The Biopsy

 

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Yesterday I checked into the Metroplex Adventist Hospital for my bone marrow biopsy. I though I would share my experience for those of you that may have one coming up, need to inform a friend of family member, or are just curious as to how it went. Everyone is different when it comes to pain and healing, so please keep that in mind. To begin, a bone marrow biopsy is done to evaluate blood cell abnormalities and other diseases in the patient. I had mine, in particular, to test for mast cell disorders as I have struggled with unexplained allergic reactions with no triggers.

0800 – Caleb and I arrived at the inpatient surgery center and got checked in. I changed into a hospital gown and socks and prepared for the hours to come.

0830 – The nurse came in and attached me to the the monitors. I had an EKG done to evaluate my heart (due to past heart trouble – atrial fibrillation & tachycardia) and the dreaded IV was put in after one painful failure.

1030 – My mom arrived to the hospital to wish me well. I was supposed to have already been taken back, but the doctor had been working on the same patient since 0730, so apparently some complications arose. Waiting is the worst part; the nerves grow, my heart raced, and I kept playing over and over about what was ahead.

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1100 – I finally was taken back. I was explained everything that would happen. I would be sedated, but might feel some pressure and the pain of the numbing sting. I went in to the Cath Lab and the completely took off my gown (that was a surprise to me), but covered me with drapes. I had an oxygen tube in my nose and was hooked up to all the necessary machines. The anesthesiologist told me he would administer the medication. I didn’t feel it immediately and began to worry it wouldn’t make me go to sleep. I told the ladies that were prepping everything that I haven’t felt the medication, they assured me the doctor wouldn’t start the procedure until I was sedated. I was “blind” since my glasses were confiscated, but I could see the outline of the needle for the lidocaine. I was trying my best to stay calm. Then I went to sleep. After that I didn’t remember a thing. Whether I was sleeping or not, I don’t remember feeling a thing until after I was awake in the recovery room.

1215 – I awoke back in my recovery room alongside Caleb and my mom; the first thing I did when I got back to the room was pucker my lips for a kiss from my man. I was a little loopy coming off the sedation leading me to make silly little videos on snapchat and saying I wanted In-N-Out over and over again. I began to feel the pain in my hip. The nurses said I had to stay for 2 more hours and I had to eat before leaving.

1300 – I was give morphine for the pain. I told the nurse it was hurting and they made me lay on my back to compress it, instead of my side (which hurt even more).

1330 – I was given a veggie burger (I told them I didn’t eat meat and they happily got this burger!) and baked crisps for lunch. I really wanted In-N-Out, so I nibbled at it and split my meal with Caleb.

1400 – I was wheeled out to Caleb’s car and discharged!

After being discharged, I went to my much needed In-N-Out; I really wanted to just get it to go, but my mom was going to head out after that, so we just ate at the restaurant. On the way home we stopped by the primary exchange to pick up my headache medication as I left the hospital with throbbing in my temples. The day of the procedure it was very painful to walk and I needed assistance from Caleb to get from place to place. This morning I awoke with a little bit of pain and had sharp stings here and there, but overall the healing seems to be going well. I can’t lift anything for 48 hours after the procedure. I can finally shower tonight and take off the bandage. Some leakage is evident, but that’s normal unless it has a green hue or looks like pus. My results should be in next week, so now I have to make an appointment with my provider to go over them. I am eager to see what the bone marrow reveals. I’ll keep you updated!

Until then,

xo,

Cass

Bachelor’s of Science 

This past May I walked across the stage at Texas Tech University and accepted my diploma after five years of intense work, tears, and way too much stress. My undergraduate started in Fall 2010 when I took a few dual-credit classes to prep me for the years ahead. I entered McLennan Community College (MCC) as a full time student in Fall of 2011 after earning my high school diploma (with honors). I continued to live at home and work part time as a waitress and a babysitter. I was inducted to Phi Theta Kappa after my first semester for my grade point average and hard work.

