I was diagnonsed with M.S.U.D. at 8 years old. I am "the first to live to 8 years old undiagnosed." The deep-line I.V. they use on some patients who are critical was first tested on me. At that time I was diagnosed, it was illegal to administer since it was untested and the FDA and AMA didn't approve it. Well, the I.V. did work, and miraculously I survived. The work and research collected on me through the years has helped others with the disease I will never meet. God grant all victims peace.
I am so glad that MSUD has a platform in which people could learn about such a rare disease. My 8 year old daughter lost her battle with it on September 18, 2009. She is greatly missed. I did, however, donate her organs and they all have been gifted to someone. so, she still lives on in many ways....Please continue to spread the word about this disease.....I've never met anyone else who has it. I would like to, though.
Hey, I made a video for biology class too, only, its more just for fun. You might want to check it out some time-it has the same title, but look for my user name: yoyodork
Hey, I made a video for biology class too, only, its more just for fun. You might want to check it out some time-it has the same title, but look for my user name: yoyodork
Wow I didn't know this was even a real disease. It sounds pretty serious too. :[
RobotnikHotCakes9000 1 month ago
I was diagnonsed with M.S.U.D. at 8 years old. I am "the first to live to 8 years old undiagnosed." The deep-line I.V. they use on some patients who are critical was first tested on me. At that time I was diagnosed, it was illegal to administer since it was untested and the FDA and AMA didn't approve it. Well, the I.V. did work, and miraculously I survived. The work and research collected on me through the years has helped others with the disease I will never meet. God grant all victims peace.
KrosanBeast315 1 year ago
paaoola science project on msud never knew about it hahahahah very sad
MoMaStAr1023 1 year ago
I am so glad that MSUD has a platform in which people could learn about such a rare disease. My 8 year old daughter lost her battle with it on September 18, 2009. She is greatly missed. I did, however, donate her organs and they all have been gifted to someone. so, she still lives on in many ways....Please continue to spread the word about this disease.....I've never met anyone else who has it. I would like to, though.
freshstart408 2 years ago
ps: it may also be under the name MSUD THIS ONE
yoyodork 3 years ago
This has been flagged as spam show
Hey, I made a video for biology class too, only, its more just for fun. You might want to check it out some time-it has the same title, but look for my user name: yoyodork
THANX
yoyodork 3 years ago
Hey, I made a video for biology class too, only, its more just for fun. You might want to check it out some time-it has the same title, but look for my user name: yoyodork
THANX
yoyodork 3 years ago