Predictably Unpredictable: My Experience with a Rare Bleeding Disorder

It's been over a year since my last update, and it's been interesting to say the least. Prompted by a variety of situations, I found myself in a position where I needed to step back from the bleeder world and focus on myself. First tour: University of Alabama. Roll Tide! I was facing my first semester back in brick and mortar school after finally working out a solid(ish) treatment plan. I was riddled with anxiety and fear that things would spiral out of control again, thus requiring me to medically withdraw. It had become the 'normal' for me where school was concerned, so I was cautious to place any expectations on my return. To everyone's surprise, my treatment plan held up and I was able to get through my first semester with it being relatively uneventful. It was great to be back with my friends and I found my groove. I also started touring colleges, something that blew my mind! There were times I doubted I would ever finish high school, let alone go on to c...

Validation- something we all strive for. Whether in our personal relationships, our jobs, or in my case, my bleeding disorder, validation is the key to making us feel whole. I've fought for years to get answers as to why my bleeding was prolonged. I've fought for years to get information as to why treatment wasn't working. I, along with my incredible mother, fought for years to get adequate treatment and to be taken seriously by physicians who, at times, had my life in their hands. To say it's been rough would be an understatement, however, I'm glad I never gave up because I wouldn't be feeling the way I am today. On October 31, 2014 I met a brilliant physician who took me seriously. He didn't dismiss my symptoms and he even acknowledged that I was long overdue for treatment. He wasn't scared to try Humate-P and possibly even platelets, which was music to my ears! He acknowledged that I was definitely not your cookie cutter case and that I was extremel...

It’s been a long, exhausting few months. I feel like I haven’t stopped. It started with my follow up appointment at UC Davis for my second opinion. My mom and I flew back out to California so they could do further testing. It was determined that I have a very rare qualitative platelet disorder, Platelet Storage Pool Defect. Essentially, my platelets don’t secret their granules, the little sacs inside of your platelets that contain hormones and chemicals that, when released, stimulate other platelets to aggregate. Storage Pool Disorders don’t have many options in regards to treatment. Stimate can work but not always. Novo7 can work, but it’s incredibly experimental. He suggested a factor IX product that might work although it’s never been considered for Storage Pool Disorders. Ultimately, I was told that my best option for all bleeding would be platelet transfusions. The news we received was initially a little defeating. I knew my current hematologist at home wasn’t open to giving...

It's been a few weeks since my appointment at UC Davis and so much has happened that I've just now allowed the information from my appointment to really sink in. I was lucky enough to spend an amazing week in Sacramento, California and catch up with friends and family. The day after we arrived was the day of my appointment and to be completely honest, I was terrified. I have had such a negative experience throughout the last few years that the thought of having to go to a hematology appointment just throws me into an anxiety tailspin. I was lucky enough to be accompanied by both of my amazing parents. Since diagnosis, it has been my mom and I primarily dealing with appointments and infusions while my dad worked his butt off to provide for us, so I was really glad that my he could be there also. Walking into the area where they hold clinic I was immediately met with positive energy. Everyone was so amazing and kind. It was a breath of fresh air. We initially met with a...

As my upcoming appointment at UC Davis for a second opinion approaches I can't help but feel a little anxious. These past few months I feel like I have been repeatedly ramming myself into a brick wall trying to get answers. I have taken notebooks full of questions into the hematologist and the only consistent word I have heard is no. There has been no explanation or reasoning behind it, just no. I am fighting tooth and nail to get an answer about what is going on with my body and what we can do so that I can start living life. Honestly, I haven't really been living. I think I've been going through the motions. I have missed out on my first two years of high school and numerous social events because of my bleeding disorder and honestly, I'm over it. I am so over living my life trapped within the world that is my bleeding disorder. I am ready to live a life where my disorder is not all of me. It will always be a part of me, I understand and accept that, but I need it to n...

There are two types of people in the world. The kind that care and try to understand the situation and those that don't. One isn't necessarily better than the other- that's just how it is. Some people are predictable. They are who they are and you know to expect that from them. There are however the instances where words fly out from left field and slap you in the face. The hardest part is when it's coming from someone who should love you unconditionally and support you no matter what. I've had my fair share of individuals close to me not understand and fail to take the time to try. I believe a major part of understanding the life of a bleeder is asking questions. I find it difficult to want to explain my day to day life to people who don't seem to care. In my eyes, it's a waste of  time.  It's hard to affectively educate as an unaffected person tells you how you're supposed to live your life. Let's all keep in mind what they say ...