Saturday, May 18, 2013

The pouch, the j-pouch.

Three weeks after surgery and I feel like a brand new person. I probably have been doing more then I should but you have to understand that for 3 years my life was taken from me ---by Ulcerative Colitis. I just want to live, I want to go back to work and doing the many things that make me Kayla. 
I'm at a point where I don't want to stay in the house anymore and recuperate. I'm tired of letting UC suck the life out of me. I'm tired of being the sick girl and the loner. Ulcerative colitis doesn't live in me anymore and  I just really love the way that sounds. 
It hasn't been quite a month since I've "taken it easy." But I hate that Ulcerative Colitis was the deciding factor of how much my body was able to take and what I can and cannot eat. 
I'm ready to live.
And in these 3 weeks, I've been living. To Disneyland, California Adventures, the movies and eating whatever my heart desires but of course in moderations. I know I don't want to end up back in the hospital, being poked and pricked, so instead of going all out like I wish I could. I'm "taken it easy" in my definition of take it easy. 
My j-pouch has given me the quality of life I've been dreaming of. I'm able to use the restroom when I want too. I'm able to hold a bowel without rushing and panicking to the bathrooms and slowly adding more foods to my diet and so far only hot dogs are --deadly. 
At night I'm trying to adjust. I'm not getting the best of sleep because the constant urge to use the restroom sometimes I'm too exhausted to get out of bed but I end up paying for it later -- but that's exactly why the invented washer and dryers right? For people who don't have a colon and have an accident. That's what I thought. 
I've added some spicy food but not too much, been eating lots of chocolate which is only going to make me fat but my j-pouch seems to have no complaints. He enjoys it and I'm loving every minute of it because chocolate and my yucky colon never got a long.
My scar is healing up // the first scab already peeled off. I almost threw up but I survived and just in a few more weeks hopefully my scar will be less visible.
So ill end with my j-pouch hasn't done me wrong yet and I'm hoping I get many more days like today-- because I deserve them. I deserve to be happy and my j-pouch is making me feel amazing and brand-new. So if you doubt yourself and think this surgery isn't for you. Maybe the j-pouch may not be your answer but getting rid of that yucky colon is. Say Goodbye, and you will live, to feel like I do right now. This is going to be the end of Ulcerative Colitis but only a new beginning for Me and my J-pouch.

Don't stop believing. 


Thursday, May 9, 2013

The emotional aspect of Colitis.

Having Ulcerative Colitis has changed the person I once was, I use to be fun, creative, motivated, willing to do anything, spontaneous, and truthful. I use to look at life in a whole different light; meeting people who have colitis, I've noticed the many things Colitis has done to them:
lower self-esteem, hard to communicate with others, not social, hard to look at themselves, hard to move on, and mostly draining where they feel as if they want to give up. You ask of course how I know this: Because I've felt those feelings. I've felt alone. There would be days I would come home from work, and just cry. I felt like I was in this bubble and I couldn't get out. There was no exit. I never did anything about it, because most of the time I was able to snap myself out of it. I looked for support groups and I looked for people to talk to, but they didn't understand. Not my best friends, not my neighbors, not my co-workers, not my family, people at church, or even a complete stranger. I would do walks for Crohn's & Colitis and would meet people who were going through the same thing, I even went to Crohn's & Colitis fundraising groups and I felt better at the end of the night, but it was never enough. I wondered what I was doing wrong, why do I feel this way? Why do I feel alone?
I became this person that would flake out on her friends, on plans made. I would hide out in my apartment or in my bedroom because I was afraid to face the world. Most of the time I was afraid to open up. I feared losing myself, depression, actually being alone or thinking the unthinkable. Days I'd have thoughts that I don't even want to mention, but that's besides the point.
There comes a point where you have to sit down and say look,
"I'm better than this, better than this disease and I will not let it defeat me." 
For me it took one absolutely amazing woman, who has been through the same thing as myself but a million times worse I think. (I wont mention her name, just in case.) but once I let her in and let her tell me her story, her feelings and her emotions. It helped a great deal, because then you know you're not alone. I would text her on my bad days, or call her when I needed just to hear "that it was going to be okay, there's going to be an end, don't stop fighting."

One day I was in my car and I was headed to a doctor's appointment right before I got there, I had this urge that I need to use the restroom and for those of you that don't know what Colitis really is, you CANNOT hold it, you must go right away. Or else you'd have an accident. Well right before I walked in front of the office door.. let's just say I didn't make the bathroom. I ran to my car and booked it home. I cleaned up, showered within 3 minutes I was headed back to my doctor's appointment, I froze. I was driving and I froze... I put on my emergency lights and I cried, and cried. I felt ashamed, I felt worthless and I felt like I couldn't live like this anymore. I picked up the phone after about 10 minutes of crying. And Called the one person that knew what it felt like.. to live with this disease. She didn't know I was crying and she didn't know what happened but after telling me I was going to be okay, I hung up the phone, turned off my emergency lights and headed to my doctor's appointment. Those simple words snapped me back to reality -- and saved me for possibly getting rear-ended by another car.

The reason I tell you that story is because God puts angels in your life. God gives you a hand to hold and a person to lean on. When you're going through something, fighting an illness, you shouldn't have to do it alone, you shouldn't have to feel you need to keep it bottled up inside. Support groups are amazing but you need to find the right people that you're able to open up too. You could have lots of friends or a huge circle but only a selected few will actually care and ask how you're feeling, and try to step in your shoes and help you find yourself again. Make you smile again, and make you realize you're a strong person and cheer you up when you're at you're lowest point.

