Individual with LGMD: Rodrigo
LGMD "ENTREVISTA EM DESTAQUE"
Nome: Rodrigo Idade: 29 yrs. old
País: Estados Unidos
LGMD Sub-tipo: LGMD2B / Myoshi Miopatia
Com que idade foi diagnosticado:
I was diagnosed with LGMD2B at the age of 24.
Quais foram os seus primeiros sintomas:
My symptoms appeared around the age of 17.
Tem outros familiares que sofrem de LGMD:
I have 2 brothers who show symptoms but have not been diagnosed.
Quais são, na sua opinião, os maiores desafios de viver com a LGMD?:
Mobility is my greatest challenge.
Qual é a sua maior realização:
My greatest accomplishment is in allowing my artistic talent to come to light.
Como é que a LGMD o influenciou a tornar-se a pessoa que é hoje?
LGMD has greatly influenced me into becoming the person that I am today. It has allowed me to see life in a completely different way. It has forced me to push myself constantly, even for the smallest of tasks, which in turn made me become resilient and persistent. It has also given me the empathy and I can sympathize with those who are struggling too. LGMD has made me appreciate every aspect of life and discard the materialistic behavior.
O que quer que o mundo saiba sobre a LGMD:
The world, first of all, needs to know we exist. Limb Girdle Muscular Dystrophy can and will be cured but not enough people know about it to care. It is a good thing it affects a small percentage of the population but we are a relatively large group of people who want to still make it in life. We are also pursuing happiness but need a lot more help from others. The world needs to know we are still contributing what we can. We struggle, even minute even putting a piece of bread in our mouth, but we have accepted these challenges and being strong has become our only way of life.
Se a sua LGMD pudesse ser "curada" amanhã, qual seria a primeira coisa que gostaria de fazer?:
I would take the fastest route to recovery. I would take off running as Forest Gump did. I would tell everyone on my path how much I appreciate moving again in an attempt to bring self-awareness of general health and point out how much we take for granted. Every step a healthy person takes for granted a person with Muscular Dystrophy wishes they could take.
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