Arizona

I live in Phoenix and I have a 24 wkr. He's now 17 mos old. Email me if you'd like to chat!
Stephanie
Oh, his name is Christian and his website is www.geocities.com/s_lynne_flores/Christian.html
 

Hi. I have a 30 weeker who is now 7. I was looking for a local branch in Yuma, and I can't seem to find one. I'm at cdominguez@yumaregional.org.

Hi. My name is Kelly Winter. I am not a mother, in fact i am only a highschool senior, but I have recently found a deep passion in myself to work to support the March of Dimes. I am a president of my highschool chapter of March of Dimes and last year we worked our tails off to raise 18 some thousand dollars for the MOD but this year have set our goals even higher (22,000!). Basically i REALLY want the about 50 students who have applied and volunteered for the March of Dimes Club to have a real reason and understanding of WHY they are raising this money for March of Dimes and who it is truly for. I think the most powerful way to get this message and importance of the march of dimes across to them is through a true life story. An amazing thing i would just be filled with joy to see is these kids who volunteer to fundraise and work, to finally really get it, to know what they want to work for and maybe in return feel more impacted and thus PASSIONATE for the cause, so that even more money can be raised to add one more success story on this site. Please consider if you or someone you know could find it in them to share their so personal story or testimonial with my highschool march of dimes club. I understand it is something possibly very difficult i am asking for someone to do..
    I go to Shadow Mountain High School. (32nd Street and SHea Blvd) And we would love to hear a testimonial anytime someone is ready to share it with us, however i think the first meeting SEPTEMBER 15, 2005 would be most productive so we can work all year with a new found purpose and raise more money for the march of dimes. Please call me if you are considering helping us in this way, have questions, are worried, anything! 602-859-4457 Again my name is Kelly Winter. thank you and god bless you

Kelly-

I would be happy to share our story with your group. My baby was born, April 19, 2005, 10 weeks early at 2lbs 3 oz and spent 47 days in the NICU.

D'Arcy

let me know if anyone would like to chat or get together. my daughter has low muscle tone, constipation, genetic issues, acid reflex, and a small head. she is having a bronchoscopy and another swallowing test done. please let me know!!

Joslyn,
Hello! My name is Holly and I live in Phoenix and would love to chat with you. My son is a 33 weeker and is doing pretty well he just has an acid reflux problem. Let me know if you would like to chat with me.

Holly

hi holly, this is joslyn's mom. my name is tina. im so glad i finally met another mom on this site that is close by. sorry if it took me a while to write you back. still learning about the site.
email me. would like to talk. tgunsolly@cox.net

tina

phone number removed for safety

Hi My name is Kimberly,
I had 32 weeker identical twins three weeks ago yesterday. My husband and I are both military, and it has been hard on us traveling back and forth to tucson. We couldn't stand having them so far away.

Angie has been home for a week and we are finally getting a schedule down. Alaina comes home today, and I am ready.

If any one wants to talk let me know.

Hello Kimberly,
My name is HOlly and I had my son in August at 33 weeks. If you would want to talk to me let me know. I am so glad to hear that your twins are home now, it is so rough when your baby is not at home with you I know that it was really hard for me.

My email address is hobear456@cs.com

Holly

My name is Stephanie and my kiddo, Christian, is now 21 mos old (former 24 wkr). I'm here to share his story and talk to other moms! I volunteer for Raising Special Kids (an Arizona based group) and also March of Dimes Parent to Parent. I go back into the NICU (never thought I'd volunteer to do that once we left, LOL!) and talk with parents who's kiddos are still in the NICU. You can read all about my kiddo at his very own website, www.miraclechristian.com.
Stephanie

hi mesa mama!
my name is tina and i have a daughter who has problems. her name is joslyn. tomarrow the 28 of nov. she has a bronoscopy done at phoenix childrens. this will determin if she still needs the ng tube or g tube or surgery for acid reflex. i have a special person at raising special kids that calls to see if im ok. her name is carol. let me know if you would like to chat. thanks!!

Hi my name is Brenda I live in Tucson I gave birth to my daughter June 4 2005. she was born at 29 weeks 6 days so 30 weeks less some hours. She weighed 3lbs 5ozs and 16 in long. She was in the NICU for 76 days. She is now 6 months and 14lbs yeah...I would like to hear from someone in Tucson.

Hi. My name is Cathy and I have a former 30 weeker who is now eight. My question is whether or not you are a part of Children's Health Services in either Phoenix or Tucson? They both have really great parents groups (Parent Action Council) that provide both support and education. Please e-mail me if you would like more information.

Cathy- cdominguez@yumaregional.org

this is joslyn mom, i just wanted to know if any one is in the raising special kids here in arizona? please let me know! they have a special day on april 1. just wanted to know if any one has gone to these special days before. im hoping to meet other parents there as well. thanks. tina

would like to have my family walk for march of dimes for arizona. how do i get info. on this? please let me know. thank you. tina gunsolly

Tina,
have you gone to the march of dimes website? If you go there is should be a big walkamerica logo, click on that. If not go to walkamerica.org if it's not org then it's com

Holly

Hi Tina! Thanks for your interest in WalkAmerica. Your participation is very much appreciated. That said, Holly's right. It's www.walkamerica.org.

best,

- James

I'm in Chandler and will be walking at the flagstaff location this year, if there is anyone who would like to walk with me or chat IM me or email me. Yahoo ID is Bailey24_owl, email is the same with @yahoo.com .

Hi , I am a mother of preemie , born 8 weeks premature . I would like to contribute in a my own small way to the organisation . I would like to know , where the walk America MOD starts, contact numbers , duration of the walk . This will help me to plan ahead , so that i can participate . My daughter is doing great . She is now 16 months and doing everything that babies her age do .

