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in Lifestyle, Uncategorized &middot January 13, 2015

How To Live At Home in Your Twenties

I don’t really talk about this on the regular – more because it just hasn’t come up than that I’m hiding it – but I’m 23 years old and I live with my parents. For those of you who are new around here, it’s due to my health, and once I hopefully get into grad school we’ll reevaluate the living situation. But today it’s all about how to live at home with your parents in your twenties.

How to live at home with your parents in your twenties - Kate the (Almost) Great

Step one: make sure you’re all on the same page and draw clear boundaries. What are your responsibilities? How do they differ from when you lived at home as a teenager? Do you need to check in if you’re staying out past 10?

Step two: give some time for new routines and adjustments. It’s going to take some time for everyone to adjust. Your parents may automatically act like they used to because it is hard to get out of those habits, so remind yourself to just let everyone get settled.

Step three: address individual concerns as they pop up appropriately. Try not to get overwhelmed with frustration and to calmly address them. After all, if you want to be treated like an adult, act like one.

Step four: remember that they are your parents and not your roommates. At the end of the day, there will be things that none of you want to talk about or see. Keep it appropriate for your relationship, even if it is a little different than it was before.

Step five: try to have some breaks from each other on a regular basis. Not only will you probably be craving a parent-free zone, they probably will want a break from you, too! After all, you are kind of cramping their style. Breaks will make the time you spend together better.

I hope these help! Anyone else living at home?

And now to introduce Kati Rose!
I’m Kati Rose! One time too many after graduating from university and wondering what I wanted to do with my life, I woke up and decided to pursue my passions. I want to spend each day surrounded by all the things I love most – the finer things in life some say. Music, travel, fashion, photography, art, entertainment and more! Kati Rose Constantly Seeking Wonder is my way to share the adventure with others!
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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. Ellen Ross // Ask Away Blog says

    January 13, 2015 at 1:27 pm

    Yes, i love this post. I moved into my own apartment when I was 22, then when I was 26 I moved back home suddenly to get out of a really bad situation with an ex and I have 4 dogs so I couldnt rent anywhere else. It's perfect tho becuase it helped me get out of debt and I'm gonna get my own house this year. But man there are struggles. my brother is 24 and lives at home too so there are 3 other people besides me. Theres hardly any room for me to store my groceries which is hard especially when you are trying to eat better. And I hate the fact that half of my things are in boxes in the basement (all the things of mine from the house i used to live in) but it's better than being homeless so I try to suck it up but it's definitely hard at times. Hang in there girl!

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  2. Chelsea Woodring says

    January 13, 2015 at 3:29 pm

    I also am 23 and live at home with my parents due to health issues. It was really hard at first because I thought going away to college meant that I wouldn't ever live with my parents again, but now that I AM living with them again, it's not really a bad situation. I am lucky enough to consider my parents my best friends, and they take care of me when they are able. I do wish that I could be independent enough to live on my own at times, but then I just have to think realistically and realize my situation would not pan out well. We have our tiffs, and sometimes I feel like I'm an adolescent again, but I know everything will work out for the best in the end.

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  3. Chelsea Oliver says

    January 13, 2015 at 5:01 pm

    This is great advice! I went from college right into grad school, so I lived with roommates and then completely alone for six straight years before I had to move back in with my parents. Six months back under their roof was enough for me. I give a lot of credit to the people my age (25) who can still live with parents while job hunting or while just starting out. It's a tough thing and an ego check sometimes too. I was thankful to have them there when I needed them but I'm more appreciative of them now that I've moved out!

    -Chelsea
    chelsandthecity.blogspot.com

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  4. Katie Kate says

    January 13, 2015 at 8:49 pm

    I lived at home until I was 26…it wasnt too bad…i guess lol It allowed me to save money and travel so that's good news! I went home for 2 weeks over this past christmas and my mom still asked me where i was going, who i was with, and when i would be home! yeesh! haha!

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  5. JBean says

    January 14, 2015 at 2:17 am

    I lived at home for almost 3 years after I graduated college. It was def trying at times Bc I felt like an adult but they often still treated me like a high school kid! It was financially necessary for me at the time and I'm thankful now they allowed me to live there until I could afford to move out. Now I've lived on my own for over 10 years and love it so much! Not sure I could ever go back at this point 🙂

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  6. Marla Rogers says

    January 14, 2015 at 6:10 am

    Seriously SO good and true and spot on. I lived at home again when I was 23-24 and it was really strange…like you said, it's like when you were in high school but also completely different. This is a FANTASTIC list, anyone that's moving back home needs to get on this!

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  7. Kati Rose says

    January 19, 2015 at 7:21 pm

    Thanks for featuring me! 🙂

    Yes to all of these. I moved back home for a short time after graduation and it was difficult, but doing things like setting boundaries and addressing things as they came up made it SO much easier.

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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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#RheumatoidArthritis #AutoimmuneDisease #Arthritis #JuvenileArthritis #JRA
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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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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⁣⁣⬛⁣⁣⁣
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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!

⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣⁣

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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⬛⁣⁣⁣⁣⁣⁣⁣⁣⁣
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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
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