In Fall of 2012, I moved to Austin to attend The University of Texas at Austin. I was accepted into the school of nursing, but switched (due to the anxiety of the competiveness of the program) to a nutrition major. I worked part time as a nanny and completed a few classes, but I grew too depressed to continue on. This was one of the worst times dealing with my depression. I became suicidal and questioned my life therefore, I returned home after the semester and took the following spring semester off to deal with my mental health. I began seeing a psychologist every week and focused on my health and diet (as I put back all the weight I lost and more due to the extreme mental agony).

Summer 2013, I returned to classes online and went back full time to MCC. I lost the weight I had gained previously to get in the best shape of my life. I got my first long-time job as a Client Service Coordinator at Banfield Pet Hospital and my GPA went back up! In May 2014 I earned two associates with honors (AA & AS).
After attending full time in the summer to get all my prerequisites finished up, I transferred to Texas Tech University as a Biology major and a Chemistry minor. I enjoyed my first year full of exciting science classes and excelled academically, but I began having health issues. I had unexplained faintness, rapid heartbeat, and chronic gastrointestinal problems. In September 2014, my heart went into atrial fibrillation and it had to be cardioverted back into rhythm after IV drugs did not work. I also began having intese allergic reactions and anaphylaxis which lead to my diagnosis of Mast Cell Activation Disorder.

Despite suffering from these issues, I was on a great path until summer of 2015. I quit my job because I was discriminated against for having depression and anxiety that did NOT interfere with my job. I was targeted by the head veterinarian (who was pretentious) along with another girl I worked alongside (she was the only black employee and she also was having a tough time). We were both basically treated unfairly and made to quit. I was told if I didn’t quit, I would be placed on leave without pay. We were thinking about getting lawyers involved for discrimination, but as anxiety goes, we both dropped it. This is when I began getting increasingly ill and I didn’t know what was wrong with me. I started having brain fog and trouble with words and times (which is maybe why they thought my depression interfered with the job, only it wasn’t my depression at all).


That summer I attended classes full time and worked part time as a veterinarian assistant, but this is when I started having extreme problems (hence the archives start here!). Some of the symptoms I began experiencing was muscle weakness, slurred speech, confusion and brain fog, daily headaches, migraines, loss of balance and coordination, and horrible neck and back pain. The pain was so intense I would lay on the floor crying. I started seeing multiple doctors (even at the emergency clinic). I was told that it must just be a muscle sprain over and over again. As my symptoms progressed, I was let go from my job for fear that I may get hurt. I got several images taken: X-ray, CT scan, and MRI. I was told everything was normal. Luckily I had my dad on my side and we would not give up until I had an answer. I got my hands on the actual MRI report which stated: patient has a herniation of the cerebellar tonsils; something my doctor did not think was important to mention to me. I made an appointment to talk to her and she said that shouldn’t affect me at all because “my flow was good.”

Arnold-Chiari Malformation: “structural defects in the cerebellum. That’s the part of the brain that controls balance.”

She insisted that I just needed a psych referral and basically disregarded my physical concerns, needless to say I fired her. I fought hard for a consult with a “Chiari Expert.” My dad actually found a doctor in Houston that specialized in neurology and did posterior fossa decompressions as part of treating Chiari symptoms. I made an appointment with him and had severe issues having my insurance cover it. My dad offered to pay out of pocket for one appointment; we arrived, cash in hand, only to be told that was incorrect and they didn’t take payment from the patient (only insurance companies). My dad begged for them to see me, seeing how badly my symptoms were progressing, but we were turned away. He didn’t stop until he talked to the insurance representatives and they agreed to cover an appointment.

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I finally met Dr. Parish in November and he immediately diagnosed me with Chiari Malformation. My hands and feet were numb due to the lack of proper flow of the spinal fluid cord and he assured me that he could successfully complete the operation with a good chance of aiding or resolving some symptoms. On December 9th, 2015, I under went brain surgery to correct my defect. I had a leg graft taken to be placed in the back of my skull to allow more room for the cerebellar spinal fluid (CSF) to flow. This was an extremely hard time for me as I finished my semester only days before having to be operated on. That semester was truly a grueling one; I had to battle ongoing symptoms of the defect while having to focus on school. The brain fog was immense and it was hard for me to concentrate and memorize. This was the start of working harder than everyone to maintain my grades. In addition to all of this, my grandmother passed away in November only a couple weeks before my operation, but I made it through.

