Hi Sienna,
This is Alissa your Cousin that lives in Albuquerque,New Mexico i just wanted to say hi and i miss you guys so much and i wish i could see you both more often. Someday i will have to go visit and all i can remember from this summer seeing you guys you and Sierra both have grown up so much. Keep up your hard work i can see that you love to sing follow your dreams. I love you!
Hi my name is Jodie & my 11yr old middle son also has a form of primordial dwarfism called Russell Silver Syndrome. I saw some of your apperence on Anderson Cooper.Feel free to contact me anytime.
Hello Sienna!
I am a brazilian boy with dwarfism and I found your blog through a news site. I really enjoyed your story and thought it was very cool its initiative to have a blog to share your experiences.
I also have a blog about dwarfism (nanismoemfoco.com) and I’m putting a link to your blog in my sidebar. I hope you can put one to my blog too.
Hugs, Joao Lucas.
Hello Sienna!
I am a Indian boy with dwarfism and I found your blog through a news site. I really enjoyed your story and thought it was very cool its initiative to have a blog to share your experiences.
I’m putting a link to your blog in my sidebar. I hope you can put one to my blog too.
Hugs, dilon kumar(dilonkumar@yahoo.com)
(dilonkumar@gmail.com)
(skype : dilon.kumar)
Hi Sienna, i´m Catarina from Portugal. I have a 4 yrs old daughter with P.D. and she´s the only case known here in our country. It´s been an interesting journey so far cause everything is new for us and her doctors. She´s as happy as she could be and brightens our life every day. Thanks for your example to.
Hi Sienna,
This is Alissa your Cousin that lives in Albuquerque,New Mexico i just wanted to say hi and i miss you guys so much and i wish i could see you both more often. Someday i will have to go visit and all i can remember from this summer seeing you guys you and Sierra both have grown up so much. Keep up your hard work i can see that you love to sing follow your dreams. I love you!
Always,
Alissa
Thanks for stopping by! I know they’d love to see you, too!!
Hi my name is Jodie & my 11yr old middle son also has a form of primordial dwarfism called Russell Silver Syndrome. I saw some of your apperence on Anderson Cooper.Feel free to contact me anytime.
So sorry I think I missed this! I’m not sure how I missed it! Are you guys part of the Potentials Foundation?
Hello Sienna!
I am a brazilian boy with dwarfism and I found your blog through a news site. I really enjoyed your story and thought it was very cool its initiative to have a blog to share your experiences.
I also have a blog about dwarfism (nanismoemfoco.com) and I’m putting a link to your blog in my sidebar. I hope you can put one to my blog too.
Hugs, Joao Lucas.
Thanks! I look forward to checking out your page! Blessings!
Hello Sienna!
I am a Indian boy with dwarfism and I found your blog through a news site. I really enjoyed your story and thought it was very cool its initiative to have a blog to share your experiences.
I’m putting a link to your blog in my sidebar. I hope you can put one to my blog too.
Hugs, dilon kumar(dilonkumar@yahoo.com)
(dilonkumar@gmail.com)
(skype : dilon.kumar)
Nice to “meet” you!!!
Hi Sienna, i´m Catarina from Portugal. I have a 4 yrs old daughter with P.D. and she´s the only case known here in our country. It´s been an interesting journey so far cause everything is new for us and her doctors. She´s as happy as she could be and brightens our life every day. Thanks for your example to.