06/10/2023
[ad_1] Resources for Spanish-Speaking Individuals Impacted by cancer/Recursos para personas
Read more
[ad_1]
Palliative and supportive care plays an important role in caring for children with cancer. Through palliative and supportive care, children and their families receive help with managing the various side effects of cancer and its treatment, including its physical, emotional, social, and financial effects.
In this podcast, Abby Rosenberg, MD, MS, MA, discusses what parents should know about pediatric palliative and supportive care, including what it is, what to expect when meeting with the palliative and supportive care team, and how this type of care helps support children with cancer and their families.
What is palliative and supportive care? [01:47]
How is palliative and supportive care different than hospice or end-of-life care? [03:20]
How can parents know if their child is ready to receive palliative and supportive care? [04:04]
How does the palliative and supportive care team provide support for children with cancer? [04:46]
What should parents and their children expect when meeting with members of the palliative and supportive care team? [05:41]
Does palliative and supportive care also include support for the parents and family members of children with cancer? If so, what does this support look like? [07:00]
Dr. Rosenberg is the chief of pediatric palliative care at the Dana-Farber cancer Institute and Boston Children’s Hospital in Boston, Massachusetts. Dr. Rosenberg has no relationships relevant to this content to disclose.
Was this podcast useful? Please subscribe, rate, and review cancer.Net Podcasts wherever you listen to podcasts. This prerecorded podcast can be listened to online or downloaded to your computer. A transcript is also available. For more information, visit the cancer.Net podcast page.
cancer.Net podcasts are edited for length and content.
[ad_2]
cancer.net/blog/2023-10/palliative-and-supportive-care-children-with-cancer-expert-perspective”>Source link
[ad_1]
Resources for Spanish-Speaking Individuals Impacted by cancer/Recursos para personas de habla hispana afectadas por el cáncer

En esta entrada de blog de preguntas y respuestas, y como parte del mes Nacional de la Herencia Hispana, la coordinadora del programa “Insights” de CancerCare y trabajadora social de oncología, Sara Grisales Jaramillo, LMSW, comenta los servicios y recursos en español de cancerCare para personas afectadas por el cáncer
¿Podría compartir con nosotros algunos de los retos a los que se enfrentan las personas y familias hispanas a la hora de enfrentarse al diagnóstico y tratamiento del cáncer?
La comunidad hispana/latina experimenta varios retos únicos. Algunos de los más importantes son la falta de acceso a la educación de salud, incluida la comprensión de qué es el cáncer y en qué puede consistir su tratamiento. El estatus migratorio es también uno de los mayores impactos en la comunidad hispana. El estatus migratorio está directamente relacionado con el acceso al seguro médico y a la atención médica. Muchas personas de la comunidad hispana luchan por conseguir servicios de apoyo adecuados, así como opciones de tratamiento adecuadas, educación sobre el plan de tratamiento y como tomar decisiones compartidas. Comunicación con el equipo medico y el nivel de comodidad de los pacientes y cuidadores es afectado por las barreras lingüísticas.
¿Qué recursos ofrece CancerCare específicamente adaptados para apoyar a las personas hispanas que están navegando por las complejidades de la atención del cáncer?
CancerCare ofrece servicios en español, tales como consejería individual, grupos de apoyo y navegación de recursos. Estos servicios abordan las necesidades emocionales de las personas hispanas que están luchando con los impactos del cáncer. Nuestros servicios también proporcionan a los individuos las herramientas para navegar por tales complejidades y recursos que abordan las necesidades básicas. Nuestros servicios capacitan a los clientes para abogar por sí mismos.
¿Podría destacar alguna iniciativa o programa culturalmente sensible que CancerCare haya desarrollado para garantizar que los clientes latinos reciban la mejor atención y asistencia posibles?
cancerCare ha desarrollado talleres en español para educar a los hispanos sobre cómo enfrentar un diagnóstico de cáncer, al igual que las formas de conseguir recursos. cancerCare también ofrece un grupo de apoyo a pacientes en español que ayuda a establecer una comunidad entre ellos. cancerCare tiene una gran cantidad de recursos dirigidos específicamente a la comunidad hispana.
