Type 1 Strong Week 1-Q&A

 

Kayla

January 8, 2018

Hi everyone! This week I have a very special person who is considered to be one of my DIABETES! Her name is Kayla and you can find her Instagram here! I met Kayla at my vest first Type 1Meet up- which honestly surprisingly enough was amazing! We all become so close to one another. She is the sweetest, most beautiful girl outthere! Our goal is to continue creating meet ups every month in SD and LA! Her positivity radiates everywhere, I love it. I had the honor of doing the Q&A with her this week! Below is a little bit about the wonderful Kayla herself.

1). When were you diagnosed? NOVEMBER 2006

2). What is your silver lining of Type 1 diabetes? MEETING THE BEST FRIENDS I COULD EVER ASKED FOR. I HAVE FELT SO LONELY WITH TYPE 1 AND THE FACT THAT I HAVE MADE SO MANY FRIENDS THAT SUPPORT ME, NEVER JUDGE ME AND WILL ALWAYS ACCEPT ME IS THE BEST FEELING.

3).Who is your greatest supporter when it comes to dealing with diabetes? MY BOYFRIEND THAT ALSO IS A TYPE 1 DIABETIC. HIS NAME IS KENNY AND HE IS MY ROCK.

4). If there was one day where you were diabetes- FREE, what would you do for that day? EAT SO MUCH FOOD UNTIL I COULDNT WALK ANYMORE. I WOULD EAT SO MUCH CANDY!!!!

5). How long have you been active in the Type 1 community via social media? SINCE MAY 2017

6). How has new technology changed the way you engage with your diabetes? IT HAS MADE ME ABLE TO REACH OUT TO PEOPLE WITH QUESTIONS AND CONCERNS THAT MY DOCTOR COULD NEVER ANSWER OR RELATE TO BECAUSE HE ISNT A TYPE 1 DIABETIC. I HAVE LEARNED SO MUCH ABOUT T1D FROM OTHER DIABETICS 

7). What would you THANK diabetes for? FOR BEING THANKFUL FOR BEING ABLE TO SEE THE LIGHT OR DAY, TO HEAR SOUNDS, TO USE MY FEET, TO DO SIMPLE THINGS EVERYONE ELSE TAKES FOR GRATED.

8). What is something you would tell others who are also dealing with this? YOU’RE NOT ALONE. ITS REALLY HARD WHAT WE GO THROUGH AND BE KIND TO YOURSELF. WE DEAL WITH ENOUGH ALREADY. EVERYDAY IS A NEW DAY WITH DIABETES SO KEEP YOUR HEAD TOWARDS THE SUN. YOU WILL SEE A RAINBOW AFTER THE STORM…I PROMISE.

9). Are you in working/going to school to be in the health field? If so, what are you aiming your career towards? If not, still would love to know what you want to achieve! I ALREADY WENT TO SCHOOL FOR A JOB IN THE MEDICAL FIELD AND GRADUATED. MY GOAL IS TO WORK FOR DEXCOM OR ANY DIABETIC COMPANY.

10). What is your favorite no insulin needed snack? IS THERE SUCH A THING?

Thank you so much Kayla, I am beyond blessed to have met you!

-xoxo S.

 

My Best Friend Knew Me

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I consider myself really lucky, yet grateful for having to met such a humble, beautiful being who shares my struggles. I met Claudia a few days after being diagnosed with Type 1 diabetes. I felt so much love the moment I met her, she knew exactly how I felt. She guided me, and helped just as other wonderful type 1’s did through this new process when my own doctor couldn’t.

There was no one else I would rather call at 3 am, when I woke up with the shakes and my bed filled with my own sweat, except Claudia. She would crack jokes about our diagnoses because she knew how it was. If it wasn’t for having met her, I know for a fact diabetes would me much harder on me. She is the one who got me to where I am. From carb counting together, to hikes, to even taking me to the ER when I was going to go into DKA- she knows me, high or low, she knows me.

Im grateful that many people don’t get to find that person who guides you to finding the OK with this disease. It’s very hard to accept the fact you have it, but at the end of the day no one can really care for yourself then your OWN SELF. She showed me the silver lining of this disease- even if it took me months to see it.

The only tip I have for you, is please go and find yourself a Claudia, because without my Claudia.. I don’t know how I would be handling my diagnosis and how I would be waking up everyday grateful for diabetes.

-xoxo S.

I am my own hero.

