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Krista Long

Moms of Special Needs Kids

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Moms of Special Needs Kids

A place for moms who deal with those special challenges in raising their kids and use social media as a way to connect.

Members: 325
Latest Activity: Nov 17

Welcome to the place for Moms raising children with special needs. I am fairly hands off in running the group, but have been known to delete comments that are clearly promotional in nature. Enjoy the community.

I dedicate this song to all of you:

Discussion Forum

Debbie Yost

Share Your Child's Abilities 13 Replies

About a year ago I started a monthly blog post on my blog called Ability Tuesday. The first Tuesday of each month I share one of my daughter's abilities, not her disabilities. Today is the first Tu...

Tagged: sharing, Abilities

Started by Debbie Yost. Last reply by Maureen Doolan Boyle Sep 24.

Krista Long

Let's introduce ourselves! 50 Replies

This is the place to talk a little bit more about our children. My boys are now 14 and 10, and Konal, the 14 year old, has multiple disabilities. We have in home support from Arizona's behavioral h...

Tagged: introduction

Started by Krista Long. Last reply by Kim Cristo Nov 11.

MiaHysteria

Twitter ID's 18 Replies

Hi everyone~ I think sometimes it's nice to be able to know that I'm (we're) not the only one going through battles through the day, keeping our heads on straight and love in our actions. There ar...

Started by MiaHysteria. Last reply by BH Aug 27.

Carrie

What is your child's (children's) special need(s)? 19 Replies

I really am interested in meeting other moms who face similar challenges as we may have to (my daughter is still undiagnosed -- waiting on a skin biopsy). I thought it might be helpful for all of u...

Started by Carrie. Last reply by Jean Myles Sep 3.

MiaHysteria

Do You Have a Special Needs Blog? 52 Replies

Hello Everyone~ I just started a discussion for twitter id's, but also thought (half way through the post for that one) that knowing each other's blogs might be nice too. I have a blog that highli...

Started by MiaHysteria. Last reply by Kim Cristo Nov 17.

Comment Wall

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Jill Comment by Jill on September 1, 2009 at 11:37am
My husband found a really inspirational story about a young woman w/ autism who started her own business: http://tinyurl.com/kkzr7v. Gives me hope for my son's future.
Jill Comment by Jill on September 1, 2009 at 6:26am
Poster giveway by husb&wife artists. Bright, unusual graphics, looks like alex girard or corita kent - comment on our blog to win! http://bit.ly/XKAu6
Jill Comment by Jill on August 29, 2009 at 3:46pm
Vaccines + autism. Link is tenuous, according to multiple studies, and I'm a bit irritated that Matt Lauer is giving airtime to Andrew Wakefield on NBC tomorrow (7pm, NBC). My thoughts on the issue: http://www.blisstree.com/autismvox/show-me-the-science/
Barbara Pontius Comment by Barbara Pontius on August 28, 2009 at 12:35pm
Hi Jean, yes the kids are in public school, but in the ESE classes. William has more mainstreaming than my girls. Since he is in 3rd. grade, he spends some of his time at school with a normal functioning class, he loves it. I think its good for the other kids, to understand him, he even made some friends. My girls are in a self-contained class. They have all of their therapiesin the classroom. But they do get to P.E. and music(which they love). My girls here 3 when i noticed William regression, at the time i thought he was mimicking his sisters behavior, i had thought about putting him in daycare so he could spend more time around a more normal setting. But as time went on the doctors wanted to have him tested also. I'm not sure if autism is genetic or not. They do need to do more research. I do think there is a connection between the MMR shot and autism. The mercury in that shot kills their immune systems, especially if there given the shot before they're 15mths.
Danielle's Foundation Comment by Danielle's Foundation on August 28, 2009 at 11:26am
Hello everyone. We are new, and I just wanted to introduce Danielle's Foundation and share with all of you a little information about us:

We are a new non-profit organization that just launched, and our goal
is to help parents of children with cerebral palsy and brain injuries gain the knowledge to secure the therapies, benefits, and resources their children so desperately need. But often times have a hard time either trying to locate or actually obtain.

Danielle's Foundation was created to honor the memory of Danielle Vick, our inspiration, who sadly passed away in 2008 at the age of 4 from complications of her anoxic brain injury.

Our goal is to build a community where parents can come together and not only offer one another support, but also help guide each other to resources and services for their children. We are working on building our team of volunteers and our community so no family has to go through these difficult and often tumultuous times alone, but instead can find comfort and support in knowing that there is hope--by banning together.

Please check our website out for more information to learn how we can help you, and to read Danielle’s story. We are also giving out a free copy of a book entitled: Getting the Therapies, Benefits, and Resources Your Child Needs: A Guide for Parents of Children with Cerebral Palsy and Brain Injury" which is a guide that provides families with the information they need and the support they want. On our site you can also find out how to get your FREE copy today!

www.daniellesfoundation.org

Thank you for your time, and I hope some of you will share your stories with us!!
Lynn Rickert Comment by Lynn Rickert on August 27, 2009 at 11:04am
ditto to Jean's comments. I just got 7 SEVEN!!! notices from emma nilsson. Not fun. feels like spam.
Jean Myles Comment by Jean Myles on August 27, 2009 at 11:00am
Sorry to be rude Emma, but this is not a place for advertising. We are a group of moms with special needs kids trying to support each other. I also work a home business and advertise, but not here.
Christina White Comment by Christina White on August 27, 2009 at 10:55am
Does any one out there no anything about the H.S. programs. I'm having trouble. getting my daughter in the right classes. & of course if you don't know the system. Teacher & Office personel won't offer to tell you the help that is there. Unless you know the right people to help. My daughter has P.D.D.
emma nilsson Comment by emma nilsson on August 27, 2009 at 9:56am
hey there!..... i came across a site http://surveycheese.com and i'm able to earn 700 to 1000$ every month by just spending 2 hrs a day.i would like to spread the word...its my extra income option..thats it
Jill Comment by Jill on August 27, 2009 at 8:03am
Even though Alex is a really picky eater, he's willing to eat in Chinese restaurants and coffee shops. We're also trying to make dentist visits smoother, and make sure that his clothes are accessible. Please, please let me know what tips have worked for you to make life easier!
 

Members (325)

Samantha Jean Myles Aimee Crayonsetc MiaHysteria carole harris Carrie JudiElise Krista Long rondata Tammy Lessick Nostalchick Amazing_Grace Kara T. Tamanini Karen Putz Ellen Karen U Debbie Yost Margaret Chaidez Kim Wirick Carrie Lindsey Kid Organizer Candace McLane Sygnet Creations stirling Becky Lynn Ann Marie Curling Michelle Todd L.Mae Wilkinson
 
 

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