PODCAST · society
Luppie Lesbian
by 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.🦋🦋🦋🦋❤️❤️🏳️🌈🏳️🌈
Episodes
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I am not paying for nails! I am not paying for hair! I am not giving gifts! Who asked? 🤔🤔🚫
Conversations starting I do not do nails I do not do hair stops me in my tracks🤔🙄🤔🙄 Seasoned women are not looking at you for that. They want you!💋💋🤏🏾🤏🏾🤏🏾Wake up or be alone you choose. However, you get more with honey than crap. I am just saying.
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Being single owes me nothing! I truly love it👂🏽👂🏽
I am in my single era and to be honest have been for quite some time. However, I have been working on me. Take the time given and make working on you a priority.. Love you all.💋💋💋
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After dark podcast...💦💦Ok, how many of you know what a 🌹 is and what ✂️ ing is. I did not🤣🤣🤣
After dark podcast about these topics the famous Rose and Sissoring what are they. Like I am and expert🤣🤣🤣. Dont judge and dont ask me for one🤣🤣
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Can you be ok with a person liking you but not wanting to date your disability. Its interesting!!
I am learning how to navigate all these new challenges. So I have given myself grace so how would I not give it to another. I am my disability however, some cant see past that. I am grateful for honesty.🌹💜❤️
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How do you handle unsolicited advice like exercise more, eat less, push yourself as you battle Lupus
Woosa you are already fighting a very hard battle do you really need negative comments????🫸🏿🫸🏿🫸🏿
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Dating.. first hour I say I want to come to your house. Do you keep your boundaries or say yes.
Diving into boundaries. Do you maintain a time limit on getting to know a person. Would you be ok with a person insisting they need to see you now or would that be a red flag. Remember you do not know this person🤔🤔🤔🫸🏿🫸🏾🫸🏾.
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One of Lupus cousins called Sjogrens has very distinct symptoms. Its not always dry mouth and eyes.
One day I pray they will find out why you can have more than one disease from Lupus🙏🏿🙏🏿🙏🏿🙏🏿🙏🏿
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Do you know what Intimacy is? I bet you think its horizontal no baby lets change that up.💋
Lets chat about Intimacy....where how and all day long 👑
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Would you ask a woman who may be MOC presenting if they are a Lesbian.?
I learned a thing of two recently. Safe space for you to be who you are.
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Do you know what is the number one Autoimmune disease....per Alexa🤔🤔🤔👂🏽👂🏽👂🏽👂🏽
Lets talk about Autoimmune diseases....Always take your meds...please❤️❤️❤️❤️
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Please dont say this to anyone who has Lupus or any illness 🤔🤔
Why you should never say this....people batteling illnesses are sponges.
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Having Lupus is not your fault!
The title says it all.🫶🏿🫶🏿🫶🏿
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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.
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.
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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.
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.💋💋
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Should you tell a friend that it's friends only when you are not interested. We are going in a rabbits hole.
Piggy backing off of friends in relationships🌈🌈💋💋
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Who told you that you can't have intimacy if you have any Autoimmune disease...well they lied!😉😉
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😵💫😵💫🥴🥴🤣🤣🤣🤣
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Please do not tell people how to grieve!!!!
Let people grieve!!!
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Medicare will cover certain GLP agonist starting July 1.
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.
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If you have more than 1 autoimmune disease which one right now is giving you a hard time? What do you think will help?
Haging multiple autoimmune diseases I know exactly which one is aggravating me...ugh🥴🥴🥴🥴
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Some fun facts about me🤣🤣🌈🌈💋
Here are questions I have compiled from my different Social Media spaces. Here are the answers!!!!
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In order for you to have a relationship do you have to be friends first...🤔🤔🤔🤔
I could never imagine being in a relationship and not being friends. How how 🤔 ❓️
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Navigating multi autoimmune diseases you will need Ɓoundaries. I truly believe in boundaries🫶🏿🫶🏿
Boundaries keep me sane not guessing. With Autoimmune diseases it can change from day to day so my boundaries keep me in ✔️ check.👂🏽👂🏽👂🏽👂🏽
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Can you have more than one Autoimmune disease? Yes you can let's talk about Sjogrens 🤔
Sjogrens is another Autoimmune disease. 👂🏾👂🏾👂🏾👂🏾👂🏽👂🏽👂🏽
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Who told you because you are disabled you can't date. Well that's a lie!💋
We are dating in 2026 and beyond. 💋#disableddating
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Having an Autoimmune Disease does not mean you cant date. Who told you that???👂🏾👂🏾👂🏾💜🦋
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.
