07/06/2015: 

이름: Ramesh  AGE: 28 yrs. old
국가: India
LGMD 하위 유형: LGMD2B / Dysferlinopathy

몇 살에 진단을 받았습니까?:
I started having symptoms at the age of 19 but was not diagnosed until I was about 22 years old.

첫 증상은 무엇이었나요?:
My first symptom was, when I was going to office suddenly I fell down. I consulted my doctor, he suggested physical therapy but that did not help much. After that, we found it might be best to consult the doctor in Bangalore (India). I had muscle & nerve biopsy and was in a cast for two months on each leg, one at a time. She sent me to a neurologist for further testing.

다른 가족 중에 LGMD를 가지고 있는 사람이 있나요?: No

LGMD와 함께 생활하면서 가장 큰 어려움은 무엇이라고 생각하십니까?:
I find that the greatest challenge in living with LGMD is that people have a hard time understanding it. It is not easy to describe LGMD to someone. Many people think that I am exaggerating or even lying about having this disease.   In addition to the condition, I find the lack of accessibility and social attitudes toward disabled people as very limiting. I wish people would be more open to learning about these diseases and understanding how get rid of this disease.

가장 큰 성과는 무엇인가요?:
My greatest accomplishment is, managing to work and keep working in my own way.

LGMD가 지금의 당신이 되기까지 어떤 영향을 미쳤나요?:
I’ve learned to appreciate people helping me, to have patience, to keep being hopeful and avoid feeling depressed, to be thankful for everything, to understand people who aren’t in the same situation as me and who are in a difficult situation, to value what I have and to be a saver, to give more love to my family each day as if it were the last.. I have learned to be patient and accept the fact that everyone needs a helping hand!

세상이 LGMD에 대해 알았으면 하는 것:
Even most medical professionals are unaware of this condition they have to aware of this and teach the patients how to be safe and challenging towards life.

내일 LGMD가 "완치"될 수 있다면 가장 먼저 하고 싶은 일은 무엇입니까?:
First of all I would like to congratulate each and every doctor who helped me, in person. The main thing is, I would like to open one blog about this disease and I will guide and support the patients how to overcome through the disease. I know how I am suffering with this disease. I will not give a chance to others suffer again.