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Holidays in the Hospital

November 16, 2011 in From the Hospital, Insider Insight by Children's Healthcare of Atlanta

By Ginger Tuminello

Child Life Specialist for Heart, Kidney and Liver Transplant Patients at Children’s Healthcare of Atlanta

The holidays can be stressful, especially if your child is in the hospital. Here are some tips on making the holidays in the hospital a little more bearable.

Acknowledge your feelings and the feelings of your child.

Being in the hospital, especially over the holidays, stinks. Recognize those feelings and say them out loud to your child. Once you’ve established that you’re both sad/upset/frustrated, focus on the things that can make being in the hospital over the holidays better. Just think, one day you may be telling stories that start, “Remember that Thanksgiving we spent in the hospital and had to eat turkey from the cafeteria…”

Continue established family traditions, or some variation of them.

As a family, identify what family traditions are most important to you and find ways to continue them. If your family always goes to church on Christmas morning, find out if the hospital chapel is having a service. If you always make holiday cookies, try making holiday ornaments instead. If your child’s favorite Thanksgiving treat is pumpkin pie, have someone make and bring it to her (if dietary restrictions allow). Or simply postpone Thanksgiving dinner until your child is feeling better and out of the hospital. There are no rules that say you must eat Thanksgiving dinner on Thanksgiving.

Create new family traditions.

Talk to your family about starting new holiday traditions. Make holiday ornaments to put on the hospital tree. Plan a holiday game night using either board games you love or finding new holiday games to play (check out http://www.coolest-christmas-holidays.com for some ideas). Make small gifts for the nursing staff. Organize a toy drive or fundraiser for hospital or organization. Your hospitalized child could always help design a flyer and plan other details.

Find out about special events and visitors offered by the hospital.

During the holidays, lots of folks enjoy volunteering and putting on special events for the hospital. Even though the local nursing home group playing hand bells may not sound very exciting, you might be surprised. Think of these events as opportunities to get out of the room, socialize, and make new holiday memories.

Start a special project with your child.

Take pictures and create a holiday scrapbook. Make holiday cards for other patients. Make gifts for family members. There are lots of inexpensive craft projects that you could do with your child that would provide hours of entertainment and bring a smile to many faces. Check out www.familyfun.com or www.craftbits.com for some great ideas.

Decorate.

Nothing says holidays like decorations. Bring a holiday blanket and pillowcases from home. Create holiday pictures and hang them on the walls. Get a small fake tree, decorate it, and put it on display. Get washable window paint and paint your windows. Wear festive clothing. If the room looks festive, you may find yourself in the holiday spirit. Just be sure to check with the hospital staff about policies regarding lights, hanging pictures, live plants/flowers, and window painting. And don’t forget to bring pictures of your loved ones at home.

Plan one small thing to look forward to each day.

The trouble with being in the hospital is that it gets boring and redundant. Plan something each day that you and your child can look forward to. Pick out an interesting location (i.e., gift shop, outdoor garden area) and plan for an afternoon walk there. Rent or borrow a new movie and plan for a movie night. Borrow a game you’ve never played and have a game night.

Create a schedule for visitors.

Hospital rooms can be tight quarters and too many visitors at once can be overwhelming. Creating a schedule for visitors can help limit the number of visitors and also allow you to schedule some quiet/alone time, which is important.

Find out the visitor policies.

During cold and flu season, some hospitals don’t allow siblings to visit. Find out these policies and ways to work around them. Is there a common area that the siblings can come to, like the cafeteria, so that you have time as a family? Could you use technology like Skype to communicate when you can’t be together? Try playing a game using Skype, making sure there’s a board on each end. Have your children at home and your hospitalized child write letters, send pictures, or record messages/stories often. Getting mail or email can really light up someone’s day.

Make time for yourself.

If someone offers to play with your child so that you can take a break, let them! Go for a walk, get a cup of coffee, or take a shower. Make sure that you are taking time to decompress and focus on yourself.

Use your team.

Your child life specialist, social worker, and chaplain are all great resources to help you and your family cope with hospitalized holidays. Be sure to let them know when you need something or just need to talk. They can be a great source of comfort and support.

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by Beth

Down Syndrome Awareness Day

October 3, 2011 in Featured, Featured Member by Beth

This post, by community member, Beth, originally ran this past March for Trisomy Awareness and World Down Syndrome Day. Given that it’s National Down Syndrome Awareness Month we decided to run it again.

