#HospitalLife – In Pictures:

I am beyond thrilled to share that I have arrived HOME!  Late last night they determined that I was fit enough to return home and all of my efforts of putting up the fight of my life, certainly seems to have now paid off.  There is quite a descriptive post in the works, to walk through my latest health journey in words and how I feel that I have once again been afforded a chance at life. This has been an entirely transformative experience and one that I never imagined in my wildest dreams.  Somehow, my strength and resilience is at an all time high and because of that I have been peacefully healing —- mind, body and soul.

Here are a few pictures of the

#HospitalLife

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My hemoglobin levels were considerably low, in which case I needed a blood transfusion.  It never really dawned on me how wonderful it is that people donate blood, something I have always been too ill to do even prior to my diagnosis as I have always been anemic.  I ended up using two units of blood which ran for about six hours.  Shortly after I felt like a completely different person; less fatigued, less cold and returned color to my face.  Thank you to those who donate!

Red Cross Blood Bank Centers

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The day of my surgery I snapped an #instax polaroid of my baby, Zoi.  It seemed obvious to me that if I had her adorable little mug looking at me with those eyes of hers, it would push me to do everything in order to make it back home to her.  Aside from all of the tremendous amounts of love I received from people near and far, my amazing friends, family and of course my husband — Zoila was the one little (but actually very HUGE) incentive to show up, kick ass and get back on the road of life and viola! here I am!

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Anyone who follows along on my Instagram knows that my baby Godson holds the actual key to my heart.  He stole it from day one.  When his beautiful mom — my lovely friend, Michele visited at the hospital the day after my surgery, she brought along a one of a kind flamingo and it instantly brought ridiculous amount of smiles — and not just from me, but all of the staff, fellow patients and anyone who saw my trusty IV monitor as I wheeled it by my side throughout my stay.

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I’ll admit, my biggest complaint about surgery is that you are forbidden the basic human need of drinking water (or anything for that matter), prior to the procedure.  In my case, I was told that I couldn’t have anything from midnight until later in the night after recovery.  Quickly, my mouth became a desert and my need for water seemed like life or death.  Of course that is an exaggeration, but it is certainly how I felt.  As soon as I got the green light, which was about twelve hours later, I ordered “sips and chips” and I felt like I stumbled upon an oasis.  Dreamy does not even begin to describe the feeling of when the ice water cooled my lips for the first time.  Sometimes it really only takes the small things to make you feel a sense of nirvana.

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Before I had even been transported to my room, my two best girls had flowers ready and waiting.  Prior to my surgery, I couldn’t find the strength to speak to them.  Distancing myself for selfish emotional reasons seemed to be the only way I could cope.  I felt that if I spoke with them, I might expose that I thought I was going to die and that we’d never have an ABC reunion again.  Without fail, they stood by my side no matter what and made sure that I knew they were there with me, showering me with their love and non-stop support.   I love you both.

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I felt so much power behind this operation.  Power from prayer and positivity and all of the amazing thoughts that were put out in the universe in honor of getting through this operation with a successful outcome.  I feel cheesy every time I say it, but there is no way I would have been able to do it without all of you.  Every single person that took it upon themselves to take the time out of their day to wish me well and include me in their conversations with whomever they have faith in.  It would be fair to say that I feel endlessly blessed.  Seeing this gleaming photo at St. Joe’s Hospital and Medical Center seemed like a fitting vision for the morning after the operation.  What a beautiful sight to see (I can even see my neighborhood if I look really close).  

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On the same glorious walk as pictured above, I was marching along the halls with the most important women in my universe.  They guide me through every struggle and challenge and proudly walk by my side, even in the darkest of hallways.  There are not many words that can do this picture justice, other than, thank you and LOVE.

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Further exploring the hospital, my home away from home, I walked past my favorite piece of art adorned on the walls in the lobby of the Oncology ward.  This particular wall decor always seems to catch my eye.  I appreciate creativity and try to search for it wherever I may be.  I can especially appreciate when it’s in unexpected spaces and places.  Well done, St. Joe’s.

