Eggless Sugar Cookie Dough (Believe me its fantastically!!)

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So… Its Shay-De foodie Friday!! And its the start of food allergy awareness month. Which means that I will be posting about it. Food allergies have been in my life since I found out I was allergic to cherries when I was a young child. But it didn’t change my life fully till I was 17 years old and my body was reacting to so much food.

I found out nine food allergies then. I now have gained more and I have over all about 22 food allergies, but thats putting some of them together. But yes I have food allergies, my body doesn’t like so many foods.

I don’t mind having food allergies, its hard to live with but its not horrible. Food allergies change your eating and it changes parts of your life but its just made me more fantastic then ever, and I love it. I don’t know why but they can for sure be highly annoying.

But since its Shay-De Foodie Friday lets get to the recipe part of this blog..

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So here is the Recipe for eggless sugar cookie dough.. (This is just to eat not cook. I do not believe cooking it wouldn’t work, but I ate mine raw and it was fantastically wonderful)

1 ⅓ cup of flour (I used oatmeal flour, as we all know oatmeal flour is my go to flour.)

½ cup butter or butter

¼ cup raw sugar

¼ cup brown sugar

1 ½ teaspoon of vanilla (extract or from bean)

 

Instructions

  1. Beat together the sugars and the butter till adorably fluffy or just fluffy if it doesn’t look adorable, do not be worried. I beat my together for sevens minutes.
  2. Add the vanilla and beat for another minute
  3. Add the flour slowly till all the flour is mixed in fully. It took me about five minutes to add it all and beat it.
  4. Put in bowl, eat enjoy!!!!

I hope your week has been amazing and if you ar staying in this weekend then I hope its amazingly fantastic!!! Make this cookie dough and eat it and then feel fantastic unless your a spoonie with stomach problems then you might feel like horridness afterwards if this is the fact then.. Well I understand.

 

Thanks for reading this has been Shay-De Foodie Fridays if you would like me to make something center let me know in the comments below!!

  Shayweaseling it!

I Won’t Fail My Failing Body

 

Today I ate lunch and then as my disease made up its mind that this food I had taken into my body was not going to stay, I went to the restroom and vomited, a few times. I tried not to make it a big deal or anything.

When I came out of the restroom, a lady stood there just looking at me and she said “Are you bulimic?” there are a few things about this question, one if the answer was yes that is not the way to ask a stranger in the restroom. But I answered “No I have a disease called gastroparesis my stomach is paralyzed and doesn’t work the way it should.” she then went “Oh well why do you have it?” I hadn’t ever had someone ask me this follow up question before. I answered “They don’t know the reason why. It might be genetics.” She followed up with this “Maybe you just haven’t taken care of yourself.” She then left the restroom and I stood there and looked into the mirror.

My collarbones have become so much more visible, its not by choice believe me. My legs are thin, my cute round face is less round theses days, even though I have a little left of my moon face from the meds a few weeks ago. I stood there and thought.

Its not fair to me, because I have a chronic illness that people feel the need to either tell me how to heal myself or tell me that I’m not taking care of myself. If I had cancer I would be brave, and cancer is hard to face, but I don’t understand why the fact that I “just” have a chronic illness that I should just deal with it. It doesn’t seem fair. I was born with illnesses and more illnesses have attacked my strong so strong body. I’ve been through more in my life health wise than most. I’ve had crazy days and I’ve been in a places where I had to make crazy hard choices.

My body is failing me. I didn’t fail it. I didn’t make myself sick. I just am sick. I’m okay with my illnesses hurting me but I’m not okay with people telling me Its my fault. I do not have cancer, no. I have an illness that is incurable. Its lifelong, Its painful. Its horrifying sometimes. I have things that are undiagnosed. I had a doctor straight up tell me that I’ll most likely be in some pain forever, and that he was sorry. I have had surgeries not many just two, I’ve had an air tumor in my nose.. What’s that? My doctors didn’t even know.

   So no I didn’t fucking give myself theses illnesses Its not my fault. You can tell me off when I’m vomiting in the restroom, but only if you will hold my hair and then give my toilet paper so I can blow my nose and get all the vomit out it. I didn’t make myself vomit, my body is not working. My stomach has just stopped. My doctors are working to either find a med that works or a feeding tube might come into play or I might have to do some other stuff that I truly just don’t want to do. I want to go and live my life. I really want to go on that long bike ride.