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What Trisomy Awareness Month means is each Trisomy gets its own day to raise awareness. For example, my daughter Lauren has Down syndrome. She has 3 copies of the 21st chromosome, so our day to celebrate and raise awareness is March 21 (3-21). My friend Marta has a 9 year old son who has Trisomy 18. Their day is 3-18.

According to Wikipedia, trisomy is where there are 3 copies of a certain chromosome instead of the usual 2. There are several different types of trisomy. The most common type is Down syndrome (Trisomy 21). The other five types are rarer. Kayden, Marta’s son has Edwards syndrome (Trisomy 18). There are trisomies that occur on the 8th, 9th, 13th, and 22nd chromosomes also.

Because Down syndrome is the most common, it also has the most awareness (but still not enough). We have Buddy Walks, World Down Syndrome Day (March 21), National Down Syndrome Awareness Month.

Lauren was born in 2007, during a blizzard. She was a week early due to my blood pressure, and I needed an emergency c-section. She was 6lbs. and so tiny. She got jaundice, wouldn’t drink water (she still doesn’t!) I was told she would never breastfeed because she “is Downs”.

I started really advocating for her when she was 6 months old. We started early intervention; I started planning our first Buddy Walk for our community. I tried to find other moms online, since the moms around our community really wanted nothing to do with us.

I learned so much about Down syndrome such as the proper terminology. Lauren has Down syndrome. She is not Downs. Also, it is Down syndrome, not Downs, Down’s. Big D, little s. It was named for the doctor who first discovered the features of Down syndrome. I really despise when Lauren is called a Downs kid, or a downie. I always try to explain that by saying you wouldn’t call a woman with breast cancer ‘the cancer lady’. That would be rude.

My name is Beth and I blog at Our Typical Life. I talk about everything from Down syndrome to taking pictures. Lauren is 3 and has Down syndrome. Avery is one and the biggest copy-cat ever. I’ve been married for nearly four years and we live in Minnesota.

 

My Great Story Campaign for Mother’s Day

May 8, 2011 in Featured, Featured Group, From Julia by Julia Roberts

A Forum to Share Her Story

NDSS & The My Great Story Campaign join together to raise awareness for Down syndrome in celebration of Mother’s Day.

Today, Mother’s Day 2011, the National Down Syndrome Society (NDSS) will celebrate the accomplishments and achievements being made by people with Down syndrome by honoring their mothers. The My Great Story (MGS) public awareness campaign seeks to ignite a new way of thinking about people with Down syndrome by collecting inspirational stories told by people with Down syndrome and their family members, friends, colleagues, and many others. NDSS has added a new section in honor of Mother’s Day. Participants share a story about their mothers, grandmothers, sisters, aunts, cousins or friends who have a son or daughter with Down syndrome. Anyone can comment or vote on the stories already in the collection. NDSS invites you to cover the MGS campaign, post, tweet and blog about it, and promote reposting, retweeting and more sharing amongst your audience.

NDSS also invites you to watch the two MGS Celebrity PSAsthat star TV Hosts Meredith Vieira and Nancy O’Dell and post them to your media outlet’s website. Vieira’s dedication to the MGS campaign stems from her relationship with her son, who has worked as a camp counselor for people with Down syndrome, and O’Dell was drawn to campaign through her fond memories of her mother’s sister, who had Down syndrome. Both Vieira and O’Dell have also submitted stories to the campaign that speak to their experiences.

Down syndrome is the most commonly occurring genetic condition, in which the individual has a third copy of the twenty-first chromosome. One in every 691live births is a baby born with Down syndrome, and it is the most commonly occurring chromosomal condition. People with Down syndrome attend school, work, participate in decisions that affect them, and contribute to society in many wonderful ways.

People with Down syndrome are living longer than ever before. The life expectancy of individuals with Down syndrome has increased dramatically in recent decades – from 25 in 1983 to 60 today. Children with Down syndrome are often fully included in social and educational settings and increasingly go on to graduate high school and attend postsecondary education programs. While placement in the workforce remains a struggle, the situation has improved and adults with Down syndrome have attained a variety of positions, bringing enthusiasm, reliability and dedication to their jobs.

We encourage you to get involved and help NDSS and mothers of people with Down syndrome everywhere to raise awareness for people with Down syndrome.