Las barreras lingüísticas pueden ser a menudo un reto importante. ¿Cómo aborda CancerCare la accesibilidad lingüística para garantizar que los hispanohablantes puedan acceder a información y apoyo vitales relacionados con el cáncer?
cancerCare ofrece todos los servicios en español. Desde que un cliente contacta inicialmente con cancerCare, se le pone en contacto con un trabajador social que habla español. cancerCare también tiene publicaciones y recursos en español. Las publicaciones en español contienen información sobre las formas de enfrentar al cáncer, los efectos secundarios, enfrentar las necesidades de ser cuidador y mucho más. cancerCare también cuenta con personal bilingüe y bicultural dentro de departamentos como la unidad de asistencia financiera y el departamento de trabajo social. Nuestro personal bilingüe y bicultural interactúa directamente con los clientes de cancerCare eliminando la barrera del idioma.
¿Qué consejos o recomendaciones tiene para las personas y familias latinas que se enfrentan actualmente a un diagnóstico de cáncer y cómo pueden aprovechar al máximo los recursos disponibles durante este importante mes de concienciación?
La experiencia del cáncer puede ser aislante cuando los clientes se mantienen conectados, se reducen los sentimientos de depresión. Mantenerse en contacto también permite a las personas sentirse capacitadas para abogar por sí mismas y tomar decisiones informadas sobre su atención o la de sus seres queridos. Conectarse a través de un grupo de apoyo también puede ser útil, ya que escuchar otras experiencias puede ayudar a encontrar maneras de hacer frente a los desafíos y encontrar un sentido de pertenencia y comunidad.
In this guest Q&A blog post and as part of National Hispanic Heritage Month, cancerCare’s Insights Program Coordinator and oncology social worker, Sara Grisales Jaramillo, LMSW, discusses cancerCare’s Spanish languages services and resources for people impacted by cancer.
Can you share some insights into the unique challenges that Hispanic individuals and families might face when dealing with a cancer diagnosis and treatment?
The Hispanic/Latinx community experience several unique sets of challenges. Some of the most prominent challenges include lack of access to health literacy, including understanding what cancer is and what cancer treatment may consist of. Immigration status is also one of the biggest impacts in the Hispanic community. Immigration status is directly connected to access to health insurance and health care. Many individuals in the Hispanic community struggle with getting proper supportive services as well as adequate treatment options, treatment plan education and shared decision making. Language barriers also impact communication with medical teams and the comfort levels of patients and caregivers.
What resources does cancerCare offer specifically tailored to support Hispanic individuals who are navigating the complexities of cancer care?
cancerCareprovides Spanish-speaking services, such as individual counseling, support groups and resource navigation. These services address the emotional needs of Spanish-speaking individuals who are struggling with the impacts of cancer. Our services also provide individuals the tools to navigate such complexities and resources that address basic needs. Our services empower clients to advocate for themselves.
Could you highlight any culturally sensitive initiatives or programs that cancerCarehas developed to ensure that Latinx clients receive the best possible care and assistance?
cancerCare has developed Spanish-speaking workshops to educate Spanish speakers on how to face a cancer diagnosis as well as ways seek resources. cancerCare also provides a Spanish-speaking patient support group that aids in establishing community. cancerCare has a plethora of resources geared specifically towards the Hispanic community.
Language barriers can often be a significant challenge. How does cancerCare address language accessibility to ensure that Spanish-speakers can access vital cancer-related information and support?
cancerCare provides its services in Spanish. From when a client initially contacts cancerCare, they are connected with a Spanish-speaking social worker. cancerCare also offers publications in Spanish. Spanish publications contain information on ways to cope with cancer, side effects and coping as a caregiver. cancerCare also has bilingual and bicultural staff within departments like the financial assistance unit and the social work department. Our bilingual and bicultural staff interact directly with cancerCare clients eliminating the language barrier.