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Just two short years ago, Steve and I spent the night at the hospital on Christmas.  It was by far one of the more depressing of holidays.  I feel very fortunate that I will be able to spend this Christmas with my family instead of inside the hospital walls.  However, they do their best to make you feel in the holiday spirit.  To those who will be spending your holiday in the hospital, my Christmas wish is that you are surrounded by love and joy.  It will get better.

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One of my favorite little cheerleaders, Kambrell joined me at the hospital a few days after the procedure.  Seeing things through her eyes and the way she expresses her love for life, makes me feel equally alive.  She is one of the most special little girls I know and I’m so grateful to be a part of her world.

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Just a few of the many gorgeous flowers I received. THANK YOU! I was able to enjoy them everyday and smile thinking of each person and the memories we have shared.  I chose to donate the flowers to the Oncology ward of the hospital once I was released.  They were all so beautiful and I wanted other cancer patients to be able to enjoy them as much as I did.  Please know that your kindness has such an impact and made many others smile, as well as me.

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Last but most certainly not least, my Steve sent this to me the second night, once he returned home to our dogs, Keg and Zoila.  He always knows how to make me laugh, as he was wearing my #ASU hoodie and my satchel to carry Zoila, all in an effort to take Keg on a walk. He takes care of all of us so very well and I am the luckiest person to have such a brave, selfless and loving man.  Thank you seems so insufficient.  What else can I say? You’re top notch, my love.

HospitalLife

More to come soon.

Love,

Britt x

Remission ☚ ☚ ☚

Remission

Ochoa, Britt- Cancer Timeline

Ochoa, Britt- 12 Chemo Rounds

If you shake me hard enough, I will appear, yet it feels as though I have been in an unceasing dream, or shall I say nightmare since July 1st, 2013. It has taken me a couple of days to regain surreal consciousness as I was sluggishly coming out of the dark tunnel that has been my existence for the last nine months. In fact, I became used to the dark tunnel, my eyes adjusted to the dimness and although I imagined the light at the end, I grew to accept my new reality as a Stage IV cancer patient. Somehow, I knew by some means I’d eventually see the glistening light but in the mean time I vigorously challenged my mind, body and spirit for the fight of my life.

My new identity and only distinctiveness became that of a Stage IV cancer patient. Prior to being diagnosed, I held a good deal of individual characteristics that made up my identity in my profile as a human being. Twenty-seven years had crafted me into an abundance of roles to which I found myself identifying with; a lover of all mediums of art, a frequent concert goer, a best friend to Crystal, wife of Steve, daughter of Karen and Tom, loyal employee of American Express, a shoe collector, a clothing coinsure, frequent traveler and student of the world. However, as of July 1st, 2013, my identity splintered and all of the things that once made me who I was, became superseded as I hastily shed my foregoing self to become a cancer patient, which immeasurably became my whole universe.

The last month had become soberly temperament in the realm of ways I was deteriorating both physically and mentally. For weeks I was vomiting between fifteen to twenty times per day and in some cases even greater than twenty. I was unable to keep anything down, even water. Much like many other times within the last nine months, I was forced to shelter myself like a recluse, as my symptoms disallowed me to be a part of the rest of the world for fear I would be sick, pass out and assassinate any remaining cool factor that I was clinging onto for my ego’s sake. Nevertheless it became very apparent that my inflated coolness was overstepped by my Exorcist’s style of retching. I passed the indications along to my Oncologist and she had many calculations as to what she believed it could be, even at one point believing that my symptoms were synonymous with the possibility of a brain tumor. Needless to say, I endlessly underwent every assessment and scan known to man in this so called game of “practicing medicine”. Fortunately, but frustratingly everything was coming back negative and to no avail we discouragingly found ourselves at a stand still. I cursed and I cried. I spent several nights in the Emergency Room and still no sign of the culprit or any form of developments in the hunt of what was remotely off beam as they were all returning to us unfounded. Conclusively, after kicking and screaming, my Oncologist decided it would be best to admit me to the hospital, and just like that I once again became an occupant of the Oncology Ward. The plan of action was to monitor me in the ongoing effort to uncover my unusual and erratic symptoms, which was liable for draining my body of any remaining strength by the minute.