About My Great Story

MGS was created pro-bono by NY based Ad Agency, Pedone. After 14 months of market analysis the Pedone team developed a campaign in an effort to shape the future for all people with Down syndrome. The online story book was developed by CT based Interactive Agency York and Chapel, who spent over 12 months developing the user friendly technology, sophisticated design and esthetics, and incorporation of the spectacular print ads shot by Zachary Scott. To date, over $5 million has been donated in national and regional ad space and services. The campaign has been seen by over 175 million people across the country and featured in media outlets such as Allure, Fortune, Golf Digest, The New Yorker, Newsweek, Time, Vogue and Wired, among other noteworthy outlets. To learn more, visit www.ndss.org/stories

About NDSS

The National Down Syndrome Society is a nonprofit organization representing the more than 400,000 Americans with Down syndrome. The mission of NDSS is to be the national advocate for the value, acceptance and inclusion of people with Down syndrome. The National Down Syndrome Society envisions a world in which all people with Down syndrome have the opportunity enhance their quality of life, realize their life aspirations, and become valued members of welcoming community. NDSS has over 350 affiliates nationwide. To learn more, visit www.ndss.org.

Cowabunga! It’s for the Mommas!

April 27, 2011 in Featured, Giveaways by Julia Roberts

We Celebrate You!

We at Cowabunga Ice Cream celebrate you for your dedication, hard work and loving support that you show your children day in and day out. We admire your hearts, your strength and your stamina. With Mother’s Day being just around the corner, we are honored to offer one of you with a little gift of luxury because you deserve an indulgence.

You are all deserving of a little pampering. We wish we could send each one of you a heaping portion of you favorite flavor of ice cream. Unfortunately, that’s just not feasible. To that end, we have teamed up with the supportive staff here at SupportForSpecialNeeds.com to run a fun little contest. The winner of this contest will receive either 4 pints or 2 quarts (flavors of your choice) of Cowabunga Ice Cream, the world’s first Designer Ice Cream.

Contest Details – In a clever 25 word or less synopsis, tell us about your favorite little luxury that you turn to when you need a bit of indulging. Leave your entries in the comments on this post. We’ll select a random winner from among the entries and they will either 2 quarts or 4 pints of Cowabunga ice cream flavors of their choice.

  • Deadline for entries: May 1, 2011
  • Winner selected/announced by Julia Roberts: May 2, 2011

There is one caveat since this contest involves shipping of frozen food. For this giveaway, we can only ship to a winner in one of the following states:

  • Maine
  • New Hampshire
  • Vermont
  • Massachusetts
  • Rhode Island
  • Connecticut
  • New York
  • New Jersey
  • Deleware
  • Maryland
  • Washington D.C.
  • Pennsylvania
  • Virginia
  • West Virginia
  • North Carolina
  • South Carolina
  • Tennessee
  • Kentucky
  • Ohio
  • Indiana
  • Michigan

Thank you to all of you for the hard work and loving devotion that you display each day. We celebrate you!

We can’t wait to read all of your entries!

ABOUT COWABUNGA ICE CREAM:
At Cowabunga Ice Cream we serve up designer ice creams and frozen yogurt that will bathe your taste buds in luxury. Our small batch (just 5 gallons at a time), handmade production methods ensure a blissful experience each time you indulge.

“This is the Louis Vuitton of ice cream.”~ NY Times Best-selling author Omar Tyree

If you’re in the area, stop in at our shop in Forked River, NJ. For those not in the area, we are pleased to announce that you can now order our high-end ice cream online and have it shipped right to your door. Please visit our website (http://cowabungaicecream.com) for more information.

“It’s easy to be skeptical of ice creamery Cowabunga’s foodie cred…but they pass the taste test.” ~ Wall Street Journal

Ten Coping Strategies for Crisis

April 11, 2011 in Book Reviews, Featured by Admin Dawn

By Linda Cole, author of Resurrecting Anthony: A True Story of Courage and Destination

1.      Recruit and accept help and emotional support through family and friends.  Do not try to weather the crisis alone.

2.      Confide in your primary physician.

3.      Be positive.  Be proactive.  Your attitude will contribute greatly to the outcome.  Educate yourself and be involved as much as possible.

4.      Recognize that “This too shall pass.”  You will have a “normal” life again, although it may never be as it was.

5.      Find your mental “get-away” for particularly traumatic moments.  Example: Envision yourself floating on calm water.  Block out all distractions and center yourself.

