• Skip to main content
  • Skip to primary sidebar
  • Skip to footer

Kate the (Almost) Great

Chronic illness blog

  • Home
  • Start Here
    • About
    • As Seen On
    • Tags & Topics
    • Popular Posts
  • Blogging Resources
  • Freebie
  • Shop the Blog
    • Products for the Chronically Ill
  • Contact & Work with Me
    • Ads and Sponsoring
  • Follow
  • Holiday
    • Gift Guides

in Health &middot July 20, 2018

Chronically Ill Tips: Preparing for Medical Appointments + Freebies To Help

Not to brag, but with anywhere from 2 to 8 medical appointments a week, I’m pretty skilled at preparing for them. In all seriousness, I have 6 chronic illnesses – 3 of which cause chronic pain – and have been actively been preparing for them since 2001. Since this fall will mark 17 years that I’ll have been chronically ill and in pain, I thought I would share my tactics for preparing for these appointments. I’ve seen doctors, nurses, and physical therapists that haven’t believed my pain, some who supported me and I saw at least once a month, fellows and residents who have never seen a patient like me, and some who were somewhere in between.

I hope that my tactics will help you, and make sure you scroll down to the bottom to check out two free printables. One is the sheet I use to keep track of medications, conditions, my medical team, and family history, and the other is one designed to help you put all of your symptoms in one place. I hope that these will help make your appointment as productive as possible!

Medical appointments can be tricky when you're chronically ill. I've been sick for 17 years, so today I'm sharing my tips to help you prepare for your next doctor's appointment.

Chronically Ill Tips: Preparing for Medical Appointments

Organize your thoughts beforehand – I think this is the most important one and everything else on this list really comes from this. If you don’t do some kind of organization, you can forget something that is important. Some questions you can ask yourself are: What do you want to get out of the appointment? Why are you going to this appointment? What does this medical professional need to know? If this is not an appointment with a new member of your medical team, then you should also take note of anything that has changed since your last appointment. If you have a condition like fibromyalgia that can cause brain fog, I strongly suggest writing some things down. Make sure you put this list somewhere that you’ll remember to bring it. I always write these lists in my planner, as I bring that everywhere.

Talk to your loved ones/people you live with about what they’ve noticed – With several of my specialists, I see them every couple of months. A lot can happen in that time, so I always ask my parents if they have any questions for me to ask or if they’ve noticed anything different. Sometimes we’re on the same page, and some times something has happened in the previous 3 months that I’ve forgotten about in lieu of other things. If you live with your partner, you might ask them if they have any questions or things to bring up, and if you live with roommates, you might ask them if they’ve noticed anything different about your health since your last appointment. While this can help you remember something that you’ve forgotten about, it can also bring up something that you may not have noticed. For example, while those of us with chronic pain are generally more in tune with our bodies and their changes, we may miss that we’ve been turning down invitations more than usual if it happened at a slow and steady pace. Getting that feedback may help you notice what you’ve forgotten.

Gather any images or test results you have – This is especially important if your doctors are not a part of the same system. What I mean is that almost all members of my medical team are based at Massachusetts General Hospital, and with technology how it is now, they can pull up all tests or imaging done at MGH. It doesn’t matter that my cardiologist is out in Waltham and the rest of my team is in Boston; she can pull up any tests that were done in Boston. So if you’re seeing someone who is at a different office or is a second opinion, make sure you have any relevant images or testing with you. Don’t have it? This is your personal medical history, so you have a right to it. You can call the office that has what you need and they will mail it to you, or you can pick it up. Make sure you leave enough time between when you call and when your appointment is because for some offices it can take a while to get to you. I’m pretty sure it’s because they don’t send you the only copy of the information; they have to make a copy for you. I did this several years ago and it took weeks for my history to get to me. Turned out it was like 100 pages that they had copies because medical bureaucracy, you know? Also I have a very long medical history shhh

chronically ill, chronic illness, chronic pain, rheumatoid arthritis, ra, rheum, arthritis, psoriatic arthritis, ja, fibromyalgia, endometriosis, postural orthostatic tachycardia syndrome, POTS, chronic anemia, asthma, chronic fatigue, fatigue, chronic illness tips, rheumatoid arthritis tips, ra tips, fibro, fibro tips, fibromyalgia, endo, endo tips, endometriosis tips, POTS tips, tips for living with RA

Write down a history of the problem you’re having – I find this especially important for issues that I’ve been having for years. When did it first start? What could have contributed to it? What makes it better or worse? How has it been recently? These are all questions that you will be asked, and you want to make sure that, when you’re seeing a new doctor for this issue, you start at the beginning and go chronologically. This is something I always mess up: I start in the middle, or I skip around, or (worst of all) I forget important details. That’s why it’s so important that you write it down before you go in. If it’s a complicated issue that has been bothering you for a long time, you might write it down to give to the doctor. The other option is to write it down just to get your thoughts in order. This will help you be prepared for the appointment and hopefully not too flustered, which is a situation I’ve found myself in too often.

