This is simply amazing! I am an artist that does donation drawings for different foundations, I am unable to donate money strait to due to our current state of economy here in America. I do donations to foundations that embrace difference and allows people to be their selves. I would love to help you out with this foundation. I am not the most experienced artist but I am willing to help however i can. I may only be 14, but i feel i can make a difference. Thank you, so much.
soy de colombia y tengo mi hijo que tiene esta enfermedad me gustaría saber que crema es buena para su pielecita y si esto tiene alguna solución físicamente y si aqui hay fundaciones muchas gracias. agradesco a la persona que me pueda dar esta información
I am a 64-year-old woman with hidrotic ectodermal dysplasia. I have problems still with people staring at my hands and thinking i have a contagious disease.
It is so good to know there is a group out there helping people like me.
I would love to attend one of the conferences. Keep up the good work.
As an ED affected male, I was never interested in being in the groups. They made me feel like I had a problem, and here's all these other people with that problem. My coping mechanism was to convince myself I didn't have a problem and that I was as normal as the next person. Now that I'm older (29) and living a full, successful life I feel like I should probably get involved in sucha group.
Oh what a great video! I am so thankful for NFED!!!! It is amazing and helped me transition so wonderfully into my daughters and my diagnosis of XLHED! I felt so alone, and then We found you!
What a wonderful video! Without the NFED, I don't know what we would do. Thank you for your tireless efforts to bring awarness of ED. Thank you, thank you, thank you!!!
Muy buen video. Espero que sirva para difundir la inapreciable tarea que desarrolla este grupo de gente. Quien pueda trate de difundir el mismo. La NFED es de inapreciable ayuda y apoyo para quienes tenemos que tratar con ED. Un saludo para todos y sigan para adelante.
where the heck was this stuff when i was a kid? i couldve used the support for sure. i mean im 18 an i have hed but i wish this stuff was around when i was young
I'm very excited to see this video. I won't try to say what NFED has meant to my family; not because I don't want to, but because I can't. What I can say is that the people involved with NFED are great people. When your child has something that you have no understanding of, having the information and support proved by NFED is a Godsend. Mary Richter is one amazing human being, and the lives of those in my family are better for her and her work. Thanks to all at NFED.
This is simply amazing! I am an artist that does donation drawings for different foundations, I am unable to donate money strait to due to our current state of economy here in America. I do donations to foundations that embrace difference and allows people to be their selves. I would love to help you out with this foundation. I am not the most experienced artist but I am willing to help however i can. I may only be 14, but i feel i can make a difference. Thank you, so much.
Cyndariss 2 months ago
soy de colombia y tengo mi hijo que tiene esta enfermedad me gustaría saber que crema es buena para su pielecita y si esto tiene alguna solución físicamente y si aqui hay fundaciones muchas gracias. agradesco a la persona que me pueda dar esta información
nando6163 3 months ago
I am a 64-year-old woman with hidrotic ectodermal dysplasia. I have problems still with people staring at my hands and thinking i have a contagious disease.
It is so good to know there is a group out there helping people like me.
I would love to attend one of the conferences. Keep up the good work.
joszyism 4 months ago
As an ED affected male, I was never interested in being in the groups. They made me feel like I had a problem, and here's all these other people with that problem. My coping mechanism was to convince myself I didn't have a problem and that I was as normal as the next person. Now that I'm older (29) and living a full, successful life I feel like I should probably get involved in sucha group.
hyperswivel 1 year ago
OMG, my friend has this and he never told us what is was now i know.
AnielloNASTASI 1 year ago
@AnielloNASTASI aniello, this is jesse, glad you finally get to see what i have. :) see how they look like me. that's why donovon looked like me.
3stepandrun 1 year ago
Comment removed
3stepandrun 1 year ago
wheeh....... i hope there will be foundation who care for the persons having HED here in philippines
22maet 1 year ago
Most awesome person in the world with HED is Michael Berryman, he is absolutely awesome!!!!
sharall 1 year ago
Thanks for the info.
I heard about HED on Iowa Public radio today, they were chatting with Bonnie Rough, who has a new book out (maybe its not new??)
Anyways, thanks for helping me to understand and accept people with these differences.
nobodymm 1 year ago
Mary you are an inspiration to us all!!!
lovemextender 2 years ago
Mary Kaye rocks....
nightshadedesign 2 years ago
Thanks so much for the video and im super excited for the summer family conference! (:
lwangsd 2 years ago
Oh what a great video! I am so thankful for NFED!!!! It is amazing and helped me transition so wonderfully into my daughters and my diagnosis of XLHED! I felt so alone, and then We found you!
angelhawk15 2 years ago
What a wonderful video! Without the NFED, I don't know what we would do. Thank you for your tireless efforts to bring awarness of ED. Thank you, thank you, thank you!!!
DHolmanJ 2 years ago
Muy buen video. Espero que sirva para difundir la inapreciable tarea que desarrolla este grupo de gente. Quien pueda trate de difundir el mismo. La NFED es de inapreciable ayuda y apoyo para quienes tenemos que tratar con ED. Un saludo para todos y sigan para adelante.
thefly2674 2 years ago
where the heck was this stuff when i was a kid? i couldve used the support for sure. i mean im 18 an i have hed but i wish this stuff was around when i was young
jd27271 2 years ago
Greate clip... Thank you for what you do... Greatings from one of about 100 in Sweden that are effected by ED....
Boorken 2 years ago
I'm very excited to see this video. I won't try to say what NFED has meant to my family; not because I don't want to, but because I can't. What I can say is that the people involved with NFED are great people. When your child has something that you have no understanding of, having the information and support proved by NFED is a Godsend. Mary Richter is one amazing human being, and the lives of those in my family are better for her and her work. Thanks to all at NFED.
excaliburno1 2 years ago
Comment removed
excaliburno1 2 years ago
Beautifully done!!!
DrewTheHalfJewPrince 2 years ago
I love this video and will be sharing it on my facebook account. Thanks NFED for everything you have done and continue to do!
fredewanuickfan 2 years ago
Great video. Very informative. Thank you.
elaine4300 2 years ago