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I had to keep reminding myself that I was faster, stronger and had more will power to overcome the negativity and insecurities that fueled that behavior. I did notice that with every large boulder, there was a much smaller and easier rock that I knew I could step on without any worry. I was able to gain mental strength and confidence from being forced to face my fears.
Eventually, getting blood drawn became a part of normal doctor visits, but I knew they helped me check my body for disease activity and helped to keep me healthy. As one would expect, I eventually came to the biggest gap between two boulders I had ever seen and I was exhausted.
I eventually found my jar of bravery, opened it up and problem-solved my way to the other side. I did take longer than the others, but I used my past experiences to help me walk my way around the dangerous gap and onto the other side, ready to continue on my path.
Eventually we all were called back as a troop to climb back to the parking lot.
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The field was much less intimidating and I found myself, almost sad that the challenges were over. Now that I am much more controlled, I sometimes find myself wondering if I received the right diagnosis or have made up all of that pain and struggle I endured a few years ago.
It can seem like you have lived more than one life as you move from chapter to chapter in the struggle against Lupus. But, then the joint pain, fatigue, body rashes, weight loss and muscle spasms rear their ugly head, bringing me back to reality. Unfortunately, I will never be able to go back to the start from where I came like I did on that Girl Scout trip.
My Lupus journey will continue to sometimes be easy and sometimes make me feel like there is no way I can survive the systemic pain.
Emily Carroll began battling the Lupus with Scleroderma overlap since , during her first semester of college. Since then she has participated in various autoimmune and Lupus awareness activities to spread awareness and offer a helping hand to others.
In her spare time she enjoys being outdoors, painting and traveling with her husband.
Lupus at the molecular level
They have two rescued fur babies: Daphne, a boxer mix and Sojourn, an Alaskan Malamute. This a journey not too many of us could endure, Emily.
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There are six opportunities to enter this giveaway.
All entries must be in this form — comments on this post do not count as entries. SHARE this giveaway on Facebook with this link , or use the social media icons at the bottom of the post.I feared that snakes and bees nests would pop out at me while I tried hopping to the other side.
Functional dissection of systemic lupus erythematosus using congenic mouse strains. I did take longer than the others, but I used my past experiences to help me walk my way around the dangerous gap and onto the other side, ready to continue on my path.
Validity of the brief pain inventory for use in documenting the outcomes of patients with noncancer pain. The impact of flare on disease costs of patients with systemic lupus erythematosus. The model was then compared with an existing SLE conceptual model developed by Gallop et al.
Han Xin Ru. Pain assessment: I eventually found my jar of bravery, opened it up and problem-solved my way to the other side.