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I’m strong. I’m really strong, but you see me as an attention seeker in some weird public restroom, you didn’t ask my name, you didn’t tell me you were sorry this happened to me, no you blamed me. My body is not my fault. My mind is not my fault. The things that happen to me are not my fault. I only get to choose how I react to them. And man I’ve reacted damn well… I’ve done pretty good. I choose to wake up. I choose to keep going because I don’t see the choose to stop.

   My body is failing me, but one thing’s for sure, I’m not failing my body.

 

This has been Wesday the day where I rant about whatever I please. And today I ranted… Don’t blame me for my illness, I will not fail my body.

Thanks for reading~ Shannon DeRose (Shayweasel)

Choose To Be Healthy

I’ve had different illnesses since I was a child. My body has never loved me. But neither has my mind. I know things about life that most people don’t even know. Because they live a life where their minds, brains, bodies and health is just something they never think about. “healthy” to most is a choice, they can choose to eat healthy food, they can choose to go on a walk for their health. But for me “healthy” was just nothing, it was just not a choice, my health has never been good, never horribly I’m about to die, but its never been good. Its always been something that I’ve had to think about through.

My brain, its always failed me. No matter how hard I would try my brain was not what I wanted it to be, or what everyone else felt it should be. But a few years ago when my brain turned fully against me and basically tried to kill me, I knew my life was going to be different after that, I knew I’d have to accept the fact that my body, my brain, my life was not going to be easy and that everything I could possibly do was be alive.

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So the strange question at hand is… What is healthy? What do I see for my future and how do I want to handle my health? My life? I want to be alive, thats the first thing. But I want to be awake and I want to be able to live happily and beautifully.

My body doesn’t seem to always enjoy doing things its suppose to do like eat food or make the necessary hormone my body needs to live. So I could choose to be upset or happy but I could and have choose to just have emotions and live as I please.

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Today I was riding in the car with my sister and a few of her friends, her friend said jokingly as he smoked his cigarette that he was only going to live till he was 50, because of all the smoking and drinking and partying he is doing now. But I knew in my heart that those sometimes or people like him or my moms biological father they are the ones who live while people like me and so many others we might not live to be 50, I’m not saying I won’t live I’m just saying I might not because of my health and its not because I don’t have the choice to either eat healthy food or not smoke or go for a run, but I don’t get to choose my heath. I barely get to choose my treatment, but I get to live, I don’t know how long I will live, I mean I could live to be 100 years old, so many treatments are available  and become available all the time.

What I’m trying to say is that if you can choose to be healthy, choose it. Because I don’t get that chance, and so many people like me don’t. And its not fair. So take care of yourself, love yourself, take care of your body, and health. Because you can lose it in a day. Or like me you can’t lose what you never had.


I’m happy I am, this blog post might not make sense, But I am Shannon DeRose this is my randomly rantingness. Thanks for reading.

Best Chocolate Chip Cookies (Gluten-Free, Corn-Free, Nut-Free)

 

Now if I’m being honest, I’d tell you that I love eating cookies, and I do it so much that I’m pretty sure I’ve found ways to make my oatmeal taste like cookies.

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And if you give me a cake I’d be like I’m good, because its not cookies, so since I love cookies so much. When I was told that I was allergic to a lot foods, I had to go out and find ways to make different things.

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Cookies being one of them. Enjoy Life chocolate chip cookies have been a lifesaver because everyone knows I want chocolate chip cookies. So I use those a lot and oatmeal. I mean man am I blessed to not be allergic to oatmeal, I do love me some oatmeal

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But back to cookies so a few days ago I was wanting some chocolate chip cookies and I wanted them bad, so I pulled together everything I had to make them, and I, being me, was trying to find a recipe to work with and I couldn’t find a good one till, well, today. I found this recipe and I had to change it a tad, but it works and the cookies I made are so amazing.

So here is how you start off

Ingredients

eggs – 1 full egg and 1 egg yolk.

2 ½  cups flour (I used one and ¼  cup oatmeal flour and one and ¼  cup tapioca flour)

½ teaspoon baking soda

1 cup Brown Sugar packed

½ teaspoon salt

1 teaspoon vanilla extract

½ cup raw sugar (you can use white sugar I used raw)

¾ cup butter (I used dairy butter but any butter works.)

