We are spotlighting two people this month who are sharing their experiences as members of the Arthritis Foundation’s Patient Leadership Council (PLC). Learn how to apply to join the PLC at the end of this post.
By Sarah Cloud | Sept. 1, 2021
关节炎的诊断可能是一种惊讶和接受,也可能是一种绝对的恐惧。这完全取决于“关节炎”这个词之前的词汇,以及你的医疗服务提供者可能会如何解释和支持你的诊断。
对于一个19岁就被诊断患有骨关节炎的人,以及一个听到“我认为你的孩子患有幼年关节炎”这句话的母亲来说,影响是很大的。随着时间的推移,我的丈夫被诊断为强直性脊柱炎,我被诊断为类风湿关节炎。不幸的是,没有改变的是当地缺乏资源、信息和关怀。我们的儿子被误诊了,甚至做了一次不必要的紧急手术,在我们听到那句可怕的话之前,“幼年关节炎”,加上“我们需要把他送到300英里外的盐湖城去。”
The doctors in our rural area hadn’t seen a patient like our son. I didn’t know another parent on this journey for over two years. In the years that followed I found an amazing group of moms on Facebook who helped us along our journey, and we became heavily involved in the Arthritis Foundation.
One night, I was reading a newsletter and there was a link for a newly forming Patient Leadership Council (PLC). The Foundation was looking for people to apply, but I almost didn’t. I had talked myself out of it. Why? Who wants to hear from a school bus driver in the middle of nowhere who has no letters behind her name? I didn’t have any formal education and no connections to the Foundation, as there was no local Foundation office. We joked at national events and online that we lived in “No Man’s Land.” We lived in Hurricane, Utah, located 16 miles from Arizona and about 40 miles to Nevada. It’s often known as “Land of the National Parks,” but not much else.
最后,几个好朋友让我去申请,因为他们最坏的反应就是拒绝。想象一下,当我接到一个电话和一封电子邮件,邀请我参加病人领导委员会的成立小组时,我有多惊讶和震惊!小小的我,没受过教育的校车司机从偏僻的地方来的我。
Being a member of the PLC has allowed me to express my voice as a mom, but especially as a rural mom, when it came to what we needed and what was considered. The care my son received was so vastly different from the care our friends in Salt Lake City received. We had the same doctors but different access. If we had a problem, it required a six-hour drive each way and a hotel room if we could afford it.
Most the time we couldn’t afford a new set of tires for the car to make the trip, let alone to stay the night. This meant that many times our son had to receive care once every six months or by phone. If we had problems, I had to email pictures to the doctors in Salt Lake City, then they would tell us what to check for and what to do. Think: pre-telemedicine. I couldn’t just schedule him for clinic. Scheduling for clinic meant a day off work, having to find a substitute, arranging transportation, gas, meals and entertainment for a then-preteen who hated car trips.
To be able to voice what was different from our perspective gave voice for every rural family the foundation serves. It allowed us as patients to say: “Nothing about us without us.” We have been asked to weigh in on many things, from the direction of events to targeted market research studies. We never know what will come our way to study and voice feedback on.
I have loved my time on the PLC. I have formed friendships with people I probably wouldn’t have met. With these friendships and support and encouragement, this mom went back and earned a college degree in patient access and we have since moved to rural southwest Missouri, where, Ironically, we face many of the same challenges with lack of resources and care, but this time I know I have a voice and resources to change that.
If you’re like me and don’t think your little voice matters, you’re wrong. Your experiences and voice are needed to shine light on what we as a collective community can do to change the access and outcomes for people everywhere.
If you’re interested in joining us, apply. The worst they can say is no.
Interested in applying to join the Patient Leadership Council (PLC)? Applications are currently open! You can applyHERE. Deadline for application submissions is 11:59 p.m. Oct. 15, 2021. If you are selected for next steps, we will notify you by early to mid-November. Thank you for your interest! And spread the word!