Its been 600 days since my diagnosis of a type 1 diabetic. Things changed dramatically, but we all knew it would have right?

The first couple months I was on top of my diagnosis. Waking up every day, making sure I have all the snacks I need to prepare myself if my sugar drops during the day. After a while, you get tired of the constant worrying if you’ll make it to the next day- you start slacking off.

At least thats what happened to me, I started slacking off with my diagnosis, My A1c went to 8.7. It was that moment that triggered my own being. I decided to start taking care of myself- because in the end all you really have is yourself, right?

As soon as I knew it, My insulin pump broke. Let me remind you, I injected myself for over a year and ever day was another day I would hold my breath because me and needles just don’t do well. Anyways, after my pump broke, I was of course admitted to the ER due to DKA-how joyful.

Regardless of all the moments where I hated myself for having diabetes, for all the moments I wanted to stop fighting because diabetes was “winning”, I stood tall and became my own hero.

I remind myself daily, everyday I wake up that I am so grateful for another day living with this disease. I nourish my body with food that benefit me and my broken pancreas. I thank God for allowing me to share my daily struggles and Wins with type 1 diabetes. Without this disease, I wouldn’t have met the greatest individuals out there from all over the world.

Were never going to have perfect numbers everyday- but we sure as hell can fight like we will. No matter what hardships I face daily, Im stronger then just letting it control me. Remember, you should never allow diabetes to control who YOU are. You’re stronger then you think you are, and your capable of all the highs and lows, all the carb monitoring, don;t ever doubt yourself any lower then that.

Regardless of T1D, I still felt strongly that no bucket list item, life goal, or brilliant idea was off limits because of my diagnosis- and because of that, I AM MY OWN HERO.

8 months as a Diabetic.

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I hit my 8 month period as a type 1 diabetic, and all I can really say is.. wow.

I remember few weeks after my diagnosis, I was told it gets easier. I would be lying to myself and others if that was actually true. Truth is, diabetes sucks the living out of you on most days. Don’t get me wrong, I have those days where my blood sugars are shinning bright, and days where I lay in bed with gallons of water.

But among the terrible days, I gain strength every single day. Diabetes is part of my life- but not my sole identity.

God has a plan for me, and a reason for my diagnosis, I turn my wounds into wisdom and allow my pain to make me BETTER not BITTER.

I’ll be honest, its hard trying to live a normal life when having to inject yourself numerous times with syringes, prick your fingers 6+ times a day. I just want you all to know that it is fine to have bad days where you just want to break down and cry, that is completely normal. But remind yourself, how fearless you are, how empowered you are because of diabetes.

To be honest, I found myself in this 8 month process, I thank diabetes for allowing me to find out who I truly am, and allow me to find the purpose of my diagnosis. It does not get easier, in fact you honestly just learn to get USED TO IT.

In this 8 month time period, I’ve learned to put aside the pain on injecting myself, to be able to LOVE and THRIVE every single day.

I promise you this- your journey ahead is beautiful.
Remain humble, shine your positive gratitude each day, and always remember never give up.

Here I am- LIVING TYPE ONE STRONG.

Don’t let it define YOU.

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Phobia of Hospitals.

All I could seem to remember was waking up with my entire body numb.

Now, if you’ve been hospitalized you know that it is nearly impossible to rest. All i wanted to know was what was going on with me. I lost about 22 pounds in 2 months. However, being that skinny made me look sick. I was not losing fat, instead I was losing muscle mass. There were days where I had no energy to get up and walk. My legs were as weak as I can imagine. I finally went into the ER, thinking all I needed to do was get blood work done, maybe even some medications.

I ended up being stuck there. I had gone into DKA and I was as weak as I could remember. If you all don’t know what DKA is, it’s when your body produces high levels of blood acids called ketones. If left untreated and sugars remain sky high, you could possibly go into a coma. I was terrified.

When I got released from the hospital, I was a whole different person, I was diabetic! Being told I was Type 1 Diabetic, just seemed to fly right by me. I couldn’t take it in. Probably because, all I needed to know was why ME?

Being told that for the rest of my life I will have to inject myself daily with a needle, frightened me. I kept telling myself this can’t be happening to ME.

I’d love to sit and tell you that it gets easier day by day, but I’d be lying if I did. Truth is, I’m still trying to figure this all out myself. I’m trying to figure out why my body doesn’t work like a “normal” body. There are days where I don’t feel like pricking my fingers 4 times a day, don’t feel like injecting myself.. but if I didn’t.. I could die.