2 cups chocolate chips (I use enjoy life chocolate chips)

 

  1. I preheat the oven to 325 degrees F (165 degrees C) line cookie sheet with butter or cooking spray or parchment paper, I only had butter so I used butter and they worked good. (I basically just put butter all over the cookie sheet)
  2. Sift together flours, baking soda, and salt, set to the side.
  3. In a bigish bowl I used my kitchen aid that makes everything easier. Butter that has been at room temperature for a while (mine was about two hours) and sugars together, I let it blend together for about 5 minutes to get that creaminess I feel it works better.
  4. Add vanilla, egg and egg yolk and beat until well blended, (I let my eggs sit at room temperature for a little while you don’t have to do this step but I think it helps.)
  5. After the eggs and vanilla are really well mixed together add the flour, baking soda and salt, Now be careful not to add it to fast. I add it slowly and then just till its blended then add the chocolate chips and let sit at room temperature for about ten minutes if its still kind of not right looking let it sit longer.
  6. Put on pan anyway you please and then bake for 10-16 minutes my cookies happen to be big so they cooked for 16 minutes.
  7. Let cool and enjoy!

So that my best chocolate chip cookie recipe!! I hope you all have a good Shay-De foodie Friday!

Come back next Friday for more food recipes and come back Sunday for randomness and come back Wednesdays for Wesday the day where I rant about whatever I please!!

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Why weekends are hard…

I hate mondays Fridays, I know what? Shay? How can you hate the weekend they are fantastic. One let me say I haven’t always hated them. And I still hate Thursdays more than I hate Fridays but for me I hate the idea of the weekend, that you have to go out and hang out with friends or if you don’t have plans then you are just going to die alone or become a cat lady.

I mean its not a big deal. I have been a nanny and my idea of a friday night was the parets going out and me making like 100 dollars thats my idea of Friday for a long time and when I wasn’t working I would sit in my living room watching TV shows or movies or I would be on tumblr for like nine hours.

So I don’t get where this you have to be busy on the weekend sleep in and go out and party or go to church on sunday. I don’t get it. I want to do what I do on a normal day. To me the weekend ends up normally being really boring and I don’t enjoy it because everyone is saying “Oh my I’m doing blah blah..” I mean even if I had a lot of friends who wanted to do stuff the weekend wouldn’t be when I wanted to hang out it would most likely be a random day.

But I want to say since my chronic illness kicked in over drive, the weekends end up being really hard on me. I feel like I am missing out on a part of live that I never knew I needed but I don’t need it. You might be someone in school or work the weekdays and when you get a free day its like fantasticness but to me it sometimes end up making me sad because I’m like I don’t have energy to do anything and its not going to change just because its the weekend sometimes I have good days but they are normally on a weird day like Tuesday and I get to make breakfast and go to the store, but my body doesn’t know that its the weekend. It does what it wants to.

So why am I telling you all this? Because I know that people with chronic illnesses might feel the same way, so if you know someone who has a chronic illness go over and watch a movie with them and don’t try and make them talk to much or anything just let them be but be there with them. It means a lot when you get a friend who can sit in the same room on their laptop as you and not talk but will say something like did you see this?

Or when we need to rant about shit you listen. Its hard because we might seem whiny but it really is that some of us aren’t around people. Don’t talk to people, and a lot of us don’t get to see very many people at all or only talk to people online.

The weekends are hard because its not just we can’t get out its that no one wants to stay in and no one wants to hang out with you.

When you are diagnosed with a chronic illness you normally lose half your friends right off the bat and it kills small parts of you. So yes, if you want to help make weekends better then just be there and say what’s on your mind.

My name is ShayWeasel and this has been a weirdish public blog post…

#spooniestrong #weekendssuck #fuckit

Internet people…

I have a problem. Its not that big of an issue, its more like well.. .Let me just tell you

I’m an internet type person, I enjoying the internet, I am not that social of a person, My sisters are mostly all very social.

They love people most the time, me? No. I can be highly rude and I sometimes would rather read blogs and watch youtube videos then talk to people. Yes this could be a problem. I like to say that this isn’t a problem at all, that this is totally normal, but lets take what I’m doing right now.

I’m sitting in a sort of dark room, my family is downstairs and I’m writing a blog post, yes I’m writing a blog post upstairs away from my family, while listening to Lady Gaga through headphones. I really fail at social things.

Today as we all sat in the living room I played YouTube videos that no one asked to watch on the TV using the chrome cast, but personally I know it seems weird that I’m not a huge social person but I do like how I am. I don’t think I’d change much about myself and the fact that I am an internet person is okay. I’ll stay up late watching YouTube videos reading blogs writing blog post and well sometimes making YouTube videos which I make private because I’m so nervous to show people.

