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in Health &middot March 12, 2021

So Someone Healthy Has Given You Health Advice

If you have experienced chronic illness or pain symptoms for longer than a month, then you have probably gotten unsolicited health advice, especially from healthy people. And if you’re like me and have had symptoms for longer than that, then you’ve gotten a LOT of it. To say it’s “pretty annoying” is a bit of an understatement.

A while ago (sorry for taking this long!!) someone requested I write a blog post about how to deal with getting heath advice from healthy people. Since I’ve dealt with chronic illness symptoms for nearly 2 decades, I have a lot of experience with it, which made me agree to write this post.

Below I’m sharing how to deal with unsolicited health advice from people who don’t know you personally and from people who do. I hope this post helps you find strategies and ways to make your life a bit easier.

If you have experienced chronic illness or pain symptoms for longer than a month, then you have probably gotten unsolicited health advice, especially from healthy people. And if you're like me and have had symptoms for longer than , then you've gotten a LOT of it. To say it's "pretty annoying" is a bit of an understatement.
Contents hide
Why is it annoying to get unsolicited health advice?
Getting Unsolicited Health Advice: When It’s Someone You Don’t Know
Getting Unsolicited Health Advice: When It’s Someone You Know (And They Mean Well)
Getting Unsolicited Health Advice: When It’s Someone You Know (And You Don’t Know If They Mean Well)
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Why is it annoying to get unsolicited health advice?

If you’re reading this post, there’s a good chance that you are someone who has gotten their fair share of unsolicited health advice.

But there’s always the chance that you’re someone who has given it, and if that’s the case, it’s important to explain why this is frustrating before we move forward.

Let’s say you’re talking to someone you know – like a friend or coworker – and you ask, “Have you tried [insert random treatment here] to feel better?” In that case, you’re basically saying, “I don’t think you’re trying hard enough to feel better. If you really were, you’d try this treatment that I, a layperson with zero medical education, have suggested.”

Let me tell you something: one of the first things you do when you’re diagnosed is turn to Google to find out everything you can. And if you’re talking to someone who has been diagnosed for years and years, they know more about the treatments out there than you do.

Free Medical Symptom Organizer

Let’s say that you’re talking to a stranger on the Internet and send a message or comment saying, “Have you tried [insert random treatment here]?” Here you’re saying, “I don’t care enough to find out what you’ve tried or what your medical history is. However, if you don’t try what I’ve suggested, then you’re settling for a life of pain/health issues and all future health issues are your own fault.”

Messages and comments from people suggesting random treatments really upset me because, as you can see here, the moral for all of them is pretty much that I’m not trying hard enough to feel better. This is true for conventional medical treatments as well as alternative ones.

There’s a chance that you meant to give advice because you care about the person! But that’s now how it feels.

Part of that is because I have gotten so much advice from people who don’t actually care about me as a person. They care about being right. They care about convincing people to buy their product. You get the picture.

4 Questions To Ask Before Sending Medical Advice on the Internet

health advice, unsolicited health advice, chronic illness, chronic pain, rheumatoid arthritis, RA, rheum, rheumatoid disease, autoimmune arthritis, inflammatory arthritis, fibro, fibromyalgia, endo, endometriosis, POTS, postural orthostatic tachycardia syndrome, dysautonomia

Now that I’ve addressed why getting unsolicited health advice is annoying in the first place, let’s talk about what to do when you get it from someone you don’t know.

Getting Unsolicited Health Advice: When It’s Someone You Don’t Know

This could be someone who has given you advice online – such as replying to a post of yours or DMing – or it could be someone who just comes up to you when you’re out and about. I haven’t gotten in-person unsolicited health advice in a while, but that’s more about how because of COVID-19 I don’t really go places and when I do go places people aren’t really coming up to me because, again, COVID-19.

At one point, to avoid unsolicited advice, my pinned tweet said something like, “Please don’t give me advice unless I specifically ask for it.” Then, in follow-up posts, I explained that I’ve been in pain for a very long time and how giving me unsolicited advice is the quickest way to anger me.

Of course, this only kind of helped on Twitter, not anywhere else.

Most of the time, I just ignore it – I don’t reply, I don’t like, etc.

On Instagram, I started getting near-spam comments on my posts when I posted health posts. To stop that, I used the “mute” function to mute comments with certain words and phrases.

When you’re in your settings, click “Privacy.” Then, under “Interactions,” click “Comments.” In the filters, I have turned on “Hide Offensive Comments” and “Manual Filter”.

Under “Manual Filter,” you type in the words or phrases that you want muted. Additionally, I have “Filter Most Reported Words” turned on, which hides comments with words or phrases that are most commonly reported.

Again, these things only work for certain types of social media and certain types of engagement.

My other suggest is to use the block and mute buttons liberally.

