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Tuesday, May 24, 2016

Usborne Books Online Fundraiser: Shop For A Cause!

Last weekend we partnered with Usborne Books for a fundraising event at Coping With LM HQ in New Jersey and guess what! The event was a HUGE success!


 

Since the fundraiser was so successful, we have extended the event so ALL of our supporters can join the fun!


Be sure to JOIN our Facebook Event and SHARE with your friends & family, the more the merrier!


HOW TO SHOP:
Click here  to shop, and as long as you see Coping With LM, you are good to order! 
UBAM ships anywhere in the US, as well as worldwide to APO's. If you are outside of the US, please be aware that you will have to have your order sent to Alycia Nolen and then shipped out at an additional shipping charge, that will be determined by the package size and weight. If you have any questions regarding this, please feel free to send Alycia a message

*This event will close on Sunday May 29, 2016*


Sunday, May 1, 2016

Mother's Day Giveaway! (CLOSED)

Happy Mother's Day to all of our strong, beautiful and fearless Mothers! 
We applaud you for standing up, letting your voice be heard and trusting your instinct.
Now we want to treat YOU with a huge giveaway!

ONE random winner will receive:
  • #LuThelamb stuffed animal
  • Limited Edition Coping With LM Thirty-One tote bag 
  • You First Journal by Lea Michele
  • John Masters Organics Essential Travel Kit for normal hair
    HOW TO ENTER:
    1. Follow Coping With Laryngomalacia on Facebook
    2. Share THIS post on your Timeline
    3. Follow Coping With Laryngomalacia on Instagram 
    4. Comment below on this blog post
      (scroll down, do not comment on the Facebook/Instagram posts):
      -Your name
      -Email address
      -Location
      -Complete the following statement:
      I am a strong mother because...

      Terms:
      1. One random winner will be chosen on May 8, 2016 at 9pm EST via Random.org
      2. Winner will be contacted via Email provided
      3. Each mother may only enter once
      4. This giveaway is open worldwide
      5. This giveaway is free of charge to the winner, the winner is NOT responsible for shipping charges but may be subject to custom charges if the winner is international. 
      6. This giveaway is only open to mothers of babies with LM, TM and BM
      7. The winner will have 24 hours to respond to the Email providing her mailing address
      8. If the winner does not reply within 24 hours, a new winner will be chosen
      9. This giveaway is not sponsored by Facebook, Blogger, Thirty-One Gifts, John Masters Organics or Lea Michele.
      10. Happy Mother's Day and good luck!



Wednesday, April 27, 2016

You are not alone. We are here.

For many babies who receive the diagnosis of laryngomalacia it is simply noisy breathing. Usually no further medical treatment is required after the initial diagnosis. For their parents, laryngomalacia becomes a forgotten word as their baby reaches milestones, 
thrives and "out grows" the noisy breathing by his/her first birthday.
 
And then there is that very small group (1-5%) of babies who are diagnosed with life threatening laryngomalacia. Parents of these babies are thrown into a world of unknown.
They must cope with hospital stays, major airway surgery, other related medical conditions and lack of support, to name a few. Life is turned upside down all because of a congenital defect that was supposed to be common, benign...no big deal.

CWL Founder & President Stephanie Hueston with daughter Seraphina.

 
Parents of severe laryngomalacia babies often feel anger, fear, unsupported, overwhelmed and alone. Unable to connect with other severe LM parents because severe LM is so rare.
This is why Coping With Laryngomalacia, Inc. is here. To provide support, strength and education for families coping with laryngomalacia, tracheomalacia and bronchomalacia.
 
Our goal is so no LM Supermom has to sit in ICU, 
watching her infant struggle to breathe and think,
 
I wish I had someone to talk too.
 
You are not alone. We are here.
 
I know how it feels to sit in ICU. To have to breathe for my baby. To wish for support. To be angry that my child had to be in the "worse case we've ever seen" category.

I know because I was there.
 
Though the journey has been difficult, life changing and oh so overwhelming... 
 I will tell you this...the good follows the bad. 
Always.

Breathe Easy, Stephanie Hueston CWL Founder & President
#LuTheLamb CopingWithLM.org
Carrier: Moby® Wrap

Tuesday, April 19, 2016

Natalie's Story

The good follows the bad.

This is my pint sized powerhouse, Natalie. She turned 3 a week ago. She had a tough road like a lot of the little ones here. She had a supra done at 6 weeks, adjusted age 1 week. We had tube feeds, tons of meds, therapies and so on. It wasn't easy on her or us. We had good days and then it seemed like we took 20 steps back. 

Natalie, age 3.


