#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.

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More to come soon.

Love,

Britt x

11.30.2015: Pre-Op Video Update

11.30.15 BKO. from Britt Ochoa on Vimeo.

It is safe to say I am fairly numb after today’s visit with one of the surgeons performing my operation on December 3rd, 2015.  My energy levels are pretty low and this is the easiest way for me to communicate with everyone at the moment.  If you’ve messaged, text, called, etc. I’m sorry for not responding — I’ve been a little emotional, as I am sure you can imagine.  But please know your love and kindness has not gone unnoticed.  All thoughts, prayers and good energy is beyond appreciated and I’ll update my blog as soon as possible after surgery on Thursday.

Love forever,

B 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

One Thing After Another…

Well, the good news is that I have lost another twelve pounds and thirty-five since my diagnosis last July. Finally, I am getting back to my normal weight, slowly but surely. It’s now fun shopping in my own closet. Things that I was unable to fit in for the last two years now fit perfectly. It’s as though I have a whole new wardrobe. I am now more comfortable in my own skin; although I still have some more weight to lose it’s motivating to see the number on the scale dropping.

Since my diagnosis I have been trying to eat healthy for the most part, with the occasional treat. However, as of late my appetite has been non-existent. Living off of bananas and cuties (you know, those tiny tangelos). While it’s been nice shedding pounds, my body is rejecting all food and I am throwing up at least seven times daily. It’s becoming so frequent that throwing up has become a part of my daily routine and I can pretty much guarantee exactly when it’s going to happen. It has become so bad that I am paranoid to go out in public, for fear that I will be sick and not make it to a restroom on time.

I had a Doctor’s appointment with my Oncologist this past Monday and I was feeling so great that day, that I completely forgot and failed to mention my beyond frequent nausea and vomiting that has been occurring over the past month. We chatted about every other subject under the sun, yet it slipped my chemo infused mind that my seven time daily spewing was affecting my life in many ways and could not be a healthy side effect.

Once I remembered my failing to share the details of my recent hurling marathon, I called my Doctor to share the information out of sheer concern. My Doctor was shocked and concerned by the amount of times this is happening daily, especially considering I was not sick in this way during my twelve chemo rounds. In fact, I wasn’t once sick during chemo, as my only side effects were achy bones and fatigue. Of course, following my chemo I was diagnosed with “almost” debilitating neuropathy, which is slowly getting better as the days pass by. Initially, I thought that my throwing up may have to do with my neuropathy and thought that it had perhaps traveled to my esophagus. Clearly, I don’t have Dr. in front of my name, but I deemed myself a medical professional via WebMD.

When I expressed this to my Oncologist, she immediately ruled out any correlation to my severe neuropathy. I could hear in her voice the level of concern and hesitation on telling me the possibilities of my recurrent vomiting. After a moment or two of silence she explained that my symptoms were synonymous with having a brain tumor. A brain tumor? How could this be? Suddenly my day went from bad to worse and I felt as though the light at the end of the tunnel was quickly dimming.

After I digested the possible thought of having a brain tumor, my Doctor advised that she wants me to get a MRI of my brain immediately, along with another PET Scan, even though I had one less than a month ago. She went on to explain that if the MRI and PET came back negative, then the next step would be to see a Gastrologist.

Heaven knows that I have already been through hell and back over the last nine months. Suddenly my weight loss seemed so minor and the thought of my daily vomiting seemed scarier than ever. I have my MRI tomorrow afternoon at the hospital, then my PET Scan on Tuesday. In the meantime I will continue to keep my upbeat attitude in hopes that it is not related to a brain tumor. I ask that you all say a prayer for me for negative results and send all of your good vibes my way. As always thank you for the ongoing love and support. I couldn’t make it through without all of the kindness and encouragement that I constantly get from all of you. I will update as soon as I have more information. In the meantime, have yourself a fantastic weekend!

RIP, Arianna ♥♡♥

#BSMHB #BrittOchoa #BeStillMyHeartBlog I www.bestillmyheartblog.wordpress.com I

To us it was just an ordinary day, the beginning to a beautiful spring weekend.  For Arianna and her precious loved ones, this third weekend in March was unlike any other and was the end of a battle that a beautiful little girl fought.  Although I never had the pleasure of meeting Arianna or her family, I discovered Arianna’s beautiful light when I was scrolling through Instagram and a close friend shared Arianna’s feat against cancer.  Unsure of her age, it is clear that Arianna was far too young to have experienced the evils of cancer.  Their is not a child on the face of the earth that should have to endure cancer; the despicable life threatening disease that takes so many children and adults lives day after day, year after year.

Although I am battling for my life everyday, I would do it again and again if it meant that children were exempt from this heinous war on their bodies.  It’s easy for me to fall victim to feeling sorry for myself time after time.  However, when I see or hear about a child that has to suffer from cancer and lose their life, it puts everything into perspective.  I was met with a huge reality when seeing Arianna’s angelic face.  There is no doubt that she was a hero, whether you know her or not.  One look at her amazing face and you know that she was a ray of beaming sunshine.

Despite your political stance, religion or beliefs, I am certain that the thought of cancer and children brings a tear to your eye.  No, I did not personally have the pleasure of knowing Arianna or her family, but they are in my thoughts, heart and prayers.  May Arianna find peace up above and watch over her family like the angel that she is.  May Arianna’s family find it in their heart to bravely bless other people with Arianna’s story and find peace and happiness to never forget and always love Arianna.

Thanks, Lulu for sharing her inspiring story.

Love,

Britt x