As Murphy’s Law would have it, I did not vomit once during the recurring visit to the hospital. Ultimately, the Doctor’s were unable to categorically figure out the vile symptoms I had been having over the last month and determined that the only conceivable cause was myself. Yes, that is correct, the medical professionals reasoned that due to all of the negative testing and scans; the unremitting vomit activity was due to my very own irrational brain, or psychological anxiety, as they prefer to define it. My brain was the dam and the levee ruptured leaving me with an overflow of anxiety and self-made symptoms that could not be contained.

Now with the understanding that the monsters in my head were making me sick, I was about to be discharged from what had become my natural habitat, but not before my lovely Oncologist entered the room. Making herself comfortable at the foot of the hospital bed, as I lay sitting up waiting for her to address any further information pertaining to my current circumstances, she reached for my hand, squeezing it in a fashion as though she was about to share something of great magnitude. I took a deep breath preparing myself for her words and she then began to speak in her soft, gentle tone, “Britt, your last PET scan came back remarkable and while there is still a small tumor, there is no evidence of disease”. Confused, yet delighted, I once again found myself emerging straight into business mode. I had so many questions and my brain was scrambling to connect all of my overwhelming thoughts. Was I cancer free? Did I beat Stage IV cancer? Is this hellish nightmare over? Did I redeem the clean bill of health I had so hoped for? I was quickly shut down on all of the above questions. My Oncologist went on to say that I am in the early stages of remission, the tumor still exists, and if it weren’t for my debilitating neuropathy I’d still be on chemo going forward. She proceeded to keep it real with me and explained that the tumor still resides in my body and that there is a high probability that the cancer could return at anytime, being that my diagnosis was Stage IV. Yet, for now it is dormant and by a small margin, I am well enough to proceed with my young life at the moment without any evidence of disease living inside of me. It wasn’t the exact way I had envisioned myself receiving such news, however to know that the chemotherapy treatments proved to be a success and I was now able to carry on with a quality of life, came to be first class news and the greatest news I had heard in almost a year.

It’s been nearly five days since I have been gifted this news and to be perfectly honest I have not been able to make sense of it all in my head. But, more significantly I am hesitant as to how I should refer to myself– Am I still a cancer patient, or now a cancer survivor, or perhaps neither? Yet, I am more than willing to accept the news and feel vigorous that I survived this war that has been waged upon my body and robbed me of good health for the last 290 days, 41 weeks, 417,600 minutes, 6,960 hours and 9 months + 16 days.

After we had finally arrived home, Steve hugged and inhaled me while whispering, “I finally have my wife back”. Tears streaming from his eyes, I kissed the salt that was streaming down his cheek. Somehow, I felt as though I was the only one who wasn’t bursting at the seams with ultimate ecstasy. Cancer had managed to take possession of my life and suddenly I didn’t know how to go back to my life after the cancer surrendered. Following a steaming hot shower to wash away my bewilderment, I stood in the doorway of our bedroom that met the living room where Steve was gleefully revealing the remarkable news with all of our family and friends. In my disoriented state of mind, Steve detected that the best news we had received since my diagnosis was not sinking in for me and he wanted me to completely take in the concept that I was now a healthy twenty-eight year old woman. Resembling that of a movie, Steve enticed me to chant and scream and repeat at the top of my lungs, “I’M HEALTHY, I’M HEALTHY, I’M HEALHY…I, Britt Ochoa am H-E-A-L-T-H-Y”. It was an unfamiliar declaration, as even so much as decent health had been a stranger for so long. Somehow, I was the only one needing convincing of this news and felt guilt-ridden that I was not reacting in a more gratified and wound up manner. Sure, I knew I should be jumping for joy, showcasing tears of happiness and taking the news in a gifted way, but I was unable to parade my sudden liberation; perhaps out of shock or perhaps because I felt unconvinced.

