I’m Still Here

Hello to all those who read this!

I know, I have been silent for some time, just have so much that I am working through in life. So many changes and new challenges to face, but that’s life. Right? I hope I have something right.

Lately, it’s been primarily adjusting and refocusing back on my college education. Yes, you read that right. I am still attending college full time while battling cancer and recovering from a transplant. I have had people tell me that I am an inspiration for continuing my education through everything, but that’s not why I do it. My education is important to me, and when I am done and conquer this battle, I want to continue my life as “normal” and have the job that I want. So, I will continue going to school and gain the education I desire.

While I am not in school during the fall and spring, I am working. Yes, you read that right, too. I am also working while battling this cancer. I am in the Air National Guard and absolutely love it. They have been wonderful working with me and my needs. I am an aircraft mechanic, so sadly I haven’t been able to do much of my job the past year, but I have still been able to contribute where I can. I wish I could do more when I work though. I feel like that’s just a constant frustration. I feel like I am so limited in what I can do because I have cancer and how the treatment affects me. I am sure I am not the only one in this battle that feels that way. I can’t take trips to other bases for weekends because I have to stay close to home. I can’t work on planes because there are too many chemicals. Take away those two things and what am I going to do? I end up doing administrative duties and the like, which I don’t always mind, but I am in the military in a demanding job and I can’t do more. I know it’s not in my control. I have to work with what I got and in time I will be able to return to work. I just gotta get there. Everything takes time and sometimes my patience is thin.

As you may have picked up on through my recent posts, I did have a peritoneum transplant. I had about 75-80% of my peritoneum replaced. I was placed on the transplant list in July and only spent a few days on it. I did not, by any means, like being on the transplant list. Yes, I am appreciative of my donor. Yes, I am honored to have it to live. But at the same time, I still question why “I was worthy of it”. Why do I deserve it over the person behind me? I guess that’s my depression peering around the corner though. At first, the transplant went really well. My body was showing signs of acceptance and circulation. That’s what we wanted. But why would any of this be easy for me? A few weeks into August, I was having some issues: fluid buildup, lots of pain, swelling, and sensitivity in my abdomen. I was also struggling with eating and digesting anything I ate. Scans and tests then showed acute organ rejection. Really?! Since there wasn’t much damage to my new peritoneum at this point, they decided to do a month of trial medication and see if the rejection would stop. I am now reaching the end of my trial month and prepping for more tests to see if another transplant is in the books for me. It just never seems to end.

At this point, I can confidently say that I am aware and accepting of my current medical situation. I know I have cancer. I know it has now been 66 weeks since first diagnosed. I know I no longer have a reproductive system. I know I will be on hormone replacement therapy for the rest of my life. I know I had a peritoneum transplant and am risking another. I know I will be on anti-rejection medication for the rest of my life. I am aware of all of this, no matter how terrifying it all is.

But there are other things that I am aware of. I know I have an amazing support system. I know what to expect when I do my final chemo round. I know I will survive this. I know I will have a life after this. I know I will find someone who loves and accepts me for me at some point in my life. I know I will have the career I want. I know I will strive to achieve everything I desire in life. I KNOW I WILL LIVE!

I don’t know when I will post again. Between school and medical necessities, my life is pretty consumed, but I will do my best to post again in the near future.

Thank you for reading!

The Big 21

I know some people who make a big deal about their birthdays every year and have to go all out to celebrate each one. I’m not saying these people are wrong to do that, but that’s not me. Sure, growing up I celebrated every birthday with a pool party and sleepover, but as I got older, I didn’t find the big deal in them. My “sweet 16” included my three best friends at the time coming over for a movie marathon. Talk about big and exciting. My 18th was pretty much the same thing, except I was more focused on leaving for basic training than I was on celebrating my birthday. So, yesterday, July 11, I celebrated my 21st by going out for dinner and drinks with my dad and enjoyed downtown Harrisburg.