I might not be social face to face, I might be shy and I might get upset when people don’t want to hear what I have to say but I like myself I’m weird as well… I’m just Shay

and I like that about me

My name is ShayWeasel and I’m an internet person if you’re an internet person let me know and we can be internet people together and maybe we can be awesome and weird as shit together from a far.

  So yea thanks for reading… I guess thats cool…

Its not “Just” the Internet

What people don’t get about team internet.

SO team internet, we are a random group of people, you have people like Grace Helbig who is having a fucking TV show come out this is a big deal, but what people don’t get is that every time I sit down at home or in a bookstore and watch a youtube video of Tyler Oakley or Mamrie Hart I feel like they are my friends, I feel like I know them. I laugh outloud and I cry from laughing so much. They don’t just act like they care they have things they care about Connor Franta raised money to build wells for people how fucking cool? Tyler Oakley raised money for suicide privitin. And Hannah Hart got people to work together in communities to help the world be better. I mean thats just a few what people or some people don’t understand is that we don’t just find people online to talk to and get in trouble with no…. we work together as an online community to make the world a better place to be alive in together. We want everything to work together. We want to live in an earth that’s more amazing than ever. I like the way we can work together.

No the internet isn’t always safe, there is a lot of bully and stuff but when you go to a youtube page, like scishow and you learn about something that in school you should have learned but you somehow you missed it or someone just didn’t talk about it. To me shows like Scishow make my life better, I love learning and people never took me (still don’t) seriously when I talk about science and when I watch these videos or have a convo in the comments it makes my world a little better.

What you need to understand is that team internet is not just a bunch of weirdness its an amazing platform that holds a bigger world than you know. Yea people are all different but the internet makes the world smaller and when I find someone that says something and I go you like the “vlogbrothers?” and they look at me like what? Thats what makes the world funnier and better because we are DFTBA!! We are working together to make the world less suckish.

My first time I got on youtube for real was in 2009 it was super late at night and I had this boredom deep in my sleepless soul. I watched a video by rhett & link and I laughed outloud in the middle of the night, my world changed I found people who lived in my state, and were making videos, Rhett & Link now live out in Cali, they followed their passion and they blew people away with the laughter of others. Thats what team internet does. They gave me hope that I could follow my weird passions even if my passion was just writing a blog post or making a weird video.

Its not that the world online is nicer or anything its that its just different. I remember when I found this girl with blonde hair and she was weird and she was surely random, Grace Helbig would become a youtube video I would watch all the time. I would laugh and I would giggle at all the weird things. I watched Juilian Smith and would not be able to stop laughing people would have no clue what I was laughing at.

I still go back and watch the video “Trees Hate You” because it makes me laugh so hard that its my goal in life to be able to be that random.

The internet and Team Internet and team DFTBA is not just a good thing its being able to say I’m hartosexual and someone going me too. And both of you being able to find a place and for me to feel like I can watch a video on the internet and I can maybe chase every dream I have.

People that make youtube videos we all know they start off really small, they make these videos because they just want to. I love being able to see Tyler Oakley and Grace Helbig on cable TV because they have been apart of my week for a long time, they have made me laugh and made me think.

I don’t think people when I say I watch Youtube videos I don’t think they get it that what real happens when I watch a youtube video mostly everyday and these people that I don’t know are like weird friends, they make me feel less like I live in a world full of people who don’t understand.

We are the people who will No we are changing the way people think, there are videos about coming out and about being true to yourself on the internet, we are team internet we are DFTBA we are amazingly fantastic and we will we are changing everything, the world needs people that understand the giggles of a miranda sings video and why I wake up 20 minutes earlier a lot of times to watch a Good Mythical Morning episode and why I like to sit on sundays and watch Danger Dolan and why when I don’t know how to do something I google it. Or when I need to feel like I am better than this I watch Sprinkle of Glitter videos and why I like the way I am because if I can be this random and no one likes me where I’m at I can be liked by some on the internet.

If you ever feel like life isn’t great or is very suckish then remember that people on the internet and all over the world are trying to make it less horrid. I know the world might not be great all the time and when people are rude or stupid you can get really mad but remember that people are working so hard to make the world less suckish. I love what Youtube has done for the world. Its brought us closer. Its made everything different in a good way.

 

You see the YouTubers you watch become friends, I remember when I found O2L videos and thought to myself these guys came together and made something wickedly random videos, they all made me laugh.