The first few days of my new “branded identity” as someone in remission did not go as expected. Unable to get myself out of bed, I found myself wanting to be completely alone and still felt as though I was in the never ending dark tunnel that I somehow became comfortable in. The thing is, as I would lay in bed over the last nine months, it became a frequent daydream as to when the day remission would be mentioned and how I would feel in that very instant. I pictured myself to feel well, feel 100% and back to the Britt that once was. But, in turn, I felt the opposite, still reeling from the brutal pains of neuropathy, as well as the poisonous chemo that remains in my body, a “welcome home” to your old self, was not arising. Were all of the nightmares over my health supposed to escape my head by the mere mention of remission? Was I supposed to peel away the mental scars and put them in a mason jar for safekeeping? Pessimistically, my head seemed to be splitting at the seams and I found myself having an identity crisis; who was I, if not Britt, the Stage IV cancer patient?

So, as I sit here now, I can honestly tell you that I am still very jumbled over how I am presumed to emote over such rewarding news. However, alongside the confusion, I am eternally grateful that I was able to go on this journey, for I truly believe that I am a better person for it, whomever that person may now be. I now understand the meaning of “life is too short”, I comprehend that life can change in an instant and that no matter the situation; you must go at it in its full entirety. I am humbled by this experience and realize that people are truly mind-blowing, ranging from close friends and family, to complete and utter strangers. When I didn’t have the strength to pray for myself or inflate myself to keep fighting, so many soldiers in my corner took it upon themselves to keep me in their pleas to God and blessed me with good vibrations. The love and encouragement will forever be in my heart and mean more to me than anyone will ever understand.

As for my next steps, I am going to focus on healing and manifesting the idea that nothing is permanent, much like my identity as a Stage IV cancer patient. I’m not sure who I am now since finding myself post cancer, or how I will come to define myself, but what I am damn sure of is that I am a relentless fighter and if cancer shows its dreadful face again, I will be well equipped to handle it and terminate its existence.

Thank you, to everyone for being an unwavering support system through this turbulent trek. I am going to get busy living and embrace the new Britt, while rekindling some of my former identities. I now revere my life similar to that of a semi colon; a sentence that was supposed to end but didn’t. My sentence in life came close to an end and I was given the opportunity for it to continue. Therefore, I will be upmost grateful for this gift called life and continue on with my life’ s story.

Until next time,

Love- Britt x

Love, Britt x

Stupid Cancer- “Get Busy Living”

The young cancer epidemic can be quite daunting. Just when young adults are getting themselves prepared for their future into adulthood, i.e.- education, career, relationships, they are grossly impaired once the discovery of cancer has been made in their young bodies. Many things can be affected when it comes to cancer in young adults and a large amount of sacrifices have to be made. For me personally, I have had to put my life on hold and with the possibility that it will never get back on the same track again according to my career goals, family plan and overall setup of my young life. Since being diagnosed in July of 2013, I have had to give up my position with a wonderful Fortune 500 Company, a position that was nearly ten years in the making as I had been with the Company since I was nineteen years old. I had somewhat of a cushy position, a work at home position, one that I revered highly and worked hard to get. In addition to having to forgo my career, I have also had to put my education on the back-burner, when I had just one year left until graduation. Seemingly, these are all replaceable things when it comes to the importance of your health and life, however nonetheless important if you have spent nearly a decade trying to get to where you once were.

As I further along in my “cancer career”, I realize that young adult cancer and the awareness needs to be at the forefront of the medical world. We are talking about the generation “now”, who is responsible for birthing the generation of tomorrow. Many times, young adults are diagnosed with cancer at a late, already aggressive stage. This can then lead to problems with infertility as well as lifelong residual symptoms of the toxins dumped into the body in an effort to keep the cancer at bay or gone completely.

I have mentioned before that since my diagnosis, it is difficult for cancer to not consume your world, as you live and breathe it daily and go through the tumultuous motions and emotions that comes with the toll. Naturally, since my world has been turned up side down, I am determined to not only fight for my life, but bring awareness and attention to the risks in young adult cancers. It is my mission to advocate for others and myself that medical awareness, even as a young adult is extremely important and most of all entirely necessary.