I tried to use my winter break to recover. I signed up for Spring classes foolishly. I was so eager to stay on the path to graduation which was planned for December 2016. After making it all the way through April, it became too much for me to deal with. I wasn’t used to studying after the operation, which is thought to be a Traumatic Brain Injury because of the invasiveness and the aftermath. I couldn’t cope with my confusion. Although my numbness and slurred speech improved, I had much difficult thinking of the right words, staying on a schedule, and had a horrible memory. The pain, which I thought had been resolved (probably masked by the incision pain?), reappeared in March. I made the choice to medically withdraw. My anxiety was incredibly high because I had never had such problems with school as I did that semester.

That summer I had so many life changes. My previous relationship ended and I met Caleb. I questioned my ability to go through another year of school, but I pushed forward. I ran into financial issues as I had to find out the hard way that financial aid is hard. I returned to school in August 2016, determined that it would be my last fall semester. I changed my minor from chemistry to health professions because I would have had to stay an extra semester for one class and I had had enough! I somehow made it through a grueling semester in which I moved and made some serious changes.

January 2017 I started my last semester at Texas Tech, extremely terrified at the course load. I’ll admit that I’m terrible at chemistry and had to buckle down to pass. I somehow managed to make it through despite facing some discrimination along the way (short story: my chemistry teacher blew up on me for forgetting how to set up and apparatus). The months were the slowest of my life. They dragged on and on and I counted the days I had left. I finished my last final on May 12th; that feeling of waking up the day after and coming to the realization I don’t have to endure this repetitive cycle of driving 72 miles back and forth to school and constantly stressing over attendance (that’s what chronic illness does) and proficiency (grades!) is over… it’s liberating, the best feeling in the world! I can’t believe I did it. Over 5 years of hard work with so many challenges and setbacks. I’ve done it! I drove to Lubbock alongside my mom, Caleb, and Dianne to accept my Bachelor’s of Science on May 19th!

So what now? Where will my life take me? I’ve spent this past month applying for jobs left and right, in hope that the perfect one will arise and be interested in my education and experience. I’ve been looking at administration jobs because I know with my chronic pain and conditions, a standing job isn’t ideal. I’ve been working hard this month: exercising, eating healthy, and attending appointments (neurology, allergy, and my PCM to manage my care). I ended up in the ER late May after some terrifying symptoms (numb and blue limbs, confusion/brain fog [worse than usual], feeling faint, & low blood pressure) occurred. It was concluded that I had complex migraine (how can this turn your limbs blue with the blood pooling?) and I got a referral for neurology to see why I am having chronic migraines and neurological issues. The ER doctor said that he saw an old lesion on my cerebellum, which makes me wonder if it is a result of the decompression or something completely different. I fainted a couple weeks later and experienced rapid heart beat upon standing, so a referral to cardiology was put in as well. Praying that I can get these symptoms under control!

Managing my health and upcoming career is stressful to think about, not to mention my endless wedding planning for our upcoming October “I dos.” I often think about my future life and what it will turn out to be. I’ve always wanted to be a mother, but I never thought chronic illness would affect me so much. I just need a steady career and some more answers and/or treatments to manage my defect and diseases. Right now I’m battling my thyroid disease as my medication needs to be adjusted (my synthyroid dose is too low). I just found this out on Friday after my biopsy consult. My doctor that had ordered this test had my results and said nothing (why you have to investigate yourself!). No wonder I’ve been feeling so sluggish, run down, and hungry. Despite working out and eating healthy, I’m not losing any weight! So many times I haven’t been informed of my test results, which is why now I will request a copy!

Here’s to my crazy life ahead (post-undergraduate)! Let’s see where life leads me! Congratulations to the Class of 2017!

