Slightely Maggie

Maggie shares her experiences of Ehlers-Danlos Syndromes awareness month and how her dissociative identity disorder alters are preparing for their first season of Pride in almost ten years. Processing leaving the Mormon church and how that is affecting her views about Pride this year.

In a long-awaited update, Maggie shares what it is like to time share one body with over 100 personalities.

So many changes coming down the line, I don't even know where to start! Join me on Friday 3/18 for a big surprise!

Maggie rants about her ROHO cushion and NuMotion and shares her recipe for Berry Sweet and Sour sauce as well as her adventures with her new KAFOs.

She is also asking for input on her hair!

Maggie describes the paradigm she is in with The Church of Jesus Christ of Latter-day Saints after almost 9 years of membership and then gives health advocacy updates about her KAFOs and sleep study. Hear about her adventures with developing recipes for these last two weeks and how they relate to a jam jar and a can of cider!

Maggie starts a new format, recording on video as well as audio. Simultaneously publishing on YouTube for accessibility and to enable her audience to check out visual elements. Added to advocacy updates is a recipe Maggie developed this week: Air-fried Mushrooms.

In the season 2 opener, Maggie catches everyone up on her ongoing projects and the accident from July in Paratransit as well as what happened with Strangers No More.

Maggie explores the healthcare advocacy work she endured through the summer that is extending into September, as well as her preponderance of social media friendships.

In her longest episode ever, Maggie updates several aspects of her health and self-advocacy efforts

Maggie catches you up with her health struggles in the month of June as well as a possible diagnosis.

Maggie wrote a quick poem about the goals she has, then she shares a dream she is working towards. All inquiries are welcome in making that dream come true.

For day 22 of MyEDSChallenge, a social media challenge that has been exhausting, Maggie shares her most vulnerable and proudest moment.

For day 18 of MyEDSChallenge, we are implored to give some advice to parents. This is a bit from me.

Many signs of my neurodivergent childhood are discusses. As is the reason for a lack of understanding about my struggles.

Although I've known I was neurodivergent for years, having been diagnosed with ADHD in my 30s, I received an additional diagnosis this week I want to share with you.

Stay tuned after Maggie gives the 411 about her most recent injury, for the results from the hearing that inspired this podcast!!

A letter, with a significant date was received a couple of days ago. What that letter could allude to has Maggie pondering and Googling.

Headed to the doctor today to check on some things. I share a few things I learned there. Ehlers-Danlos Syndrome, gastroparesis, and biliary colic are some of the things discussed.

In this podcast, Maggie opens up about her chronic pain and what having a right upper quadrant pain crisis has delayed her life.

On the day I was planning to record a video about how excited I am to have my rehabilitative power chair, I was met with professional ableism. I do not abide with shame.

Ever wonder what Maggie Slighte's Sundays look like? Well, here's a great description!!

Looking back at some of my previous life choices over the past few decades, and realizing when I need to request help. And then following up!

Yesterday, I started a podcast. Today, I share some details about some of the things we discussed yesterday!