Self-Advocacy Resources Menu
- Video Shorts-Tips for Talking to Your Doctor
- 10 Things to Do Before Your Next Doctor’s Appointment
- Video Shorts-Medication Advice from a Pharmacist
- 10 Things to Know When Starting a New Medication
- Resources to Help With Medication Costs
- Self-advocacy tips and stories of successful self-advocacy experiences from others who are living with vasculitis.
- Links to reliable websites that can help you increase and deepen your advocacy skills.
- Additional Self-Advocacy Resources
These resources were developed by VOV ambassadors, who, like you, navigate their lives while living with vasculitis.
Advocating for Yourself
You’ve been a self-advocate for most of your life. As a child, you probably advocated for a later bedtime. As a teen, you likely advocated for being allowed to use the family car. Now, as a patient with vasculitis, you must advocate for yourself in the medical world. This world includes long hallways, multiple exam rooms, lots of tests, and a parade of healthcare personnel speaking in what seems to be a different language: medicalese. And, adding to your challenges, this advocacy role starts at a time when you’re not feeling well.
What does effective medical self-advocacy look like? It’s going to a medical appointment with questions at the ready. It’s educating yourself about the latest vasculitis research advances and clinical/survey studies, and the Vasculitis Foundation is an excellent source. It’s listening to yourself about how your journey with vasculitis is going and what you want your future as someone living with vasculitis to be. Complementing medical self-advocacy are emotional/mental well-being and physical activity, both addressed in other sections of the website.
Please let us know what topics you’d like to see included.
Each of us is on a personal journey with this disease, and together we can help each other in our own Victory over Vasculitis.
Welcome to exploring your self-advocacy skills.
Vasculitis Medications: What Your Pharmacist Wants You To Know
Important Questions
Mitch Horowitz, a registered pharmacist who is living with MPA vasculitis, shares the questions you need to be sure to ask your doctor when you are prescribed a new medication.
How Will I Know?
Mitch Horowitz, a registered pharmacist who is living with MPA vasculitis, shares why it is so important to ask your doctor how you will know if the medication is working.
When Should I Be Worried?
Is this a normal side effect? Should I call my doctor? Mitch Horowitz, a registered pharmacist who is living with MPA vasculitis, explains how to deal with side effects, what side effects to look for, and when you should notify your doctor about a side effect you are experiencing.
Ask Your Pharmacist
Your pharmacist can be an excellent resource. Mitch Horowitz, a registered pharmacist who is living with MPA vasculitis, shares that your pharmacist wish’s you knew.
Cost Control
Medications can be expensive, especially if you have a chronic illness. Mitch Horowitz, a registered pharmacist who is living with MPA vasculitis, shares tips for controlling medication costs.
You Can’t Just Swallow a Handful of Meds Once a Day
Mitch Horowitz, a registered pharmacist who is living with MPA vasculitis, shares the important questions you should ask your doctor or pharmacist about how to take your medications.
Vasculitis Medications and the Timing of Vaccines
Mitch Horowitz, a registered pharmacist who is living with MPA vasculitis, shares important questions to ask your doctor about the timing of vaccines.
10 MEDICATION TIPS
Mitch Horowitz, Registered Pharmacist
Questions for the doctor. Be prepared when the doctor prescribes a new medication. Ask questions when you are in the doctor’s office.
WHY are you prescribing this medication for me?
WHAT should I expect this medication to do for me?
- Control/resolve vasculitis symptoms? (Treat active disease? Maintain remission? Treat a flare?)
- Control/resolve side effects? (Sleep issues, GI issues, high/low blood pressure, peripheral neuropathy, etc.
- How can I tell if what I am feeling is a side effect of the medication or a symptom of the Vasculitis?
WHAT’S NEXT?
- How long will I have to take this medication?
- How long will it take for the medication to start working?
- How long do we wait to determine if the medication is not working? What then?
- Who do I contact if I think I am having a problem – filling the medication, getting insurance approval, having a side effect?
WHEN should I take this medication?
- Morning/afternoon/evening
- With food? On an empty stomach?
- With other meds? By itself?
- Are there any food, drink, or drug interactions I should consider, most commonly with statins, citrus, or foods with high calcium content (dairy products)?
HOW is this medication given? Ask about other options.
- Pill – can you swallow big pills? Can it be split?
- Injection – needle phobia? Will someone teach me how to inject myself?
Infusion – outpatient infusion centers or hospital?
Ask about the TIMING of medications and vaccines such as flu, pneumonia, shingles, and COVID-19.
Medication COST
- Ask how much the medication costs, if insurance covers the medication, if it requires pre-approval, is there a generic available? The doctor may not know the answers but can direct you to someone in their office who can help. You may need to call your insurance company directly to ask questions.
- If you are in the hospital all medications will be dispensed by the hospital pharmacy.
- Pharmaceutical companies may have patient-assistance programs although it can take time to process an application and eligibility differs based on each company.
KEEP A LIST of your medications, doses, and schedules so you can track how long you have been on a medication.
