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The little lupus girl
1. Chronic Illness Report
Courtesy of Annie 12/27/2011 [Edition 1, Volume 1]
The Little Lupus Girl
The story of a brave girl who fights an autoimmune
disorder without a definite diagnosis and with scrutiny Fibro
from her friends.
Fibromyalgia is another thing
Hi, I’m Annie. I’m the Little All they cared about was that I fight. Yes, it’s another
Lupus girl. Yup, that’s me. I’ve making sure I suffered for invisible disease. It causes
been dealing with symptoms of missing their class. extreme pain all over the
Lupus since I was 10 years old. body.
Of course then I didn’t realize Eventually I graduated and
that there was something went on to college. And it was Sometimes it can cause
wrong with me. Nope, I just there that I really got sick. Of intense muscle spasms that
thought it was normal to have course…. It was there that I cause pain all over. I have it
achy joints, sensitivity to the got the fractions of answers more on the higher level of
sun, hurting lungs, a rash in the that I never really wanted.- the mild end.
shape of a butterfly, and all
I was diagnosed with Although it may seem like I
have it on the more severe
end because I claim I am sick
“…I was willing to endure the pain as long as I a lot…. My Fibro is a actually a
could get better…” lot better than it was in the
past.
that other fun stuff. Fibromyalgia…and I had a horrible doctor who
autoimmune arthritis. The treated it in the past. She
I didn’t know there was a second diagnosis could mean didn’t really know how to help
problem. I used to dip my Lupus or RA (Rheumatoid me. And she made me angry
hands in a bowl of cold water Arthritis). Not good news because of that.
to help my hands stop swelling. either way. Both are bad.
The summers were brutal. People want competent
A lot of my “friends” didn’t doctors for their chronic
I was always so tired and believe that I had Lupus. They illnesses, for the inner wars
fatigued. I just always wanted all thought I was faking and they face, but sometimes
to know, at the back of my making it all up. they don’t always get them.
mind, what was “wrong” with
me… They were the types of people
I shut out. And there were
As I grew older I missed a lot of many of them. So it was hard
school. And a lot of teachers to shut them out.
were unforgiving about that.
They didn’t care that I was sick.
2. But eventually I managed to. It I am “going home” now and I
was hard though. So many feel rather good about that…
people thought that I was Because I think “home” is
making it up. It hurt. But I was where I need to be. Not with
willing to endure the pain as the unbelievers or the people
long as I could get better. who don’t give a damn about
me. I need people. And I will
And I did endure the pain. I get it.
endured it for so long; I didn’t
know how much longer I could We all need to “Go HOME”.
endure it. But I did.
Manic World
Living with Bipolar Disorder
People are more and more you to think about death and I know some people have to
seeing things on Bipolar other frightening thoughts. disagree because their lives
Disorder. I am glad that there Who would have thought! have changed for the worse…
is more awareness going on but my life changed for the
out there. Bipolar Disorder is a People with Bipolar Disorder better and I have to write this
horrible mental illness and aren’t crazy; they just have an down.
needs more coverage. imbalance in their brains that
make it so that it is harder for I speak out because of all the
I have Bipolar Disorder. I get them to be stable. ignorance that goes around.
horrible depression and mild And because I am kind. And
“highs”. The highs make me I have that same imbalance. because I don’t know…because
extra talkative and creative. I And I am not crazy. I consider I feel like someone has to do
feel like life is beautiful and myself to just be Annie. The it….
amazing. same Annie I’ve always been.
Nothing has really changed. I’m And besides… why not?
But crashing is not fun and can happier now that I’ve gotten
be the worst pain you will ever my diagnosis.
feel in your entire life. It causes
3. Information about “Autoimmune Disorders Do Not Label Me”
Ann
Autoimmune Disorders Do Not Label Me is a Tumblr blog about
Chronic Autoimmune/Related diseases, Mental illnesses,
Costochondritis, and Pleurisy. It is also about the Environment,
and Going Green.
****
Dear Court,
Hope you liked this :) I tried doing this for you so you could see
some of my artwork
![Chronic Illness Report
Courtesy of Annie 12/27/2011 [Edition 1, Volume 1]
The Little Lupus Girl
The story of a brave girl who fights an autoimmune
disorder without a definite diagnosis and with scrutiny Fibro
from her friends.
Fibromyalgia is another thing
Hi, I’m Annie. I’m the Little All they cared about was that I fight. Yes, it’s another
Lupus girl. Yup, that’s me. I’ve making sure I suffered for invisible disease. It causes
been dealing with symptoms of missing their class. extreme pain all over the
Lupus since I was 10 years old. body.
Of course then I didn’t realize Eventually I graduated and
that there was something went on to college. And it was Sometimes it can cause
wrong with me. Nope, I just there that I really got sick. Of intense muscle spasms that
thought it was normal to have course…. It was there that I cause pain all over. I have it
achy joints, sensitivity to the got the fractions of answers more on the higher level of
sun, hurting lungs, a rash in the that I never really wanted.- the mild end.
shape of a butterfly, and all
I was diagnosed with Although it may seem like I
have it on the more severe
end because I claim I am sick
“…I was willing to endure the pain as long as I a lot…. My Fibro is a actually a
could get better…” lot better than it was in the
past.
that other fun stuff. Fibromyalgia…and I had a horrible doctor who
autoimmune arthritis. The treated it in the past. She
I didn’t know there was a second diagnosis could mean didn’t really know how to help
problem. I used to dip my Lupus or RA (Rheumatoid me. And she made me angry
hands in a bowl of cold water Arthritis). Not good news because of that.
to help my hands stop swelling. either way. Both are bad.
The summers were brutal. People want competent
A lot of my “friends” didn’t doctors for their chronic
I was always so tired and believe that I had Lupus. They illnesses, for the inner wars
fatigued. I just always wanted all thought I was faking and they face, but sometimes
to know, at the back of my making it all up. they don’t always get them.
mind, what was “wrong” with
me… They were the types of people
I shut out. And there were
As I grew older I missed a lot of many of them. So it was hard
school. And a lot of teachers to shut them out.
were unforgiving about that.
They didn’t care that I was sick.](https://image.slidesharecdn.com/thelittlelupusgirl-111228224436-phpapp02/85/The-little-lupus-girl-1-320.jpg)
