Members Archive : Page 7 of 8 : Becker Muscular Dystrophy

To be seen, understood and celebrated for the brilliance we carry forward in tackling every day.

Becker Community Member

60532

I wish that this community keeps growing in size and strength! So wonderful to see people connecting and sharing experiences.

Becker Community Member

80302

Community bonding and healing!

Becker Community Member

90012

Love.

Becker Community Member

92503

More social activities, movie night, pizza night, outdoor adventures.

Becker Community Member

32609

Community, Resources, Friendship.

Becker Community Member

34771

To continue to research for the cure.

Becker Community Member

08723

I have Becker and was diagnosed at age 5. My form of Becker is thankfully relatively mild but I know many of the same struggles living with a chronic condition that can be unexpected. I have also engaged muscular dystrophy as a researcher. As a Fulbright scholar, I studied exon-skipping therapies for Duchenne, an approach based on Becker. It is my hope that people with Becker can move past barriers, especially in employment, and involve themselves as scientists and clinicians. Overall, I wish for a more accessible world for people with many different abilities, including people with Becker.

Becker Community Member

97035

My wish is for future generations to be able to recode DNA so rare diseases, and especially muscular dystrophy, will be problems of the past.

Becker Community Member

95330

My wish is for a cure or even a treatment to give us hope. May the insurance companies also not deny coverage so our boys have a chance at the life they deserve.

Becker Community Member

53083

My wish for you is a happy, long life where you can achieve all of your dreams. Also, may a drug come out that’s safe to help make your life easier. We love you!! We support you. We see YOU.

Becker Community Member

30071

Social support for young children living with Becker.

Becker Community Member

30004

Hear from the community