Organize your medical history and medications beforehand – This is one of the most important things you can do. How is this different than above? If you take more than 3 medications, it can be difficult to remember the exact dosages of them. It’s also important to share allll of your medical history and not just what you’re seeing that doctor for. You might not know if one chronic illness could influence a different part of your health or vice versa. Additionally, you need to include your family’s health history. For example, my aunt and cousin both have other autoimmune diseases. My cousin was diagnosed a few years ago, and his doctors needed to know that I and our aunt both have autoimmune diseases. We all have different ones, but that family history made sure that his doctor considered him having an autoimmune disease. You might not know that a family history of x condition could cause the same of different condition in you. And this usually takes pre-work, such as calling different family members and making notes of who has what. How can you keep track of it all? Download the free printable medication and medical history organizer. This is my #1 thing that I always have. I have a copy of it folded in my wallet. I print out new copies to give to my medical team – especially because medical offices usually only give you a couple of lines to write medications and family history. Get it here.

Organize your symptoms beforehand – How is this different than the other things mentioned in this post? I think it’s important to do a person inventory on all of your symptoms that the medical professional should know about. Many offices will give you a form to check out any symptoms that you might have, but if you’re in a rush or the doctor is in a rush, something might get missed. It’s important to figure it out before you go into your appointment. To help you, I’ve pulled together a free large symptom organizer to help you figure things out beforehand. It includes how long you’ve been having symptoms, what makes them better or worse, and more. Check out the symptom organizer here.

Why You Must Track Symptoms of Your Chronic Illness + Freebie To Help

Free Medical Symptom Organizer

What do you always do to prepare for medical appointments if you’re chronically ill?

Like this post? Share it and check out these:

Preparing for Chronic Pain Medical Appointments, Answering Questions about Being Chronically Ill, Hacks for Living with Chronic Conditions, 5 Items Every Immunosuppressed Person Needs

Kate Mitchell

Kate Mitchell is a blogger, chronic illness patient, and advocate who helps people understand chronic illness and helps chronic illness patients live their best lives.

Share this with your family and friends:

  • Share on X (Opens in new window) X
  • Share on Facebook (Opens in new window) Facebook
  • Share on Pinterest (Opens in new window) Pinterest
  • Email a link to a friend (Opens in new window) Email
  • Share on LinkedIn (Opens in new window) LinkedIn
  • Print (Opens in new window) Print
  • Share on Tumblr (Opens in new window) Tumblr

Related

Previous Post: « How Blog Traffic Reports Can Get Traffic to Your Blog
Next Post: My Workwear »

Reader Interactions

Trackbacks

  1. POTS and Heat Intolerance | Kate the (Almost) Great Boston Lifestyle Blog says:
    December 27, 2021 at 11:31 am

    […] Chronic Illness a Disability?, Chronically Ill Tips: Preparing for Medical Appointments + Freebies To Help, Hacks for Living with Chronic Conditions, College Tips for Disabled Students, 30 Things about […]

    Loading...
    Reply
  2. Chronically Ill Tips: What To Do When a Doctor Isn't Listening to You says:
    October 15, 2022 at 3:51 pm

    […] Chronically ill tips: preparing for medical appointments […]

    Loading...
    Reply
  3. How Chronic Illness Affects Relationships | Kate the (Almost) Great says:
    May 18, 2024 at 4:12 pm

    […] To Actually Rest When You Take Breaks, Is Chronic Illness a Disability?, Chronically Ill Tips: Preparing for Medical Appointments, Questions Not To Ask Someone with a Chronic […]

    Loading...
    Reply
  4. 120 Resources for Living with Chronic Illness says:
    July 20, 2024 at 3:25 pm

    […] Chronically Ill Tips: Preparing for Medical Appointments + Freebies To Help […]

    Loading...
    Reply
  5. Holiday Gift Guide: Gifts for Chronic Illness Patients - Kate the (Almost) Great says:
    June 30, 2025 at 4:48 pm

    […] All gift guides, Caring for Rheumatoid Arthritis Patients, Chronic Illness and Mental Health, Is Chronic Illness a Disability?, Chronically Ill Tips: Preparing for Medical Appointments + Freebies To Help […]

    Loading...
    Reply

Leave a ReplyCancel reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Primary Sidebar

Kate the (Almost) Great® is a chronic illness lifestyle blog. It is a resource for chronic illness patients and their loved ones.