Often times those who are effected by young adult cancers have a late stage diagnosis, as well as life threatening stakes as many young adults fail to get proper screenings until symptomatically they are forced to go to the Doctors. This then leads to assertive treatment, which then contains many after effects. Through my many hours of research on young adult cancer, I stumbled across a website specifically for the cause; StupidCancer.org. Stupid Cancer is dedicated to young adult cancer, awareness, resources, tools and a bevy of helpful implements. Moreover, it is wonderful to connect with other young adults suffering from cancer and who are busy living despite their prognosis.

Stupid Cancer holds a convention each year and also offers meet up’s throughout the country; in an effort that the cancer patients can stand up to cancer with one another and no one has to go at it alone. Just watching the below video gave me the boost I need to get up on my feet and declare war against my cancer and my peer’s cancer. We can all learn from one another and help one another through the process; if there is a will, there is a way!

Additionally, there will be a Stupid Cancer Convention called OMG2014, which will be held in Las Vegas, Nevada on 04/25-04/27.  If you would like to register please visit OMG2014 Summit.  “The 7th Annual OMG! Cancer Summit for Young Adults is the premier oncology conference and social networking event for the young adult cancer movement. The largest gathering of its kind, OMG2014 will bring together hundreds of survivors and caregivers to connect, get educated, build community and unite to drive the change we wish to see.”

Love,

Britt x

S⬆2C – World Cancer Day 💜

Stand Up 2 Cancer I I #BSMHB #BeStillMyHeartBlog I www.bestillmyheartblog.wordpress.com

Stand Up 2 Cancer

I’m a little late in the day to recognize what an important day it is.  Today, February 4th is World Cancer Day, a day that brings global recognition to cancer as well as awareness to everyone, despite their relationship or affiliation to cancer.  It is wildly important to ensure that you and your loved ones are “in the know” about the disease, as well as get screened, know your family history and most importantly listen to your body.  Cancer, although it’s a touchy subject, is something that each and every person has to stand up to.  On that note, happy World Cancer Day- may you all stay happy and healthy!

Here are some myths about cancer, please read and think about each area as it pertains to you.  If nothing else, it will make you think twice about the disease and how it may effect you or someone you love.

Myth 1: We don’t need to talk about cancer.

Truth: While cancer can be a difficult topic to address, particularly in some cultures and settings, dealing with the disease openly can improve outcomes at an individual, community and policy level. The American Cancer Society has lots of pointers for talking about cancer, whether it’s with friends and family, your doctor, or others.

Myth 2: Cancer… There are no signs or symptoms.

Truth: For many cancers, there are warning signs and symptoms and the benefits of early detection are indisputable.

Myth 3: There is nothing I can do about cancer.

Truth: There is a lot that can be done at an individual, community and policy level, and with the right strategies, a third of the most common cancers can be prevented, according to the UICC. Avoiding tobacco, maintaining a healthy body weight, eating right and getting enough exercise, and getting appropriate cancer screening tests can all make a significant difference.

Myth 4: I don’t have the right to cancer care.

Truth: All people have the right to access proven and effective cancer treatments and services on equal terms, and without suffering hardship as a consequence. The American Cancer Society is committed to fighting cancer worldwide.

Cancer represents over 100 diseases and is basically abnormal cells that have grown out of control. Half of all men and one-third of all women in the U.S. will be diagnosed with cancer in their lifetime. The cancer mortality rates for African Americans is higher than any other group of people.  These are the facts. So since this disease affects our whole community, we need to take detection and prevention very seriously. And while the number of cancer cases is very alarming, the number of people surviving cancer today gives us what we need to know that progress is being made.  The American Cancer Society, one of the largest health-based organization in the world and second largest fund:

Show your support for World Cancer Day by turning your Facebook and Twitter profile pictures purple, and Chevrolet will donate $1 to the American Cancer Society, up to $1 million. You can also “like” World Cancer Day on Facebook.  Purple is the color for all cancer awareness, so help spread the Power of Purple!er of cancer research next to the U.S.. government, tells us that sixty years ago, 1 out of 3 people diagnosed with cancer survived. Today 2 out of 3 will survive.  It’s time to finish the fight.

Reference:  http://michronicleonline.com/2014/02/04/world-cancer-day-2014-what-you-should-know/

Love,

Britt x