Here’s the thing, I couldn’t have alcohol yesterday. I’m the “rare” person who doesn’t drink on their 21st, and that confused a lot of people that didn’t know my situation. What the waiter or bartender didn’t know is that I can’t drink for two different reasons: going through chemo for cancer and recovering from a transplant. Don’t get me wrong, I would have loved to have a drink last night to celebrate, but I don’t feel like I missed out. If all goes as planned, I’ll be able to celebrate later, and I’ll be celebrating more than just turning 21.

When I was first diagnosed, it didn’t really hit me that I had cancer and would be going through treatment until a few weeks in. Starting that journey included many changes in my life including my diet, especially when my diagnosis was changed to stage 2 and chemo started. Towards the end of my “first round of cancer”, my diet was down to eating rice and fighting to keep it down with an NJ feeding tube to give me the nutrients I couldn’t eat. I lost the most weight at this time, and all I wanted was to be able to enjoy the food. I was in this state for a total of 3 months. It made me realize the difference in the mental state when I couldn’t feed myself by eating and had to “feed” myself through a tube. I was the girl on campus with a mask from my immune system being so down, a feeding tube from my backpack to feed me, and another two lines (one for fluids and one to monitor readings) leading to my arm. I was connected to my bag 24/7 and hated every minute of it. I was known on campus for what was seen, and I hated that too. “Oh, you were the one in a face mask and all the tubes/lines.” Yes, that was me. Glad that’s how you remembered me.

After I reached remission after my surgery, relapsed, and was able to eat a variety of foods (2 months after my last chemo), I went out with a few of the people I’m closest with on campus for lunch. I had a steak, and it was wonderful. I enjoyed every bite of it because I just went through 44 weeks of chemo and had no clue when I would be able to eat another steak after learning that I relapsed. At that lunch, we all made the plan that we’d do it again once I was back in remission. I didn’t realize at that point that I wouldn’t be able to drink on my 21st, so I guess I’ll be getting a steak and a drink when I get in remission. That’ll be a nice thing to celebrate, but I won’t be celebrating my 21st, I’ll be celebrating remission. I gotta get there first.

I never thought I’d be in this position. Never thought I’d be in many positions: rape, child loss, loss/suicide of those close to me, and cancer are the top situations. Here I am. I’m still alive. I may not always feel alive, but I’m still living, breathing, moving, and eating. I’m surviving. I don’t think life was meant to ever be easy. I have learned so much about the people around me and myself through everything that I have faced, good and bad. I have grown so much as an individual from going through what I have. Yes, I hated every bad situation and still do, but I know that they have matured me and taught me so much that has made me the person I am. This is me. I will be honest, raw, and open about what I faced to help someone else because I know what it’s like to feel like there’s no one else who knows what you’ve been through. If you feel alone, you are not. I promise you that.

So, here’s to being 21. I’m ready to see what the world holds for me, at least as prepared as I’m going to be.

A journey within a journey

For me, it always seems as though every journey, whether trial or triumph, has smaller journeys involved in the process. My journey through cancer diagnosis and treatment has had a multitude of journeys including, but certainly not limited to, diagnosis, different treatments, remission, and relapse. Each journey required learning, adapting, and overcoming. This past week started a new journey for me that I never expected.

After my most recent surgery including a complete hysterectomy and a peritonectomy, my stomach continued to grow more distended. I was in excruciating pain, couldn’t keep food down from said pain, didn’t fit the majority of my clothes, as well as a whole list of other related issues. I was able to gain access to some more wonderful medication that helped ease the pain and allow me to eat enough to sustain myself without another feeding tube.

I was scheduled to have an MRI and more blood work done to figure out what the complication was. Last week I got the results: my organs do not have enough support to function properly, nor do I have the proper circulation needed for the fluid buildup that was happening. Back track a bit, after my surgery, they did not replace my peritoneum because they calculated that my body would be able to adapt to this change. Well, they were wrong! So here I sit with supports in my abdomen to temporarily hold my organs in somewhat order until I can get in for another procedure to replace.