Youtube, people who blog… People who have a job through the internet is amazing. Just so you know, life sucks but we together can try and make it suck less…. Just like the vlogbrothers say

 

The world is made up of all kinds of people, let the world be better, and also let them be amazing. Life will get better….

 

I love finding people on Youtube like ServiceDogVlogs (Tatianna) who has the awesome videos and a great singing voice and she talks about stuff like shit people say to service dog handlers and you have people like The Clairty Project (Clare) who makes videos on what its like to be awesome with a chronic illness and she just talks she did theses reviews of red band society and made me want to watch the show so I could keep up with her reviews. Both Clare and Tatianna make videos on life with chronic illnesses. Its how you look at it. And they are amazing,

 

We are going to change the world, we are changing the world. We make everything so different and the way people start off real small give people hope that maybe we can all be awesome people, because we are all awesome person but every now and then we forget that we are awesome and that we make the world more amazing by just breathing in. People like Sam Pottorff I have randomly laughed at his videos but he also talks seriously about things and he seems so raw sometimes, as a lot of the YouTubers do.

There are things like VidCon and playlist live and all kinds of things because we as a whole make the world weirder more random and we are learning as team internet that we don’t have to agree on everything but we have to care and love each other. We don’t want hate and I think team internet will be the ones to change that. I think we will laugh as the videos we watch and all the blogs we read have made this world a more easier place to live. Its hard to know where to stand on everything but we have the world at our finger tips and its amazing. So here is to team internet and all the people who are all about being as random as fuck. This people is how you team internter YouTuber style, thanks for making videos keep it up

(Shout out to AConMann, Anastasjia Louise, Bunny HopkinsThe Clairity ProjectServiceDog Vlog,)

The Medical World Has failed

This post should really bother you, if it doesn’t….

 

The medical world has failed horridly for people with chronic illnesses, they have failed us. I as someone who has multiple chronic illnesses I know. Because as the doctors talk to you like you are either stupid or like you are suppose to understand everything. I have health issues and the doctors they act like I’m suppose to put up with being in pain and being sick because they have no fucking clue how to live with chronic illness, when I go to the doctor and I say well I had one good day last week and then I say “I only threw up twice all day.” Yea thats a good day, I’m fed up with doctors treating people with chronic illnesses like its our fault, and oh they do.

in the medical world you sometimes have to wait nine weeks to nine months to a few years to get to see the only doctor who has any clue what they are doing, people are either misdiagnosed or they are called insane and sent home, or better yet put somewhere like an mental hospital when they have a physical illness that needs to be treated by a doctor who will listen.

Living with an illness is hard but personally what’s harder is hearing the words “It is all in your head” “You are already on the treatment” “the medicine I put you on is suppose to help”

My sarcastic answers to these questions are much easier for me to say then really dealing with another doctor and another treatment that didn’t work. The medical world is not helping because out of the 7000 rare diseases there are only 200 that have cures and most of the rare diseases don’t have treatments, theses diseases are unknown and so most of them are undiagnosed so you have a ten year old child whose body parts body out of place and everyone just says she is loose jointed and then they go on and act like this is fine and then when she is 15 her body hurts and other weird things keep happening but what happens when that same girl gets in a car crash and she is rushed to the ER and she is talking and all is fine but then she dies her heart burst because she has EDS and it wasn’t on any of her paperwork and she didn’t even know, because no doctor put all the pieces together, what happens then?

They die, okay lets go back a little, sometimes doctors want to put us into small little boxes when in reality some of us have multiple rare diseases, and we don’t fit into the boxes of us, well the people with EDS might be able to fit into small boxes but not health wise. The medical world needs to admit they failed the people with chronic and rare disease.

It needs to change, we don’t need to be treated like we are insane every time we walk through the door, my stomach when I throw, I just throw up like a gush of water, if you didn’t want to know that then I’m sorry, but it seems the doctors they don’t want to know either, because as soon as they come into the room, they have made up their minds, when are blood test show we are normal, maybe you aren’t doing the right blood test, maybe its you doctors, because every chronic illness person thinks its there fault, and I don’t know where doctors got this idea that everyone is making up their illnesses, but they aren’t. Maybe five people are but most of them aren’t and you need to deal with the fact that maybe you doctor have no clue what is wrong but do tell me that you know something is wrong, tell me you believe me, even if you can’t help me, just be honest with me and say you can’t because as the person with the illness, I’m not just trusting you with my illness, I’m trusting you with my life.

