Saturday, August 27, 2016

Caged Animal: Part 1

For this post, I’m going to do something that is completely out of character for me. I’m going to tell you how I REALLY feel instead of how I want to feel. It’s never easy for me to disclose what’s really going on with my health; I’d much rather paint a pretty picture and leave it at that. I don’t want to be judged for having bad days. I’m supposed to be a superhero, and superheroes don’t have bad days, do they? But, I want to be honest this time. I don’t want to hide behind another pretty picture. I don’t want to be a superhero if it means I can’t be honest.

A caged animal. That’s literally what you begin to feel like when you have to live your life within such tight boundaries. I mean, I guess it’s OK in the beginning, when you’re still oblivious.
I was tested for food allergies way back in elementary school. After the test results confirmed an allergy to dairy, I immediately stopped eating dairy. I remember having sushi for lunch sometimes and all the other kids were like, “EEEEWWWW. What IS that????” Yeah, I was that weird kid who ate something unusual for lunch. BIG DEAL!!!! It bothered me a bit, but I didn’t have the capacity to consider having to be that “weird kid” all the way into adulthoodDespite our efforts, eliminating dairy from my diet wasn’t enough. It didn’t stop me from throwing up ALL of the time. In restaurants, out in the parking lots of restaurants, in public bathrooms, malls, shopping centers, in our friends’ cars, friends’ houses, family outings, anywhere in our house all night long…EVERYWHERE. Of course, this was in addition to chronic pink eye, chronic strep throat, endless trips to the school nurse, bizarre rashes, chronic stomach aches, the mumps, tons of absences, cyclic vomiting… The whole nine yards. There were even times when my family and I would get into our car to go out and once we reached the intersection at the end of our neighborhood, I would tell my mom to turn around because I was going to be sick. BUT, I was too young to see the big picture. My world was still so tiny. I only saw what was two feet in front of me. Then came middle school. More broken bones. More chronic stomach aches. A wicked case of pneumonia. A cough so serious that I was forced to get help from a speech therapist. I needed someone to help me stop coughing because the principal was angry about my disruptive coughing. Double ear infection. Sprained ankle. RSD diagnosis. Tick bite (that would not be acknowledged or addressed for another 10 years). Pain. Lots and lots and lots and lots and lots and lots of pain. Humiliation. Misunderstandings. Frustration. Sadness. Anxiety. Confusion. Disbelief. Dropping out of the eighth grade due to the unbearable amount of pain I was in, plus the fact that it was hard for me to even walk. Homeschooling. No friends. Moving to Philly. A month spent at Children’s Hospital of Philadelphia in an inhumanely rigorous and intense physical therapy program (in an effort to squash my relentless RSD that was spreading throughout my body like wildfire). I remember my very first day. I was answering basic questions from some gentleman, and I remember telling him that I was so excited/happy to be there because it meant I could get better. The guy gave me a strange look and said, “It MUST be your first day.” I thought, why would he say that? What’s so wrong with me feeling happy about being here…? There were times during the program that I wanted to die. The pain was so intense that I couldn’t stand being alive. RSD is pain, so basically I worked out whilst in excruciating pain. I would tell my PT I was having my period so that I could get off the treadmill, but what I really did was run to the bathroom and call my mom. I lied on the floor of the bathroom and called her, telling her to get me the hell out of the program. And my PT would come to the bathroom, pull me out, and put me back on the treadmill. When I would come home in the evenings to our little row house in downtown Philly, my mom would have to basically carry me up the stairs because I was in too much pain to put one foot in front of the other. Every day was filled with EIGHT long, never-ending hours of hardcore, hellish, militant-like physical and occupational therapy. Every night ended in tears. Every morning began with tears and dread. Kids at my middle school thought I was dead. Food limitations? HA! Those were the least of my worries at the time. I was too worried about losing my ability to walk since the RSD had spread from one ankle to the other, as well as up my legs to the rest of my body. The pain was debilitatingI’d say it was almost paralyzing. It was like I was spending my life in a torture chamber, and there was no way out. 
*To be continued* 
Love and healing light, 
Allie 
XOXOXOX 