The hope is that I will not need an artificial replacement. This is where that journey comes into play. My information was submitted to be placed on the transplant list. I know quite a few people that needed different organ transplants and I never thought I’d be on that list, but here I am. I got the official notification that I was on the list yesterday. If I can’t get a transplant in a month, then I will have to get an artificial because it could cause too much damage to my organs if I wait longer than that. The fear is that my body won’t accept the artificial due to previous issues, plus they’d have to remove more of my peritoneum instead of attaching the transplant to what still exists. This is still sinking in. For me, I need a peritoneum without damage and ,of course, matches my blood type with some other specifications. This isn’t something I can go ask someone alive to get tested, why would it be that easy? I actually have to wait for someone that matches what I need to die. I find that a bit out there for me. I never thought I’d be in the position where I’d be waiting for someone to die just so I can get their abdominal cavity lining. Then again, I never thought I’d have cancer either, yet here I am.

With all of this this past week, there was a positive that came out of it. I was able to start back at work this week, which is a massive blessing, even if I can’t do anything and just sit all day. Having an income will be wonderful to help ease the impact of upcoming costs. It will also give me the ability to pay bills and not worry about food for the month. No, I won’t be able to live a thrilling and filled life, but I can go to the extra appointments to help alleviate pain and discomfort and other symptoms and not worry about not having the money to pay the copay.

I have two different parts to me right now: (1) I am ready to call it quits because it’s been over a year since my first diagnosis and I am tired of fighting, and (2) I’ve made it this far, I’m going to keep fighting till the end. I’m trying to stay optimistic. I’m trying to look for the future. I’m trying to enjoy what I have in my life. It’s so hard! It just feels like every accomplishment is followed by another trial.

I’m exhausted all around. I’m drowned in bills and loans. I’m in pain. I don’t want this. This is not the life I want to live, but I’m not going to end it. I know that as long as I’m able, I will fight. I will survive this. I may not know how, but I will.

As always, thanks for reading.

The good with the bad

WARNING: this post may cause triggers related to sexual assault

Welcome back!

I know I’ve been MIA for a bit, but life just keeps on going. There has been good news mixed in with the bad, and that’s what’s running through my mind. Lately, my life has not been the easiest. I have been given more bad news than good, but I’ve adapted and continued on.

May 31 I had my procedure to remove the rest of my reproductive system as well as the majority of my peritoneum. The procedure went well without complications (good), but the healing process has been long and hard with complications after surgery (bad), but I’m still going. Two days post-op, I was still bleeding heavily and later found that I ended up tearing stitches again and would have to have another procedure to close up and place a drain. Once this was completed, I was placed on restricted bed rest and was not able to move for 72 hours to give my body a chance to catch up. Let me just say, not moving for 3 days definitely tested my sanity, especially since I can’t personally do visitors.

My goal with this blog is to be able to open up about what life has given and taken from me to help others, so with that, here’s some background with visitors for me:

This does not come from a bad experience with visitors for me, per say. My parents ended up divorcing when I was 13. After the divorce, my dad came out gay, and back then it was terrible for anyone who was gay, or, in my case, related to a gay person. I lost majority of my friendships from either them or their parents not wanting them to be around gay person or someone related to a gay person. This left me very isolated and in search of any acceptance. I had one friend who stayed with me and I thought it was out of true care and support for me; his name is Jake. Jake was someone I thought I could always trust and felt safe around. I’d hang with him at his house or out-and-about and enjoyed his company. One night, I went to his place like normal to talk about the divorce and how I was managing it. He gave me a glass of water like normal and woke up a few hours later tied to his bed, naked, with him standing over me; I was drugged. That night, Jake raped me, beat me, and did everything his heart desired. He never loosened the restraints during the rape, he just told me all he wanted to do to me and proceeded to follow through with his words. How can someone who has always been there for me tied me to a bed and rape me?

