Advertise on podcast: Luppie Lesbian

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Life of a differently-abled Lesbian Woman of color living with Lupus/Sjgournes and other autoimmune illnesses. In my podcast we will talk all things from. Lupus Lesbian spilling the tea on ♥️💨relationships while being disabled.💋 Dr's appointments Navigating the medical world You will hear how I use my tool box of ideas to navigate staying connected to this earth.. staying happy..finding love in me and others. So please come along it's going to be a great ride....Love you guys...thank you in advance.💋💋💋

Podcast episodes

Check latest episodes from Luppie Lesbian podcast

Welcome to the Lupus Community.🦋🦋🦋🦋

2026/01/06

Let me reintroduce myself and welcome the Autoimmune Queens/princesses and Kings to our community. 🦋🦋🦋🦋🦋

Do you have a type...Date them all until you figure it out.💋💋💋

2025/11/28

Lets talk about Lesbians and dating. Do you have a type? Do you you adhere to dating them all until you make a decision on who suits you. You dont need to be alone. Have fun life is short.💋💋💜💜💜💜💜💜💜💜💜💜💜💜

Its time for you to get up and live. I say this because I had to do it. Girl get up!!!🫶🏿🦋💜

2025/11/27

After months in my bed, sick sad depressed I got up. I did it sad mad upset alone scared, but I did it. You will be isolated during this journey. However, know you can do it. #teamlupuswarrior

Luppie Lesbian is back🦋💜🦋 Happy Friendsday. I missed you guys.💋💋 #teamlupuswarrior

2025/11/27

After a longggggg break I am back. #Lupuswarrior

You are not alone on your Autoimmune Journey.

2025/07/10

You are not alone on your autoimmune journey. We are here. I am here.....

Lupus requires you to have things in place. If you stay ready you won't have to get ready.💥💥💫💫💫

2025/06/12

Yup I have lupus and her cousins. I am the auntie who will tell you bluntly this is not for the faint of heart but that you can do it. If you stay ready you do not have to get ready. 💥💫💥💥💥Love you more.

Let's talk about how I found out I had Lupus and the things that happened prior. 🦋🦋🦋🌈🌈🌈🌈🌈

2025/06/09

It was like any other day until I fell and that's when my mind started 🤔wondering Lupus can take years to get a diagnosis as you will hear. However, it will eventually be discovered. It is a very frustrating time to be sick and not know what is wrong. We are more than a diagnosis!!!!!!

Luppie Lesbian is back. I missed my Lupus Warriors. Let's talk about where I have been♥️🦋♥️🌈

2025/06/09

This is my first podcast since my new diagnosis of Sjogrens Syndrome. Life has not been the same since this diagnosis. However it picked the right one cause I am a fighter. So you get in here so I can spill the tea....ps.....you will make it♥️♥️♥️🌈🌈🌈🌈🌈🌈

Update on this Chemo!

2024/07/30

Yes some of us take Chemo for autoimmune diseases. It is working however, this week I have side effects.

My little take on family members who are negative towards you during and illness.🤦🏾‍♀️🤦🏾‍♀️

2024/07/24

I will dish the tea on this topic!!!

Update on my plastic surgery🤪😷🤦🏾‍♀️🤦🏾‍♀️🤦🏾‍♀️💕

2024/07/24

Update on my cryolesion removal from my face

As a lupus warrior you will be tested to make tough decisions.

2024/07/22

I am in a place to make tough decisions as my Lupus progresses. We all will have to make them.

Lupus and your skin….

2024/07/22

Lupus can attack anything even your skin always get it checked out. Let’s talk about Cryrosurgery which I had on lesions on my face.

Do you know when you are starting a flare?

2024/07/18

I can tell now when my body is off and going into a flare. We must pay attention to our bodies.

Here is a list of things to help you with a long long flare with a chronic illness.

2024/07/15

Coming back from this flare has taught me so much. I hope I am able to share with others how to stay in your home and stay safe as you deal with your flare