6.      Focus on others.  Do not internalize.  Who else needs your help during this crisis?  How can you help those around you?

7.      Stay busy.  This is a bad time to be idle.  Don’t sit home alone.

8.      Exercise regularly.  Walk, run, bicycle thirty minutes every other day.  The endorphins released will help you mentally and emotionally.  Your sleep will improve.  Your body will be stronger and you will feel more in control.

9.      Sleep.  Get a good night’s sleep.  Your body and brain need the recuperation times.  If you are exhausted, you will be less effective at a critical time.

10.  Eat well.  Eat well-balanced meals, lots of fruits and vegetables, good proteins and complex carbohydrates.  Your body and mind are in a state of hyper-stress.  They need useful nutrients, not chemicals, processes and additives that sap your strength.

Finally, you will have moments that you can’t avoid.  Find a place; mine was in the closet, where you can really cry.  Let it come.  But set a limit, perhaps 4-5 minutes.  Afterward move on.  Do not dwell.

Linda co-authored her first book, Resurrecting Anthony: A True Story of Courage & Destination, which tells the story of her 12-year-old son’s heart attack and brain injury. A look back over the decade since the event helps the reader see how her once perfect family survived the devastating loss of a child and how a new family has come to be. Linda is also CFO of Anthony Cole Training Group, a successful company that builds sales cultures within organizations nationwide.

Tony graduated from the University of Connecticut with a degree in Education. A scholarship athlete, upon graduation Tony leveraged his experience to coach Iowa State University and University of Cincinnati athletic teams. He then spent more than 15 years in sales and sales management positions in the exercise equipment and insurance industries.

This unique combination of coaching and selling led Tony and Linda to launch Anthony Cole Training in 1991. An immediate success, by the end of 1998, the little company of two grossed half a million dollars. However, when their twelve-year-old son became severely brain injured the company down shifted for several years. In 2003, having adjusted to a new life and family, the company began to grow once again. Tony is CEO and President of Anthony Cole Training Group, which serves companies nationwide, bringing new life to sales organizations.

They Like Us, We Really Like Them

April 6, 2011 in Featured, From Julia, Roylco by Julia Roberts

During our Great Big Wish List Giveaway this past November we were lucky enough to work with some great companies and we formed a special relationship with Roylco.

Roylco has a heart for children and their educators and they have some great products for kids with special needs (typical kids, too). We have started a mini-site for our reviews and information! We promise to give you honest opinions (they are providing free toys for community members review) and if we can we’ll throw in how they could be good for kids with differences.

We’ve found that they’re a terrific company to work with and their people are nice. You know how refreshing it is to work nice people who “ooooh” and “ahhh” over your ideas? Yeah, it’s pretty good. We hope you’ll like seeing their products from our real world perspective and we hope you’ll feel inspired to check the toys out for yourself or for someone you love.

So please check out this special site! We’ll also let you know on the home page, on our Facebook page and Twitter feed when there’s something new up!

We’re working on bringing other partnerships like this one to our community as we seek out companies to join us! We hope you enjoy getting to know more about Roylco and their products.

Four Things That Stifle Caregivers and Kill Their Dreams

March 28, 2011 in Community Wisdom, Featured by Michelle Howard

Oftentimes caregivers view their lives with tunnel vision. Questions like “Who are you?” is met with the common response of “I’m a caregiver of a special needs child.”

While that statement is true, it’s also incomplete. Just because you have the huge responsibility of meeting and supporting the special needs of another, does not mean that’s what defines you.

Caregivers have dreams too. Sometimes those dreams are related to being a caregiver. Many times, they are not.

Being a caregiver birthed a dream of me becoming a physical therapist. I wanted to help children like my child to become more mobile. That dream has since fizzled out. Not because I’m no longer interested but because I allowed situations and circumstances to stifle it.

What is it that you are allowing to kill your personal dreams? Are you allowing circumstances unique to care giving, stop you from fulfilling them?

There are four enemies to your dream becoming a reality. They will stifle hault, thwart or whatever you want to call it.

Lack of Self Confidence

Just because you are caregiver, doesn’t mean that’s the only thing you can or should do well. What were you passionate about before you became a caregiver? Reach back to that point in time and refocus on what it was that made you good enough back then to accomplish those goals.