After he was done with me, he got up and walked away. He came back a little while later and threw a sheet over me, untied me, and carried me out to his car. I fought with all the energy I could muster, but he easily managed to restrain me in his arms. At this point, I was terrified of where he’d take me and what he was going to do next. Is he going to rape me again? Is he going to kill me? I was honestly terrified for my life because this guy I thought I knew just took advantage of me.

We drove for about 30 minutes and he seemed to debate on what he should do. We eventually stopped in a place I was not acquainted with and he pulled me out of the car and drove off, leaving me in a heap of blood and tears with only a sheet to cover myself on the sidewalk. It was around 0200 at this time. I stayed there for what seemed like forever until someone finally stopped and helped me; thankfully it was a women. I cannot remember any of the conversation we had that night. We only had to walk two blocks to the nearby hospital where they admitted me and started the tests and screenings they needed to perform. I left a few days later with a hairline fracture in my cheek bone, a severely bruised jaw, and various cuts and bruises covering my body; when I left, I was told I was not impregnated.

During this time in the hospital, I only saw my parents when they had to sign papers and take me home. They didn’t visit me when they had the chance and wouldn’t look at me when they signed the papers. I’d understand if they didn’t want to see me, but my mom refuses that I was ever raped and my dad just doesn’t talk about it. This is how it has always been and continues to be.

I’ve eventually accepted this for what it is. I am more independent than I ever thought I’d be, and I’ve become very good at managing all my medical necessities on my own. But with Jake destroying my trust and my parents, the people who should always be there for their kids, not giving a shit and showing up, I no longer feel that I can trust anyone that enters my hospital room. Also, being in a hospital bed puts my PTSD on high alert for anything out of the ordinary. So with all this considered, it is easier for me to not have visitors during my hospital stays.

Going back to the beginning of this post, I spent a total of 12 days in my most recent hospital stay. It consisted of everything needed for recovery and provided an environment for me to focus on what I needed to do to recover the quickest and healthiest. I’m now at a little over two weeks post-op. I have received news that surgery removed everything that was needed out (good), but I’ll have to have more tests and scans to figure out why my stomach is still as distended as it is (bad). But, all I can do is keep going and do as I’m told to recover and be able to continue living my life.

I will live and I will be a survivor. To me, that is not a choice. I have to put all I can into fighting this fight so I can live the life that is in front of me. I know I have so many opportunities in front of me. There are things I want to do and so many places to see. That is my motivation to push through and win this fight. I will win, even if I lose parts of me along the way.

Finish, Process, Prepare

Hello!

It’s been a few weeks since I’ve posted anything. The past few weeks have been my time to finish, process, and try to prepare as much as possible. That’s how life goes. You’re always trying to complete or finish a task at hand. You’re always trying to process your current situation, good or bad. You are always trying to prepare for the future, whether it’s known or not.

May 11, at 8 AM, I completed the last final of the sophomore year; I had four finals that week. This final was for Anatomy and Physiology: Head, Neck, and Thorax. I put hours I couldn’t even count into studying for this final and hoping for the magical 75% on the final to keep a B in the class. A 75% may seem easy, but I had a 60-something on all of my lab exams, and my lecture exams were in the 70s. The only grades that kept me at an 80.5% in the class were my intro exam, quizzes, and bonus points. In the weeks approaching my final, I was the student walking laps around campus while talking to myself to review for this final. I did every suggested study technique I could think of because I was going to achieve that grade. I went to the class to take the test with my hundreds of flash cards in hand prepared as best as possible to pass this test. When I completed it, I turned it in and walked out feeling exhausted. It wasn’t even a sense of relief. It wasn’t until the following day that I received the email that grades were posted; this was the moment of truth. At this point, I received the grades for the three other classes I took, and I got As in all three. I logged into BOLT where grades are posted and learned that I got an 84%! This was where relief set in. I just passed A&P with a B! This professor even suggested after I explained my cancer situation at the beginning of the semester, that I should drop the course as I would not have been able to handle it. Well, I just handled it. This past year has been the farthest from easy as I spent only a handful of weeks not pumping poison into me, yet I ended the year with a 3.5 GPA. Life may not be easy, but there are still accomplishments to be made.

