Luppie Lesbian

Society EN ↓ 208 episodes

Life of a Lesbian Woman living in a Pre/Post Pandemic with Lupus/Fibro. I love to spill the tea on Lupus, Lust, Love, and living as a Differently-abled Woman of Color during a Pre/PostPandemic.🦋🦋🦋🦋❤️❤️🏳️‍🌈🏳️‍🌈

Author

Luppie Lesbian

Episodes

Having Lupus is not your fault! 05.07.2026 10:02

The title says it all.🫶🏿🫶🏿🫶🏿

I am putting the phone down, getting off of social media and going out in the big beautiful 🌎. People want to see you. We are warriors one minute at a time. 05.07.2026 25:07

I promised myself that no more living on phones. When I am able I am going out. Life is not a dress rehearsal. 💋💋🌈🌈🌈🌈. Do small things until they become big things.

I am not delusional loving a MOC women. Femme women who are into MOC women whole heartily love them. This is one trend or narrative that I am in no agreement with. 29.06.2026 14:25

I have loved MOC my whole life and I am not delusional. We should celebrate the diversity in our community. Ladies you are loved just as you are.💋💋

Should you tell a friend that it's friends only when you are not interested. We are going in a rabbits hole. 29.06.2026 17:33

Piggy backing off of friends in relationships🌈🌈💋💋

Who told you that you can't have intimacy if you have any Autoimmune disease...well they lied!😉😉 27.06.2026 17:07

It is absolutely possible to have one active love life and have Lupus. You will have to navigate some things but yes it is doable! Yup I said it without telling my business😵‍💫😵‍💫🥴🥴🤣🤣🤣🤣

Please do not tell people how to grieve!!!! 27.06.2026 12:13

Let people grieve!!!

Medicare will cover certain GLP agonist starting July 1. 27.06.2026 9:47

If you are on a GLP currently and on Medicare with part D talk to your primary to get on the Medicare GlP bridge gap program to pay the reduced program rate of 50 dollars.

If you have more than 1 autoimmune disease which one right now is giving you a hard time? What do you think will help? 27.06.2026 12:16

Haging multiple autoimmune diseases I know exactly which one is aggravating me...ugh🥴🥴🥴🥴

Some fun facts about me🤣🤣🌈🌈💋 26.06.2026 17:05

Here are questions I have compiled from my different Social Media spaces. Here are the answers!!!!

In order for you to have a relationship do you have to be friends first...🤔🤔🤔🤔 16.06.2026 22:45

I could never imagine being in a relationship and not being friends. How how 🤔 ❓️

Navigating multi autoimmune diseases you will need Ɓoundaries. I truly believe in boundaries🫶🏿🫶🏿 14.06.2026 24:20

Boundaries keep me sane not guessing. With Autoimmune diseases it can change from day to day so my boundaries keep me in ✔️ check.👂🏽👂🏽👂🏽👂🏽

Can you have more than one Autoimmune disease? Yes you can let's talk about Sjogrens 🤔 14.06.2026 23:36

Sjogrens is another Autoimmune disease. 👂🏾👂🏾👂🏾👂🏾👂🏽👂🏽👂🏽

Who told you because you are disabled you can't date. Well that's a lie!💋 13.06.2026 14:44

We are dating in 2026 and beyond. 💋#disableddating

Having an Autoimmune Disease does not mean you cant date. Who told you that???👂🏾👂🏾👂🏾💜🦋 23.05.2026 8:08

Dating with an autoimmune disease can be challenging, but you deserve love also. I want to tell you my take on dating. We all deserve ❤️ love.

Thank you for the 5000 listens on mutiple platforms. We are Lupus Strong💜💜🦋🦋 06.03.2026 7:09

This is just a short thank you from me thanking you all for the 5000 listens. I am just a Lupus warrior who does not want anyone to think they are alone fighting this insidious disease alone. We are warriors🦋💜🦋💫

Welcome to the Lupus Community.🦋🦋🦋🦋 06.01.2026 11:35

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.💋💋💋 28.11.2025 34:36

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!!!🫶🏿🦋💜 27.11.2025 19:41

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 27.11.2025 20:23

After a longggggg break I am back. #Lupuswarrior

You are not alone on your Autoimmune Journey. 10.07.2025 17:32

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.💥💥💫💫💫 12.06.2025 12:00

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. 🦋🦋🦋🌈🌈🌈🌈🌈 09.06.2025 26:53

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♥️🦋♥️🌈 09.06.2025 14:18

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! 30.07.2024 11:06

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.🤦🏾‍♀️🤦🏾‍♀️ 24.07.2024 16:48

I will dish the tea on this topic!!!