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𝕄𝕒𝕪𝕒 𝕄𝕚𝕔𝕙𝕖𝕝𝕝𝕖

@mayaa.michellee

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EXTRA! EXTRA! Read all about it! 👀

A NEW ARTIST HAS ENTERED THE CHAT! 🎤

I can’t even begin to explain how excited I am to be announcing my debut as an artist! Definitely feel like I owe it to myself AND GOD(we’ll get into this later lol) to put the time and effort into this craft that I love so much. Out of all the things that I’ve gotten into, music has been the only constant. There’s no way I could go without it and I wish I was exaggerating!

I cannot wait to take y’all on this journey with me! Dying to share what I’ve been working on. Hoping to get something out to ya’ll REAL soon ❤️

LET’S WORK! You ready??!

xoxo -
Maya Michelle
——————————————————————
📸: @snappedbytia
💄: @myaxmuaa
💇🏾‍♀️: @mydastouchwigsllc

#musicartist #singer #ctartist #ctmusicartist #rnb #debut #mayamichelle by @mayaa.michellee

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a year ago

Good morning beautiful people! 💜🦋

Wow.. can’t believe it’s going on three years since joining in on the #WalktoEndLupusNow. It honestly feels like it just happened yesterday. In the past two years we, yes WE, have been able to raise over $1,600 towards Lupus research. WHAT?! I know, crazy right?
The amount of love and support shown doesn’t ever go unnoticed! I’m just happy we all can be part of the mission to find a cure.

This post is not only to invite you to join us on Sept. 26th, but to ask you to join our efforts in raising money and awareness to this mysterious disease. We’re currently sitting at $405 with a goal of $1200! I know we can accomplish that!

Please find the link to donate in my bio! Anything helps.. $5, $10, $25! Literally anything! If you’re unable to make a donation, I’d be happy to just see a familiar face walking with me. Please do not hesitate to ask questions! 💜🦋 Hope to see you soon!

Maya 💜

#lupus #sle #lupusawareness #ct taken in Lupus Awareness by @mayaa.michellee

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a month ago

Chronicles of a Resilient Lupie💜🦋 Episode: Good Riddance!

11 days post op!! IT’S A LONG ONE, but I promise it’s worth the watch. I tried to trim it down, but there was so much I wanted to say! 😂 So buckle in, get comfortable, because we’ve got some GREAT news! Thank God!!

Resilient Lupie out💜

#chroniclesofaresilientlupie #lupusawareness #sle #lupus #lymphnodes by @mayaa.michellee

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2 days ago

Soo.. I did a really cool thing! I was a panelist at the Connecticut Lupus & You Empowerment Conference!

If you know me, you know talking about my journey with Lupus has become second nature. I’m always happy to provide insight and love how sharing my story allows me to take my power back!

It was refreshing being in a room full of people who know exactly what it is you’re going through. Although, our stories are not the same, we’ve all lived the same struggle. From the continuous and seemingly never ending doctor’s appointments, hospital stays, and frequent bloodwork panels to the constant fatigue, joint pain, and brain fog! We show up even when it’s extremely hard to, and that is what makes us ᴡᴀʀʀɪᴏʀꜱ.

I want to thank the @lfa_northeast for putting together such an amazing event! We left informed, inspired, and having built some new connections. I hope to see you all at the walk! Can’t wait for next year’s conference! 💜🦋

#lupusawareness #lfanortheast #sle #lupus #lupusandyouempowerementconference by @mayaa.michellee

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4 days ago

AHHH! What is actually happening?!

Extremely ecstatic to announce that I will be a panelist at the Lupus & You Empowerment Conference! 💜🦋 Wow, wow, wowwww! Ahh, I’m so excited! 😊 If you want to learn more about what Lupus is, how you can support someone living with Lupus, or just want to build your own community, please attend!! I hope to see you there!!!!

This is a FREE event, but you MUST REGISTER to attend. Registration link can be found in my bio! Also feel free to comment “attend” and I’ll send the link to you directly💜

Details:
🗓️Date: Saturday, July 18th
🕙Time: 10am-2:30pm
📍Location: UConn Health - Rotunda
Address: 200 Academic Way (Parking - Academic Lot A4), Farmington, CT, 06030 US

#lupusandyouempowermentconference #lupusawareness #connecticut #lupus #sle taken in UConn by @mayaa.michellee

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24 days ago

Good eats, great vibes, and better company 🫶🏾 — Quick(not really) road trip 🚙 with the girlies this past weekend! Charlotte owes me nothing but some sleep! Why didn’t y’all tell me Charlotte was that fun? taken in Charlotte, North Carolina by @mayaa.michellee

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a month ago

Better late than never I always say.. I promise I won’t make y’all wait this long next time🤣🫶🏾

As always, I want to thank @tunesummit for creating a space for artists of all backgrounds to come together and share their art. Thank you for holding space for us to create freely, openly, and unapologetically. We need more spaces like this, ESPECIALLY here in CT, my goodness!

#mayamichelle #connecticutartist #ct #aspiringartist #jazminesullivan by @mayaa.michellee

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a month ago

Man.. if 13 y/o Maya could see me today, her jaw would be on the floor 😭 This may not seem like much to some, but baby, we’ve come a long way! When I tell you, I used to walk on stage, smile, and patiently wait for my cue? Mmmmmyea. I don’t think people realize how hard it is to get in front of people and be comfortable owning the space. ESPECIALLY being the shy and introverted girl.

Nowhere near where I want to be.. there’s still so much to learn and so much to be done.
🫶🏾
#tunesummit #mayamichelle #singer #stagepresence by @mayaa.michellee

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2 months ago

LUPUS FOG + social anxiety is a TERRIBLE combo 😭 I can’t tell you the number of times I’ve stumbled over my words… EMBARRASSING AHH😭😭

Did you know that 70-80% of people with Lupus experience brain fog at some point in their lives? If you have instances of not being able to think clearly, issues with memory, or stumbling over your words, you might be experiencing “brain fog” or “lupus fog”. You aren’t alone! Be patient with yourself and have a laugh!

The more you know!💜🦋

#lupusawarenessmonth #lupus #lupusfog #autoimmunedisease #brainfog taken in Lupus Awareness by @mayaa.michellee

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3 months ago

MAY IS LUPUS AWARENESS MONTH! — prepare to be sick of me 💜🦋

All jokes aside.. this is quite literally why this disease is known for being an invisible disease. When you present well, no one knows that your body is constantly attacking itself. No one knows that you’re quite literally in a fight with your own immune system! So to that I’ll say, “just because we may carry it well, does not mean that it isn’t heavy”…

Happy Lupus Awareness Month! 💜🦋
#mayislupusawareness #lupusawareness #lupus #lupie #autoimmune by @mayaa.michellee

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3 months ago

❤️ by @mayaa.michellee

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3 months ago

Y’all ready for this experience…❕✨
Tune Summit Pt 2 Showcase spring show is now here check out our reel 😊 thank you everyone that came out to support TUNE SUMMIT 🗣️stay tune for more…
#tunesummit #explore #recap taken in New Haven, Connecticut by @mayaa.michellee

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3 months ago