More than 50 countries, including the United Kingdom, Australia, Canada and all 28 countries of the European Union, have banned the use of asbestos. The United States is not one of them.
This document discusses managing side effects of mesothelioma treatments through nutrition. It covers common treatments for mesothelioma like chemotherapy, immunotherapy, radiation, and surgery. Each treatment can cause side effects that impact quality of life. Side effects from chemotherapy include nausea, low blood counts, and neuropathy. Nutrition strategies like eating small, frequent meals can help manage immunotherapy side effects. Radiation side effects include fatigue, and packing portable protein snacks is advised. Surgery side effects involve risks of infection, which nutrition before and after can reduce. Unintended weight loss from treatments can be prevented by meeting calorie and protein needs.
Over 75 different occupational groups have exposed workers to asbestos. Repeated asbestos exposure puts workers at risk of numerous cancers and serious pulmonary diseases, including mesothelioma and asbestosis.
A cancer diagnosis shouldn't stop patients from exercising (if approved by their oncologist.) In fact, exercise can improve a patient's quality of life. Benefits of increased exercise during cancer treatment include less fatigue, stress and anxiety. Over multiple studies, it was shown there was a link between exercise and decreased cancer recurrence. Learn what types of exercise should be incorporated into a cancer survivor's fitness routine.
Cancer is a topic no one wants to learn how to talk about. Mesothelioma is a new experience that can be challenging to navigate socially. Not only we affected by a cancer diagnosis, but so are our family and friends.
Research shows talking about it helps people adjust to the reality of a situation. By talking about it, our brains begin planning and problem-solving to better cope with the situation. We are better able to get our needs met if we communicate how we are feeling and what we need from our loved ones.
With that being said, it is important to remember that we don’t have to share everything with everyone all the time. It's our choice.
Clinical trials are changing the face of mesothelioma treatment. While researchers and physicians continue to search for a cure, patients can enroll in clinical trials in order to access the latest medical advances available for treating mesothelioma cancer.
Choosing to join a clinical trial is a very personal decision that patients must consider with their caregivers, family members and medical team. Learn more about the pros and cons of mesothelioma clinical trials and find out how to decide if a clinical trial is the right fit.
Many people think of anger as a negative emotion, but that's not the case. The reality is that most cancer patients feel anger at times: At diagnosis, when treatment is delayed and even after treatment finishes. Anger can actually be a helpful and motivating emotion if channeled properly.
Anger is a very normal and healthy emotion in life as well as when you or a loved one has mesothelioma. Actively engaging with the feeling and finding healthy ways to express it is key to good anger management.
A mesothelioma diagnosis can drastically change your life. Your days often become focused on appointments with doctors, chemotherapy sessions and routine testing. When you are no longer undergoing active treatment, it can be hard for you and your loved ones to adjust to this "new normal." Learn how to overcome the challenges of adjusting to life after mesothelioma cancer treatments.
Self-esteem is the value that we have of ourselves. It also includes how we perceive our value in the world and to others. Being diagnosed with a serious, chronic illness such as mesothelioma may lead to a decrease in self-esteem. Sadly, many people with chronic illnesses or disabilities feel “less than” others who may be healthy or able-bodied.
Our value in life is not tied to how much money we make, how many things we build, how clean our home is or how good our lawn looks. Our value is what we mean to others. Cancer does not change what we mean to others.
This document discusses managing side effects of mesothelioma treatments through nutrition. It covers common treatments for mesothelioma like chemotherapy, immunotherapy, radiation, and surgery. Each treatment can cause side effects that impact quality of life. Side effects from chemotherapy include nausea, low blood counts, and neuropathy. Nutrition strategies like eating small, frequent meals can help manage immunotherapy side effects. Radiation side effects include fatigue, and packing portable protein snacks is advised. Surgery side effects involve risks of infection, which nutrition before and after can reduce. Unintended weight loss from treatments can be prevented by meeting calorie and protein needs.
Over 75 different occupational groups have exposed workers to asbestos. Repeated asbestos exposure puts workers at risk of numerous cancers and serious pulmonary diseases, including mesothelioma and asbestosis.
A cancer diagnosis shouldn't stop patients from exercising (if approved by their oncologist.) In fact, exercise can improve a patient's quality of life. Benefits of increased exercise during cancer treatment include less fatigue, stress and anxiety. Over multiple studies, it was shown there was a link between exercise and decreased cancer recurrence. Learn what types of exercise should be incorporated into a cancer survivor's fitness routine.