What advice or recommendations do you have for Latinx individuals and families who are currently dealing with a cancer diagnosis and how can they make the most of the resources available during this important awareness month?
The cancer experience can be isolating. When individuals stay connected, it reduces feelings of depression. Staying connected also allows individuals to feel empowered to advocate for themselves and make informed decisions about their or their loved one’s care. Connecting through a support group can also be helpful, as hearing other experiences can help with finding ways to cope with the challenges and finding a sense of belonging and community.
[ad_2]
Source link
[ad_1]

The population of childhood cancer survivors in the U.S. is increasing, with an overall childhood cancer survival rate greater than 85% five years after diagnosis. However, survivors can still be at increased risk of various health conditions, including second cancers.
Using data from the Childhood cancer Survivor Study (CCSS) and the St. Jude Lifetime Cohort Study (St. Jude Life), scientists at St. Jude Children’s Research Hospital have identified a genetic explanation for why a small proportion of survivors is more likely to develop second cancers and why these cancers may be more severe or deadly.
The findings, which will inform genetic counseling, testing and adoption of personalized cancer screening and prevention strategies, were published today in The Lancet oncology.
The St. Jude group showed that survivors with pathogenic (damaging) genetic variants in specific genes, called cancer-predisposing variants, are at an increased risk of developing second (subsequent) cancers as adults, and those cancers are more likely to be severe and deadly.
The scientists had previously identified that survivors with pathogenic variants in one of 60 different cancer-predisposing genes or 127 DNA damage repair genes were more likely to experience a second or subsequent cancer. This study extends that research to show a direct connection between cancer-predisposing variants and increased second-cancer-related mortality.
Many of these genetic variants are known to be causally linked to cancers. For example, the tumor suppressor gene TP53 is one of the 60 genes included in the analysis. The key to the discovery’s utility is that these variants are present in the DNA of patients when they are diagnosed with cancer as children, allowing for an individualized medicine approach to be developed early in life for each survivor.
By promoting better understanding of the effect such genes can have on future cancer risk and its outcome beyond the primary childhood cancer, the study will help inform efforts to prevent second cancers and improve the outcomes in these individuals.
“Our study pinpoints that clinical genetic testing to screen for and identify if survivors are carriers of these pathogenic variants could lead to screening and early interventions for those at higher risk to develop deadly second cancers, potentially saving their lives,” said senior corresponding author Zhaoming Wang, Ph.D., St. Jude Department of Epidemiology and cancer Control.
The total number of childhood cancer survivors who develop second or subsequent cancers is small (<10% based on current studies), and the percentage of survivors who carry cancer-predisposing variants is low (about 6%). Together, these factors have made it extremely challenging to study and understand the genetic risks for second cancers and their outcome in this population.
To reach statistically meaningful results, Wang and his collaborators combined whole genome/exome sequencing and clinical data from over twelve thousand survivors of childhood cancer. The study combined data from North America’s two largest survivorship studies, the CCSS and St. Jude LIFE cohorts.
“This is the first comprehensive study looking for the genetic reason for late mortality—specifically late mortality due to second cancers,” Wang said. “Now we know that cancer-predisposing variants contribute to the risk of death from second cancer.”
Increased surveillance may help limit the impact of these cancer-predisposing variants as childhood cancer survivors grow into adulthood. By knowing which survivors are at greater risk, health care providers may be able to recommend personalized cancer screening, which may lead to the detection of additional cancers at their earliest and most treatable stage.
These variants are part of the inherited (germline) DNA with which people are born. This means they can be detected in children when they are first diagnosed with childhood cancers, arming survivors with the knowledge they need to lower their risk later in life.
“Even before finishing childhood cancer treatment, clinicians can recommend referral to do genetic counseling so that survivors with these variants can seek cancer prevention strategies later on,” Wang said. “Depending on the gene harboring the variant, survivors that are carriers may be able to implement prevention strategies to safeguard their long-term health.”
More information:
The Lancet oncology (2023).