People not respecting your boundaries? Block. People who seem to mean well but just can’t get the message that you don’t want their suggestion? Mute ’em.

Don’t feel guilty for kicking people out of your space if they only seem to care about being right. If they don’t seem to care if you want to hear from them. If they don’t seem to care if you don’t want people giving you unsolicited advice.

Kick. Them. Out.

Plenty of people will say that you shouldn’t block or mute people for “just giving you advice.” Those people clearly don’t have the experience of getting unsolicited advice regularly for decades. They don’t understand, and they can’t understand unless they live it.

It’s one thing to get unsolicited advice from someone who you don’t know, but it’s something else entirely when it’s someone you do know. Let’s first talk about when it’s someone you know and they mean well.

Getting Unsolicited Health Advice: When It’s Someone You Know (And They Mean Well)

This is the easiest one to answer!

If someone in your life – who you know means well – keeps giving you unsolicited health advice, at some point you need to say something to them before it gets to the point where you are actively angry.

If their advice is something like, “You should try [whatever thing]!”, at a certain point, you could say something like, “I know that you mean well when you give me health advice, but it’s something I get a lot from a lot of random people, and I would rather leave my health to my medical team.”

If they keep giving you the same advice over and over again, you could say something like, “I know that you really believe in [repeat treatment], and if I try it I’ll let you know. But for now, I would appreciate if you stopped suggesting it.”

If they are confused or hurt, you could explain to them that you get a lot of advice from a lot of different people. You could explain that, while they mean well, you get a lot of unsolicited advice from people who don’t mean well.

Something else to try is to see if they are suggesting a treatment or if they are curious if you’ve tried a treatment. Maybe they are wondering if something actually works, but their phrasing isn’t clear. If you wonder this, it’s definitely worth asking them, “I know you suggest I try [repeat treatment] a lot. Are you suggesting it or are you wondering if it has worked? It’s unclear.” Then you can go from there.

Getting Unsolicited Health Advice: When It’s Someone You Know (And You Don’t Know If They Mean Well)

Maybe this is a co-worker or a classmate or a new friend or someone in your family.

I’m going to assume that this is someone who you are going to have to see again or at least for the foreseeable future.

It’s always best to start with being police and nice. I’m not always good at this, but I try to smile and answer with a yes or no if they ask, “Have you tried [treatment]?” or the less-nice version of “Have you considered trying [treatment]?” (That second version is very condescending.)

If they are persistent and either in the moment or later ask you about other treatments, then it’s time to step it up. At that point, I would ask that person a question: “Just so I’m clear: are you wondering if I tried something or are you suggesting I try something?”

If they say that they are wondering, then deal with those questions how you want. Answer them all at once, tell them that you would rather not discuss your medical history, tell them to mind their own beeswax, etc.

If they are suggesting, then tell them that you would rather they didn’t. Tell them that having chronic illness or pain is confusing and difficult enough without getting advice from classmates/coworkers/family members/etc. Tell them that you hope that they mean well, but there are plenty of people who don’t mean well that it’s hard to tell sometimes.

If they insist on asking you questions or giving you advice, then tell them to stop. Use the word please, phrase it as a question, swear, whatever you feel is necessary.

What it all comes down to is the fact that we get a LOT of unsolicited advice. So sometimes, I feel a bit snippy about it! If you mean well, just know that we’re probably good without your advice. If you don’t mean well or you don’t know the person you’re talking to well, just know that we really don’t care what you have to say and you should just keep it to yourself.

Chronic patients: what do you wish people knew when they gave you health advice?

Like this post? Check out:

What Is Self-Advocacy? An Answer + Strategies To Help, Living Life with Chronic Illness: Common Problems & Their Solutions, The Impact of Chronic Illness on an Individual, How Chronic Illness Affects Relationships

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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Comments

  1. Kelly says

    March 13, 2021 at 10:40 am

    Thank you for sharing your perspective! I can’t imagine how annoying and frustrating that can get. I’m not one to really dish out health advice, but I’ll definitely be considering all your points going forward.

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  2. Emily Bendler says

    March 15, 2021 at 10:19 am

    I’m not a medical professional, but I am constantly doing research on improving health. I’m relatively disciplined, and try to make health a priority. On the other hand, I try to never give anyone advice unless solicited. I feel like the things I do with my lifestyle shows that I have studied health and wellness a lot, so a lot of people do ask me things, but I never bring it up. I assume if people wanted my opinion, they’d ask.

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  3. April Smith | The Thriving Spoonie says

    August 8, 2022 at 1:37 pm

    This is such a helpful post! It’s something I’ve dealt with, too, and having tips and different perspectives to draw from for how I choose to respond will definitely help things go more smoothly in the future. Thanks so much for sharing!

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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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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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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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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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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

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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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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.

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