Cancer is a topic no one wants to learn how to talk about. Mesothelioma is a new experience that can be challenging to navigate socially. Not only we affected by a cancer diagnosis, but so are our family and friends.
Research shows talking about it helps people adjust to the reality of a situation. By talking about it, our brains begin planning and problem-solving to better cope with the situation. We are better able to get our needs met if we communicate how we are feeling and what we need from our loved ones.
With that being said, it is important to remember that we don’t have to share everything with everyone all the time. It's our choice.
Clinical trials are changing the face of mesothelioma treatment. While researchers and physicians continue to search for a cure, patients can enroll in clinical trials in order to access the latest medical advances available for treating mesothelioma cancer.
Choosing to join a clinical trial is a very personal decision that patients must consider with their caregivers, family members and medical team. Learn more about the pros and cons of mesothelioma clinical trials and find out how to decide if a clinical trial is the right fit.
Many people think of anger as a negative emotion, but that's not the case. The reality is that most cancer patients feel anger at times: At diagnosis, when treatment is delayed and even after treatment finishes. Anger can actually be a helpful and motivating emotion if channeled properly.
Anger is a very normal and healthy emotion in life as well as when you or a loved one has mesothelioma. Actively engaging with the feeling and finding healthy ways to express it is key to good anger management.
A mesothelioma diagnosis can drastically change your life. Your days often become focused on appointments with doctors, chemotherapy sessions and routine testing. When you are no longer undergoing active treatment, it can be hard for you and your loved ones to adjust to this "new normal." Learn how to overcome the challenges of adjusting to life after mesothelioma cancer treatments.
Self-esteem is the value that we have of ourselves. It also includes how we perceive our value in the world and to others. Being diagnosed with a serious, chronic illness such as mesothelioma may lead to a decrease in self-esteem. Sadly, many people with chronic illnesses or disabilities feel “less than” others who may be healthy or able-bodied.
Our value in life is not tied to how much money we make, how many things we build, how clean our home is or how good our lawn looks. Our value is what we mean to others. Cancer does not change what we mean to others.
People vary in their ability and comfort in having conversations about health, illness and emotions that can accompany a cancer diagnosis. This can lead to communication challenges throughout a mesothelioma battle.
Mesothelioma patients and caregivers may notice that some relationships temporarily changed after a mesothelioma diagnosis. That's normal.
To overcome these changes and challenges, survivors should try to have frequent honest conversations about expectations, thoughts and feelings, so misunderstandings and frustrations don’t lead to more serious relationship problems.
Many cancer patients experience fatigue at before, during and after treatment. Studies show that 20-90% of cancer patients on active treatment experience symptoms of fatigue, and 20-80% of survivors report fatigue after finishing treatment.
Cancer-related fatigue can be unpredictable because a patient may feel energized one day but fatigued another without any change in activity or rest patterns.
When you or a loved one has mesothelioma, it can seem like there is so much to worry about. That's normal. It is a misconception that all worrying is distressful and unproductive. There are healthy levels of worrying that motivate us to do what we need to be happy, successful and healthy. When worrying becomes overwhelming and feels uncontrollable, then most people experience distress and feel anxious. Obviously, the challenge is to keep our level of worry at a range that motivates us, not give us anxiety.
After being diagnosed with an incurable disease such as mesothelioma cancer, it can be difficult to be hopeful. It's important to understand that with all the recent advancements in mesothelioma treatment, it is realistically hopeful to look forward to surviving longer and with a better quality of life.
The document discusses the challenges of caregiver burnout, noting that 60% of caregivers are female and 40% report high stress levels. Caregiver stress can occur when the demands of caregiving outweigh a person's ability to meet those demands, potentially leading to burnout if stress is not managed. The document provides tips for caregivers to minimize stress such as asking for help, prioritizing self-care, exercising, and connecting with other caregivers.
Every mesothelioma survivor is different, which means each story is unique and provides a distinct insight into life with this type of cancer. There are many benefits to sharing your mesothelioma story, but it is also important to prepare for any reactions that may come from hearing your story.
Cancer patients experience a myriad of emotions before, during and after treatment. Emotional effects therapy, such as meditation, can help patients cope with their cancer in everyday life.
This document discusses exercise recommendations and options for cancer patients during bad weather. It provides an overview of the benefits of exercise during and after cancer treatment, including improved sleep, decreased fatigue and treatment side effects, and reduced anxiety and depression. However, certain chemotherapy drugs can make patients sensitive to temperature changes and increase fall risks. As such, the document recommends indoor exercise options when weather is poor, such as using home exercise equipment while watching fitness videos, or exercising at indoor locations like malls, yoga studios and gyms. It emphasizes that staying active is important for cancer patients' emotional and physical well-being.