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Thank you for the 5000 listens on mutiple platforms. We are Lupus Strong💜💜🦋🦋
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🦋💜🦋💫
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Welcome to the Lupus Community.🦋🦋🦋🦋
Let me reintroduce myself and welcome the Autoimmune Queens/princesses and Kings to our community. 🦋🦋🦋🦋🦋
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Do you have a type...Date them all until you figure it out.💋💋💋
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.💋💋💜💜💜💜💜💜💜💜💜💜💜💜
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Its time for you to get up and live. I say this because I had to do it. Girl get up!!!🫶🏿🦋💜
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
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Luppie Lesbian is back🦋💜🦋 Happy Friendsday. I missed you guys.💋💋 #teamlupuswarrior
After a longggggg break I am back. #Lupuswarrior
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You are not alone on your Autoimmune Journey.
You are not alone on your autoimmune journey. We are here. I am here.....
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Lupus requires you to have things in place. If you stay ready you won't have to get ready.💥💥💫💫💫
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.
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Let's talk about how I found out I had Lupus and the things that happened prior. 🦋🦋🦋🌈🌈🌈🌈🌈
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!!!!!!
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Luppie Lesbian is back. I missed my Lupus Warriors. Let's talk about where I have been♥️🦋♥️🌈
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♥️♥️♥️🌈🌈🌈🌈🌈🌈
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Update on this Chemo!
Yes some of us take Chemo for autoimmune diseases. It is working however, this week I have side effects.
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My little take on family members who are negative towards you during and illness.🤦🏾♀️🤦🏾♀️
I will dish the tea on this topic!!!
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Update on my plastic surgery🤪😷🤦🏾♀️🤦🏾♀️🤦🏾♀️💕
Update on my cryolesion removal from my face
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As a lupus warrior you will be tested to make tough decisions.
I am in a place to make tough decisions as my Lupus progresses. We all will have to make them.
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Lupus and your skin….
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.
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Do you know when you are starting a flare?
I can tell now when my body is off and going into a flare. We must pay attention to our bodies.
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Here is a list of things to help you with a long long flare with a chronic illness.
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
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Sending prayers for my Luppie Listeners impacted by the storms in Texas.
Sending love ❤️ to the Luppie Warriors impacted by the storms in Texas.🙏🏾🙏🏾🙏🏾
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I have had a rough few months. New diagnosis new debilitating symptoms but now better Yes!
I am feeling so much better. Thank you God……..I love life I truly do!
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What is it like living with a disability,
How has being disabled affected my Love Life….Get in here to hear this🤣🤣🤣🤣😜😜😜😜😜
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What do you do when illness comes knocking at your door?
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💜💜💜
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Date with your brain. your brain will decide when you give access to your 💜 heart.
Dating and courting is difficult. However, when you date with your brain it will decide when to give access to your 💜 heart.
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Cougars do not want to woke up at 2am are you up.😝🤪
Do you answer a text from your young thang you gave your number at 2am….we are Cougars and that’s a cub😂😂😂😂😂
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Let’s talk about heavy legs….is that normal or is it Lymphedema or Lipidema
Let’s talk about Lymphedema and Lipedema.
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So your heart was broken by the supposed love of your life….now what
Moving on from being broken up by the supposed love of your life….let’s chat
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I am letting you know who Luppie Lesbian is so go and listen.
Have you wondered who I am….. so have I. So just listen and follow me.
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ABOUT THIS SHOW
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.🦋🦋🦋🦋❤️❤️🏳️🌈🏳️🌈
HOSTED BY
Luppie Lesbian
CATEGORIES
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Frequently Asked Questions
How many episodes does Luppie Lesbian have?
Luppie Lesbian currently has 185 episodes available on PodParley. New episodes are automatically indexed when they're published to the podcast feed.
What is Luppie Lesbian about?
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.🦋🦋🦋🦋❤️❤️🏳️🌈🏳️🌈
How often does Luppie Lesbian release new episodes?
Luppie Lesbian publishes regularly with 185 episodes available. Check the episode list for the typical release schedule.
Where can I listen to Luppie Lesbian?
You can listen to Luppie Lesbian on PodParley by clicking any episode. We provide an embedded audio player for direct listening, and you can also subscribe via your preferred podcast app using the RSS feed.
Who hosts Luppie Lesbian?
Luppie Lesbian is created and hosted by Luppie Lesbian.
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