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in Lifestyle &middot December 30, 2013

That Time the Christmas Tree Fell on Me

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in Lifestyle &middot December 30, 2013

That Time the Christmas Tree Fell on Me

I’m back from my vacation! I was up in central Maine at my family’s house for Christmas and also seeing family I haven’t seen since June or July. It was great to be up there and to unplug for 5 days. I’m back in Boston now, and will be here for the rest of the week. My next infusion is next Monday, and then next Tuesday I head back to Nashville.

I have pictures to recap my time off … and a story that you can probably guess the outcome of based on the title of this post.

The 12-foot Christmas tree – check out the story below the pictures!

The centerpiece of the Christmas dinner that I was too sick to eat – beef tenderloin wrapped in bacon.

It was a teensy bit chilly in Maine. (Also, that alarm is for medication, so don’t worry, you read that right.)

A bit blurry, but a cute picture of Gus (the Berner) and Piper (Cavalier King Charles spaniel) cuddling.

My dad picked these up for me (and a matching one for my sister) when he was at the series-winning game. I’m so glad to have this memorabilia! 

No trip to the Bangor area is complete without stopping in at my uncle’s pub/restaurant, known for their “American eats and Irish treats.”

It was a beautiful white Christmas for sure.

And now for the story …

My mom and sister went up to Maine last Saturday to get the house ready for Christmas before my dad and I joined on Tuesday after my infusion and mass in the Portland area. They picked up our beautiful, 12-foot tree on Sunday, but they needed the dump truck to bring it from the farm to the house. They got it all decorated with the big ornaments that normally can’t be hung because they’re too big for the size of the tree and the size of the branches.

They met my dad and me in Portland on Tuesday (Christmas Eve), where we had lunch and went to church before driving up to the house in the Bangor area. Christmas Eve and Christmas day everything was fine. We opened presents and hung out in the living room near the tree for most of the day on Christmas, and on the day after Christmas.

The day after Christmas, my grandmother was at my house when she got a call that her generator stopped running. (If you have watched the national news this week, you’ve probably heard that Maine got hit by an ice storm last weekend, and it was a pretty bad one that left 120,000 people out of power on Christmas Eve. Less than 4,000 people are still out of power now.) Without her generator, her water supply for the entire winter could freeze. Both she and my dad hustled out of the house to get over to her place to try and get it running. I spent most of my day reading and relaxing, including sitting on the couch in the living room.

Around 6:15 Thursday night, I sat on the couch reading when all of a sudden the tree started to fall over, headed directly at me. Based on the speed it was falling and how slow I’m moving right now, there was no way that I could get out of the way. As the tree headed towards me, I put my right hand up and caught it.

My mom came running out of her bedroom as my sister and I screamed, and they picked it off of me. They tipped it back up into the stand and I moved out of that seat as quickly as possible.

Luckily, I’m okay. It was terrifying and I was extremely shaken up, but I wasn’t hurt too badly. The unfortunate thing is that it takes almost nothing to hurt me because of my arthritis. Catching the tree did not break any bones or strain/sprain my wrist, thank goodness. But I have been in a lot of shoulder pain over the past 3 days, to the point where it hurts to move my arm or carry things. I’m not too concerned, especially because I see my Mass Gen rheumatologist this week anyway.

Anyone else have a harrowing experience over Christmas?

 photo ScreenShot2013-06-12at83901AM_zpsfbca4448.png

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. Rebecca says

    December 30, 2013 at 1:20 pm

    So basically what you're saying…is you're superwoman? I mean, I already knew that…but you caught a tree with one hand. Yup. You have super powers.

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  2. Kim @ HappyPrettyBlog says

    December 30, 2013 at 1:27 pm

    I'm in New Brunswick, Canada so being attached to Maine, we got hit by the storm too! Thankfully we had our power the whole time! I'll stop into that pub next time I'm in Bangor! I go a few times a year!

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  3. Kim @ HappyPrettyBlog says

    December 30, 2013 at 1:27 pm

    I'm in New Brunswick, Canada so being attached to Maine, we got hit by the storm too! Thankfully we had our power the whole time! I'll stop into that pub next time I'm in Bangor! I go a few times a year!

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Trackbacks

  1. Kate the (Almost) Great | Boston Lifestyle Blog - Memories of Christmases Past - Kate the (Almost) Great | Boston Lifestyle Blog says:
    December 21, 2016 at 8:00 am

    […] tree – If you’ve been following this blog for a while, then you might remember this story. I was sitting on the couch when a movement caught my eye, and when I looked up, the tree was […]

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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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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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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
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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⁣
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Wear a mask whenever I leave the house⁣
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Work from home⁣
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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! 

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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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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
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