Luppie Lesbian

Luppie Lesbian

Society EN ↓ 219 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.πŸ¦‹πŸ¦‹πŸ¦‹πŸ¦‹β€οΈβ€οΈπŸ³οΈβ€πŸŒˆπŸ³οΈβ€πŸŒˆ

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Author

Luppie Lesbian

Category

Society

Podcast website

podcasters.spotify.com

Latest episode

Sep 28, 2026

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Episodes

Thank you for the 5000 listens on mutiple platforms. We are Lupus StrongπŸ’œπŸ’œπŸ¦‹πŸ¦‹ 06.03.2026

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 warriorsπŸ¦‹πŸ’œπŸ¦‹πŸ’«

Welcome to the Lupus Community.πŸ¦‹πŸ¦‹πŸ¦‹πŸ¦‹ 06.01.2026

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

Do you have a type...Date them all until you figure it out.πŸ’‹πŸ’‹πŸ’‹ 28.11.2025

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.πŸ’‹πŸ’‹πŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œπŸ’œ

Its time for you to get up and live. I say this because I had to do it. Girl get up!!!πŸ«ΆπŸΏπŸ¦‹πŸ’œ 27.11.2025

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 backπŸ¦‹πŸ’œπŸ¦‹ Happy Friendsday. I missed you guys.πŸ’‹πŸ’‹ #teamlupuswarrior 27.11.2025

After a longggggg break I am back. #Lupuswarrior

You are not alone on your Autoimmune Journey. 10.07.2025

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.πŸ’₯πŸ’₯πŸ’«πŸ’«πŸ’« 12.06.2025

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. πŸ’₯πŸ’«πŸ’₯πŸ’₯πŸ’₯Love you more.

Let's talk about how I found out I had Lupus and the things that happened prior. πŸ¦‹πŸ¦‹πŸ¦‹πŸŒˆπŸŒˆπŸŒˆπŸŒˆπŸŒˆ 09.06.2025

It was like any other day until I fell and that's when my mind started πŸ€”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 beenβ™₯οΈπŸ¦‹β™₯️🌈 09.06.2025

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 itβ™₯️β™₯️β™₯️🌈🌈🌈🌈🌈🌈

Update on this Chemo! 30.07.2024

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.πŸ€¦πŸΎβ€β™€οΈπŸ€¦πŸΎβ€β™€οΈ 24.07.2024

I will dish the tea on this topic!!!

Update on my plastic surgeryπŸ€ͺπŸ˜·πŸ€¦πŸΎβ€β™€οΈπŸ€¦πŸΎβ€β™€οΈπŸ€¦πŸΎβ€β™€οΈπŸ’• 24.07.2024

Update on my cryolesion removal from my face

As a lupus warrior you will be tested to make tough decisions. 22.07.2024

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

Lupus and your skin…. 22.07.2024

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? 18.07.2024

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. 15.07.2024

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

Sending prayers for my Luppie Listeners impacted by the storms in Texas. 09.07.2024

Sending love ❀️ to the Luppie Warriors impacted by the storms in Texas.πŸ™πŸΎπŸ™πŸΎπŸ™πŸΎ

I have had a rough few months. New diagnosis new debilitating symptoms but now better Yes! 09.07.2024

I am feeling so much better. Thank you God……..I love life I truly do!

What is it like living with a disability, 02.07.2024

How has being disabled affected my Love Life….Get in here to hear this🀣🀣🀣🀣😜😜😜😜😜

What do you do when illness comes knocking at your door? 30.06.2024

I sound so upbeat however, it’s not easy to live with being Chronically 😷 I’ll. For the best of my life it will be tough that’s the card I pulled in life. We can do this…..we canπŸ’œπŸ’œπŸ’œ

Date with your brain. your brain will decide when you give access to your πŸ’œ heart. 30.06.2024

Dating and courting is difficult. However, when you date with your brain it will decide when to give access to your πŸ’œ heart.

Cougars do not want to woke up at 2am are you up.😝πŸ€ͺ 30.06.2024

Do you answer a text from your young thang you gave your number at 2am….we are Cougars and that’s a cubπŸ˜‚πŸ˜‚πŸ˜‚πŸ˜‚πŸ˜‚

Let’s talk about heavy legs….is that normal or is it Lymphedema or Lipidema 30.06.2024

Let’s talk about Lymphedema and Lipedema.

So your heart was broken by the supposed love of your life….now what 30.06.2024

Moving on from being broken up by the supposed love of your life….let’s chat

I am letting you know who Luppie Lesbian is so go and listen. 27.06.2024

Have you wondered who I am….. so have I. So just listen and follow me.

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