Never heard of this. Thanks for the info. My heart and prayers go out to each and everyone of those family members and to anyone suffering from this disease. Hope they can soon find a cure!!
Like many others in this thread, I too have been ignorant as to this disease. My thoughts and prayers are with those who have this and whose families must live with it. Thank you so much for creating awareness.
Thinking of all who suffer or have children who suffer with it. Its good to be made aware of illnesses and the things other ppl have to go through just to live day to day.
Thanks all for the support on this Let's try and keep this thread alive And post a for support if you don't know what write
Way to raise awareness to DMD Honey. Prayers love and hope to the families and children suffering through this. Also to the doctors and researchers looking to find the cure/treatment.
I met a guy back when I was younger he had DMD and he was the kindest person I ever met
Have a niece with SMA (Spinal Muscular Atrophy). She is 14 years old and probably has another 7-9 years left to live.
Much support for this. We are so blind to so much that is around us. Always pay attention and be aware. Amazing thread as always Honey. Thoughts and prayers go out to the family and young one affected by this.