05/14/2016:

Intervista a riflettori accesi sulla LGMD

Nome:  Dave    Età:  27 yrs. old

Paese: Australia

Sottotipo LGMD: LGMD 2A / Calpainopatia

 

A che età è stata fatta la diagnosi:

I think I was diagnosed around the age of 14.  I know that it was while I was in high school.

Quali sono stati i primi sintomi:

I would go to golf every Saturday and when I would come home I would have to go and have a sleep for a few hours.   I would be sore all over.   So, my mother took me to the doctors to see why I was tired all the time.

Avete altri familiari affetti da LGMD:

I am the only member in my family who has any form of Muscular Dystrophy.

Quali sono, secondo lei, le sfide più grandi da affrontare nella convivenza con la LGMD?:

The biggest problem I had was explaining my Muscular Dystrophy to people ( family, friends and strangers) and not have them completely believe me. They just thought I was tired because I was lazy.

I spent a night in hospital with massive cramps in my leg which I could not calm down. I could not walk properly for 3 weeks and still had to work in pain.   I’ve always had a problem with stairs and carrying heavy things for long periods of time.

Qual è il suo più grande risultato:

My greatest accomplishment is getting married this February to my wife Rebecca.   She has become my strength and motivation to keep moving.  I am a second generation truck driver in Australia and it is something which I am very proud of!  Although, my job can sometimes become rather physical and it takes a toll on me.   My wife, Rebecca, helps me through it all.  She is my wonder woman.

In che modo la LGMD l'ha influenzata nel diventare la persona che è oggi:

I have learned to listen to people about their condition. I have made a lot of great friends on Facebook who I keep in touch with. I listen to their concerns and problems and ask them for advise also. Most of all I have learned that it is okay to ask for help when I need it — instead of trying to do everything on my own.

Cosa volete che il mondo sappia della LGMD?:

I want the world to know that Limb Girdle Muscular Dystrophy exists!!!    It is incredible the amount of times I’ve had to explain my condition to people and they almost don’t believe me.   They don’t understand that my LGMD  cannot be fixed or cured by going to the gym.   There are no cures or treatments for LGMD.  We have no control over our condition, it is a part of us….a part which we struggle with but it is what makes us who we are.

Se la vostra LGMD potesse essere "curata" domani, quale sarebbe la prima cosa che vorreste fare?:

My personal goal apart from having a family….would be to play basketball again. I loved it growing up. I would definitely get back out onto the court and run for as long as I possibly could.

 

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