Thursday, March 24, 2016

HaPpY 5th BiRtHdAy, SoUpEr DoUpEr SCDer!!!! :D

I have started and restarted this blog post over a million 
times since 9:30 p.m. -__-
The cat's got my tongue. *a-hem!* 
I really don't know what to say. 
MY BLOG TURNS 5 TODAY?! 
Are you for real? 
Or, are you just being a heel?
You better be certain before you speak. 
Unless you're being honest, 
I wouldn't let my mouth spring a leak.
Turning five is no small thing. 
Heck, I'm so excited about this that I may have to sing! 
I've learned SO much over the last five years. 
When I think about all that's happened and all that I've learned, 
I am practically brought to tears.
 All the people I've met...
All the hard lessons I'll never forget...
They've changed me. 
After all this time, I feel like I'm finally able to see. 
I see that if you want to win this fight, you have to reach out.
Of this, I have no doubt. 
I've also discovered that you have to thank people 
who've helped you along the way. 
Trust me when I say that it'll make their day!
Thank you, Elana Amsterdam (from Elana's Pantry), 
for being my light when I needed it the most. 
I can honestly say that you are the greatest woman on the
 entire west coast.
I started my blog because of you, my dear.
You taught me to push forward and have no fear. 
 To my family, I love you with all of my 
heart for constantly 
standing by 
my side through thick and thin. 
   Supportive: that's all you've ever been.
To my outstanding teachers from high school and MC, thank you for helping me succeed during some of the HARDEST years of my life thus far. 
I think you know who you are!!!!!  
To my friends, I love you for coming into my life and for 
making me realize that 
I'm not the only 
one with tummy issues. 
However, when I think about how many of 
us there are in my support 
group, I'm tempted to grab a box 
of tissues. 
To my darling fiancé, I cannot thank you enough for taking 
care of me, for loving me, 
for supporting me, 
and for bringing so much joy into my life
I am SO excited about someday 
becoming your WIFE! 
NOW, I think it's finally time for this post to come to an end.
Thank you for taking the time to listen to me rhyme, my dear friend. 
:) 

Lots of love and healing vibes, 
Allie 

P.S. HAPPY BIRTHDAY, you precious blog.❤︎ You truly saved my life. I can't believe we've been at this game for five years now. I hope this magic continues and we celebrate your birthday year after year for a LIFETIME. And yes, to my followers who didn't know, I'm ENGAGED!!!! :) 


Monday, February 1, 2016

Chronic illness + social life? Here's how to have BOTH! P.S. We need a little help from our friends. ;)

When you're fighting a chronic illness, hanging out with friends can be quite tricky. In fact, getting out of the house can be nearly impossible
It's not that we don't want to see you, or meet you for coffee
It's not that we don't care about your presence in our life
It's not that we don't appreciate your kind gesture
It's not that we don't want to have FUN with you
Sometimes [most of the time], our inability to see you is 
completely out of our control
Why, you ask?
That's easy!! One word:
U-N-P-R-E-D-I-C-T-A-B-L-E.
Our bodies are simply and relentlessly unpredictable. 
We almost never know when we might stumble into a flare. 
It could be related to...
eating something other than the mere FIVE foods we tolerate, 
foul weather, 
stress, 
side effects from a treatment, 
a full moon [yes, this is a real trigger], 
the fact that it's a Tuesday and not a Wednesday, 
putting on mismatching socks, 
rubbing our tummy and patting our head at the same time, 
sticking to our regiment so well that it's time to be punished...
In other words, 
something completely regular and meaningless can set off a flare. 
Flares don't have to be triggered by a typical trigger
It can be ANYTHING or NOTHING that sends us into a miserable flare.
 {As if that wasn't enough, our a-n-x-i-e-t-y shoots through the roof once we're in the middle of the flare.
 That doesn't help, either. 
We'd prefer not to end up at the local Starbucks with you as our sweat stains reach our WAISTLINE
We'd rather not be at the movies with you if we can't sit still due to severe joint pain from our hips, or the fact that our stomach looks like we've swallowed a watermelon
It's embarrassing for us to feel so poorly in front of others, so we just avoid contact to escape humiliation. 
-SO, you're probably wondering how you will E-V-E-R be able to hang out with us, right?-
Phone calls, 
FaceTime,
Skype,
a cup of coffee at our house,
a yummy lunch in our kitchen that's entirely "gut-friendly", 
LITERALLY show up at our front door, 
a Hollywood hit in our at-home movie theater where we can accommodate our position for any joint pain, 
a gentle walk around the neighborhood for some fresh air instead of chemical-rich air in a mall...
In other words, 
you may have to prepare yourself to take charge of the situation.
We may never feel well enough to make an adventure happen, so you might have to help us out a little bit. ;) 
That's all we ask of you. 
Please, please, please [with cherries on top!] bear with us so we can enjoy your company. 
We promise to repay you in some way, possibly with a BIG BAG of... homemade, 
gluten-free 
COOKIES? :) 
[If that sounds reasonable to you, 
you ROCK!!!!!!!]
XOXOX
~Souper Douper SCDer~