Welcome!

This blog is to show people what it's really like to live with Rheumatoid Arthritis at 18. When I was diagnosed, I searched the web and found very few accounts showing the difficulties of dealing with this disease at such a young age. On top of this, there were NONE that described the college experience living with RA, which has inpired me to start this! I hope my account can provide hope and support to RA fighters of all ages, and especially to those who have just been diagnosed!

Thursday, April 5, 2012

Gladiator Run

As I mentioned before, I decided to run a 5k race while I still can. It was the Phoenix Gladiator Rock'N Run autism fundraiser and I was actually pretty nervous to see how my joints would react.

The race included a mountain run, and 17 obstacles including a mud craw, fire put jump, and rope wall that we had to climb. It was a strain to be able to do some of the events, but overall not bad! I was surprised to see how well my body handled it, and had very little swelling and pain the next day. It has really encouraged me to start being more active, and I'm hopefully going to be signing up for a half marathon soon.

Here are some pictures from the race. We were team "Tutu's and Tata's".



Monday, March 12, 2012

Spring Break

So excited to be home! My and my mom are planning T-shirt designs that we will hopefully be making soon. I can't wait to get them out to start fundraising for OA. I'll post them on here as soon as they are finished!


Also, since being home, I have noticed that weather actually does seem to have an effect on my joints. The heat seems to really be helping them, which is great considering I will be moving back here next year!


 My kitty!
Camel ride at the Renaissance Festival! 

Monday, March 5, 2012

Gladiator Rock'n Run!

I must be insane for singing up for this, but me and a few friends have started a team for the Phoenix Gladiator Rock'n Run! It's a 5k race with 17 obstacles, including a mud crawl, freezing water swim, and a rope course. I know my joints will probably hate me the next day, but I might as well participate in things like this while I can! Our theme is Tutu's and Tat's and I will post pictures after the event! It is on March 17th, and here is the link for anyone who is interested http://www.gladiatorrocknrun.com/


Interview

I was recently asked for an interterview about living with ra, to assist a university in Malaysia with a product development. So excited! Just thought i'd let you all know :)


Also, I want to create ra shirts with the profits going towards the national arthritis foundation. Would anyone be interested in purchasing one if I did?

Monday, February 20, 2012

My Mom Is Awesome!

She found an arthritis walk in Phoenix and has become a team captain. If anyone is interested in donating or walking please check out her team link!

http://pazarthritiswalk.kintera.org/faf/donorReg/donorPledge.asp?ievent=492030&supid=352665300

Cool Things!!

I recieved an email from a Cornell student asking me if I would help her with a project. Her aunt had RA, and she is designing a piece of furniture for people living with RA and wants to ask me questions. So cool!


I'm glad people are finding this blog.

Enbrel

I started Enbrel about a month ago, and recently took pictures of the process. My Rheumatologist told me that the methotrexate and plaquenil were not enough anymore. 

I was incredibly hesitant to start the shots, considering they are weekly injects and I completely DESPISE shots. I originally wanted to do the monthly IV drip, but somehow my rheumy and parents talked me into doing the weekly injection. I chose the pen version, and the weekly dose will be better to provide constant medication.

Knowing that I was living away from home, they even sent me a brand new bright red hazardous waste bin that I get to keep in my dorm. YAY.............. try explaining that to your ra or friends.

The Shot (The Pen) 


First of all, I want to note that before each injection, I ice my leg for about 3 minutes, clean it with an alchol pad, and then proceed. I find that the ice helps to numb the skin, making it hurt less. My dad reccomended I do this, considering he takes the weekly humira for psoriasis and it has helped him.


  • The directions tell you to first clean your hands, and pull the skin apart with your index finger and thumb to make area tight. If you don't do this (which I have done) the needle tends to go through more skin, causing it to bleed more afterwards. 
  • When you place the pen onto the area, you have to push it down first, so the rubber tip sinks down a bit. It almost seems like a spring, you push it down until you can't and are ready to basically shoot your leg. 



Yes, I took pictures of the one time I forgot to pinch the skin. 

Also, please excuse my messy room. Although I think it really shows the college life haha.

  • This was me right before I pushed the button. You can see that I am pushing it down into my skin (the spring like thing I mentioned)The cap is a dark blue cap, and it you have to push it all the way down in order for it to work. 
  • Once you click it, there is a lound snap noise, and the needle in inserted.
  • It stays in for about 30 seconds, until you hear another click, and it is safe to pick the pen up. When it is in however, you want to keep your hand as still as possible, because the needle is in fact about 2 inches in your flesh. And moving your hand would not be pleasent. When the medication is going in, it slowly inserts, and there is a slight pain or burning, but it's not bad at all. 
Afterwards

The redness on my leg is from the cold ice pack!


  • It will start like a small dot of blood like this, but be cautioned, it spreads very quickly. I'm not sure if this is because my blood is thin from other medications, or from the enbrel. I usually wipe it off with a tissue or gauze, and place a bandaid on it. (However, often times I have to change it due to the amount of blood) 

  • You might want to note the brusie from last week. That's one downside of the weekly shots. I always have small unfortunate looking bruises on my leg.
My Review

I really didn't notice a difference in my joints at first, but over time I have realized that I haven't had any swelling in the past month. I'm not sure if this is because I have gone back to school or not. However, I am working at the same job I was over break, so this should not be the case. 

What I DID notice right away was my energy level. While on methotrexate, my energy is always shot. I never have energy to do anything, and with a daily 8:00 am class, I thought this would be a problem. However, since being on enbrel, I have noticed a tremendous increase in my energy. I am more active and more awake for nearly everything, and I absolutely love it!!

Overall, I'm obviously going to stick with it to see what happens, but so far so good!