LGMD "SPOTLIGHT INTERVIEW"

 

NAME:  Michele   AGE: 52 Yrs. Old

PAYS: États-Unis

LGMD Sous-type:   LGMD2A – Calpainopathy

 

À QUEL ÂGE AVEZ-VOUS ÉTÉ DIAGNOSTIQUÉ ?:

I was initially diagnosed with an unspecified form of muscular dystrophy at the age of 25 years old.  I received confirmation of my LGMD2A diagnosis at the age of 43.

QUELS ONT ÉTÉ VOS PREMIERS SYMPTÔMES :

In my late teens I developed an awkward waddle when walking and in my early 20’s began limping.

AVEZ-VOUS D'AUTRES MEMBRES DE VOTRE FAMILLE QUI SONT ATTEINTS DE LA LGMD :

Yes, one sibling has LGMD2A but the other does not.

WHAT DO YOU FIND TO BE THE GREATEST CHALLENGE IN LIVING WITH LGMD:

To be blunt, the worst part is dealing with public restrooms because the transfer to/from a wheelchair is physically difficult and the restrooms are not always adequately set-up so I am always worried about drinking water or coffee while I’m out.  Sometimes it feels as though my life revolves around fluid management!

QUELLE EST VOTRE PLUS GRANDE RÉALISATION ?:

Professionally, my greatest accomplishment is my involvement in the creation and management of Coalition to Cure Calpain 3 (C3) which is a non-profit group focused on funding high potential research to cure LGMD2A (also known as Calpainopathy),and educate the global community about the disease.

Personally, my latest accomplishment is solving a New York Times Mini Crossword puzzle in 15 seconds,
HOW HAS LGMD INFLUENCE YOU INTO BECOMING THE PERSON YOU ARE TODAY:

On the plus side, it has made me more empathetic and given me the opportunity to show my children that it is important to take action when you are frustrated with the state of things.  Don’t complain; be an agent for change.

On the down side, it has made me adjust my daily life as my mobility has worsened, and while I certainly make the most of my life and am generally happy and productive, it certainly presents its challenges, and that can get tiring physically and emotionally.

QUE VOULEZ-VOUS QUE LE MONDE SACHE SUR LA LGMD ?:

We need more funding for research and more scientists engaged in finding a treatment or cure.

IF YOUR LGMD COULD BE”CURED” TOMORROW, WHAT YOULD BE THE FIRST THNG THAT YOU WOULD WANT TO DO:

Ride a bike (preferably a pink Schwinn with a basket on the handlebars and a thermos of coffee) to the beach and walk along the jetty with my family.

 

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