Lack of Resources

Don’t allow money to be the determining factor for not pursuing a dream. There are a ton of resources at your disposal. You just may not be aware of them. It will take some research but you CAN find financial help. As a matter of fact, you may find help that others are not privy to BECAUSE you are a caregiver.

Allowing Other People’s Opinions to Matter

Sure, you don’t want to disregard others around you – especially those close to you. Yet, you don’t want to allow other people’s opinions to weigh in heavier than your own (unless their name is 3 letters, begins with G and ends with D :-)

Sometimes people can’t catch your vision. That’s OK. Just don’t allow their negativity or ignorance to stop you from doing what you know in your heart you were born to do.

Fear

This is a powerful word and can stop anybody cold in their tracks. If you find that you are not following your dreams because you fear the outcome or even fear success, you must find a way to push on – even in the face of fear. Otherwise, your dreams will die.
Being a caregiver doesn’t have to be the be all and end all of your existence. If you have dreams, don’t let these 4 things keep you from reaching them. Do what you are good at, have passion for and long to do. You just may change someone else’s life.

About Michelle: Michelle H Smith is a mom of a child with multiple special needs. She helps other caregivers find ways to balance their lives by sharing stress reduction tips and resources on her blog Stress Relief for Caregivers. She also offers a line of pain and stress management products in her online store, http://www.antistressandpain.com

Supporting your Sensory Child through Spring Break

March 14, 2011 in Featured, Insider Insight by Carolyn Dalgliesh

For “Sensory” kids – those with anxiety disorder, sensory integration dysfunction, learning challenges, ADD/ADHD, obsessive/compulsive disorder, high- functioning autism, Asperger’s syndrome, or other sensory challenges – this can be a time for year filled with uncomfortable experiences like changes in routines, lots of people visiting, and travel to unfamiliar places full of unfamiliar faces. As a professional home organizer and the parent of a sensory and a typical child, I know the importance of coming up with a few simple ways to provide extra support during the holidays to help your “sensory” child and the whole family enjoy the season. Pick the one or two things that are the hardest for your “sensory” child and create extra support to target those challenges.

Preparing for Changes in Routines

Preparing our “sensory” child for what is coming is a one way to support them in their day-to-day experiences all year round. This is especially true this time of year when there are frequent changes in their regular schedule. Create a visual support whenever possible before the change is coming. Explain in pictures and/or words the new schedule making sure to highlight what they have done before successfully or people that will see that they enjoy. Make sure to include a few options of what can be done when your child is overwhelmed or needs an break.

Visits and Interactions with New People

Spontaneous visits can happen very frequently this time of year. Try to set the expectation of more visits and social interactions. For younger “sensory” kids, try making a story about “People we see during the spring break and the holidays”. You can also talk about the social expectations of these visits in the book – saying “hi” and introducing yourself to the visitor. For older “sensory” kids, make a laminated sheet that explains what you expect them to do socially with visitors, how long they need to stay and “visit” and when they can go do their own thing.

Make Travel Easier

Again, preparation ahead of time is key to making holiday travel easy on yourself, your family and your “sensory” child. Give your “sensory” child a visual of where you are going via online sites, pictures of the family home you will be staying and the people you will be seeing. For younger sensory kids, make a trip book that explains what will happen during your travels. During your visit, set-up a space for your child that is their “escape and regulate” spot. It can hold the toys or things that are calming and relaxing for your “sensory” child.

Creating Routines during Vacation Week

The lack of regular structure during the holiday vacation time can also be a challenge for most “sensory” kids. Create a special calendar for vacation week and write in a loose schedule of what is happening. Have a list to the side of the calendar that will give your “sensory” child options of what you might do when during your free time. Be sure to write in the things that will hard for your child so the expectation is set and they will be prepared to be successful.

Take some of the stress out of the holidays for you, your family and your “sensory” child. Create a few simple supports to prepare them for new routines, to set expectations for frequent visitors and more social interactions, and to make holiday travel successful. Happy Holidays!

Carolyn Dalgliesh is the owner of Simple Organizing Strategies and Systems for Sensory Kids. She can be reached at Carolyn@simpleorganizingstrategies.com or (401)413-2811.

 

Welcome to New Members

March 11, 2011 in Around the Site, Featured by Admin Dawn

Gail Curran: Gail works at the Arizona Centers for Comprehensive Education and Life-Skills. Are you in Arizona? Look Gail up!

