Luppie Lesbian
Luppie Lesbian
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.🦋🦋🦋🦋❤️❤️🏳️🌈🏳️🌈
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Auteur
Luppie Lesbian
Catégorie
Site du podcast
Dernier épisode
28 sept. 2026
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Épisodes
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!!!
Update on my plastic surgery🤪😷🤦🏾♀️🤦🏾♀️🤦🏾♀️💕 24.07.2024 6:02
Update on my cryolesion removal from my face
As a lupus warrior you will be tested to make tough decisions. 22.07.2024 12:25
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 10:14
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 11:20
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 26:08
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 5:51
Sending love ❤️ to the Luppie Warriors impacted by the storms in Texas.🙏🏾🙏🏾🙏🏾
I have had a rough few months. New diagnosis new debilitating symptoms but now better Yes! 09.07.2024 10:38
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 21:56
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 16:32
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 can💜💜💜
Date with your brain. your brain will decide when you give access to your 💜 heart. 30.06.2024 21:29
Dating and courting is difficult. However, when you date with your brain it will decide when to give access to your 💜 heart.
Cougars do not want to woke up at 2am are you up.😝🤪 30.06.2024 11:03
Do you answer a text from your young thang you gave your number at 2am….we are Cougars and that’s a cub😂😂😂😂😂
Let’s talk about heavy legs….is that normal or is it Lymphedema or Lipidema 30.06.2024 19:25
Let’s talk about Lymphedema and Lipedema.
So your heart was broken by the supposed love of your life….now what 30.06.2024 17:27
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 15:12
Have you wondered who I am….. so have I. So just listen and follow me.
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