Tips & Rewards For Going To Healthcare Visits With Your Loved One

Tips & Rewards For Going To Healthcare Visits With Your Loved One

For many people, having a trusted friend or family member join them during a doctor’s visit or test (in person, virtually, or by phone) can be a great source of comfort and practical help. Sitting in may also bring you some peace of mind.

Photo of Caregiver and patient

Besides being there for support and a second set of eyes and ears, you may also be that person’s advocate—gathering and sharing information with the healthcare provider, collecting information for them, and following up after the appointment to ensure continuity of their care. Knowing what to do before, during, and after a medical appointment can help safeguard the health and well-being of your loved one.

 

The Bag It Cancer’s Bag contains a nifty take-everywhere binder that was designed to help people get prepared for their medical appointments, keep track of information and records in an organized manner, and accompany them to each visit.  Here are some of the tips from the binder.

Prepare for the appointment

  • Set time aside with your family member or friend to discuss the primary purpose of the appointment. Is this a check-up? Follow up visit? Possible new medical condition? Together make a written list of questions, notes, or updates to share with the provider, keeping it to a single page and leaving room for the answers). This might include new symptoms, possible side effects of medications, or a new medical condition since the last visit. Also, discuss how they would like you to assist them during the appointment so you come to an agreement about your role.
  • Star the three top priorities on your list to discuss in case you don’t get to all of them. Some people prefer to make an extra copy to hand directly to the doctor at the start of the visit.
  • Gather everything needed for the appointment. Use Bag It’s My Companion Guidebook to store and record all your information in the tabbed sections and on the helpful patient forms. You will need:
    • Day/date/time of the appointment. (Note that providers often ask you to arrive earlier to complete paperwork.)
    • Name, address, phone number of the provider’s office.
    • Driving directions if needed. If someone is attending virtually or by phone, make sure you have the log in or call-in details in advance.
    • Insurance cards and copays due at the time of service.
    • Copies of your medical records, including medical and family history.
    • A notebook, pen or a recording device such as a smart phone with recording app.
    • A complete and accurate list of current medications, vitamins/supplements, and over the counter medicines being taken.
  • If lab work, tests, imaging, or other procedure needs to be completed so the doctor can review the results at your appointment, schedule them in advance and with enough time for the report to be available to the provider. Call to make sure the results have been received by the doctor’s office. Or pick up a copy of the results and bring it with you to your appointment, if needed.
  • If communication with the provider will be difficult for the patient due to a language barrier, request that a professional interpreter be present during the appointment. Relying on a family member or friend to perform this role is not the best choice when complicated medical terms may be used to discuss the patient’s diagnosis and treatment options, or difficult treatment decisions may need to be made.
  • If you decide to go online to research the patient’s disease or condition, avoid misinformation by visiting only reliable medical websites. Download our tips on how to evaluate medical websites. Always discuss with the provider any information you find online to make sure it is appropriate for your loved one and their situation.

 

The information and forms are just what is needed to assist with recording your cancer journey. The guidebook gives information to help explain and understand what to expect and record for the future.  The bag helps you feel more comfortable speaking up for yourself by providing forms to write down questions and concerns which will help to explain at future doctor appointments.

–Caregiver, California

 

During the appointment

  • Introduce yourself to the provider if you have not met them and explain your role and who you are to the patient. If you will be attending appointments on a regular basis, begin to build your relationship as a member of the patient’s care team.
  •  If your loved one is unable or hesitant to actively communicate with their provider, speak up on their behalf early in the conversation if this is what was agreed to by you and the patient.
  • Verify the doctor has received the results of testing or procedures completed since the last visit. Provide a copy of the results if they have not been received.
  • Address the priority concerns and questions on your list. Be direct, honest and respectfully assertive when speaking with the provider.
  • Listen carefully. Take notes and write the down the answers to the questions asked. Another idea is to record the conversation, with the provider’s permission. There are apps to download onto a smartphone, or use another recording device.
  • Before the visit concludes, make sure any information relayed to you is well understood, including how to perform any medical tasks required at home. If not, ask for it to be explained again in a different way or using everyday language. Ask follow-up questions as needed. Repeating or rephrasing the important parts back to the provider are good ways to confirm you interpreted the information correctly.
  • You can also ask for information to be provided to you in writing so you can refer to it at home. This is especially helpful for instructions on how to perform home care tasks.
  • Review the patient’s current medications. Understand why any new medications are being prescribed, and make sure you are clear on how, how much and when the medicine should be taken to avoid medication errors.
  • Find out the best way to communicate if a non-urgent matter arises between visits. Some offices prefer a message sent through the portal, some use email, and some will ask you to call a specific member of the health care team. If your loved one agrees, consider giving the provider your phone number and/or email as another point of contact.
  • If there wasn’t enough time to address all the questions and concerns with the doctor, ask if a nurse or other member of the healthcare team can help you further that day, or follow up with you after the visit. You can also ask to make another appointment to continue the conversation.
  • Request copies of any test results, reports or other medical records related to the appointment if not given to you automatically. If they are available online through the patient portal, confirm you have the correct URL for the website and instructions on how to set up a user name and password.
  • Before leaving the office make any follow up appointments needed, if possible. Be sure any orders for lab work or other testing or procedures are given to you or sent electronically to the medical facility. This also includes any referrals to other providers.

