Dragonflies for Hope

Dragonflies for Hope Epilepsy and Autism support for families and caregivers. Feel free to reach out! You can either conta

We are committed to providing resources for epilepsy patients and their families. Also to promote awareness and understanding of chronic diseases of the brain.

02/03/2023

International Epilepsy Day 2023 is Monday February 13th encouraging others to !

Epilepsy stigma exists in all cultures, impacting educational and job opportunities, and social acceptance.

Stigma is found throughout several communities globally due to lack of medical knowledge.

Make your plans now to join the global effort on Epilepsy Day. Downloadable resources are available at: https://internationalepilepsyday.org/resources/

International Epilepsy Day is a joint initiative of International Bureau for Epilepsy and ILAE - International League Against Epilepsy.

02/03/2023

Jon shares his experience as a caregiver to his daughter who has epilepsy. Read about their family's time learning about epilepsy, balancing self-care, & more.

11/19/2022

I know I have posted this before but it is such a perfect way to explain how overwhelming and exhausting it is sometimes.
This is all the things we feel every day but never say...

Here's what most people just can't understand about being the parent of a child with extra needs...
We are never honest with you.
Not all the way.
It's nothing personal.
It's not for a lack of trust in you.
It's not because you did anything wrong.
It's because we are certain you won't understand.
And that's okay.
We don't expect you to...not fully.
See, when a parent of an extreme child says "I'm tired," what we really mean is that we absolutely cannot anymore.
We have nothing left.
We are a brand of exhausted they don't even have human words to adequately describe.
The idea of self-care feels hilarious to us.
Not because we mean to diminish your hair appointment or long run, we want that for you.
But because it can legitimately take DAYS for us to relax enough to begin to breathe normally, much less actually recharge who we once were as human people before extreme parenting.
Our kids remain our greatest gift.
We love them with a ferocity many can't fathom because we HAVE to fight for them.
For their accommodations,
For their meds,
For their appointments,
For their equity,
For their basic human rights.
And we might share that side with you, friend.
Because most parents can understand and support another mama's desire to advocate for her kids.
But the fight at home, when everyone else is riding bikes and enjoying popsicles on the sidewalk this summer, those are the things we don't fully share.
Because it can be ugly,
And messy,
And scary,
And shameful.
It shouldn't be.
But it is.
Because so few really 'get it'.
It is rare to find another human who lives every minute of every day 'on' because if they rest--even for a second--it could mean danger for their child or someone else.
Maybe our kid is lower functioning so they risk a fall or exploring an outlet with a fork.
Maybe our kid has behaviors so they may become impulsive and things get broken.
Maybe our child is emotionally disregulated and they can cause harm to themselves or others.
Maybe our child's anxiety gets triggered and their reaction is so loud we are in constant fear of a call from the police or DCS or our landlord.
No matter what our specifics, we NEVER fully rest.
When our kids aren't with us, we exist in a sort of paralyzed sense of fear for when they may need us or the phone might ring or something may happen.
Friends, it is exhausting in a kind of way we don't share because we truly don't expect you to understand.
But even without really living it, you can be kind.
You can offer an ear (without judgement).
You can come sit with our kids so we can shower or nap.
You can send a coffee gift card or a text of support.
You can hold our hand while we cry and sit in the silence with us.
Because this life isn't what we chose,
Its not what we expected,
Its not something we'd wish on anyone
Or expect others to embrace,
But we also wouldn't trade it for anything.
Because as much as extreme parenting
Pains us,
Exhausts us,
Stretches us,
Pushes us,
Scars us,
Lies to us,
Convinces us we are failing,
We aren't.
Our kids, in all of their struggles, desperately need us.
No matter how many times our extreme children yell hurtful things, thrash and throw stuff, or insist they hate us, they don't.
They will continue to come back to us because we are theirs.
And mamas, that is sooooo hard.
It's so tiring.
It is endlessly maddening.
But it is ours.
And we're in this life together. 💜
-B.
Credit: The Mama On The Rocks

Nothing worse than the sound of crashing and hitting the floor when your child has a seizure.
11/05/2022

Nothing worse than the sound of crashing and hitting the floor when your child has a seizure.

10/31/2022
Halloween is always so much fun for me. Unfortunately Nick doesn't remember any holiday, except Christmas, from year to ...
10/31/2022

Halloween is always so much fun for me. Unfortunately Nick doesn't remember any holiday, except Christmas, from year to year but that usually doesn't stop us from going out and getting some treats!
What are you Halloween plans? We would love to know!

10/31/2022
10/31/2022
Happy Halloween!!
10/31/2022

Happy Halloween!!

I always seem to forget how long ago we started this page. Until November rolls around and people start sharing our post...
11/08/2021

I always seem to forget how long ago we started this page. Until November rolls around and people start sharing our posts (thank you for that).

2013 seems like a life time ago, so much has changed, and so much has not.

We have definitely been blessed in a lot of ways, although seizure control is not one of those ways.

Long story short...we started Dragonflies 4 Hope not just to advocate and educate, but because we wanted to help. To make a difference no matter how small. To let people know that they are not alone..

In honor of Epilepsy Awareness month I would love to do a fundraiser. But it's extremely important to me that the money goes where it is going to make a difference so I am requesting your help..

There are a lot of non profits related to Epilepsy..

Which one is your favorite? Which one would you like to see the money go to? Which one do you think would benefit the most people?

Or do you know of a family that is struggling?

Please let us know!!! We would love to hear from you ❣️

Epilepsy and Autism support for families and caregivers. Feel free to reach out! You can either conta

https://onehopewine.com/event/417036bc-a4d7-454a-a904-c1ebe89aa193We have teamed up with One hope wines to do a fundrais...
03/29/2021

https://onehopewine.com/event/417036bc-a4d7-454a-a904-c1ebe89aa193

We have teamed up with One hope wines to do a fundraiser for the Epilepsy Foundation!!
All you have to do is ✔️ the link and shop!

ONEHOPE Wine is a world-class vineyard in Napa Valley that makes a positive impact on the world with every bottle sold. See whatʼs in store! Indulge. Do Good. Wine Not?'

01/18/2019

Sould be an exciting weekend. Full moon and lunar eclipse. Starting off with a bang. So far today he has had 3 generalized seizures... the worst was in Michael's while shopping. Results were a busted lip, bruised arm and broken glasses. Employees came over and offered to call 911, but luckily it stopped before that was necessary. One thing that you learn early as an Epilepsy parents. Never leave home with out the emergency meds!!!
Wishing everyone a safe and seizure free weekend. Full moons suck!!

Address

Atlanta, GA

Website

Alerts

Be the first to know and let us send you an email when Dragonflies for Hope posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Practice

Send a message to Dragonflies for Hope:

Share

Share on Facebook Share on Twitter Share on LinkedIn
Share on Pinterest Share on Reddit Share via Email
Share on WhatsApp Share on Instagram Share on Telegram