Amber living with Dystrophy's video: We Need To Talk

Hello my Loves!!! It's been over 7 months since I last uploaded a video and I am happy to announce that I am back and super excited to start up my channel again! I have been through a lot and this video will talk about what I have been through . It is a VERY sad subject, so please , anyone who gets triggered easily turn into a different video or be sure to come back again later for happier videos and tutorials. I want to say thank you to everyone who stayed and subscribed even though I wasn't posting new content at that time . I love you all so much and I am so beyond thankful for your kindness and support ! With all my heart thank you my darlings ! For Business Inquires Please Contact Me Here: amberslwd@gmail.com www.amberslwd@gmail.com *You can also find me here: Instagram: https://instagram.com/amber_kohaku_chan 37.1k Tumblr: amberlivingwithdystrophy.tumblr.com Blog: amberlwd.blogspot.com ALL MUSIC IS 100% COPYRIGHT FREE, 100% ROYALTY FREE AND PROVIDE BY THE ARTISTS THEMSELVES FOR USES ON ANY YOUTUBE VIDEO! ALL FALSE CLAIMS WILL BE FOUGHT AND REPORTED! My Short Story: I'm considered to be a Living Doll not only because of my looks but because of my rare disease that affects my body's muscles called Becker's Muscular Dystrophy. It affects my legs and my arms for now but it is a progressive disease without any known cure for now. This disease makes me like a doll even more because I'm very weak and It's hard for me to do different tasks like standing up on my own and I have to walk with a cane & at times I need assistant to walk. But I won't EVER let this get me down What helps me -other than my wonderful husband and his amazing family and my amazing Supporters on my Instagram- is my love for art/painting, makeup effects, tattooing, anime &cooking!! Making these videos and communicating with all of you make me so happy now as well & Please know that life and love goes on after a major diagnosis so please Always Enjoy Life and Loved Ones!! If you have any questions about Muscular Dystrophy you can watch my video on it here http://youtu.be/xumsoCd5bEQ or visit www.mda.org for more information or to donate to families and research for a cure All my videos are filmed and edited on my iphone by Me :) (Amber