So if anyone is following along, you may have realized from my previous post that I relapsed the week before finals week. Not the best timing of news. My oncology team pushed to discuss treatment options right away, but I decided against and to wait until after finals week. At this point I wasn’t sure what my future was going to look like. I knew I needed to focus on my academics before I scheduled anything for treatment. So an appointment was scheduled for May 11 in the afternoon to discuss my treatment options. After I completed my final, I packed up my remaining things in my apartment and sent off for home. I got home around lunch and dropped my things off at my mom’s house before heading to the front street of Harrisburg to walk and process. There were so many questions: Why me? Why now? Did I miss something? Could I have done more? Is this how my life will end? I know the last may seem dramatic, but at this point in my life, I’ve faced too many negatives and trauma that I didn’t know how much more my body could take. The time comes for everyone, whether it be age, illness, or something else. The questions previously mentioned constantly run through my mind and still do with an end that probably won’t come. I spent about 2 hours on front street until I found my car and made my way to my appointment. The options provided were previously discussed when I was first diagnosed: either some form of treatment or no treatment at all. I’ve always been and will always be a fighter, so the later option was really not an option for me. I will fight for my life. So, with the decision to continue treatment, chemo and surgery were scheduled with another PET scan and more blood work to check for any changes. The scan and blood work came back with the same results which provided some relief that it hasn’t metastasized more. With that, my “first” chemo was scheduled for this past Friday, May 18. I felt so defeated walking back into the clinic for treatment. I knew my chances of returning were high, but it’s only been about 2 months. This chemo really kicked my ass. It was the heaviest I’ve ever faced and it really took a toll on my body through this past weekend. I knew it wasn’t going to be easy. I know none of this will be easy. I DO know that I will fight and do everything I’m told and everything I can do to make it to the end. I will get through however many chemo treatments it takes (number isn’t set yet) and I will go through surgery next Thursday. I will constantly be trying to process all of this, but I have a wonderful support system in my life that I know will be there for me throughout this process.

With everything that I have faced (more will be discussed in the future), there is always something to prepare for, whether it’s academically, health, or life in general. You can never prepare for everything. No one knows what life will hold next. So when I say I’m preparing, I mean I’m preparing for what I know. I know I’ll have more treatment to go through. I have accepted this for what it is. I have gone through treatment before, so I have an idea of what to expect. I can mentally prepare for the toll this will take on me. I know there’s a chance I will be attending college in the fall, so I am preparing by planning my apartment and the things I’ll need to complete another year. I also know there’s a chance that I won’t be able to attend college in the fall, so I am also preparing for that by discussing my options with my advisor. I’m the President of the Student Veterans Association on campus, so I’m also preparing for that by scheduling the events and preparing the Vice President in case I can’t be there. Then there’s the filler events that I know and can prepare for like work, birthdays, and trips. There is always something in life to prepare for; it’s just never known until you get there if life allows for it to happen.

Finish, Process, Prepare

We all do these three things, whether they’re noticeable or not. And we all do things differently. Life is filled with so many ups and downs that we can’t all finish, process or prepare, but as long as you keep fighting to get through, then I think you’re doing it right.

Relapse…

I don’t know how to start this blog. My mind is running a-mile-a-minute, and I am trying to comprehend things. This is not an easy conversation, and I am flooded with emotions, so please stay with me as this will not be my best writing.

There are words that no one ever wants to hear: death, infertility, and cancer are just a few. June 1, 2017, I heard the word cancer come from my doctor. I had no clue how to take it, and I was in such shock that it took a few weeks for it to fully sink in. When it finally sank in, it hit me hard.