I hope that one day I can become that person for you, for me, and for the millions of people fighting Ulcerative Colitis. Because I know what you're feeling, I know it's hard. You're crying and you probably don't know what to do next.. BUT if I could be that person you'll listen too. Just know the fight is almost over, and the way you're feeling wont last forever. Please don't ever give up on yourself, you're stronger than you think.

This is for you.

Take my hand
and hold me close

Walk with me
and I'll walk with you

I'll carry you
when you're low

I'll even stand right below.

just in case
you might fall

I'll be right here
or down the hall.

I'll hold your hand
and wipe your tears

please have no fears
for you are not alone

you're stronger then a stone.
you must know.

I'm not GOD
but I'm just like you

a girl who fought a disease
I am too

a Colitis fighter
and I'm here for you.

and help you find the brighter
side of you.






If anyone has questions, concerns, fears.
Or just needs someone to talk to.
I am always here, you can connet with me on facebook/kayla.escobar.332
or email me mis_kaylove5@yahoo.com

I wish I had someone who really understood what I was going through 3 years ago, but now that I have all this support.. I'm finding who I really am again, and things about myself I didn't even know. My circle has only became bigger and of course I've realized the people who are really there at your bedside when you need them. You'll never know what I went through unless you asked me. Even just a faeebook message to say you read my blog, or a text message after surgery impacted me. Made me want to be a better person, and I'll be there for you when you need me. Ulcerative Colitis you were once apart of me, but not anymore. This is my life and I'm so ready to have it back.

"Alone we can do so Little, together we can do so much."
"Never be afraid to help others, in their time of need, you never know when you may need that shoulder to lean on."


and last but no least.

"Do not judge a girl on what you can see, she may be fighting cancer, or an incurable disease, she could be a girl in chronic pain. She comes in many forms. She is breathing, but she is hurting. She may look young, but she feels decades older. She smiles, but her heart sobs. She walks, she talks, she cooks she cleans, she works when she can, and sometimes when she cant. She is, but she is NOT all at once. She is here, but part of her is missing. She fights a battle you will never see. But if you can take a moment to look beyond the smile, you might see that girl is me."


Thank you for the support. xo

Friday, May 3, 2013

Dr. Fleshner

I don't know if I will be able to look you in the eyes and tell you this tomorrow but I am beyond thankful for you. Even if I've been stubborn throughout this entire process and I've cried many tears in front of you. I thank god everyday for a man like you. You're my life saver, my hero.
The man I can always count on and say he made a difference in my life.
Dr. Fleshner, I wish there were more people like you.
"It takes a great doctor to pull off what you have, but you made it look so easy. You're a doctor I'll always remember. You not only imprinted my heart, but I have a body part that was reconstructed by you."
"The mama with no colon can point fingers at you, but not because i'm angry, but because I'm thankful beyond measure for you."





God.
"You have helped me see the light of things, you have given me strength I never knew I had, you watched the hands of Dr. Fleshner as he operated on me. You gave me people in my life that would go above and beyond for me. My parents who have struggles of their own, be there by my bedside as I recover. Eating hospital food and spending money on hotel rooms.
My brother and sisters who travel hours to be with me, you were there so they arrived safely and you were there on their return home. My aunt and uncle who take time off to just be there and make me laugh and Malia's father who hasn't been the best of a man but is making up for it. You have helped me fight when I didn't even think I had a fight left in me. You've given me new friends. Megan Freda- battles the same illness as I do. And even though we live miles away and never met.. we are connected because of you and we always will be. I'll always wonder where she's at, how she's doing, and if her new life is bringing her happiness. And that's all because of you. The man of many miracles."

You all may think I'm strong, and you make think I don't cry. But God has given me the strength everyday to wake up and live. He's told me I'm amazing, he's
Told me I'm better then what I give myself credit for. He's even given me Malia when I was only 21 years old, but he knew I was capable of being a great mommy. That's all I'll ever strive to be now.

Ulcerative Colitis you are no longer apart of me anymore, and I'm thrilled. It's amazing to think someone could live
Without a colon, but in replace of it, is given a j-pouch: that warns you when you have to go to the restroom but it doesn't hurt. See with ulcerative colitis- it hurt and sometimes it would be so bad, I would bleed, I would throw up and I'd would curl into a ball and just want to scream. You couldn't hold it and if you tried.. Believe me, you'd only be angry at yourself. There would be POOP everywhere. Hopefully you have black on. But with your j-pouch it just lets you know when it's full and it's time to release. So far I've been able
To hold it and that's a week after surgery and I'm able to say that. I still wear protection just in case but hopefully that's only for a little while until I have full control
Of my bowel and trust my j-pouch. You do get irritated down there but you find creams and things that suite you, and make you comfortable. So far.. I have no
Complaints with my j-pouch.
I've introduced watermelon and honeydew to my j-pouch today and I felt fine. I was able to be active today, so I cooked and cleaned. An had about 5-6 bowel movements but nothing to drastic. I could manage that, as long as there is no pain.. I don't care how many bowels I have. Just getting use to my new friend. And I'll update you as time passes. Just trying to heal up my battle wounds and get rid of all these bruises so I can enjoy some free-time. Also give me a few more weeks and I'll have a name for my j-pouch.

Love you all, and thank you for reading.