All i really seem to understand at this moment is that my pancreas doesn’t produce insulin, so my cells are not absorbing the nutrients I need.

When it finally sunk in. 

Diabetes got the best of me. I was confused at this entire situation and just kept asking myself why? Trying to understand everything possible about being Type 1 diabetic frustrated me. I was stubborn and didn’t want to be educated. Until it was like something came and slapped me across the face. You live with it now. I was finally realizing that I would have to put in that extra work that was needed for being a Type 1 diabetic. I realized that this is my life. I will always have to inject myself, I will always have to count my carbs. And I will always have those days, where I would either have perfect numbers or bad numbers! It has been the most challenging time, but ultimately it has made me much stronger.

Take it day by day. 

I want you to know that you are not your diabetes, you are so much more. Yeah, it demands for a new lifestyle, but YOU can handle it. And always remember…

Have a support group. They are there for a reason. Talk to them! I am surrounded by love and endless support, and I can’t thank them enough. It’s not easy, but having people surround you who help you get through it makes it a whole lot easier. Don’t allow this disease to get the best of you. Don’t let it consume you. You are still the same person, just with a little extra work to do.

You control your diabetes, it doesn’t control you. Make this diabetic journey be one hell of a journey. This is my journey on accepting every aspect of my diabetes, in hopes to find its silver linings and hopefully inspire and support others.

And don’t forget.. Live your life. Having diabetes shouldn’t stop you from doing what you love. If anything, let it be a motivation to become more self aware and tune in with your body.

Continue do THRIVE, TO LOVE, TO LIVE.. live to inspire.

It’s a lot to handle, but Diabetes has empowered me and i hope it will for you as well. You still have the best years of your life ahead of you, don’t lose hope!

I am a type 1 diabetic and this is my story!

Stay strong, xo


Living With Hashimoto’s Disease

Let me back track just a few months prior to being diagnosed as a Type 1 diabetic.

I was in a frightening car accident late August of 2014. While in the hospital waiting to get released, they did more blood work to make sure everything was fine. Eventually 6 hours later they released me.

About a week after, I got a call from my Doctor saying I needed to do an ultrasound of my thyroid because they “found something”.

Results are In.

My thyroid test came back with everything registered within the normal range. I felt good, I didn’t feel hopeless anymore.

Fast forward to when my entire life was changed.
Not long after being diagnosed as a Type 1 diabetic, my Doctor ordered another thyroid test to be done. I figured it wouldn’t change much since I took the test only a few months ago.

However, she explained to me that individuals who are type 1 are more likely to develop other autoimmune disease’s, just like thyroid disease.

Let me first explain what your thyroid does. Our thyroid is a small gland that produces a thyroid hormone, which is essential for our body’s metabolism. There are two different types- underactive thyroid (Hashimoto’s disease) and overactive (grave’s disease).

One day, I found myself in class dazing off and I felt so confused. I felt something was completely off, so I called up my doctor to see if my results were in by now.

Shortly after, she had called me telling me my TSH level was extremely high (A test that evaluates your thyroid function). She indicated that I have an underactive thyroid gland, resulting in Hashimoto’s disease. Apparently my immune system is not allowing my thyroid to do its primary job and had begun to attack it.

My thyroid wasn’t producing the hormones that my body needed.(Much like my pancreas isn’t producing insulin anymore).

Handling Diagnosis

I believe hearing your diagnosis and accepting it is the hardest part in dealing with a chronic condition. And that was entirely true in my case.

I would have never imagined that at age 19, I would be diagnosed as a Type 1 diabetic and living with Hashimoto’s disease. But just like everything else in life, we stumble over obstacles.

However, please don’t let those obstacles interfere with your everyday life.

I live with Hashimotos disease, and it is now velcroed into my daily life.

The only advice I can give to anyone who may be dealing with thyroid disease, with or without another autoimmune disease, is that its up to you. The power is in the palm of your hand.

You define the way you live, and I hope that you can remain strong in any given situation.

We live everyday in a daily battle between our health and our chronic disease taking over. Know you are not alone, and know that the current battles we face will make us stronger in the end.

Always remember… Half the battle is accepting you have it, and being strong enough to overcome it.

You are you.. and you are strong.

Here I am, living with Hashimoto’s disease.