In the beginning, I was diagnosed with stage I ovarian cancer. After going through 2 hormone transfusions and 2 laser therapies, I was rediagnosed to stage II ovarian cancer. After receiving the new diagnosis and beginning the multiple rounds of chemo and radiation was when the reality hit me: I have cancer…

Since the final diagnosis, I have undergone 17 PICC line chemo transfusions, 10 oral chemo treatments, and 13 radiation treatments. None of it was easy. I was in pain, couldn’t eat anything and had to get an NG tube, couldn’t keep myself hydrated and became IV fluid dependent, and I felt so alone at the beginning of it.

I never had support at home, and I have always struggled trusting people. It wasn’t until halfway through my fall semester when I realized that I may not physically be able to stay the whole semester. I might have to drop out. That was when I finally started talking to people and letting them in. That decision has changed everything for the better; I now have a support system that I could not go without. They have supported me through all of my treatment and continue to stand with me.

March 30, 2018, I finally reached remission! After 43 weeks, I was in remission!

I had two weeks after the news that I struggled with acceptance of what my life now consisted of including infertility and an overly high possibility of relapse. After those two weeks, I felt myself again. I was able to eat actual food and hydrate myself with drinking water. I was getting more sleep than I did before. I was not in pain anymore. I was finally in relief from the hell I faced. These two weeks of relief were well cherished.

May 1, 2018, I received the news that I relapsed…

First of all, I am beyond livid.

Second, is this real?

I feel defeated. I am not sure there is really another word to encompass how I feel right now. I am trying to just deny it for the next two weeks to get through my finals, but how? I did everything right. I did everything I was told to do and then some. I took multiple loans out to cover extra costs of suggestions that weren’t covered by insurance. I have 10s of thousands of dollars in loans to cover everything I went through, and I relapse?! How? This isn’t right. This isn’t fair. This is not how it should be. So why is it? Were 43 weeks not enough?! What did I do to deserve this? There are so many questions that run through my head with this news, but I know that they don’t have an answer. Why now? What did I do wrong? WHY ME?!

There are all these emotions rushing through me that I don’t know how to cope with: anger, confusion, denial, and lost are a few. I need to focus on my studies because I need to do well on my finals, I just can’t get myself to focus. How can I?

There is so much more that can be said about my current situation, but I am struggling to find words to honestly describe how I feel. For now, this is all I have to say. With time, I will be in a better mental state where I can express more of my feelings and be able to better describe what I am facing. If you have any suggestions or questions, please leave a comment.

Until next time, thank you for reading.

The Journey Begins

This is something I have never done: write a blog. It was suggested by two good friends of mine to start a blog and share my story with others. So, let’s see how this goes.

I am 20 years old and am currently a college student making her way to a bachelor’s degree. At the end of my college degree, I hope to obtain my doctorate degree in Audiology. I still have some years to go for that achievement, but it is a goal nonetheless. Through this journey called life, I, like everyone else, have faced many trials and triumphs that have all been learning experiences for me. I have learned who will stay by my side and who I really am. Life is one big learning lesson; it may not all be enjoyable, but there is always something to learn.

I plan to use this blog as a way for me to talk about the trials and triumphs in my life in hopes to help myself and/or others. Some topics may lead to laughter while others may lead to tears, but I am tired of putting on a mask and acting like everything is great. Life is not always easy, and it’s not fair. We have all faced some sort of challenge in our life that made us question “why?” or “how?” and those questions don’t always get an answer. I know I don’t always want the answer, but there is always a positive that comes out of every experience.

This blog is not a means for me to complain, nor is it my way to put myself in the spotlight. I am writing this blog in hopes to help myself or someone who can relate to anything I post. It can be terrifying to say, “yes, I went through that, too, but I feel so alone.” You are not alone, and I say that because I am here, and I am sure that I am not the only one. We can get through this thing called “life” together.

So, with that being said, please feel free to follow along. I cannot guarantee a blog every week or every month as I do not know what life has in store, but I am ready to give this a shot.

Thanks for joining me!

Good company in a journey makes the way seem shorter. — Izaak Walton

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