I remember her being 9 months old and having to syringe feed her for days because she wouldn't eat. I just sat in the hallway crying. This group saved us and my sanity. We will always be grateful for you. Even though it felt like it would never end, things got better....slowly. We don't have symptoms now unless she gets sick. She no longer has anymore therapies or special instructions to help get her caught up on her milestones. She's ahead at this point! As bad as it seems, one day it will get better.
 I love my pint sized powerhouse! 
(She picked out this shirt. It's her favorite)

-Laryngomalacia Mom, Cynthia 

Thursday, March 24, 2016

Coping With Laryngomalacia, Inc. HONORED AS 2016 TOP-RATED NONPROFIT

For Immediate Release:
Coping With Laryngomalacia, Inc. HONORED AS 2016 TOP-RATED NONPROFIT 

GreatNonprofits.org Award is based on Positive Online Reviews

Port Monmouth, New Jersey (March 24. 2016) –Coping With Laryngomalacia, Inc. announced today that it has been honored with a prestigious 2016 Top-Rated Award by GreatNonprofits, the leading provider of user reviews about nonprofit organizations.






“We are excited to be named a Top-Rated 2016 Nonprofit,” says Stephanie Hueston, Coping With Laryngomalacia, Inc.'s Founder & President. We are proud of our accomplishments this year, including our very popular Breathe Easy Care Package Program. Since the start of the year, we have sent over 25 care packages from Texas to Australia.The care packages are a symbol of hope to our families. They are weathering a very dark storm, I know because I have been there. I hope that they find comfort in knowing they are not alone."


 The Top-Rated Nonprofit award was based on the large number of positive reviews that Coping With Laryngomalacia, Inc. received – reviews written by volunteers, donors and clients. People posted their personal experience with the nonprofit. For example, Jennifer wrote, “I was so thankful to find Coping with LM after my daughter's diagnosis. I learned so much about her condition and knew what to ask her doctors. I am thankful to know we are not alone in dealing with this.”

Hueston's daughter Seraphina-age 6- assembling care packages for her fellow Pint-Sized Powerhouses'.






While the Top-Rated Awards run through the end of October, Coping With Laryngomalacia, Inc. was part of the inaugural group to qualify for the year. In addition, they’ve been added to GreatNonprofits #GivingTuesday Guide—an interactive guide to top nonprofits throughout the years. Look for this near the holidays.

“Savvy donors want to see the impact of their donations more than ever,” said Perla Ni, CEO of GreatNonprofits, “People with direct experience with Coping With Laryngomalacia, Inc. have voted that the organization is making a real difference.”








#LuTheLamb has been traveling the world providing support, love and smiles to his Pint-Sized Powerhouses'.  


Being on the Top-Rated list gives donors and volunteers more confidence that this is a credible organization. The reviews by volunteers, clients and other donors show the on-the-ground results of this nonprofit. This award is a form of recognition by the community. 




Supporters painted their nails light blue for laryngomalacia on World #AirwayDefectsDay, July 10, 2015.


About Coping With Laryngomalacia, Inc. 
Coping With Laryngomalacia, Inc.'s mission is to  provide support, strength and education for families coping with laryngomalacia, tracheomalacia and bronchomalacia. Coping With Laryngomalacia, Inc. offers 24/7 online support, educational resources, worldwide programs, local meet-ups and more. Supporters can visit CopingWithLM.org for more information on laryngomalacia and how to help.
 

About GreatNonprofits.
GreatNonprofits is the leading site for donors and volunteers to find reviews and ratings of nonprofits. Reviews on the site influence 30 million donation decisions a year. Visit GreatNonprofits.org for more information.

Media Contact

Stephanie Hueston, Founder & President. CopingWithLM@yahoo.com

Wednesday, February 24, 2016

Together We Can Move Moutains

When Seraphina was born (six years ago) our family was thrown into a world of unknown. Up until her birth, we had no reason to think she would not be okay. So when our newborn was born-blue, breathing with a stridor and having significant retractions, we were shocked, lost and in need of support and education. It took five long weeks before we were able to finally get a diagnosis- laryngomalacia. This common, begin, condition was slowly killing our daughter and emergency airway surgery was needed. We spent the next two years living in and out of the hospital (New Jersey to Pennsylvania). Long nights in PICU, showering at the Ronald McDonald House and piles of medical bills became our new norm.
Throughout our journey with LM, I made a promise to myself- I would dedicate my life to helping others who have walked the same journey. I would do whatever I could to make sure no mother has to sit in ICU, watching her baby breathe and think, "I wish I had someone to talk to."

Coping With Laryngomalacia, Inc. is a 501 (c) 3 nonprofit organization, all donations- monetary or goods- are tax deducible. Everyday, CWL provides support, strength and education for families who are coping with airway defects such as LM because of it's generous donors. As an award winning, 100% volunteer organization, donors can feel confident in supporting such an important cause. 
 
Seraphina at age four months old recovering from airway surgery then at age six, thriving!
 

Want to help?
First, share this post- your share may be the reason why a concerned mother makes an appointment with an Ear, Nose, Throat doctor to see why her baby is breathing so oddly.