  • Bluesky
  • Email
  • Facebook
  • Instagram
  • Pinterest
  • Threads
  • TikTok
  • Twitter

Categories

Health
Lifestyle
Writing & Blogging

Pages To Start With

  • About Kate the (Almost) Great®: Meet the Health Blogger
  • As Seen On
  • Contact & Work with Me
  • Follow
  • Health Blog Resources I Actually Use + Recommend
  • Newsletter
  • Popular Posts
  • Privacy Policy & Disclaimer Policy
  • Products for the Chronically Ill: My Recommendations
  • Shop
  • Start Here
  • Tags & Topics

Search

As an Amazon Associate I earn from qualifying purchases.

This blog uses affiliate links. Thank you for supporting Kate the (Almost) Great!

Sign Up for the Newsletter

Please wait...

Thank you for sign up!

Most Popular Posts

  • What Every POTS Syndrome Patient Needs for the Summer
  • 9 Arthritis Products That Help My Rheumatoid Arthritis
  • Seronegative Rheumatoid Arthritis Diagnosis: What I’ve Learned
  • The Products I Loved (And Wanted) in Grad School
  • What Is the Difference between Osteoarthritis and Rheumatoid Arthritis?
  • What Does Arthritis Pain Actually Feel Like?
  • What Sjögren’s Syndrome Is: A Beginner’s Guide
  • The Lifestyle Changes I Made for My Rheumatoid Arthritis
  • Beginner’s Guide: Rheumatoid Arthritis Flare Up


Bluehost.com Web Hosting $3.95

Health Union Patient Leader Certification

Support KTAG

If you like what I do, please support me on Ko-fi.




Footer

Sign Up for FREE Instagram Challenge

Get 25 FREE Instagram prompts for chronic health creators!

You can unsubscribe anytime. For more details, review our Privacy Policy.

Thank you!

You have successfully joined our subscriber list.

Get your FREE Instagram challenge here 

and 

For just $5 get your copy of my ebook Take Your Blog (And Income!) to the Next Level with code "greatest".

.

Kate the (Almost) Great

Chronic health lifestyle blog

Lets Go!
  • Facebook
  • Instagram
  • Pinterest
  • Twitter
July is: ⁣ - Disability Pride Month ⁣ - Juvenile A July is: ⁣
- Disability Pride Month ⁣
- Juvenile Arthritis Awareness Month ⁣
- the anniversary of when I was diagnosed with autoimmune arthritis at age 19 after 9 years of symptoms ⁣
⁣
As you can imagine, that makes me very aware of my disability via juvenile arthritis⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
ID: Screenshot of a Bluesky post. The background is dark teal, and it's written by Kate Mitchell | Kate the (Almost) Great with the username katethealmostgreat.bsky.social. ⁣The text reads what's above the first black box.⁣⁣⁣⁣⁣
⁣
#DisabilityPride #JuvenileArthritis #RheumatoidArthritis #AutoimmuneDisease
There are a lot of reasons why you shouldn't doubt There are a lot of reasons why you shouldn't doubt someone's chronic illness, but this is one of them. ⁣
⁣
I'm always amazed by how people can have the exact same illness or set of illnesses and still have different experiences. Sure, there will be similarities, but which symptoms are the worst, what medications you respond to, and your quality of life can vary significantly. ⁣
⁣
It doesn't mean that one person is necessarily worse off than another; they're just different.⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
ID: Kate takes a selfie. A white text box reads "Chronic Illness Looks Different in Each Person"⁣
⁣
#ChronicallyIll #RheumatoidArthritis #Endometriosis #Fibromyalgia #POTS
This basically sums up my summer so far: Harley, a This basically sums up my summer so far: Harley, a sewing project, and my foot in a cast⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣ ⁣
⁣
ID: Harley the golden retriever has his head on Kate's lap. Also on her lap is an in-progress needlepoint project and Kate's leg (in a walking cast) is elevated.⁣
⁣
#Osteoporosis #RheumatoidArthritis #GoldenRetrievers #Needlepoint #Needlework
Week 28 of 2026 Weekly A very busy week! 1️⃣ Foo Week 28 of 2026 Weekly

A very busy week!

1️⃣ Foot checkup! Walking boot is on occasionally from now until September 
2️⃣ Boston 
3️⃣ IVIG
4️⃣ Dentist 🦷 All good! 
5️⃣ Not a filter - this was the Boston area the second half of the week 
6️⃣ Physical time!

⬛⁣⁣⁣⁣⁣⁣⁣⁣

I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.

