Different Governmental Strategies For Cancer Survivorship Care Essay

Moving forward, it would be essential to begin the interaction with compassion, and honesty. Additionally, every attempt should be made to develop a trusting relationship. B. B. was at a greater risk of breast cancer due to her obesity, sedentary lifestyle, and alcohol intake (Ferri, 2017). Therefore, screening practices needed to be conveyed and understood. Moreover, education related to minimizing risks needs to be incorporated into the plan. The strategies for this could include genuine caring dialog that allows time for listening and

Breast cancer affects one in every nine women in Britain, 45,000 women every year are diagnosed with it in some form or stage of development. Life style and cognitive interventions, i.e. counselling and psychotherapy can play an important part in how the patient deals with cancer in their lives and how they recover.

Pain is one of the most common and feared complications of cancer. It is exacerbated by stress, anxiety, fatigue, and malaise which accompany advanced cancer. Pain is generally absent in the early stages of cancer, but it is a significant factor as the illness progresses to advanced stages. Cancer-associated pain can arise from a variety of direct and indirect mechanisms including direct pressure, obstruction, and invasion of a sensitive structure, stretching of visceral surfaces, tissue destruction, infection, and inflammation (McCance 2010). Pain is generally accepted as whatever the patient says it is, wherever the patient says it is. Treatment of pain and its associated symptoms is a primary responsibility of the healthcare team. Treatment modalities for pain include the use of opioid analgesics, patient-controlled analgesia, psychological interventions, and preventing recurrence of pain. Reinforcing the reporting of pain by the patient is important, as is a respect for the social and cultural differences with respect to pain perception.

The study was composed of two groups. The control group received the usual breast cancer care. The experimental group received the usual care and some additional components including four teaching sessions completed within the first month and regular follow-up calls. Intervention

Breast cancer is most common cancer among women. Any woman can get it despite not having family history of breast cancer. It is important to study cancer to fully capture the mystery that is cancer. The journal “Understanding the Experience of Dominican American Women Living With Late-Stage Breast Cancer: A Qualitative Study” gives us a look inside what a cancer patient goes through.

Women may experience a range of emotions with the diagnosis as well as throughout the treatment as a result of breast cancer, such as: sadness, anger, fear and guilt. Therefore, it is essential to closely monitor the client for their psychosocial adjustment to the diagnosis and treatment, and identifying those that need further psychological interventions (Boehmke & Dickerson, 2006). This includes being aware of the impact the diagnosis will have on the family members and loved ones; as their support is warranted as possible caregivers during the process. Appropriate nursing diagnoses for a woman with a new verdict of breast cancer may include (but not limited to): disturbed body image related to loss of hair due to chemotherapy; fear related to the diagnosis and prognosis of the disease; and knowledge deficit of cancer treatment options and reconstructive surgery. Other diagnosis will be added and removed as the patient decides if she wants treatment; and the psychological, psychosocial, and physical changes that may affect her quality of life. For instance, after a mastectomy the patient may have a nursing diagnosis of: risk for disturbed body

According to the Agency for Healthcare Research and Quality (AHRQ) despite the evidence that consistently indicates that palliative care and provision of access to hospice is essential to end-of-life comfort and quality of life in the final stages of terminal illness, it is still not used effectively or sufficiently (2012). In fact, Ctarlson et al., (2010) determined that in spite of the fact that there has been a 41% increase in the total number of hospice service providers in the United States since 2000, that at least 60% of terminally ill Americans still die without the benefit of hospice services. This is because a variety of factors can create an availability gap, or make it increasingly difficult for individuals to access hospice care. These factors generally include: geography, race, age, and socioeconomic capital (Silveira 2011). Each of these factors can be individually examined, as they relate to care accessibility.

An article for “Coping (with Cancer) Magazine” and, any former science teachers are raising their eyebrows in disbelief, but articles for Environmentalists for Nuclear Energy and Go Nuclear, Inc. I’m also working on another children’s book. The little girl I titled Tickles Tabitha after is all grown up and a talented artist. I’d like her to do the illustrations. Unfortunately, this may take a while as she received a fellowship to UNC, and has way too many internships and school related professional grad school functions to work for free for her mother.