Living with a terminal disease is never easy, but when it is also a rare disease such as mesothelioma, it can be even more challenging as there are additional obstacles to overcome like finding reliable resources, connecting with a specialist and learning about the latest treatment options.
Many people wonder whether a cancer patient's attitude or personality type can impact their prognosis. In this SlideShare, Dana Nolan, a Mental Health Counselor, takes a closer look at how personality, attitude and cancer relate for our August 2016 support group session.
Learn what the American Institute for Cancer Research says about a diet that helps prevent cancer or ease symptoms of those diagnosed with the disease.
This document discusses factors that can affect sleep for those with mesothelioma and non-medication strategies to improve sleep. It identifies potential causes of sleep problems including treatment side effects, psychological factors, disease symptoms, and lifestyle habits. It then outlines different types of insomnia and recommends trying behavioral strategies before medications. Specific behavioral strategies described are stimulus control, sleep scheduling, relaxation techniques, and establishing a regular sleep hygiene routine.
This document discusses the roles of ancillary healthcare providers who assist in caring for patients with mesothelioma during and after treatment. It describes how doctors and nurses require support from professionals like physical therapists, dietitians, mental health counselors and others to address issues like pain, weakness, nutrition and psychological well-being. These ancillary providers have advanced degrees and certification in their specialty areas. The document also outlines what conditions different providers treat and how home health care and insurance coverage factors into ancillary care.
Choosing hospice care program can be an extremely difficult decision for many patients and families. Whether looking to improve pain management, lessen caregiver burden or maximize quality of life, the decision to pursue hospice is never hard and fast.
This document discusses ways to improve communication between cancer patients and their oncologists. It notes that while oncologist training in communication has increased, there is still room for improvement. A common issue is "collusion", where patients hesitate to bring up difficult topics and doctors don't ask, resulting in important conversations not occurring. The document provides examples of questions patients may want to ask their oncologists about various topics like prognosis, diet, exercise, medical care, travel, insurance, and sex during/after treatment. It emphasizes that oncologists can't be aware of all patient concerns, so patients should take the initiative to ask questions about integrating treatment into their daily lives.
Guided imagery (GI) involves a focus of the imagination and the senses. It is a form of relaxation that promotes harmony between the body and mind. It's a therapy that may be useful for caregivers, cancer patients and those dealing with mesothelioma.
The document discusses the benefits of exercise for mental health. Regular physical activity can help reduce anxiety and depression and improve mood and cognitive functioning. Exercise causes chemical changes in the brain that may help boost feelings of calmness and well-being.
Caregivers often run into situations where they may need financial or emotional help while caring for their loved ones. The Mesothelioma Center provides some resources for caregivers.
People vary in their ability and comfort in having conversations about health, illness and emotions that can accompany a cancer diagnosis. This can lead to communication challenges throughout a mesothelioma battle.
Mesothelioma patients and caregivers may notice that some relationships temporarily changed after a mesothelioma diagnosis. That's normal.
To overcome these changes and challenges, survivors should try to have frequent honest conversations about expectations, thoughts and feelings, so misunderstandings and frustrations don’t lead to more serious relationship problems.
Many cancer patients experience fatigue at before, during and after treatment. Studies show that 20-90% of cancer patients on active treatment experience symptoms of fatigue, and 20-80% of survivors report fatigue after finishing treatment.
Cancer-related fatigue can be unpredictable because a patient may feel energized one day but fatigued another without any change in activity or rest patterns.
When you or a loved one has mesothelioma, it can seem like there is so much to worry about. That's normal. It is a misconception that all worrying is distressful and unproductive. There are healthy levels of worrying that motivate us to do what we need to be happy, successful and healthy. When worrying becomes overwhelming and feels uncontrollable, then most people experience distress and feel anxious. Obviously, the challenge is to keep our level of worry at a range that motivates us, not give us anxiety.
After being diagnosed with an incurable disease such as mesothelioma cancer, it can be difficult to be hopeful. It's important to understand that with all the recent advancements in mesothelioma treatment, it is realistically hopeful to look forward to surviving longer and with a better quality of life.
The document discusses the challenges of caregiver burnout, noting that 60% of caregivers are female and 40% report high stress levels. Caregiver stress can occur when the demands of caregiving outweigh a person's ability to meet those demands, potentially leading to burnout if stress is not managed. The document provides tips for caregivers to minimize stress such as asking for help, prioritizing self-care, exercising, and connecting with other caregivers.
