ALD Connect . . . ions

There are many things I expected to discuss when we became part of the ALD community nearly two decades ago.

Bone marrow transplants? Sure.
MRI results? Absolutely.
Adrenal insufficiency? Unfortunately, yes. Sharing stories with a screen full of people about peeing myself in public? That one was not on my bingo card.

And yet there I was, with a bunch of ALD folks on the last ALD Connect mental health call — sharing stories, sharing tricks to masking pee stains, and in some cases — laughing with everyone until we all considered whether a quick trip to the bathroom might be wise.

It was perfect.

Not because urinary incontinence is glamorous (spoiler alert: it’s not), but because there’s something incredibly healing about being with people who truly get it. The ALD community has a remarkable ability to turn even the hardest, most awkward, most human experiences into moments of connection.

Nobody had to pretend. Nobody had to be cool. Nobody had to hide the realities of living in bodies that sometimes do unexpected things.

Instead, we laughed.

And beneath the humor was something deeper — safety. That’s exactly what this community has been for our family over the years – a safe place. ALD is heavy. There’s no way around that. But somehow, together, we are able to create spaces where we can all breathe a little easier, laugh a little louder, and feel a little less alone. In the last few months this ALD Mental Health call has included topics like Laughing Through the Leaks, In the Bowels of ALD, Carrying the Invisible Weight of ALD: Fear, Guilt and Resentment, Allowing Anger, Boundaries During the Holidays – Protecting Your Peace — all important topics, all raw topics and all difficult to discuss without feeling safe.

And now ALD Connect is encouraging more ALD connections — opportunities for people in the community to gather in person, share stories, and simply spend time together outside of hospitals, conferences, and Zoom screens.

Grab a sun hat, a bathing suit, and your fav summer shirt and join JackO for some summer fun!

Our family is excited to host one of those gatherings at our home on June 20th.

We would love for ALD folks who live in or near NJ to join us for an afternoon around our pool — eating food, sharing stories, relaxing, and yes, probably laughing harder than our bladders can handle.  Whether you’re a newborn screening family or a family with a beautiful boy with CALD or someone who has lost a loved one to ALD/AMN or a man or woman with ALD/AMN – all ALD folks are welcome!!! And, our house is comfortably accessible for any who may have mobility issues.

No perfection required — just people showing up exactly as they are. Which, in my experience, is where community begins.

Love, Jess

At the end of the mental health call, we always share a guided meditation. Here’s a bit from this month’s script:

Because community is not built through perfection. It’s built through honesty. Through vulnerability. Through laughter… Life is heavy sometimes, but laughter lightens the load. And community reminds us that we never need to carry it alone.

It’s not easy bein’ BLUE

It’s not that easy bein’ green
Having to spend each day
The color of the leaves

When I think it could be nicer
Bein’ red or yellow or gold
Or something much more colorful like that

Kermit the Frog

It’s not easy being BLUE either.

ALD makes a lot of people in our community blue. It’s a disease that effects 1/17,000 people worldwide and causes symptoms including adrenal insufficiency, loss of vision and hearing, learning disabilities, seizures, loss of speech, fatigue, bladder and bowel issues, loss of mobility, and if not treated early (** and without a certain amount of luck) can lead to death.

While there’s so much to make us all blue, there is reason for our community to celebrate.  ALD is a disease that has made some HUGE strides in the last few decades – improved treatments, new treatments, and newborn screening. The momentum is has started and we can’t let it slow down.

A year ago, my friend – and ALD warrior, Janis Sherwood, – had a magical idea. We always discuss possible ways of how the ALD community can better spread the word about our disease. Blue being the color connected to leukodystrophy awareness, Janis’s plan was — ALD Makes Me Blue. She wanted to turn our ALD blues into ALD BLUE — Dye our hair BLUE, paint our nails BLUE, wear BLUE, paint our whole darn bodies BLUE. She wanted our community to turn BLUE and then pass it on, like a dare. 

Janis didn’t stop there with her plan. She wanted to have a way for the public to learn more about ALD and even make a small (or HUGE) donation to one of the many ALD organizations.

ALD organizations connected. A website was created. ALDMMB got itself onto social media. Some sore of fancy filter was put on Instagram: https://www.instagram.com/ar/538958721328767/

Today is the day!!!

February is Rare Disease Month and it’s time to turn the world BLUE!! Our family is going to start our month of BLUE and we want you – our duct tape – to do the same. Make yourself BLUE and don’t forget to take a photo and post it on Facebook and/or Instagram and TAG friends!!! 

Please take a peek at the site, learn more about ALD, be BLUE, and make a donation.

CLICK HERE — ALD MAKES ME BLUE

GO BLUE!!!

Love, Jess