To date, The Project Medishare breast cancer initiative has provided care to 139 patients with breast cancer in nearly 2 years, becoming an integral part of the oncology community in Port-au-Prince. Project Medishare has worked in Haiti since 1994 and has partnered with Hospital Bernard Mevs since 2010 to provide trauma and critical care services, making the location an ideal place to implement a program involving chemotherapy. Before the implementation of this program, neither Project Medishare nor Hospital Bernard Mevs provided any kind of breast cancer care apart from mastectomies. The program has also helped provide the necessary infrastructure to begin collecting data on the epidemiologic profile and tumor biology of breast cancer in

There are different types of standard treatments that can be used such as the following: surgery, sentinel lymph node biopsy, radiation therapy, chemotherapy, hormone therapy, and targeted therapy (“Treatment Option Overview”). Although these are standard treatments, there are constant clinical trials going on to improve standard treatments or discover a new type of treatment that would benefit breast cancer patients even more (“Treatment Option Overview”). Once there is a chosen course of therapy, the patient will be put through several stages of cancer treatment—some making them thirsty or super sick. Ultimately, each and every cancer patient will need to have follow-up doctor visits to make sure the treatment is working (“Treatment Options Overview”). Everyone will heal at their own pace. It’s up to us, as family members, to be thoroughly educated on our loved ones’ treatment. We can better understand what they’re going through and it would make the healing process go by much faster. Medical treatment is important, but loving support from family heals anybody faster than any medical treatment that is

It is common for patients to experience feelings of anxiety and sadness, due to fear of the unknown. Patients may feel distressed and overwhelmed by their breast cancer diagnosis. As a nurse, it is important to encourage patients to express their feelings and to involve patients in their care and treatment. First, helping patients to understand their diagnosis and available treatments. Educating patients about their breast cancer type, location of the cancer, and what to expect during treatment. An intervention that may help patients cope with treatment includes exercise. According to Nursing and Health Sciences, “The longer people can maintain exercise habits, the greater the overall benefits for symptom relief” ( Narophong W, Lane A, Schafer

Breast cancer affects so many of us. Most of us will know someone who has been diagnosed with breast cancer. It may be our grandmothers, our aunts, our moms, our sisters, our best friends, our spouses, or ourselves. Breast cancer even strikes men. The likelihood is fairly high that we know someone who has been diagnosed with breast cancer. The shocking statistic is that breast cancer occurs in 85% of us who have no history of breast cancer in our family. Despite medical advancements, early detection, and the pink ribbon campaign every October, breast cancer is still the 2nd leading cancer cause of death in women.

The growing need for better quality cancer care (IOM, 2001) requires the understanding of the interacting factors (e.g. screening) and outcome (Lemon et al., 2003). Disparities in breast cancer care exist (Goss et al., 2011), moreover, patients with this disease fail to receive high-quality end of life care (e.g. pain and symptom management, end of life decision-making) (Katz & Hofer, 1994). Leaders in the care field need to create new strategies for the organizations in order to increase the care quality through the cancer treatment while maintaining the increased performance (Lemon et al., 2003). The IOM (2001) offer quality areas, dimensions to consider.

For many cancer survivors in the local community, hair loss may be difficult and can be very emotional. The emotional impact of hair loss can correlate with a person’s self-esteem, especially if their self-worth has been based on physical attractiveness. Wigs are helpful coping tools for cancer patient with hair loss. The Wig Drive left a possible emotional impact on the local cancer survivors in the community. Despite their initial concerns over the impact of hair loss, the local cancer survivors felt that the Wig Drive was empowering. Donating the wigs gave them a new image of themselves. The Wig Drive served as a support group for cancer survivors. It allowed survivors to build their confidence and gain their self esteem. The Wig

While the completion of treatment is excitedly anticipated, many cancer survivors would still be disturbed by the emotional and physical tribulation of their breast cancer trajectory (Surbone & Peccatori, 2006). This is because, the impact of cancer remains long even after treatment ended. Besides the common issues that accompany any cancer diagnosis, breast cancer survivors also have to deal with exclusive concerns such as decreased sexual function, relationship issues, fears about genetic inheritability of cancer and complications from this disease such as lymphedema (Hodgkinson, Butow, Fuchs, et al., 2007). Therefore, the completion of treatment does not equate to lesser need for health care. Long term health issues related to breast cancer survivors have thus emerged as a public health concern.