KEEP TRACK of anything unusual that happens. These could be side effects.
- What did you notice and when did it start?
- How often is it happening?
- Is it better or worse at a particular time of the day?
- Take pictures of any visible signs (rashes, swelling, etc.)
- Contact the doctor’s office if necessary and be prepared to provide a clear description of what you have observed.
Always contact your doctor right away if:
- You think you are having side effects
- You are unable to take your medication for ANY REASON (side effects, cost, insurance issues, prescription approval, medication shortage, etc.)
- Your vasculitis symptoms are not getting better or are getting worse
What your pharmacist wants you to know. Ask questions when you pick up your medicines. Pharmacists are happy to answer your questions. If possible, work with one pharmacy. All pharmacies have drug interaction software to ensure that patients aren’t prescribed two medicines that might interact with each other.
How To Advocate For Yourself With Your Healthcare Provider
The 12 Second Rule
How to communicate important information to your healthcare provider.
You’ve Only Got 15 Minutes
How to come prepared to make the most of visits with your healthcare provider.
Be Honest With Your Doctor
How to tell your healthcare provider what they need to hear.
Did You Hear Me?
How to tell if your healthcare provider is listening to you.
Just One More Thing
How to ensure you cover what is most important.
You’ve Only Got 15 Minutes-Make It Count.
Preparing for a visit with your healthcare provider? Make sure you have these ready to go:
- List of current medications, refill requests, lab tests you need to schedule/discuss.
- Your main goals for the appointment (no more than three).
- A summary of how you are doing (be brief and HONEST).
- Any problems (side effects, insurance, expenses, ANYTHING stopping you from carrying out the treatment plan).
- List of any questions you have that only the doctor can answer.
Some Possible Questions:
- Why are you recommending this test/treatment?
- Why do you think this treatment will work for me?
- How will we know if the treatment is working?
- What are the other options?
Ask yourself, is this the right doctor for answering my question?
Before you leave, make sure you:
- Schedule your next appointment.
- Know your homework (bloodwork, tests, referrals).
Our Self-Advocacy Experiences
I am my own advocate when interacting healthcare professionals. My wife comes with me to help me advocate for myself. If I have questions, I write them down so I don’t forget them. I research the answers before I go so I know what to expect. I’m not afraid to tell my doctor what I think.
I ask what this medication does, and how does that help me; are there any side effects; are there alternatives. I have dietary restrictions, so I tell to my friends if invited to dinner. Same thing for restaurants.
– Mitch Horowitz, diagnosed with MPA in 2021.
“Very early in my journey I learnt the value of being my own advocate regarding my health and well-being. You are the one experiencing the symptoms and often these symptoms do not have physical signs for the medical specialists to see. It is so important to be your own advocate for your health and well-being as no one else will hold the value of this higher than you do.”
– Emma White, MPA, New Zealand
Additional Self-Advocacy Tips from Emma
- My rheumatologist has always been supportive of my curiosity and my research; however, he did encourage me to take caution with what I was reading and to raise any questions with him so that he could provide medical feedback based on my condition.
- Ahead of every appointment with my rheumatologist I make a bullet pointed list of the issues and observations since my last visit, as well as any requests such as specific blood tests I would like done or review of my medications.
- I also keep a folder of photos on my phone of any physical items that seem unusual, which I go through with my rheumatologist. If there is anything that I need to contact my rheumatologist about between appointments, I am very lucky in that I can email through to the nurses, and they pass this onto them.
“Self-Advocacy is so important when dealing with a complex disease like Vasculitis and the complex health care systems today. Having self-awareness and taking responsibility to identify and communicate your needs to your health care team, then together making informed decisions so that you get the quality health care you deserve.
I use daily documentation to keep track of my medications, symptoms and activities. This allows me to then trend and summarize the information for my doctors’ appointments to keep those visits organized and productive for both the physician and myself.”
– Cheryl Schmitter
“I advocate for myself by looking for and participating in clinical studies such as the one at the National Institutes for Health, and donating blood for a research study for vasculitis by Sanguine Bio. I am happy to help the medical community research the disease to hopefully find out what causes it, as well as better treatments for people with giant cell and Takayasu’s arteritis.”
– Cindy Orlandi
Provides education, resources, and advocacy for people living with chronic illness.
- Click here for a list of some of the charitable organizations that can help with medication related expenses.
- The National Organization for Rare Disorders (NORD) offers resources that can help with medication costs. They can be contacted by calling 1-800-999-6673. Find more information about NORD’s Help and Support line including hours of operation, services offered, and how to contact them online by clicking HERE. Si deseas hablar con alguien en espanol por favor llame al (844) 259-7178 para asistencia.
- Most pharmaceutical companies offer prescription cost assistance programs. Ask your doctor or pharmacist about these programs or do an online search for the manufacturers contact information/website.
- If you are prescribed a new medication while hospitalized, ask to speak to the on-staff social worker or patient advocate before leaving the hospital. They can help you access programs that can help with the cost of medications.
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