NAIL October Theme 2: Autumn Leaves

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Below is my submission for the second theme in the Nail Art Ideas Link-up hosted by Eeeek! Nail Polish! and CraftyNail!

 

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I used two coats of Urban Decay “Naked” as the base.

For the detailing I used Milani “Dark Coffee” and “Foxy Lady”Zoya “Suvi”Color Club “Wham! Pow!”; and Urban Outfitters “Westside”.

 

Hi, my name is Monica and I have RA.

Halloween Nail Art Contest

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Short and Sweet in Texas is holding a Halloween Nail Art contest and I decided to submit a picture!

I am so excited about this because I incorporated the marbling and sugar-spun techniques. Spiders terrify me so after I finished taking pictures I just ignored my thumb.

 

I hope you enjoy it and please vote for my submission. I believe it is the 3rd picture in the album.

https://www.facebook.com/media/set/?set=a.592089537519139.1073741830.540216189373141&type=3

 

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Bases:

Ring: Color Club “Wham! Pow!”

All others: Sally Hansen Xtreme Wear “White On” covered by butter London “Knackered”

Detailing:

Water-MarbleOrly “Bonder”Wet n Wild “Black Creme”

Sugar-Spin: Essie “No Place Like Chrome”SpaRitual “Bismuth”

Free-hand Spider and WebMilani “Black Swift”Essie “No Place Like Chrome”SpaRitual “Bismuth”

The bat was a water decal purchased from the Born Pretty Store. I am not sure if I applied it correctly because the sticker came off white.

 

Hi, my name is Monica and I have RA.

Dumb Sh*t People Say: RA Edition – Series One, Part Three

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“But you don’t look sick…”

 

The silver lining. The very vain silver lining: I don’t look sick!

The visible symptoms would be side-effects of the medications I am on:

  • I bloat on prednisone
  • My hair thins, loses its shine, and falls out on methotrexate
  • If I forget to take my painkillers I pale
  • I break out like mad
  • My eyelashes fall out

The list is extensive.

So is my beauty/skincare regime and so is my diet.

I wrote a couple of posts on my skincare regime earlier. I am very proud of my skincare.

It is nice to know that something in that line-up is working!

After all, if I did not follow it to a tee, I would look very unwell.

 

Part One explains why this comment is not ok.

Part Two contains my reaction.

 

Hi, my name is Monica and I have RA.

Will I Learn?

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I know I have physical limitations.

 

Sometimes:

I cannot pick up my cat.

I cannot carry the ceramic dog bowls.

I sit on the floor and cannot get up…

 

Let me preface by saying I climbed today after work. YAY! I rock-climbed after almost two months! Serious YAY!!!!

I climbed two climbs. I sat down to put my shoes on for the third climb and I got stuck. I could not roll over and get up. I tried to use a floor anchor to pull myself up and ended up doing a somersault. It was very comical.

Red flashing lights: MONICA! YOU ARE DONE FOR THE NIGHT. DO NOT CLIMB ANYMORE! STOP! STOP! STOP!

If I am stuck on the floor and cannot get up on my own I should not climb. For that matter, I should not do anything at all.

The best course of action was to stop.

Instead, I decided to hop on the climb that I knew was well out of my range for the night. I might have actually said: “What is the worst that can happen?”

 

 

I did not complete the climb and I tweaked my hip and knee.

Whoops.

My doctor, my friends, and my dad always tell me I should take better care of myself. I get in trouble with my doctor because I know what the consequences are.

 

I amaze myself. Generally, I am a very calculated person. I never do anything without reason.

I go through periods when I am more careful than usual:

I only take the infusion once a month. If I flare up I can only increase the prednisone. That is not an option.

Everyone is sick. I stay away from them. I cannot afford to get sick.

I am having trouble getting out of bed. Let me rest today and nap a lot.

Then

I go through periods when I do things I am not supposed to and I honestly have no good reason for it:

Maybe this time will be different.

Maybe I am daring my body to break down.

Maybe I am just angry.

 

When will I learn?

(Maybe I should start a “Dumb Sh*t Monica Does” Series…I definitely have enough material for that. Hah!)

 

Hi, my name is Monica and I have RA.

Dumb Sh*t People Say: RA Edition – Series One, Part Two

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“…but you don’t look sick!”

 

I struggle with my physical limitations but I also struggle with the new and unfamiliar mental strain.

The thoughtlessness behind this comment always reminds me of the demons lurking at the back of my mind:

 

How much does the disease actually affect me?

vs.

How much does stress or over-though affect me?

 

(These ideas will come up again in another series)

I am battling an invisible illness. Everyone bases their opinions, ideas, and plans of action on how I feel.

 

Maybe I cannot brush my teeth or pick up my pets because I am more stressed. After all, the mind is a very powerful tool.

But it is not powerful enough to create an entire disease, right?

An over-active imagination cannot allow my immune system to destroy the cartilage around my joints, right?

…Right?

 

And when people say this and suspend belief at their convenience, I realize no one sees what I am going through.

I feel alone.

I feel like a hypochondriac.

 

Part One conveys why this comment is not ok to say.

Part Three contains the silver lining.

 

Hi, my name is Monica and I have RA.

Dumb Sh*t People Say: RA Edition – Series One, Part One

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“But you don’t look sick!”

 

Thank you?

I am glad I am not a walking billboard for the disease.  I am relieved there is no huge neon sign above my head flashing “PERSON WITH RHEUMATOID ARTHRITIS RIGHT HERE!”

I know people mean this as a compliment. Unfortunately, this comment bothers me the most.

It alludes to the fact people may not believe I am truly ill. The misconception remains that most illnesses have outward symptoms.

That is not the case with RA.

Rheumatoid arthritis is a silent illness. It is an inflammatory disease that affects the cartilage around the joints. It also affects other organs and systems in the body. Generally, there are no visible signs of the disease.

So, people with RA do not look ill.

In the beginning people are concerned, after all, they know it is a disease and it is chronic. That much they understand. As time passes, the people who were most concerned are also the people who get the most annoyed.

 

They think:

‘She is probably fine’

‘She is making excuses’

‘It’s all in her mind’

‘It’s probably just stress’

 

This one thought, that is meant to sound supportive, is the gate-way to more misguided ideas of what it is like to have this disease.

It allows people to suspend belief when most convenient. They choose not to care when it suits them. They are able to place blame on the sick person because they do not understand the nature of the disease.

 

Part Two explains my personal feelings on this comment.

Part Three contains “the silver lining”.

 

Hi, my name is Monica and I have RA.

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