Second, follow Coping With Laryngomalacia, Inc. on Facebook, Instagram and Pinterest so you can stay up to date with how your donation is making a difference.

Third, read this (http://tinyurl.com/gvmsrpw) blog post on different ways you can help- from making a secure, tax deductible donation online (http://tinyurl.com/phnrrpa) to starting a blanket drive within your community, this post will inspire you and your friends to make a difference.

Lastly, know the symptoms. The most common symptom of laryngomalacia is stridor- noisy breathing. Difficulty feeding, poor weight gain, reflux, apnea and blue spells are also signs the baby needs medical attention. Most symptoms are present at birth and worsen with the following weeks.

Thank you for taking the time to read this and supporting a cause so close to my heart. Together, we can move mountains.

~Stephanie Hueston, CWL Founder & President.
CopingWithLM.org
CopingWithLM@yahoo.com

Tuesday, February 16, 2016

Penny's Journey With Laryngomalacia

Written by: Naomi, Penny's Mom.
 
When we started on this journey little over a year ago I didn't know just how hard it was going to be. I became numb from it all because it was the only way to cope with everything that was happening.

I fought to be seen by the hospital because I knew something wasn't right and I knew it wasn't mild laryngomalacia and that Gaviscon (reflux medication) wouldn't fix this problem like the doctor said it would.
 
Penny with her Breathe Easy Care Package blanket and hospital gown.
 

I'd turn away and my precious little baby would be gray and lifeless. Fast asleep as if she'd passed away. I'd hold her in my arms and rub her to wake her up, she'd gasp and be back with us again. It was the scariest time of my entire life. Hoping that each time she would
come around yet fearing that she wouldn't with each time it happened. 

The first time the doctors attached her to the monitors, I sat staring at the numbers. Terrified each time they dropped and the alarms would sound. I've never felt so alone as I did watching those monitors.


Feeding became torturous for both her and I. Each bottle I made up, knowing she'd gag and struggle, forcing her with each mouthful so she would stay strong. Pushing her till she'd had enough but still pushing her more because a mother is meant to be able to feed her baby. To nourish them. It's a normal, natural thing to be able to feed your baby yet I couldn't, she couldn't anymore.
 
Penny, in the hospital.
 

After so many hospital visits we were told she needed surgery. I was terrified yet relieved they where going to help her get better. 
She was only 8 weeks old when this was decided. When everyone else was enjoying there new babies I was searching desperately for reassurance that she would be okay.
Researching everything because I didn't understand all the big words they where using at the time. 

She started to give up and slept all day. Only waking for small feeds then sleeping again. In the end I was feeding her tiny amounts with a syringe and that's when I couldn't do it any longer and she couldn't cope any longer being forced to feed. She was tired out with it all.
The hospital decided to tube feed her. This was all foreign to me. 
It was so hard seeing her pinned down and tubed. Each time she screamed and it was a totally different scream than you ever hear your baby doing. It was heart wrenching. 

Surgery day came and it was like no other. Handing your baby over to anesthesiologist. Terrified that she would be OK. I'm not religious but my god did I pray that day. Pray that my beautiful baby girl would stay strong and fight and by god she did me proud that day. She's a fighter, my Penny.

When I was taken to her in recovery I couldn't even hear words that anyone was saying to me. They where speaking to me but i couldn't comprehend the information
they where telling me. All I could focus on was her and her screams of confusion and pain. Her chest was making an awful sound and she was struggling so needed oxygen. I held her in my arms tightly and never wanted to let go again. 

After a rough night she recovered really well but still struggled with feeding for a few months afterwards.  I didn't care how she was fed anymore as long as she was fed. 

She did all of her 'firsts' in hospital. First smile, first time she sat up, rolled, her first tooth. Even her first taste of food.  Instead of the excitement I sat and longed to be home as a family again. We missed Christmas and birthdays, I missed my eldest daughter incredibly. I was torn in half.

It was a hard journey getting her off the tube feeds. Starving her to make her hungry so she would eat. She was scared of people near her when she was eating because of all the tube changes. She wanted to be left alone and so would you wouldn't you after all she'd been through. But she did it and she became tube free. She absolutely loves food now. 
You would never be able to tell she was tube fed now. She made me excited just watching her. I longed to be able to spoon feed her but she just wanted to be left to it. 
After a few weeks she eventually let me and I felt like a real mammy again. I could feed my own baby again!

Penny, enjoying lunch!

We've still had reflux issues but she is getting there, she is strong and she is a brave baby. She is the toughest baby I know and on days where I don't feel strong I look at her and she makes everything perfect. 

She still struggles at night and can't settle and has a terrible tracheal tug but one day she will be completely over all this. I know this because she can do anything if she got through the past year and I certainly couldn't have got through this last year without her.