Every mesothelioma survivor is different, which means each story is unique and provides a distinct insight into life with this type of cancer. There are many benefits to sharing your mesothelioma story, but it is also important to prepare for any reactions that may come from hearing your story.
Cancer patients experience a myriad of emotions before, during and after treatment. Emotional effects therapy, such as meditation, can help patients cope with their cancer in everyday life.
This document discusses exercise recommendations and options for cancer patients during bad weather. It provides an overview of the benefits of exercise during and after cancer treatment, including improved sleep, decreased fatigue and treatment side effects, and reduced anxiety and depression. However, certain chemotherapy drugs can make patients sensitive to temperature changes and increase fall risks. As such, the document recommends indoor exercise options when weather is poor, such as using home exercise equipment while watching fitness videos, or exercising at indoor locations like malls, yoga studios and gyms. It emphasizes that staying active is important for cancer patients' emotional and physical well-being.
Living with a terminal disease is never easy, but when it is also a rare disease such as mesothelioma, it can be even more challenging as there are additional obstacles to overcome like finding reliable resources, connecting with a specialist and learning about the latest treatment options.
Many people wonder whether a cancer patient's attitude or personality type can impact their prognosis. In this SlideShare, Dana Nolan, a Mental Health Counselor, takes a closer look at how personality, attitude and cancer relate for our August 2016 support group session.
Learn what the American Institute for Cancer Research says about a diet that helps prevent cancer or ease symptoms of those diagnosed with the disease.
This document discusses factors that can affect sleep for those with mesothelioma and non-medication strategies to improve sleep. It identifies potential causes of sleep problems including treatment side effects, psychological factors, disease symptoms, and lifestyle habits. It then outlines different types of insomnia and recommends trying behavioral strategies before medications. Specific behavioral strategies described are stimulus control, sleep scheduling, relaxation techniques, and establishing a regular sleep hygiene routine.
This document discusses the roles of ancillary healthcare providers who assist in caring for patients with mesothelioma during and after treatment. It describes how doctors and nurses require support from professionals like physical therapists, dietitians, mental health counselors and others to address issues like pain, weakness, nutrition and psychological well-being. These ancillary providers have advanced degrees and certification in their specialty areas. The document also outlines what conditions different providers treat and how home health care and insurance coverage factors into ancillary care.
Choosing hospice care program can be an extremely difficult decision for many patients and families. Whether looking to improve pain management, lessen caregiver burden or maximize quality of life, the decision to pursue hospice is never hard and fast.
This document discusses ways to improve communication between cancer patients and their oncologists. It notes that while oncologist training in communication has increased, there is still room for improvement. A common issue is "collusion", where patients hesitate to bring up difficult topics and doctors don't ask, resulting in important conversations not occurring. The document provides examples of questions patients may want to ask their oncologists about various topics like prognosis, diet, exercise, medical care, travel, insurance, and sex during/after treatment. It emphasizes that oncologists can't be aware of all patient concerns, so patients should take the initiative to ask questions about integrating treatment into their daily lives.
Guided imagery (GI) involves a focus of the imagination and the senses. It is a form of relaxation that promotes harmony between the body and mind. It's a therapy that may be useful for caregivers, cancer patients and those dealing with mesothelioma.
The document discusses the benefits of exercise for mental health. Regular physical activity can help reduce anxiety and depression and improve mood and cognitive functioning. Exercise causes chemical changes in the brain that may help boost feelings of calmness and well-being.
Caregivers often run into situations where they may need financial or emotional help while caring for their loved ones. The Mesothelioma Center provides some resources for caregivers.
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We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
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These lecture slides, by Dr Sidra Arshad, offer a simplified look into the mechanisms involved in the regulation of respiration:
Learning objectives:
1. Describe the organisation of respiratory center
2. Describe the nervous control of inspiration and respiratory rhythm
3. Describe the functions of the dorsal and respiratory groups of neurons
4. Describe the influences of the Pneumotaxic and Apneustic centers
5. Explain the role of Hering-Breur inflation reflex in regulation of inspiration
6. Explain the role of central chemoreceptors in regulation of respiration
7. Explain the role of peripheral chemoreceptors in regulation of respiration
8. Explain the regulation of respiration during exercise
9. Integrate the respiratory regulatory mechanisms
10. Describe the Cheyne-Stokes breathing
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