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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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SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣ ⁣ I sh SHARING YOUR HEALTH EXPERIENCES PUBLICLY⁣⁣⁣
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I share my personal health experiences online, which I find it somewhat easy to do because I've been talking publicly - albeit to a smaller audience - since my health problems started in 2001. ⁣⁣⁣
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If you share something online, you need to be prepared for people to ask questions or argue with you. Should they? No. Will that stop them? Also do. ⁣
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That's one of the reasons that talking online about what can be trauma is not easy or for everyone. That's why it's important to practice self-care and to consciously think about what you want to share online before you do it. ⁣⁣⁣
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For example, I generally only talk publicly about a health situation once it has passed, especially if it's an emergency. I also make sure that I'm in a good place mentally before I talk about it. That way, I don't share things I'll regret sharing publicly later. It also helps me be less anxious about sharing these details.⁣⁣⁣
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And I don't share everything! There's lot of stuff that I haven't talked about not only online but with people in real life. It might seem like I share everything I've experienced, but I don't. ⁣
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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: Kate works on a laptop offscreen. She's a redheaded white woman wearing a beige-and-navy striped sweater, silver Claddagh necklace, and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #ChronicPain #Endometriosis #SjogrensSyndrome
Week 18 of 2026 Weekly 1️⃣ Cross-stitch and IVIG Week 18 of 2026 Weekly 

1️⃣ Cross-stitch and IVIG 
2️⃣ Another trip to the foot doctor. We’re officially in Try To Avoid My 6th Foot Surgery mode 🤞🏻 
3️⃣ At least there were lilacs?

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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 down at Kate’s lap. Tubes are coming out of her shirt. She’s working on a cross stitch.
2️⃣ Kate takes a selfie in a doctor’s office. She’s wearing a lilac mask.
3️⃣ A lilac bush

#IVIG #CrossStitching #ChronicIllness #ChronicallyIll #InvisibleIllness
FAQ: Have I Tried Yoga for My Pain? This is a se FAQ: Have I Tried Yoga for My Pain? 

This is a series where I answer questions I frequently get about my rheumatoid arthritis. I am not a medical professional and this is not medical advice - just saying the truth about my body in particular. 

Video: Kate speaks to camera. There are captions. A black text box reads “FAQ: Have I Tried Yoga for My Pain?” 

#RheumatoidArthritis #AutoimmuneArthritis #Arthritis #ArthritisAwarenessMonth
May is Arthritis Awareness Month, which is the per May is Arthritis Awareness Month, which is the perfect time to remind people of these facts. Here's today's fact.⁣
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Like, comment, and share to spread awareness 💖⁣
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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: Fact or Fiction? Let's Check! ⁣
Fiction⁣
Arthritis only affects people as they age.⁣
Fact⁣
Arthritis can affect anyone at any age, including kids as young as 3.⁣
katethealmostgreat⁣
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#ArthritisAwareness #Arthritis #RheumatoidDisease #RheumatoidArthritis #ArthritisAwarenessMonth
I’ve been on IVIG since September. So what does su I’ve been on IVIG since September. So what does success look like? ⁣
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*This is all just for me and my case!*⁣
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1️⃣ I haven't gotten sick at all since I started, not even a cold. ⁣
2️⃣ My lungs are clear of any ground glass opacities, which was what pushed us over to finally doing IVIG regularly. ⁣
3️⃣ We feel better about saying that I don't have any infections. Because symptoms are often signs of the body fighting an infection, we couldn't always trust that I wasn't sick because I didn't have symptoms. ⁣
4️⃣ Because of all of this, we're increasing my next Rituxan dose! This will mean better RA symptoms and hopefully no new illnesses for a few years.⁣
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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 bunch of IVIG supplies, including a pump. ⁣
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#ChronicallyIll #ChronicIllness #ChronicPain #AutoimmuneDisease #Autoimmune
Week 17 of 2026 Weekly 1️⃣ Making some real progr Week 17 of 2026 Weekly

1️⃣ Making some real progress with this cross stitch
2️⃣ Walking casts have multiple uses, including holding down your mat! (Don’t worry - I only did broken-foot-compatible things) 

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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 An in-progress cross stitch. You can see that Kate stitched 2 bears.
3️⃣ A walking cast lies on a black yoga mat 

#CrossStitching #CrossStitcher #RheumatoidArthritis #Osteoporosis #LoopsAndThreads
Can we talk about fatigue for a sec? ⁣⁣⁣ ⁣ Fatigue Can we talk about fatigue for a sec? ⁣⁣⁣
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Fatigue is so much more than being tired. It's sleeping 10 hours at night and then struggling to stay awake during the day. It's trouble focusing because, even though you just had 3 cups of coffee, you're thinking about sleep. It's needing to factor rest in during the day because you have plans at night. ⁣⁣⁣
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It's a lot. ⁣⁣⁣⁣
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It's no secret that I have multiple chronic illnesses. But did you know that all of them - all 11+ of them - have fatigue as a symptom? Sometimes the fatigue is worse than the pain and, uh, I live with a lot of pain.⁣⁣
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This picture was taken when I was super anemic and waiting for 4 iron infusions. Now, months later, I can see it. And I also don't know how I got through the months of that anemia. ⁣
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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. She's a redheaded white woman wearing a gray sweater and pink glasses.⁣
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#ChronicallyIll #RheumatoidArthritis #Fibromyalgia #Endometriosis #POTS
Week 16 of 2026 This week had EVERYTHING 1️⃣ Cr Week 16 of 2026 

This week had EVERYTHING

1️⃣ Cross-stitch during virtual mass 
2️⃣ Tuesday featured a 90-minute meeting during work and then an hour advocacy work call after my day job (both were good!)
3️⃣ Wednesday started at my foot doctor’s office and I left in a walking boot. Hopefully these 3 fractured bones will heal correctly this time 🤞🏻
4️⃣ Thursday started back at MGH for my annual neurology appointment + foot CT scan
5️⃣ Then I went up to Maine … 
6️⃣ to celebrate my grandma’s 85th birthday! 

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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 In the foreground is an in-progress cross-stitch piece. The background shows an open laptop streaming Catholic mass.
2️⃣ Kate takes a selfie. She’s a white woman with auburn hair and green glasses.
3️⃣ Kate takes a selfie in a doctor’s office. 
4️⃣ Kate takes a selfie in a car.
5️⃣ Kate takes a selfie snuggling with a golden retriever.
6️⃣ Kate and her cousins stand with their grandmother in front of a sign saying "Happy Birthday." 

#CrossStitch #ChronicPain #ChronicallyIll #InvisibleIllness
My face comes with subtitles, so .. ⁣ ⁣ ⬛⁣⁣⁣⁣⁣ ⁣ I My face comes with subtitles, so .. ⁣
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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 drinks coffee giving side eye. White text box reads "My Face When Someone Says 'You Shouldn't Need a Cane At Your Age'" ⁣
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#ChronicPain #ChronicallyIll #RheumatoidArthritis #PosturalOrthostaticTachycardiaSyndrome #Fibromyalgia
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