⁣⁣⬛⁣⁣

IDs:
1️⃣ Kate takes a selfie in a doctor’s office
2️⃣ Looking at TD Garden, the bear statue for the Bruins, and Zakim Bridge in the background 
3️⃣ Looking at tubes coming out from under Kate’s clothes. There’s a Kindle on her stomach
4️⃣ Kate takes a mirror selfie before leaving
5️⃣ Medford Square looking like there’s a yellow filter over it
6️⃣ Kate takes a selfie in a doctor’s office

#ChronicallyIll #InvisibleIllness #AutoimmuneDisease #Bostonian #IVIG
Also, if this is how you’re finding out, I’m sorry Also, if this is how you’re finding out, I’m sorry. I’m fortunate enough to have a lot of people who care about me and this is the fastest way to tell everyone. 

Video: Kate talks to the camera while putting on makeup. There are captions. 

#RheumatoidArthritis #AutoimnuneDisease #ChronicIllness #Arthritis #ChronicPain
Week 27 of 2026 Weekly (Delayed because last Sund Week 27 of 2026 Weekly

(Delayed because last Sunday was baaaaad)

1️⃣ Due airport difficulties, we got a few more days with Emma. Harley was THRILLED!
2️⃣ Beautiful bird/squirrel visitors
3️⃣ A beautiful Maine summer day

⬛⁣⁣⁣⁣⁣⁣⁣⁣

I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.

⁣⁣⬛⁣⁣

1️⃣ Harley the golden retriever putting his front legs up on Emma’s legs to demand hugs.
2️⃣ A bird feeder and hummingbird feeder on a deck. There is a hummingbird at one and squirrel at the other.
3️⃣ A barn, a pond, and the Maine woods

#207 #MaineLife #MaineTheWay #NewEnglandSummer #IGMaine
Reminder: you can be proud of your disability comm Reminder: you can be proud of your disability community while wishing your body cooperated more⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
 ID: Screenshot of a thread post. The background is dark teal, and it's written by katethealmostgreat. ⁣The text reads what's above the first black box.⁣⁣⁣⁣⁣
⁣
#DisabilityPride #ChronicallyIll #InvisibleIllness #Disabled #Disability
I don’t know the exact date of my RA diagnosis, bu I don’t know the exact date of my RA diagnosis, but this is from right around then in July 2010. ⁣
⁣
When I was diagnosed, I had been having symptoms for 9 years. ⁣
- 9 years of foot pain (partially from tarsal coalition)⁣
- Arthritic damage in said food⁣
- Carpal tunnel off and on for several years⁣
- And more⁣
⁣
I was finally diagnosed because I woke up one morning and was unable to open my jaw more than 8 mm. It turned out that I had horrible arthritic damage to my TMJs, which got me off the waiting list at MGH rheumatology. I left that appointment with an autoimmune arthritis diagnosis. ⁣
⁣
The fact that July is not only my diagnosis anniversary but also Juvenile Arthritis Awareness Month has always seemed right. I may not have been diagnosed with JA, but given the amount of arthritis I had along with my many years of symptoms, it's generally accepted that I had it. ⁣
⁣
This year marks 16 years since diagnosis and this fall marks 25 years since my symptoms started. It's pretty weird that so much time has already passed!⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
ID: Kate at 19 at Fenway Park for a Red Sox game. ⁣
⁣
#RheumatoidArthritis #AutoimmuneDisease #Arthritis #JuvenileArthritis #JRA
Dos and don'ts for when someone in your life is di Dos and don'ts for when someone in your life is diagnosed with autoimmune arthritis! What are some that you would add?⁣
⁣
⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
⁣
I’m Kate, a chronic illness patient and advocate sharing what my life is like with 10+ chronic illnesses. Follow me for more and check out my blog at katethealmostgreat.com⁣⁣.⁣
⁣
⁣⁣⬛⁣⁣⁣
⁣
ID: "So someone you know was diagnosed with Autoimmune Arthritis". Under the Do column (indicated with a green checkmark) is:⁣
"As how they feel about it⁣
Offer specific ways to help⁣
Treat them normally⁣
Ask follow-up questions⁣
Wear a mask around them when sick."⁣
Under the don't don't column (indicated with an x in a red circle) is:⁣
"Say “At least it’s not xyz!”⁣
Say that and not follow through⁣
Assume nothing about their lives has changed⁣
Conflate autoimmune arthritis with osteoarthritis⁣
Pass your cold to an immunosuppressed person".⁣
⁣
#AutoimmuneDisease #RheumatoidArthritis #PsoriaticArthritis #AnkylosingSpondylitis #JuvenileArthritis
Follow on Instagram

Copyright © 2026 · Kate the (Almost) Great · Design by Studio Mommy

%d