We have illnesses, we aren’t fakers, we are sick, so dear medical world right now you are failing the people with chronic and rare illness/diseases, and we know that we may never get better but we want some help. So please help us.

  As always I might be a spoonie for life but I just hope I’m not always in pain.

Chronic Illness living…

I thought today about how I feel like people don’t understand what a chronic illness means, I mean I have an illness that I will always live with. But the physical pain isn’t the worst part of having this illness its the emotional pain, sometimes you feel like you talk too much about it, other times you want to just not talk about it for the rest of your life. Its the way people act to you. Its hard to know do I talk about my illness or do I want other people not to know or am I allowed to say blah blah or is that wrong? Its not something I’m okay with, I don’t want people to feel sorry for me I want people to just I don’t know understand.

In my first blog post on here I talked about oversharing and it comes into play here as well, how much do they want to know, part of me really does want to talk about it not because I’m obsessed but because at least seven times a day I’m vomiting or feeling weak or I bend down and feel as if my heart rate went up. Its because every part of my day I’m dealing with the illness inside me. I am having to deal with it, but I don’t want to just deal. I want to be alive and I want to live, but living is hard, so I am sorry sometimes when I have a bad pain day or just feel really yuck I might overshare and tell you to much, but I hope you understand that this pain I feel doesn’t go away I either numb it with pain killers or I go out through my day. I know I’m not going to be cured and I know life isn’t easy but I just want you to understand that I’m living with a chronic illness.

 And guys my fellow spoonies, know that most people aren’t going to understand its not going to get easier, but you will have to deal with people being rude, but every now and then you are going to get this person who will change everything, it might be a spoonie friend or someone who just tries and understands, or someone who has dealt with illness and they are going to be your friend.

 We spoonies have to stick together through the misdiagnoses and through the mean doctors to all the people who are just “dumb bitches” we will no matter what get through this!!

Health is amazing!!

when you get diagnosed with anything, you have some options, you can make up your mind that you are going to just “deal” with it. You can try and find a cure. Or you can make up your mind that you aren’t just going to “deal” with it or try and find a cure but you are going to have this disease or syndrome or allergy or other health issues and say “Welcome to my life.” It’s not that you want this illness or whatever to stay and hurt you, but you aren’t just going to “deal”

No I’m not battling any illnesses, I’m living and I’m blessed to have problems, I know I sound like a Pollyanna (overly glad person) but you can’t let something, like a health problem or something like food allergies and things that could possibly kill you.

Tomorrow I could go to the store and not purposefully touch a walnut on my way to the restroom and pass out from anaphylactic shock in the restroom and die. Thats a possibility. Its something that could happen. Life can kill you or it can make you scared to live or you can just live. You can live with anything.

WE as humans can adapt to anything, we will learn to be happy without anything. People die and we have to keep going on.

So you’ve been diagnosed with something that in time will either kill you or you have a possibility of dying from it. Think of it like this

Yesterday morning your great-grandma who was 105 years old passed away, you have to feel sad and go and lie her body in the ground. After you have lied her in the ground you have a strange choice, you can either go on or just sit and cry, so take a moment and remember what life was like with them and then get up and go on.

Walk the miles you want, do what you wanted to do before all this, but you will just have to do it differently, yes everythings going to change but its okay. Its good change. You will miss things you will cry moments of life will fall and you won’t get to be apart of it. But life can be fantastic.

Illnesses, health “problems” are just random things that happen, if you didn’t have this health thing or whatever you would have something else that would make you complain and make your life annoying. This isn’t going to be easy, I mean seriously nothing is easy. Which I personally am happy for.

It took me a long time to really understand how blessed I am to be able to understand people who have things that aren’t a bump in the road no they are a random hill thats really nice to have met along the way. I like my bumps, I like my holes, and I like the things that make my life hard because without them, I wouldn’t be Shay, I wouldn’t be okay with how much change can happen in a moment or a day or just a minute. Life changes everyday we have to deal with things.

 

I’m not right about half the stuff I say, but its what I think and what I think is what I think and no one else can think it for me, so if you don’t like it, then you don’t have to read it or hear it. I’m glad people are all different, I’m glad that we can life at stupid stuff that happens, remember that not everyone is out to get you. And that some are.

So welcome if you are newly blessed with a health issue, because this world is a beautifully artful place with randomness all over your face but it is amazing. Its just amazing.