Saturday, February 11, 2017

"Life is Better When You're Laughing"

NEW! People You Should Know Podcast: had the wonderful opportunity to share my story for a new podcast. Click here to take a listen Megan King- Ehlers-Danlos Syndrome Make sure you listen to the other podcasts that are featured. There are so many amazing individuals with amazing stories that you'll most definitely want to take a listen to.

June 25, 2016
It's my birthday! Honestly, I'm not a big birthday celebration person. Usually I dread them; more so since my initial injury because I am yet to accomplish the things I want too. Also, I had a great childhood that I miss. This birthday was different though. There was much to celebrate. I was alive all because a knowledgeable neurosurgeon listened, and stabilized my neck so it wouldn't move in ways it shouldn't due to the Ehlers-Danlos Syndrome (EDS). To celebrate we went out to dinner. My sister knows I hate attention, so she told our waitress it was my birthday and to do whatever she can to get all the people that were sitting on the patio by us involved. This led everyone singing me happy birthday...I was so embarrassed.
Post-embarrassment picture after everybody sang to me. The dessert was good; I like my sweets. One thing people might not know about the halo is that the pins can sometimes irritate the nerve that supply the eye muscles. This can cause the eye to droop down a little bit; this is why my left eye (R side of picture) is slightly drooping. 

June 30th, 2016
It was a warm summer day. Despite it being hot out it was important to me to go to the park with my nieces and my mom. As luck would have it, there were multiple kid's camps going on. This led to many stares. In this type of situation, you can't take it to heart. They're kids. Probably none of them have ever seen a halo before. So what do you do? You smile at them, and go about whatever you're doing. When the kids saw me playing with my nieces, I wasn't as scary looking and a couple came over to play, and some were inquisitive and asked questions. Use the halo as a learning experience for them. All you have to say is, "I hurt my neck, and this is a crazy looking brace to help my neck heal by keeping it from moving". After explaining, my nieces and I played bocce ball. Since I can't throw, I played by kicking the ball.

Once my nieces and I got tired of playing bocce ball, or should I say, the tops of my feet started becoming bruised from kicking the bocce ball, we decided to work on our balancing skills.
July 1, 2016
It was doctor day with my neurosurgeon, Dr. F. My appointment was to discuss my upcoming halo removal. We already had a tentative date of July 14, 2016. I did not want my halo removed; yes, I know, probably the only person in a halo that says this. There's a reason I didn't want it removed though. My neck felt good in the halo, and I was concerned my upper C spine was unstable from my skull-C2. The other reason I didn't want it removed was because my mom and I were heading back to Colorado so I could do some physical therapy, and my nieces were coming with. I wanted to feel good while we were there. Dr. F said it was okay to keep the halo on until I got back from Colorado, and that it was also a good thing because it would allow my C3-T2 fusion to heal more. The new halo removal date was set for August 25, 2016. 
Legitimately happy to have my halo time extended.
July 2, 2016
I was going on my first big outing since my halo application, and surgery in April. My family and I went to the zoo. It was so hot out, but it was worth it. I will say, my body was so sore the next day. The halo is 7-8 pounds. My legs and rest of me was so sore. It was still a fun day, and ended with a beautiful sunset. 
My niece Emily and I. We tease that a bull is my inner spirit animal because it has horns, and my halo has "horns". Emily is pretending to have them; hence the reason her fingers are sticking up by her head.
Neighborhood sunset

I very much believe this

July 4, 2016
Happy 4th of July in the U.S. Our tradition is to go watch the fireworks by the lake. It's typically crowded so my biggest concern, along with my family is that I would get bumped into once it was dark out. Fortunately, my family is creative, and having my nieces living with us meant we had glow sticks. We got to the lake early to get a seat and in the meantime my nieces decorated my halo in glow sticks. This worked out perfectly when it was dark because nobody bumped into me. 

My family and I

Never thought I would be decorated in glow public. They did a good job though. It looks like I have headphones on. 
July 6, 2016
It was an exciting day. Since May I had been bringing my dog Daisy to become certified as therapy dog so we could volunteer and bring a little happiness to people. Her trainer said she also qualifies as a service dog for my needs. Daisy has been around my medical since she was a puppy. On July 6th she passed her test and graduated. There is a lot that I can't do, and there is a lot I want to do. I want nothing more than to help people. If that means bringing Daisy to the nursing home, or hospital etc. then it's a good thing. I've always wanted to work in the medical field; orthopedics specifically. Since I don't see that happening at this point in life, for now I'll try to help in other ways. 
Congratulations Miss. Daisy. You're official!!
July 14, 2016
It was 3 days before my mom, nieces, and I would start the drive to Colorado. My nieces have never driven cross-country before like this so my mom and I were excited to show them. We took them out to lunch to talk about the drive, and we made a list so they could double check that they had all the things they'd need. 
Emily and I
I want people who are in any kind of brace to know that they can still help other people. You might have to dig deep to overcome your fears, or whatever it is that makes you self conscious, but you can do it. In doing so, you can potentially help a lot of people. 

* *If you have a Facebook account, click here and "LIKE" my page: Meg's EDS Medical Journey
** Follow me on Instagram:
**Please share, and follow me on Google +
As always, if you wish to communicate you can email me at To those that are shy to email me, I can tell you now, you are not the first!


  1. This comment has been removed by the author.

    1. Up until this year I felt bad about birthdays. This past year has been eye opening, and despite missing out on things, and not accomplishing what I had hoped by now, life is still worth celebrating. I'm sorry you have Pots/eds too. Hopefully they'll be a cure one day :)

  2. Nice look back! I've never (ever) been a big birthday person, birthdays don't really bother me so much (except on in my 20s where I was too I'll to even leave the house my parents had to go to some meeting in the evening and then when they came home we played rummikub and my dad didn't even go easy for ONE game. Mean dad day!) I hate new year though. It's when I got ill, and it's also when I got my shoulder diagnosis and worstly, it's when EVERYONE celebrates. I'm the grinch of new year!

    Although this year I opted to view it as a f*** off 2016 celebration, that was slightly better!!

    I remember the stares I used to get going round the mall (or wherever but lots of people of people in malls) in a wheelchair from toddlers in buggies(strollers). I used to think it was hilarious, it was like they knew they'd see little kids in buggies but suddenly there was this new thing to see - they'd totally twist their heads as they rolled past to keep staring.๐Ÿ˜„

    Good quotes ๐Ÿ’ช๐Ÿ‘

    1. I feel the same exact way about 2016!! haha
      Kids are funny usually. I've gotten some pretty funny looks; if only I had a camera for every look. I could make a photo book :)

  3. We could be twins. Lol. We look alike!