here. Hope you read it one day.

Thank you

CypressCynthia's picture
CypressCynthia
Posts: 2359
Joined: Oct 2009
March 28, 2011 - 12:11pm

You are so very welcome. I enjoy doing any little thing I can do to help and, if this helps, I'll continue. So thank you for letting me know that it is useful for you. I'm basically a nerd and can't help myself ;-)

laughs_a_lot's picture
laughs_a_lot
Posts: 1144
Joined: Mar 2011
March 28, 2011 - 3:04pm

Insurance companies are of course not wild about the idea of providing another service that would be most helpful. From the standpoint of my history in mental health, I am for the idea of pallative care. After all the impact of this diagnosis on not only the person themselves but also thier family members can create complicated issues for even a family who's mental health issues are at a minimum. Our lives are much like a mobile. When one part of the mobile has extra weight put on it (from cancer, bankruptcy, or any number of tragic events)the mobile moves in a differnent fashion and sometimes crashes into other parts of the mobile until it reaches a new equalibrium. I am very aware of the circle of impact that this disease places upon my spouse, children, grandchildren, co workers, and church members. We are not an island, we live in community.