Achieve Beyond: Achieve Beyond specializes in nationwide pediatric therapy and autism services for children ages 5 and under including states like California, Illinois, New York, Virginia and Conencticut. Achieve Beyond uses a family focused approach in providing early intervention speech therapy, occupational therapy, physical therapy, ABA/autism therapy and psychological counseling. We strive to serve our patients and their families by providing services and evaluations support in their predominant language, at both the home and community settings. We also offer private pay / insurance services, educational workshops for parents and therapists as well as translation / interpretation services at several of our branches.

Denise Moberg: Retired from 30 years as an SLP in the public schools. Currently have a part time private practice.

Kyra: I am a stay at home mother of 4 kids. 2 are Special Needs. My 7 yr old has ADHD, Auditory Processing Disorder, Sensory Modulation Disorder, and Dyspraxia (the last 3 are very new to us). My 2 yr old has Apraxia and Sensory Modulation Disorder. My other 2 kids are just in special need of special attention. I am on a leave of absence from school right now so that I can get a better handle on my family and concentrate more on them than me.

Julie Fick: I am a full time mom to my son who has DiGeorge Syndrome. We live in Woodstock, GA.

Alisa Ricketts: I have been married for almost 20 years and I am a SAHM of two teenagers, one of whom is a special needs child.

Patricia: I have a 7 yr old with odd severe, conduct disorder, ocd tendencies, generalized anxiety disorder, separation anxiety disorder severe

Ayoca Freeman: I have two beautiful daughters; their ages are 8 and l year old. My oldest was blessed with an extra chromosome better known as Trisomy 21, one of the types of Down syndrome.

Jennifer McMahan: Mom to 2 beautiful daughters. The youngest one has Dravet Syndrome. I am actively involved as a volunteer in the IDEA League, the only organization that provides advocacy, support, education and research for Dravet Syndrome. Their website is http://www.Idea-League.org. It is my goal to help raise money for research as well as educate the public on this very rare syndrome.

Amanda L.: Mommylebron is the slightly diabolical leader of Lefam (just don’t tell LeDaddy, he thinks he’s the leader, riiight). She is a snarky & sweet mom on a mission! Once she attains her goal of world domination she will educate all its poeple on pediatric mental illness and erradicate stigma. All while wearing a really cute apron. This domestic diva, kitchen queen, laundress extraordinaire also enjoys writing, reading, movies, scrap booking, word puzzles, kiddie cuddles, wet kisses, big brown eyes……Oh, and, during her “on time” she molds the only-slightly-less-diabolical-minds of 4 year old’s (aka preschool teacher).

Stephanie LeMieux: I have a boy with HFA and Tourette’s

We Were In Real Life

March 9, 2011 in Featured, From Julia by Julia Roberts

Rody, Our Mascot!

One of the important things about this site is the connection. Connecting with others who can relate is by far one of the best things about coming here and sharing. Here, you can support and be supported. We love to see people talk in the groups and help each other.

One of our 2011 initiatives was to bring that connection to life by hosting small events. Atlanta seemed like the logical choice and so we set out to plan. We knew we wanted it to be educational. Casual. Affordable. We didn’t want it to start to early or end to late. We talked about future childcare options. Large locations, central to Atlanta. Again, affordability. We ended up settling on a 3 speaker format and the theme of Relationships. Personal, medical and educational relationships and navigating them better in a special needs world.

I’m proud and happy to say our inaugural IRL event in Atlanta was a huge success! Thank you to our sponsors that made it affordable for attendees ($15) and muffins and lunch were deliciously provided by Babette’s Cafe.

Presenting sponsor: Celebrate Calm

Additional sponsors: Hewlett-Packard, and Spin Master

How do we define success?

  • Everyone moved in from seats around to gather for lunch to talk.
  • Everyone loved the format of speakers then lunch then speaker then an hour before we left for the day.
  • Everyone asked when the next one was going to be held.
  • Everyone asked to be put on our mailing list.
  • Many people hugged when they left.

We hope to bring this type of event and others to other cities where we have members. If you think you’d like to have one in your city, let us know! With Dawn in Ohio and several community members there as well, it’s the next logical location…and of course, BlogHer! But that’s another type of event altogether.

Thanks for letting us create a different kind of community. One where we can grow and learn from each other and one where we can figure out what kind of community we want! Thanks Atlanta!

 

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