After the Appointment

  • Recap the visit with your loved one. Finish writing any notes or instructions you didn’t jot down in the office. Listening to the recording of the visit would be helpful here.
  • Update the patient’s file with any new reports, test results or other documents you received during the visit. Download and print a copy to file if they are online in the patient portal.
  • Fill all prescriptions promptly. Verify the pharmacy has a complete and accurate list of all the patient’s medications to avoid drug interactions. Report to the doctor any new symptoms or side effects that could be related to new medicines the patient is taking.
  • If any lab work, tests or procedures, or referrals to other doctors were ordered during the visit, schedule these appointments in a timely manner. Ask when and how you will receive the results. Be sure to follow up with the office if you do not receive the results within the expected time frame –do not assume “no news is good news.” If you do not understand the results, reach out to the provider’s office for an explanation of what they mean.

We hope that these tips guide both you and your loved one to better health and more peace of mind.

 

How Would You Rate Your Healthcare Literacy Skills?

How Would You Rate Your Healthcare Literacy Skills?

Photo of Bag It Bag contents 2022October is Health Literacy Month. A study by Health & Human Services Office of the Surgeon General showed that only about 12% of Americans have proficient health literacy skills. Unfortunately, many adults lack good knowledge about their medical condition and treatment, and don’t know how to get information that is presented in a way they can understand. People report having difficulty completing medical forms and relaying important details to their doctor about their health. They may not be able to accurately read directions to take their medicines as prescribed. Each of these common situations can be linked to poor health outcomes.

Bag It Cancer is committed to expanding health literacy for all populations. Our Bag It Bag is all about making sure that anyone with cancer can find, understand and use reliable information to make decisions about their health and guide them through a complex cancer care system.

For nearly 20 years we have worked with healthcare providers who make it a practice to give Bag It Bags to their patients at diagnosis. Having a bag of printed, clear, easy to understand materials from trustworthy cancer organizations, with customizable tools to make it their own, helps people get involved in their care and feel a bit more in control.

 

Let’s Start with The Basics in The Bag

  • My Healthcare Team. Knowing who is on your healthcare team and what their role is points you in the right direction for your questions or other assistance.
  • Cancer Words. There’s a short list of definitions for common cancer words, including cancer treatments, that you may not be familiar with but need to know.
  • Lists of Questions to Ask. Asking the right questions at the right time helps you to get the info you need about your care and other areas of your life affected by a cancer diagnosis.
  • Making Treatment Decisions. The bag walks you through what to consider as you make decisions about your treatment and care, including sources for more information about your cancer type and life situations.
  • There’s a Lot to Keep Track of…medical records, appointments, business cards, questions and notes for the doctor, and lots and lots of paperwork. My Companion Guidebook has places for everything plus checklists to simplify the steps.
  • Easy Tips and Hacks to Use Like these:
    • If you’re not sure you understand what is being said to you by your healthcare team, ask for it to be explained again in everyday language (and in your preferred language). Then repeat the information back to the person to make sure you got it right.
    • Bring someone to your appointments to listen and write down the information, or ask permission to record the visit. This will help to ensure accuracy and saves you from trying to remember everything that is said to you. Another idea is to ask for the information to be given to you in writing (and in your preferred language) so you can read it again at home.
The Bag It Bag — Reviewed.  Refreshed.  Renewed.

The Bag It Bag — Reviewed. Refreshed. Renewed.

Every 18 to 24 months, we gather a committee of cancer survivors, care partners, oncology care providers, and nonprofit partners to conduct a review of the Bag It Bag. They assess how the current bag content and design are meeting the needs of people with cancer, their care partners, families, and the healthcare providers who care for them. The group also considers how the Bag could be improved.

Review, Refresh Renew graphic

The feedback we received from our recent review was thoughtful and insightful, as always. The consensus was that the significant revisions made to the Bag in 2019 continue to benefit the quality of the materials. Some helpful suggestions on ways to refresh and enhance some of the content were also offered.

