Chronically Ch(ill)🎙️

Official Twitter Account for the Chronically Ch(ill) Podcast 🎙️

[Chronically Ch(ill)🎙️ @ChronicallyChll]

Meet the faces of the #chronicallychill #Podcast 🎙️!

@alove_1980 @LingMendoza00 @LordBeeBrain @jazmen829 @bigjazz_724

Check out their bios on the official site (link in bio)

[@[email protected] @Imani_Barbarin]

What people don’t realize is that even prolonged use of mobility aids can disable you further (not the way the Ableds think).

Like I’ve been displaying signs of arthritis in my hands and shoulders since I was 25 because I started using crutches at 5.

[Candace D. @DiaryofaSickGrl]

If you can’t even spell my illness or give me a quick summary of what it is you DEFINITELY shouldn’t be giving me advice about it.

[ThePOTSPostman @ThePOTSPostman]

Things you shouldn’t say to someone who has chronic illness.

"People your age don't get that sick”

"It can't really be that bad”

“You are just being dramatic”

“If you just stopped thinking about it, it would go away”

What else do you hate hearing?

[Brain Ablaze @BrainAblaze]

One can still be disabled but not qualify for disability benefits. #EpilepsyAwarenessMonth #NEAM

[Jasi ❤️🔱🖤 @JasGetsCrazy]

Proud of myself for not letting this drag me into a depressive state. I'm too antsy to go back to bed, though.

[@[email protected] @Imani_Barbarin]

Just a reminder that disabled people need rides to go grocery shopping, doctor’s offices, to the bar, to the cafe���not just to cast a ballot that impacts you.

[Chronically Ch(ill)🎙️ @ChronicallyChll]

Due to recent events, the members of the Chronically Ch(ill) Podcast will be taking an undisclosed sabbatical to regroup.

We promise we won't be gone for too long!

Until then, everyone be safe and be blessed! 🙏

[LGS Foundation @LGS_Foundation]

Today is International LGS Awareness Day™! 💜

Join us as we shine a light on #LennoxGastautSyndrome (LGS), a rare and severe form of #Epilepsy. By spreading awareness, we can support families affected by LGS and work towards better treatments and understanding.

#NeuroTwitter

[Daphne Ward @MeandEpilepsy]

#epilepsyawarenessmonth

[Chronically Ch(ill)🎙️ @ChronicallyChll]

@seizedandshaken @jazmen829

[Chronically Ch(ill)🎙️ @ChronicallyChll]

From our very own, Jeanie 💜💜💜
#EpilepsyAwarenessMonth
#EpilepsyAwareness
#ChronicIllness
#Seizures
#Epilepsy
#ChronicallyChill #Podcast

[𝓙𝓮𝓪𝓷𝓲𝓮✨💋♒️♍️♋️♥️✨ @alove_1980]

It has now been 16 yrs since being diagnosed with #epilepsy. Being diagnosed later in life was a shock and also a challenge I wasn’t ready for. I love being able to help others learn more about epilepsy because I’m still learning as well. #EpilepsyAwarenessMonth 💜✨💪🏾#letsdothis

[Chronically Ch(ill)🎙️ @ChronicallyChll]

https://t.co/8vSDo6zCxo

Episode 3 of The Chronically Ch(ill) Podcast is here!

“Me, My(self-advocacy), and I” can be watched now on YouTube!

Hope you enjoy! 💜🗣️🎙️

[Chronically Ch(ill)🎙️ @ChronicallyChll]

10 more minutes to go! 💜

[Chronically Ch(ill)🎙️ @ChronicallyChll]

Hey, everyone!

Chronically Ch(ill) Episode 2 drops Friday, 12am EST!

Catch the premiere here: https://t.co/RYNpsTm7OF💜🗣️🎙️

[Chronically Ch(ill)🎙️ @ChronicallyChll]

Hey, everyone!

Chronically Ch(ill) Episode 2 drops Friday, 12am EST!

Catch the premiere here: https://t.co/RYNpsTm7OF💜🗣️🎙️

[Han 🖤 @spoonfulofhan]

Controversial opinion (apparently):

Disabled people should be able to afford luxuries on top of just surviving. A new phone, clothes, the chance to go to a concert, etc. We deserve to live. Not just survive.

[Chronically Ch(ill)🎙️ @ChronicallyChll]

WE'RE LIVE!!!

https://t.co/ilMw6jQO6s

[A Chronic Voice @AChVoice]

“I think the most frustrating part of living with fatigue, is that people don’t get it..But my body doesn’t work like that, sleeping does not give me energy back, I don’t wake up with full energy again": https://t.co/giAxp7pXUw by @bloomingmindxx #ChronicFatigue #InvisibleIllness

[Epilepsy Scotland @epilepsy_scot]

.Our volunteer Dave, recently had a video telemetry stay at the Clinical Neurophysiology Department, Royal Infirmary in Edinburgh. He kept a diary of his experiences.

You can read part one of his diary on our website: https://t.co/h9hHjFLPZx

#VideoTelemetry #EEG #Epilepsy