Saritha,

Go to www.walkamerica.org and you can register there. First you'll need to decide if you'd like to sign up as a family Team (that means your spouse, kids, parents, in-laws, friends, neighbors,etc as a group) or if you will be an Individual.

The second page will allow you to choose to
Join a team
Start a new team
Sign up as an Individual

From there, just follow the prompts and when you choose your local area, it will give you the location, time and distance. it will also set up your very own webpage which can take donations for your team or your efforts.

To find your local division office information:
go to www.marchofdimes.com
either enter your zip code
or search for chapters by state

Good luck on your Walk America efforts. It really is a special day.

Hope the helps,
Darcy

Hi there,
In March of this year my husband and I lost our first daughter, Amelia, when I was 19 weeks pregnant. We were crushed. All of the hopes and dreams we had for her were suddenly gone.

We decided to create a Family Team for the March for Babies which was held on April 18. This was one of the best decisions we made. We felt like we were able to do something for other babies in memory of our own precious angel.

I was also asked to join the Family Teams Committee for March of Dimes. I have met some amazing mom's in the group, each has a story that makes the mission of the March of Dimes more personal.

We are working on a lot of great things for the next year and we would love your help! July 18 the Phoenix Mercury is hosting March of Dimes Day; the awards ceremony for the Family Teams will be held at the game. We are also planning "Picnic in the Park" in November.

If you are interested in joining the AZ Family Teams committee or in creating your own Family Team, please contact me! We would love to get to know you and hear your story.

Please also look for us on Facebook (MOD Families Arizona)!

I look forward to hearing from you!

Michele

Hi Michele-

You and I lost our babies just days apart back in March of 2009. I hadn't met you at the time, but I think I remember seeing you and your husband hug and share a moment near the Family Teams Tent. I am just now rereading some of your blog posts. You should update with pics:) I'm glad to work alongside you in the FTC. I hope that you are doing well and look forward to another year of MOD fundraising!

Yes indeed, if anyone is interested in joining the FTC, we'd LOVE to have you. Meetings are held monthly at the Phx MOD office.

Lindsay

Hi AZ-

I am a mom to three preemie boys: 32 weeker (2005), 34 weeker (2007), and a 30 weeker (2009). My 30 weeker was born sleeping in the early morning hours of March 6, 2009. He weighed 3 lbs. 6 oz. and was 16 inches.

I was high-risk and knew the symptoms of preeclampsia all too well. I was seeing the same OB for all three pregnancies until the first week of Jan. in 2009. I was about 21 weeks along, going in for a routine appointment, and picking up my signed bedrest letter to give to my employer. I was hit with the most unfortunate and unexpected news I could receive. Due to the economy, and the fact that my OB hadn't invested, he was being let go from the practice! I was looking forward to delivering at a particular hospital and there was only one person at the time who had rights to deliver there. I asked if this person was good and was told yes. I think the opinion was skewed based on the goings on in the practice. Who knows?! Come to find out later, not so much experience with high risk and was in over her head:(

I had an unwanted transfer of care. I had two, yes, two prenatal appointments with my new OB in February. At my second appointment, I was 28 weeks along and I mention very seriously the swelling that was going on. No concern whatsoever. No looking at my chart to see the Dec. recommendation from the peri stating that "if your patient has not yet had a 24-hour protein screening," she should have one. This is STANDARD procedure folks! Didn't even have me come in the following week just to be sure. Nothing. I should've gone to the hospital then, but I didn't. For whatever reason, my next appointment was scheduled more than 2 weeks out. I never made it.

Two weeks later and 4 days shy of my next appointment, I call my OB to tell her my concerns of severe swelling and pain down below. She can't remember anything about me. Couldn't recall whether or not I was working, what I did for a living, anything! She tells me "it's still too early, drink plenty of fluids, rest, put my feet up, get help with the kids during the day, and to do some hydroptherapy if I belonged to a gym." About 6 hours later, I call her back and tell her that I'm going to the hospital and that something is very wrong. I wanted to urinate, but couldn't and I was shaking uncontrollably. I drove myself to the hospital nearly before midnight. My water starts to break on the freeway and I'm doing my kegels to keep it all in. As soon as I park and get to the sidewalk approaching maternity check in, my water breaks and I brace myself. A good samaritan runs to get me a wheelchair and takes me where I need to go. I'm talking incessantly to the nurses at the wait station about my medical history, my current gestation, what just happened, my OB's name (the good one and the new bad one). Stripped off my clothes and there's blood everywhere (wore black pants that night so didn't know the sight until it was before my eyes). Within minutes, a fetal heart monitor was brought in. No heartbeat. Completely devastated. I had a placental abruption coupled with a blood clot. I also had severe and undiagnosed preeclampisa!!!

It's just heartbreaking to go through something like this:( This Share site has been my saving grace these past 2 1/2 years. I miss my little boy terribly. I want very much to have a rainbow baby and "complete" my family, but it's a long journey and we're treading slowly. I am still very angry about our loss and getting those feelings out sure has helped.

If anyone ever needs to share, vent, or BOTH, I'm here to listen. I encourage you to post YOUR STORY, start a blog, and stay in touch. I've met so many wonderful people through this site and it's been helping me find my way as I journey through my "new normal."

One day at a time,

Lindsay

P.S. I happened upon Lanee's Legacy (www.laneeslegacy.org). This story was featured on Channel 12 news a few months ago. Her AZ organization makes memory boxes to be given to other parents experiencing infant loss.