Xo,

Cass

Let’s Talk

Gemma Correll has inspired me to talk about something that is a heavy topic for most people: mental health (how amazing are these images she drew up for Mental Health America?). Just this morning I had a panic attack which includes an endless cycle of “I have so much to do” and “why even bother, nothing I do is good enough.” I often have these all-or-nothing thoughts and it’s extremely difficult to break this repeating cycle. In planning my upcoming wedding, I have been overwhelmed with self-loathing thoughts: “no one will want to come” and “no one cares enough about me to be by my side,” but the truth is I do have wonderful people on my side. It may not be one-hundred, fifty, or even twenty people there to support me, but the people who are there, are the ones I WANT there. Those who love me unconditionally and understand my struggle with physical and mental illness and YET (yes, yet) still WANT to be involved in my crazy life; Those who are in my court through not only my ups, but my overwhelming lows.

I have struggled with major depressive disorder, anxiety, social phobia, and PTSD for years now and so many times I have felt ashamed, that I must hide these mental illnesses from society. [I think that] They will judge me, thinking “that girl is crazy”, “I don’t want to be around her”, or “she may snap at any moment”. The fact is: loads of people suffer with these issues of feeling inadequate at what they do. We are told not to express these emotions because we will appear weak and vulnerable, but holding on to them is what makes us weak and vulnerable in the first place!

I will honestly say that my anxiety is becoming unmanageable. I have tried so many different medications in order to feel more relaxed, but the ones that work are too sedative and/or they don’t last long enough; because of this, it is time for me to go to the next measure: a service dog. It was suggested to me in 2015 that I should obtain a dog for support (whether it be a service dog or a ESA) by my psychologist; I have always responded well to animals and grew up with a full house of five main animals (and some of them had various litters!). My pets have always gotten me through the struggles through the years: I grew up in not so favorable situations. I was abused as a child and the victim of severe bullying (this went on for over six years). I often spent my days hiding inside when I wasn’t forced (I begged to be homeschooled) to go to a school (and take the bus which was just as horrible if not worse) where I was constantly harassed. My only safe place was in the comfort of my own bedroom with my furry friends and dolls; even then I was tormented by my older brother and cyber stalked (even after I moved away from the hell of Newport, North Carolina) by the same cruel people I went to school with. These cruel girls thought it would be so “cool” for them to go to my social media platforms and save my photos so that they could go back and forth on Photobucket saying how ugly I was and that I was just a fat poser. I never understood the cruelty I received. I was brought up in a Christian household and taught to treat people like you want to be treated. I truly believe I have upheld this moral and proceeded through life with honest and compassionate intentions. I never bullied anyone, not even those who bullied me. I put my faith that God would lead me to a successful life, rich in love, which I have now obtained.

I got Mavis in March of 2016. After years of wanting a pug and a dog of my own, I finally received the gift of a lifetime in the form of this spunky, curly-tailed girl. I began training her at 3 months as a service dog, but with the stress of finishing my last semester and my first hard break-up, I took a [much too long] hiatus from the weekly training. Now that I somehow managed to graduate from Texas Tech and my heart is mended and found love, I am ready to get back on track! I want to use Service Dog Express to train Mave and get her into tip-top shape for her aiding in my life and the public access test (the test Service Dogs must pass before being deemed certified). I know anxiety will continue to play a big role in my life (although I wish it wouldn’t) and I’m tired of being afraid to go into public alone. I truly believe that I may have a shot of living a healthier life with her by my side. If you would like to get involved with our campaign, YouCaring is donating $500 to a fundraiser: It’s completely free, quick, and easy to do:

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Here is an example done by the wonderful Caleb (aka my fiancé) and my darling girl, Mave. This took five minutes to draw and take, so it’s super easy and affective. #SignedwithLove & @youcaring is all you need to include on your post! The opportunity to help will pass soon as it ends on JUNE 14TH.

or if pictures aren’t your style…

You can purchase one of the many cute clothing options available featuring “Mave Saves” on our Bonfire. The sales remain until JUNE 29TH.

Don’t want a hoodie or tee?…

The last option is to make a donation! You can do this through our Youcaring with a no end date or through our Paypal!

Here is our links: YouCaring, Bonfire, Paypal, & Facebook Page.

• • • • •

Struggling getting through the day? Call 1-800-273-TALK (8255) if you need someone to talk to. We’re here for you, 24/7. 💚📲

Never give up ladies and gentlemen.

You are so much more than your illnesses and we need to fight together to end the stigma!

xo,

Cass & Mave

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