Citation:
Host genetics helps explain childhood cancer survivors’ mortality risk from second cancers (2023, October 2)
retrieved 3 October 2023
from https://medicalxpress.com/news/2023-10-host-genetics-childhood-cancer-survivors.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no
part may be reproduced without the written permission. The content is provided for information purposes only.
[ad_2]
cancer-survivors.html”>Source link
[ad_1]
cancer Awareness Month: Expert’s Advice on Gynecologic & Blood Cancers Hindustan Times
[ad_2]
Source link
[ad_1]
Alexandre Chan, PharmD, MPH is a chair and professor of clinical pharmacy at University of California, Irvine (UCI). He is affiliated with the UCI Chao Family Comprehensive cancer Center as well as the National cancer Centre Singapore. Dr. Chan has worked with people with cancer for almost 20 years, and he has conducted a wide array of research in supportive care, toxicities management, and cancer survivorship. Quinton (Ding Quan) Ng, BS (Pharm)(Hons), is a PhD Candidate at UCI and a registered pharmacist from Singapore. Mr. Ng’s research expertise spans across domains of epidemiology, biostatistics, and biomarker analysis, with a primary focus in treating and preventing adverse health outcomes in people with cancer. You can follow Dr. Chan and Mr. Ng on X, formerly known as Twitter. View disclosure information for Dr. Chan. Mr. Ng has no relationships to disclose.
Over the past decade, the use of electronic cigarettes, also called e-cigarettes or vaporizers, has become a popular substitute for tobacco products in people looking to quit smoking. You may hear the use of e-cigarettes more commonly referred to as “vaping.” However, there is a growing amount of research to suggest that e-cigarettes contain many harmful substances, including chemicals that can cause cancer. In one study conducted by the Centers for Disease Control and Prevention (CDC), it was found that almost all the e-cigarettes sold within the United States during the study contained nicotine.
Vaping has become especially common among young people, as flavored e-cigarettes and strong marketing tactics have been used to make vaping more appealing to teens and young adults. This could be problematic, as one survey showed that teenaged e-cigarette users were 2 times more likely to smoke tobacco cigarettes compared to those who had never used e-cigarettes. These are worrisome trends as e-cigarettes continue to gain tremendous popularity, particularly among younger people.
It is important to know that e-cigarettes are not currently approved by regulatory authorities, including the U.S. Food and Drug Administration (FDA), as a method to help people stop smoking. Even more importantly, questions regarding the long-term health problems of vaping in people with cancer and survivors remain unanswered at this time. If you are using or considering using e-cigarettes during cancer or survivorship, it is important to talk with your health care team about how vaping could affect your overall health.
There is a common belief that e-cigarettes are safer than traditional cigarettes, but it’s important to know that studies involving the long-term use of e-cigarettes have shown that they can negatively impact brain and heart health. E-cigarette vapor also contains many harmful chemicals that are released during the heating of the liquid propylene glycol or glycerin, which are commonly used to dissolve the active nicotine ingredient found in vaping products. Nicotine in e-cigarettes may also negatively impact brain development and lead to addiction in children, teens, and young adults.
As e-cigarettes are a fairly new phenomenon, our knowledge on their long-term health effects is relatively lacking at this time. Human studies with follow-up periods longer than 5 years are needed to better understand how e-cigarette use may impact the health of people with cancer and survivors. In fact, the American Society of Clinical oncology and the American Association for cancer Research have called for more research to be done on e-cigarette products, including around their potential health impacts.
Regardless, because of the toxic substances found in e-cigarettes, people with cancer and survivors should talk with their health care team about avoiding using e-cigarettes as a quitting-smoking tool or as a remedy to reduce stress or improve attention, thinking, or memory problems until more is known about the effects of e-cigarette usage.
Many people with cancer may turn to using e-cigarettes because they think it could help them stop smoking. In one study published in Psychooncology, people with cancer expressed their preference for e-cigarettes over nicotine replacement therapy as a treatment for quitting smoking. However, over 70% of people with cancer who used e-cigarettes reported that they did not inform their cancer care provider that they used e-cigarettes.
