It has been a while since my last
post. The past few months have been going really well since my symptoms have
gotten more under control. There have been a few bumps in the road during the
summer, but the new obstacle that has come up is my extremely depleted
iron. On Thanksgiving, my body began to
get really achy, which I have never experienced before. As the day went on, the
aches kept getting worse, and by the afternoon I ended up passing out and going
to the hospital. I figured they would give me fluids and I would go back home
to eat some (gluten-free) pumpkin pie. Usually after one bag of fluids I feel
much better, but my heart continued to race, I was still achy, and still very
potsie. I was kept overnight and they continued to give me fluids, which was
not helping. The next day they took some blood work and found that my iron was
severely depleted, and my electrolytes were on the low end of the spectrum.
After coming home from the hospital, I still wasn’t feeling great and stayed
home from school for a week. I was given prescription iron supplements and ate
a high iron diet, but I am still extremely fatigued. Since being in the
hospital, my symptoms have not improved. I have days where I feel a little
better, but for the past two weeks it has been rough. I am weak, exhausted, and
do not have the energy to do anything.
It’s anxiety provoking to have setbacks
when you have been doing well for so many months. POTS is like a roller
coaster, you will have months of controlled symptoms and then all of a sudden
there can be a drop. It’s the downfalls where you have to be strong. It’s easy
to give in to symptoms and give up. The day after I left the hospital, I was so
upset that I was having a relapse and I was ready to stop going to school and
give up. My mom reminded me of how far I’ve come and how far I still have to
go. POTS is a life long journey of ups and downs, you never know when you will
have a flare or when a cold can turn into a relapse. It’s easy to fall into the
cycle of always fearing the worst, of always being paranoid that that single
sneeze will cause full-blown autonomic failure. I am typically not a half glass
full kind of person. I usually look at things from a more pessimistic point of
view because I hate disappointment and like to be realistic. Throughout the
past two years, I realized I couldn’t handle POTS like I’ve handled other
things. You need to be optimistic and enjoy the little things in life. It’s
very easy to fall into a black hole of desperation; it’s easy to look at how
terrible it is to be stuck with a chronic illness, but you need to find your
source of light. I found my source of light through my family. Having a big
family with 5 nieces and nephews has really helped me get through the
obstacles. My sister texted me a few
days after getting out of the hospital and told me my nephew said that they
should get me comfy pjs for Christmas because the doctor said I need to stay
warm. Its small things like this that make me keep pushing through the symptoms
and try to live a normal life.
Hope is an important factor when
living with a chronic illness. Once you lose hope, you lost your battle. I’ve
learned that hope and determination are the two most important factors that
will get you through anything. There will always be downfalls in whatever you
do, but you have to hold on to the hope that you will get better and will live
a normal life. You have to be determined to fight through your symptoms no
matter how tired or weak you are. It is easy to give up, but the easy way out
will never get you anywhere. Sometimes when I start to lose hope, I picture
happy things and a bright future. I have days where I feel like I can’t do it
anymore and days where I question why I am pre-med since what are the chances
of being a good doctor when my health is not under control. It’s those days
that I take a deep breathe and remember why I want to be a doctor. I want to be
a better person; a person that can help sick people and a doctor that I wish I
had. I want to be a doctor that doesn’t give up on her patients and helps them
fight through the bad days. Sometimes you don’t achieve your goals, but without
goals, what are you living for? I have ambitious goals and my goals of becoming
a doctor has helped me fight through the bad days and will continue to help me
fight through my symptoms.
I really enjoyed reading this post as I totally get everything you are saying! I find it hard to cope sometimes when everyone around me do not understand what I am going through, its always reassuring I am not the only one <3 Thanks for sharing! Also I think it is amazing that you want to become a doctor, we need more like you! When I get better I'd love to work for a charity or just do something to help people :)
ReplyDeletefindyourownhope.blogspot.com