Luppie Lesbian

The title says it all.🫶🏿🫶🏿🫶🏿

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 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.💋💋

Piggy backing off of friends in relationships🌈🌈💋💋

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😵‍💫😵‍💫🥴🥴🤣🤣🤣🤣

Let people grieve!!!

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.

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

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

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

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

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

We are dating in 2026 and beyond. 💋#disableddating

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.

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🦋💜🦋💫

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

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.💋💋💜💜💜💜💜💜💜💜💜💜💜💜

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

After a longggggg break I am back. #Lupuswarrior

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

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.

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!!!!!!

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♥️♥️♥️🌈🌈🌈🌈🌈🌈

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

I will dish the tea on this topic!!!