Several other studies have evaluated the patterns of e-cigarette usage among cancer survivors. One study analyzed data of more than 8,000 cancer survivors from the National Health Interview Survey (2014–2018) and observed more e-cigarette usage among cancer survivors identifying as White compared to other racial and ethnic groups. Other studies have also observed that e-cigarettes are often used together with conventional cigarettes.
We recently studied the relationship between adverse health behaviors, including vaping, and cognitive problems in young adult childhood cancer survivors, which was published in JCO oncology Practice. Cognitive problems can include trouble with thinking, paying attention, and remembering things. Our study included 1,106 young adults who had survived childhood cancer who were ages 15 to 39 when they entered the study and were at least 5 years out from their cancer diagnosis. We observed that the use of e-cigarettes was 2 times higher among survivors with self-reported cognitive impairment compared to other survivors. Those cognitively impaired survivors were also found to have poorer physical and mental health. Although the exact reasons for vaping were not captured in the study, we speculated that these survivors were vaping for stress relief, smoking cessation, and potentially to seek improvement of short-term alertness and concentration.
Ultimately, it is important to always talk with your health care team before using e-cigarettes so they can help address any questions you may have around vaping.
For people with cancer and survivors who have quit smoking traditional cigarettes and are using e-cigarettes solely for smoking cessation, they should consider seeking the help of a pharmacist. Many community pharmacies provide smoking cessation services and can help redirect them to other evidence-based methods to stop smoking, including nicotine replacement therapies and medications such as varenicline (Chantix) and bupropion (Wellbutrin, Zyban). Talk with your health care team for a referral to a pharmacist who can help with smoking cessation.
Research is also currently ongoing to evaluate new strategies for improving the effectiveness of quitting smoking approaches, including individualized health educational programs, peer navigators, and mobile health applications to help people stick with their plans to quit.
Your pharmacist can work closely with you to personalize a quitting smoking plan that is best suited for your needs and lifestyle. Even if you are thinking about quitting but you are not fully ready, your pharmacist is still a great resource to turn to as you navigate this decision.
[ad_2]
cancer.net/blog/2023-09/what-people-with-cancer-and-survivors-should-know-about-vaping-expert-perspective”>Source link
[ad_1]

As fall approaches, children, teens and their families prepare for the upcoming school year. Getting new school supplies is on many families’ minds and can be especially difficult for families coping with cancer.
Now in its eighth year, cancerCare for Kids’ Back-to-School Program provides backpacks full of new school supplies for students affected by cancer in pre-K through 12th grade throughout New York, New Jersey and Connecticut. cancerCare’s social workers and facilities team worked to pack and ship age-appropriate school supplies, including books, calculators, notebooks, folders, pens, pencils and art supplies, to 223 students from 98 families.
cancerCare’s Back-to-School program allows families impacted by cancer to spend time with their loved ones and prepare for the upcoming school year without worrying about the money and time it takes to get new school supplies.

One parent shared, “I wish you could have seen my kids’ faces when they opened the boxes! They were all so excited with everything.”
“Each item is appropriate for each of our children’s age and will really go to good use,” said another parent. “You took a big load off of us not having to think of preparing the kids for the new school year!”
“The supplies in the backpack were exactly on the kids’ supply list for school,” another parent added. “Not having to go out and look for supplies also gives me extra time with my family. As you can imagine, time with a loved one diagnosed with cancer is priceless.”

cancerCare for Kids’ Back-to-School Program is open to children and teens diagnosed with cancer, who have a loved one diagnosed with cancer or who have lost a loved one to cancer and who reside in New York, New Jersey or Connecticut.
Thank you to all of our supporters and dedicated staff who make our Back-to-School Program and all of our free services possible!
Learn more about cancerCare for Kids and how we help children, teens and families affected by cancer. You can also call our Hopeline at 800-813-HOPE (4673) to speak with an oncology social worker or email cckids@cancercare.org with questions.
[ad_2]
Source link