The Covid-19 pandemic did not prevent us from completing this important process or continuing our work. For the Bag It Team, the challenges it brought reinforced that this valuable resource is critical for those dealing with cancer, renewing our commitment to our mission of educating, supporting, and empowering those impacted by cancer.

2022 Bag It Bag Updates

Paths to Survivorship Booklet

We added new information about dealing with potential cancer treatment side effects such as hot flashes, bone health, and genital and urinary problems, which are common for some types of cancer. It is important for people to understand all of their rights and options to best navigate their situations related to work, disability and health insurance, and managing finances. Triage Cancer provided valuable content on these legal and practical issues. 

Paths to Survivorship CoverAn overview about genetic and biomarker testing explains what they are and, when ordered by your doctor, how the test results can help your cancer care team offer you the most tailored options for effective treatment of your cancer. Your doctor will determine if this type of testing is appropriate for you.

This booklet includes helpful lists of questions you can ask your healthcare team based on where you are in your diagnosis and treatment:

  • Questions to ask your healthcare team about your diagnosis
  • Questions to ask your healthcare team about cancer treatment
  • Questions to ask your healthcare team about follow-up care
  • Questions to ask your healthcare team about late and long-term side effects
  • Questions to ask your healthcare team about living with chronic or advanced cancer

Here are printable versions of the questions to take with you to your appointments. You’ll also find other Self-Advocacy Tips and A Survivorship Checklist. 

Paths to Survivorship (and all the booklets and forms in the bag) can be downloaded for free on our website. Want to share this great publication with others? You can email it in PDF format or send them the link to the Bag it Bag.

My Companion Guidebook

It goes without saying that there’s a lot of information coming your way when you or someone close to you is diagnosed with cancer. It can be overwhelming. A great deal of paperwork is given to you by your providers, and there is much to keep track of in an accurate and consistent manner. 

My Companion Guidebook photoMy Companion Guidebook is a helpful way to organize everything in one place to ensure you have access to what you need, when you need it. We’ve made some tweaks to make it easier to sort and store your records in the various sections, and added more tips on how to make the most of your appointments.  There’s also a handy new page to keep a running list of your questions for your next doctor visit.

Blank copies of the forms to print or the fillable PDF format can be found on our Bag It Bag page

Resources, Resources, and More Resources!

Did you know Bag It’s online Resource Center houses over 150 vetted websites covering a wide range of cancer topics? Whether you want education about your cancer type or to find support services out there that can help you or your family along the way, we’ve done the legwork to save you time and to bring you resources you can rely on.

At the same time, we also realize that not everyone has equal access to or is as comfortable using the internet. That’s why we added two new pages to My Companion Guidebook listing many helpful organizations to assist with some of the most common and pressing needs that cancer can bring. (Phone numbers are also listed in case you prefer to call and speak to someone there.)

Topics include:

New Companion Book Topics 2022

To order a Bag It Bag for yourself or someone else, visit our Bag It Bag order page

 

Cultural Sensitivity Is More Than Language Translation

Cultural Sensitivity Is More Than Language Translation

Bag It Cancer continually reviews the Bag to ensure it is as helpful as it can be for those living with cancer. This spring we conducted research through a series of interviews and focus groups of Latino and Hispanic survivors, caregivers and other stakeholders for input on how to better address their values, beliefs, language, and culture in the Spanish Bag.

We heard about a variety of topics that would be beneficial to include in the Spanish Bag, or address in a different way in the Bag.

Photo of Spanish Bag It bag contents

For example, to many people, cancer=death. If someone is diagnosed with cancer, the only possible outcome is death. We hope to dispel this commonly-held misconception and others by educating Bag users and families about the evidence-based facts about cancer. We gained more insight about the importance of family in the Latino and Hispanic communities. Family members often take part in the decision making about treatment. Their involvement in that process, and as caregivers, can have huge impacts on a patient’s wellbeing.

We also learned that if nutritional information in the Bag isn’t tailored to culturally relevant foods, patients and caregivers may not make necessary changes to their diet during and after treatment. We plan to include recipes from Latina kitchens that adapt favorite Latin dishes to make them healthier – lower in fat, richer in fiber and vitamins, but still tasty.

Latinos and Hispanics are disproportionately affected by poor conditions of daily life which are shaped by a variety of structural and social position factors (such as income, education, occupations, cultural values, and social support systems), known as social determinants of health. These factors impact their cancer care and survival. We can’t overcome all of these barriers, but we can do our small part by educating and guiding Latinos and Hispanics with a more culturally-tailored Bag It Bag.

We look forward to introducing the new bicultural Bag It Bag to you and your patients at the end of the year.