患有 LGMD 的个人: Katsuya
09/28/2015:
国家: Japan
LGMD 子类型: LGMD2B / MMD (Dysferlinopathy)
您在几岁时被确诊:
I was diagnosed at the age of 24.
你最初的症状是什么?
I was not able to jump.
您是否有其他家庭成员患有 LGMD:
Yes
您认为 LGMD 患者在生活中面临的最大挑战是什么?:
It is to support a researcher.
您最大的成就是什么?:
I have established PADJ (Patients Association for Dysferlinopathy Japan) which was established for the communication between Japanese and international patients with dysferlinopathy (Miyoshi myopathy, Miyoshi muscular dystrophy 1 (MMD1) and limb-girdle muscular dystrophy type 2B (LGMB2B), development of early treatment for dysferlinopathy aimed at a complete cure.
LGMD 是如何影响您成为今天的自己的?
I had to change a dream. It was a very difficult problem. However, I was able to meet the friend who was in the world.
您希望世界了解 LGMD 的哪些方面?:
The dysferlinopathy (MMD/LSMD2B/ DACM)) is a rare disease. I do not know the exact number of dysferlinopathy patients in Japan.
It is a form of LGMD. Let’s do our best together.
如果您的 LGMD 明天就能 "治愈",您首先想做的是什么?:
I want to celebrate with family and friends.
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