Recently Diagnosed or Relapsed? Stop Looking For a Miracle Cure, and Use Evidence-Based Therapies To Enhance Your Treatment and Prolong Your Remission
Multiple Myeloma an incurable disease, but I have spent the last 25 years in remission using a blend of conventional oncology and evidence-based nutrition, supplementation, and lifestyle therapies from peer-reviewed studies that your oncologist probably hasn't told you about.
Click the orange button to the right to learn more about what you can start doing today.
“If the doctor gives you a Multiple Myeloma diagnosis during your appointment and you don’t understand what it is or if you have any questions at al, feel free to ask additional questions…”
The NYT article linked and excerpted below is about a medical diagnosis in general. I am using it to discuss what people should do when diagnosed with my cancer- a multiple myeloma diagnosis.
A multiple myeloma diagnosis
(MM) is one of the greatest challenges you will ever face in your life. While all your appointments with your oncologist are important, your first appointments are the most relevant to your understanding of your multiple myeloma, your prognosis, your therapy plan and your life going forward.
The issue may not be myeloma yes or no, the issue may be how aggressively to treat your diagnosis. For example MM stage at stage 1 is almost a different disease than MM stage II. Elderly MM is treated completely diferently.
Is is never too early to hear what your oncologist has to say about any surgery, chemotherapy or radiation you may have to undergo.
Have you been diagnosed with multiple myeloma? What stage? What symptoms are you experiencing? Scroll down the page, post a question or comment and I will reply to you ASAP.
If you’ve received a multiple myeloma diagnosis, scroll down the page and ask for the MM CC nutrition and the questions guides. I will send these guides to you for free ASAP.
Being a patient is stressful. Receiving a multiple myeloma diagnosis is stressful. These strategies will keep your mind clearer when you are dealing with a medical diagnosis…
PREPARE FOR YOUR APPOINTMENT
To ensure you have the best possible experience with your doctor, it’s best to come prepared…
ASK QUESTIONS
We’re taught to listen to what the doctor says, and while in most cases that’s a good idea, in order to be our own advocates, we also have to speak up and ask questions. Remember: There is no such thing as a stupid question. If something comes up that you hadn’t considered, ask about it. If you don’t understand something, say so. This includes having the doctor explain any complex medical terminology.
But direct your questions appropriately.
Questions about scheduling appointments? Ask the front desk.
Getting ready for a hospital stay? Ask the nurse (not the doctor) about what clothes to bring.
Have a specific medical questions about your diagnosis or treatment? Ask your doctor. Chances are you’ll come up with additional questions as soon as you leave the appointment. Ask the doctor or nurse for the best way to contact them with these follow-up queries…
KEEP TRACK OF THE ANSWERS
A multiple myeloma diagnosis is complicated. When you’re in the doctor’s office because of a health problem, you may feel anxious or rushed — either way, it’s helpful to record the answers to the questions you ask your medical team, as well as the other information they give you. Bring paper to your appointment (or if you forget it or a pen, just ask the receptionist) to take notes of everything that is said during the appointment. If you’d feel more comfortable having an audio recording of the appointment, ask your doctor if you have their consent to record the office visit. There’s no need to purchase any equipment: most smartphones come with a free recording app, like Voice Memo. Depending on the nature of the appointment, it may be helpful to have a family member, friend or partner either go with you for a second set of ears, or call in on speakerphone so they can hear and take notes on everything being discussed…
MAKE SURE YOU ARE HEARD
A doctor’s appointment should feel like a conversation, and it’s important for both you and your physician that your voice is heard. Asking questions is one thing, but it’s also necessary to speak up when you don’t think you’re being heard or understood. There is no rule saying that the doctor’s opinion is the be-all and end-all. They are capable of making mistakes or, in some cases, simply ignoring patients and their concerns, which can be especially true when the patients are women or people of color. Therefore, it’s very important that you leave the appointment believing that your doctor is taking your pain seriously.
Be as specific about your symptoms as possible. The more information you’re able to provide to your medical team, the better your chances are of getting an accurate diagnosis. If the doctor is still being dismissive, calmly and respectfully express your concerns, and let them know that you don’t feel as though you’re being fully heard. If this doesn’t work, it may be time to change doctors or get a second opinion…
MAKE SURE YOU UNDERSTAND
If the doctor ends up making a diagnosis in the appointment and you don’t understand what it is or what it means, feel free to ask additional questions. Don’t hesitate to ask the doctor to refrain from using medical jargon when explaining what is happening to you…
WHEN YOU NEED (OR WANT) A SECOND OPINION
Some medical conditions have routine, straightforward treatment procedures. Other times, there are multiple ways to treat a patient, and it can be difficult to determine which option would be most beneficial. That may mean it’s time to get a second opinion. Moreover, if your doctor recommends a procedure that is invasive or your diagnosis is severe, that’s another good time to get a second opinion…”
Leave a Comment:
23 comments
Debbie Kintigh says
a couple of days ago
I would like the MM CC nutrition and question guide. My doc is totally upfront with me. I was diagnosed a year ago. I also have hemochromatosis and anemia.
[…] invite you to read Multiple Myeloma Diagnosis- A How To Guide- Years of researching myeloma and working with newly diagnosed patients have taught me the most […]
