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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

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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.

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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?⁣
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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⁣⁣.⁣
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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".⁣
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#AutoimmuneDisease #RheumatoidArthritis #PsoriaticArthritis #AnkylosingSpondylitis #JuvenileArthritis
Weekj 26 of 2026 Weekly Scenes of a summer week Weekj 26 of 2026 Weekly 

Scenes of a summer week in Maine! So glad I work from home, which means I can work from my real home (Maine, if that wasn’t clear)

1️⃣ Lots of Harley time
2️⃣ Working from home means saving my PTO for fun things!
3️⃣ Lots of duck families (📸 my dad)
4️⃣ What a lot of my days look like - Harley and my current project (needlepoint). And, yes, I’m still in a cast.
5️⃣ Learned how to play Mahjong, which my parents love
6️⃣ Lake views on the 4th

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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⁣⁣.⁣⁣⁣⁣

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IDs:
1️⃣ Harley the golden retriever on a deck as seen through some plants
2️⃣ Kate takes a selfie
3️⃣ A duck with little ducklings following on a lake
4️⃣ Harley coming up to Kate. Her legs are out on an ottoman, 1 foot in a walking cast, and an in-progress needlepoint project
5️⃣ Looking down at a Mahjong table with the game set up
6️⃣ A kayak on the shore of a lake 

#MaineTheWay #MaineSummer #Needlepoint #MaineLife
Living with chronic pain is really hard. You’re wi Living with chronic pain is really hard. You’re winning every day you’re still here.⁣
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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⁣⁣.⁣
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ID: The background image is a lake at sunset. Text reads what's above the first square and also "katethealmostgreat".⁣
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#ChronicIllness #ChronicPain #RheumatoidArthritis #Fibromyalgia #Endometriosis
I've been spending a fair amount of time at my foo I've been spending a fair amount of time at my foot surgeon's office this year, and boy has it been messing with my head. ⁣
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I spent a lot of time from 2001-2010 dealing with my left foot. Long story short, it took until this foot surgeon saw me in 2010 after fixing this foot for me to be diagnosed with rheumatoid arthritis. But I spent those 9 years going from doctor to doctor, having surgery after surgery, trying to figure out what was causing my pain and to fix it. ⁣
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Was it the tarsal coalition? Did I have another chronic health issue? Etc. ⁣
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I spent from age 10 to 19 unsure what exactly was wrong with me and in huge amounts of pain. We thought we figured it out, and then something else happened. ⁣
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We know exactly what is wrong with this foot this time around: in 2024, I got 3 stress fractures, and no one put me in a boot. They almost fully healed before breaking in 2025, and then the same thing happened in 2026. ⁣
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This is a different part of the foot than I used to deal with, but any problems with my feet and especially my left foot messes with me. While this doctor eventually fixed the problems and even got me diagnosed with RA, every time I go back to his office, I have to fight not to become 17 again. ⁣
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PTSD is a bitch.⁣
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(PS - if you want to know why I'm going back to this guy when it messes with me, it's because I don't trust anyone else to fix my foot.)⁣
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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⁣⁣.⁣
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ID: Kate takes a selfie in a doctor's office. ⁣
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#PTSDAwareness #ChronicallyIll #TarsalCoalition #RheumatoidArthritis #Osteoporosis
Week 25 of #2026Weekly Happy to be in Maine for Week 25 of #2026Weekly 

Happy to be in Maine for a few weeks! I didn’t get up to a lot, so another week of very few pictures

1️⃣ IVIG 
2️⃣ Lots of beautiful birds have been coming to my mom’s bird feeder!

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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⁣⁣.⁣⁣⁣⁣

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IDs: 
1️⃣ Looking at Kate’s lap. Tubes are coming out from under her shirt and there’s a Kindle
2️⃣ Birds arriving at a bird feeder as seen through a window

#ChronicallyIll #InvisibleIllness #ChronicPain #IVIG
What do you have to do every day for your chronic What do you have to do every day for your chronic illnesses? ⁣
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For context, I have rheumatoid arthritis, fibromyalgia, endometriosis, POTS, heart disease, osteoporosis, and more. ⁣
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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⁣⁣.⁣
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ID: ⁣
Things I Do Every Day for My Chronic Illnesses⁣
Take pills at least 4 times a day⁣
Don’t eat gluten, dairy, corn, soy, or eggs⁣
Sleep 7+ hours a night⁣
Consume 80-100 grams of protein, 120 mg of calcium, 5-10 grams of sodium⁣
Wear a mask whenever I leave the house⁣
Do pilates 4+ days a week⁣
Work from home⁣
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#ChronicallyIll #InvisibleIllness #RheumatoidArthritis #Fibromyalgia
Filmed this back in April (hence the sweater) but Filmed this back in April (hence the sweater) but it applies to whenever I have appointments! 

Video: Kate talks to the camera while holding a purse. She holds up individual items mentioned in the video before putting them in the bag. There are captions. 

#ChronicallyIll #RheumatoidArthritis #Osteoporosis #ChronicPain
There are a lot of medical advancements that I'm g There are a lot of medical advancements that I'm grateful for, but one of them is the ability to do IVIG at home. ⁣
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I'm on IVIG - or, in my case, subcutaneous immunoglobulin replacement therapy - because I have to kill the better part of my immune system. There are, in fact, some parts of my immune system that don't attack me, which is why we add them back in. This helps reduce my chance of serious infection and also made my rheumatologist feel comfortable enough to increase my Rituxan dose. ⁣
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This is a weekly treatment that I do, but it's so much better that I can do it at home than going into the hospital. It takes around 2.5 hours from taking my pre-meds to tossing my needles into a Sharps container. While it's another thing that I have to do, because I do it at home, I don't have to risk exposure to infections at the hospital or deal with Boston traffic, which would add another hour to the process. ⁣
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I can finish my treatment and then go about my day, which I'm very grateful for.⁣
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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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⁣⁣.⁣
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ID: A Kindle on Kate's legs. There are tubes for an infusion coming out of her shirt.⁣
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#IVIG #ChronicallyIll #RheumatoidArthritis #Autoimmune #AutoimmuneDisease
Weeks 23 and 24 of 2026 Weekly! The last two wee Weeks 23 and 24 of 2026 Weekly! 

The last two weeks were prepping for my infusion, having/recovering from my infusion, and getting caught up after. This meant things were very busy but also I don’t have a lot to show for them. 

1️⃣ New glasses! I really like having multiple pairs so I can switch them as I want.
2️⃣ One of my current projects. I got this standing hoop for my birthday and I’m working on an alphabet (uppercase and lower, although I’m still working on the lower) with extra floss.
3️⃣ Infusion time! I got my higher dose so hopefully my symptoms improve a lot in the upcoming weeks🤞🏻

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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⁣⁣.⁣⁣

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IDs: 
1️⃣ Kate takes a selfie. Her new glasses are thin silver circles
2️⃣ An in-progress cross-stitched alphabet in a special hoop stand that Kate is sitting on.
3️⃣ Kate takes a selfie in an infusion chair.

#ChronicallyIll #RheumatoidArthritis #AutoimmuneDisease #CrossStitcher
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