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in Health, Lifestyle &middot November 23, 2016

Chronic Medical Conditions and Family Discussions over the Holidays

One of the classic elements of the holiday season is conversation with family members you haven’t seen or talked to in a while about what your life is like right now. This can be uncomfortable to anyone but it is especially so for people with chronic medical conditions. Sometimes there are problems with answering “normal” questions, and sometimes there are problems with health questions. Our problems with these questions are a bit different than those of healthy people; sometimes we quite literally do not have the energy to answer them, and sometimes we just don’t know how to answer them. Regardless of what problems you have, I hope that this helps you.

You might also enjoy – Common Spoonie Conversational Issues + How You Respond

Looking forward to the holidays but not looking forward to family discussions about your health? Here is how you deal with those conversations.

“What are you up to?” – If nothing much has changed since the last time you saw them, you’re not doing much other than going to medical appointments, or your health is doing worse, you can quickly pass over yourself and then redirect the conversation back to the person who asked. Tell them, “Oh, I’m up to the same. How are you? How is work? Are you still doing [insert their favorite hobby here]?” If something is coming up, you can always talk about that.

“Have you tried [etc.]?” – When you have a chronic illness or condition, often people who don’t know much about it will turn to good ole’ Google. This can be great in some cases, but it can also mean that you have many conversations that focus around information from basic internet research. Often, this leads people to act as though they know your medical condition better than you do. I’ve been able to shut people down by saying someone along the lines of, “If it’s a treatment for RA, I’ve either tried it and it didn’t work for me or my rheumatologist doesn’t believe it will work for me.” Then, I move on. If you haven’t tried many treatments, you can always say, “That’s interesting! I’ll have to look into it.”

How to respond to questions from family about your chronic medical conditions during the holidays

“What are you looking to do after your degree?” – This is a question I’m dealing with a lot right now, especially since humanities degrees don’t have any obvious career after completing them. Unfortunately, this is also the most emotionally difficult for me to answer. I studied secondary education in undergrad and I loved teaching, but I had to quit my job after my first year because my health was bad. I’m terrified of setting my heart on another career and then my health getting in the way again. One way to answer this question without getting upset (hopefully) is to say, “I have several ideas but I’m not positive what I’m going to do yet.” If you have no idea what you’re going to do, you could say, “I’m not positive yet, but my school/advisor has some ideas.”

“Are you doing better?” or “I hope you get better soon!” – This is probably the hardest question to answer unless you are doing better. The people who ask this care about you, and they don’t want you to feel worse. If they ask how you’re doing, you can say, “I’m hanging in there!” or a simple, “Thank you – that means a lot.”

How do you deal with family discussions when you’re chronically ill?

[bctt tweet=”How to talk about your health with your family over the holidays” username=”kmitchellauthor”]

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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  1. Round-up: Pie, Blogging, Literary Heroines, and the Holidays! - Second Breakfast says:
    November 29, 2016 at 10:51 am

    […] How to talk to friends and family about your chronic health issues. This one’s hard for me. I don’t talk about my issues much–I didn’t tell anyone about it for the first four years!–but sometimes you need to. Your family wants to know what’s going on, how you’re doing, and Kate has some great tips for how to talk to them about it. […]

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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
Week 22 of 2026 Weekly 1️⃣ Off to see my foot doc Week 22 of 2026 Weekly

1️⃣ Off to see my foot doc … and my foot is healing! Yay!
2️⃣ A very cool notification to get!
3️⃣ This is 35 🎂
4️⃣ Featuring Harley snuggles 
5️⃣ And then it was my mom’s birthday! 
6️⃣ With Harley again 

ID: 
1️⃣ Kate takes a mirror selfie 
2️⃣ a notification from WordPress saying “Receive views from 150+ counties. The United Nations has nothing on you!”
3️⃣ Kate smiles for the camera in a cafe 
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Lifestyle Changes I Made for My Rheumatoid Arthrit Lifestyle Changes I Made for My Rheumatoid Arthritis⁣
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While these are not my treatments, they have made my life better in some ways. ⁣
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What lifestyle changes have you made, for RA or another condition?⁣
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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: ⁣
A series of pictures. Each has a text box on them related to the picture. ⁣
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1️⃣ Lifestyle changes I made for my rheumatoid arthritis⁣
2️⃣ Wearing a mask⁣
3️⃣ Using a cane⁣
4️⃣ Changing my diet⁣
5️⃣ Working from home⁣
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What helps you mentally get through a tough time?⁣ What helps you mentally get through a tough time?⁣
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I'm struggling right now with my broken foot, which brings back a lot of tough memories. That plus being due for Rituxan and the heat starting up has made things hard. ⁣
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Here are somethings I do: ⁣
▪ Stick with my routine⁣
▪ Make recipes that I really enjoy⁣
▪ Work on embroidery projects so I can do something productive that involves stabbing fabric⁣
▪ Cut myself slack ⁣
▪ Get Harley hugs⁣
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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 and Harley the golden retriever hugging. Kate is a redheaded white woman wearing a black dress, pink sweater, and round pink glasses.⁣
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Week 21 of 2026 Weekly 1️⃣ First real cross-stit Week 21 of 2026 Weekly 

1️⃣ First real cross-stitch project: done! 
2️⃣ The magic machine that is hopefully healing my broken foot 
3️⃣ When your 2 refrigerated medications are delivered on the same day

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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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1️⃣ A completed cross-stitch project, which shows 2 bears walking past a lake, trees, and mountains.
2️⃣ An Exogen machine showing use 13 days in a row
3️⃣ A couple of styrofoam refridgerated containers for medication

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You guessed it, I'm one of that 25%. ⁣ ⁣ May is Ar You guessed it, I'm one of that 25%. ⁣
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May is Arthritis Awareness Month. 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⁣
You only have rheumatoid arthritis if your rheumatoid factor tests positive.⁣
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As many as 25% of RA patients test negative, which is called being seronegative.⁣
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Things are tough (all over pain, heat with POTS, i Things are tough (all over pain, heat with POTS, in a walking cast waiting to see if I need my 6th foot surgery), but so am I.⁣
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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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Week 20 of #2026Weekly 1️⃣ IVIG + Kindle reading Week 20 of #2026Weekly 

1️⃣ IVIG + Kindle reading 
2️⃣ Almost done!!!!!

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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 Infusion tubes coming out from under her shirt. There’s a Kindle on her lap.
2️⃣ An almost-finished cross-stitch project

#IVIG #ChronicallyIll #CrossStitcher #CrossStitchersOfInstagram
FAQ: Have you tried [insert supplement here]? As FAQ: Have you tried [insert supplement here]?

As with all things, what’s true for me might not be true for others. I’m sure there are plenty of RA patients who do respond well to supplements; I’m just not one of them. 

Additionally, at one point, I refer to being on chemo since 2012. As always, the chemo I’m referring to is Rituxan, which is my RA treatment. I do not have cancer nor have I ever claimed to. 

Video: Kate talks to the camera. Text at the beginning reads “FAQ: Have you tried [insert supplement here]?” and other text later reads “*24” to correct when she says “symptoms for 21 years”. There are captions. 

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