You are not alone.................
Life. It seems to get in the way sometimes. Trying to juggle school, friends, family, work, illness and everything in between, I sometimes forget what it is all for. My purpose. This week I recieved a lovely e-mail from a mother whose daughter has been suffering for many years. It could not have come at a better time. It reminded me of how I felt not too long ago. Scared, alone, desperate for answers. I had this disease but couldnt find anyone to relate to. My head was spinning. That is when I decided to start this site. To provide a place were other girls like myself can find hope. Without hope I would not have gotten through all this. I feel more and more like my old self everyday. It is not without sacrafice and sick Carrie is a completely different person than healthy Carrie. I dont get it right all the time, I sometimes do things to my body that I know I shouldnt. But this is how I live a life that still feels normal. A life that is not filled with pain and fatigue. I hope that you all know, we will survive, we must. There is no other option but to go forward. When those around us dont understand what it feels like to writh in pain. To want nothing more than to wake up in the morning with energy. To live a day where the smallest amount of stress doesnt send waves of pain thorough your body. Those moments when you struggle to breathe from inflammation but say nothing as you fear just speaking of it will send you into shock. If I have learned anything, I have learned that only the sick understand what it is to be sick. Others can say they understand, but they dont. It was hard for me to not fault others for this, but now I have learned my purpose. My purpose is to care for the sick in any way possible. Be it as a nurse, as a friend, or as someone who will for the rest of my life, be sick.
7/29/2013 09:17:57 pm
I love you post. Its a one kind of motivation for me. I just want to say that I learn one important thing from your post.
6/27/2018 09:40:48 pm
Lord knows I can relate to this post. On my worst days, I tend to find myself getting mad at others who want to compare my RA to their knee pain. Or my mom's friend who has a bad back but is in her 60's and her back issues started in her 50's. She tells me all the time, wait until you get old then you'll know pain, YOU ARE TOO YOUNG TO HAVE THAT: ARE YOU SURE YOU HAVE A SMART DOCTOR (if I had a dollar..), you can't be in pain because how much I see you move, if it causes you pain then why do you do it..
Leave a Reply.