INDIVIDUAL WITH LGMD: Vicki

LGMD "焦点访谈"

名称:  Vicki   年龄: 44 yrs. old

国家: 加拿大

LGMD 子类型: LGMD2A / Calpainopathy

 

您在几岁时被确诊

I was diagnosed at the age of 22.

您最初的症状是什么?:

I was having difficulty climbing stairs.  The Doctor told me that the tendons in my ankles were short, he then sent me to a neurologist for a second opinion to see if there was an underlying condition as to way they were short.  My neurologist sent me to have a muscle biopsy in Montreal.

您是否有其他家庭成员患有 LGMD: 

No, I am the only person with LGMD in my family.

您认为 LGMD 患者在生活中面临的最大挑战是什么?

There are many challenges; to stay independent alone in my home, and to stay active in my community and with friends.  It is challenging when planning to go somewhere new.  I have to ensure it is accessible for a wheelchair and I have to ask about the washroom facilities.  It is also challenging to stay positive- when you can’t perform an ordinary task, go somewhere you want to go, or just see others moving so easily in public. 

您最大的成就是什么?:

My family is my first great accomplishment- My husband, Dean, and our son, Tyler.  They make my life worth living; they make me feel like I can do anything.  I am very blessed.  I also take great pride in my MD fundraising.  In the past, I have organized a yearly auction, online FB auctions, yard sales, raffles, etc.  My latest idea has been making and selling felt ornaments.  I started making them January 2016.  I design a pattern, cut it out on felt, hand sew them together then market them on Facebook. They have their own FB page: “Vicki’s Handmade Ornaments for MD”.  My husband and I have donated all the supplies to make them, I have even gotten business cards.  ALL proceeds from the sale of the ornaments go to MD Canada every year in June for our Walk for Muscular Dystrophy.  Since starting I have sold ~$4000 worth of ornaments.  My fundraising goal for the walk for MD has been $6000 for the past many years.  I always find a way to exceed my goal.

My husband and I started a healthy eating regime back in March.  We have both gotten lighter, and healthier because of it.  I was able to stop taking the 3 medications I was taking for inflammation, pain and high blood pressure.  We feel great and I love to spread the word about it!

LGMD 是如何影响您成为今天的自己的? 

I am learning more and more about myself every day.  My challenges and past experiences have made me learn so many things about myself.  I have learned to love myself for who I am and not for what I can or cannot do.  I have become a strong, self-confident person.  I have realized that I am who I am and the wheelchair does not define me!  I also belong to a local disability group.  We go into middle schools every Spring and talk about living with a disability, and how you can help people with disabilities.  My public speaking has come a long way because of this. 

您希望世界了解 LGMD 的哪些方面?

It is rare but it is also a common disability.  Some of us liked to be offered a helping hand, some like to do it themselves however difficult it may be.  Everyone is different.  Ask before helping someone and never be turned off by someone with a negative attitude or personality.  I always smile because I know what I have in my life and LGMD cannot take my smile away from me!

如果您的 LGMD 明天就能 "治愈",您首先想做的是什么?

There are probably many things that I would do: travel, swim, run, go shopping on my own, work, exercise, visit my friends’ houses with stairs, get in and out of the bathtub, clean the house, I am sure I could come up with a long list…  A lot of these things I can do now, but in a modified way.  It would be nice to do these things without thinking, in a more carefree way.

 

* * * 欲了解更多 "LGMD 聚焦访谈",或自愿参加即将举行的访谈,请访问我们的网站 https://www.lgmd-info.org/spotlight-interviews