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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.

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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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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 ⁣
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As you can imagine, that makes me very aware of my disability via juvenile arthritis⁣
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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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#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. ⁣
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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. ⁣
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It doesn't mean that one person is necessarily worse off than another; they're just different.⁣
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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. A white text box reads "Chronic Illness Looks Different in Each Person"⁣
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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⁣
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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: 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.⁣
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#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⁣⁣.

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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
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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. 

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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

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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 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⁣
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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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#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. ⁣
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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⁣
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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. ⁣
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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. ⁣
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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!⁣
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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: Kate at 19 at Fenway Park for a Red Sox game. ⁣
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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:⁣
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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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