Mood:  celebratory

I have just won my number 49 award. I am one away from 50. I

am so excited. The most awards for any new site. This is

another international one to boot. In 9 months of having my

site up. How does a person with HD do this? I started this

when I was sick. Go full on to what you want. I never let HD

rule my life. Never let HD rule your life. It is yours to do what

you want. Live your dreams.That is why my dreams are

coming true. I wanted to make a positive site that changes

lives. I also wanted to make an award winning site. That is

secondary. I always try to win awards for my Mom and Dad.

Dad pays for my site. He paid for my schooling. I have HD. I

could never pay them back. Especially with early onset. I also

 help us get the word out about HD by winning these awards. I

 am internationally recognized. I am bringing in other people

that do not about HD. I am getting word out. I am helping us

get more people to know about HD by winning all of these

accolades. It will always be that way. Daily hope is what I

started this for. I do not care if I am immobilized and can’t

move. I will never stop this. There is nothing else for

everyone with HD to get hope from. I understand having HD

how bad no hope is.  I know there are people that want me

too stop. I am not naming names. The person that came out

with that article saying we would never get cured. Two days

after mine. Do not listen. We are going to get cured. It will

happen. I started my hopeful revolution.  Will never stop ever.

My home support workers know that too. I have it too. It does

not go telling us matter of fact. We need more. We need

actual hope. Need it so bad. We also need people to know

how hard this is. Everyday how brave we all are. We know.