Luppie Lesbian

I learned a thing of two recently. Safe space for you to be who you are.

Lets talk about Autoimmune diseases....Always take your meds...please❤️❤️❤️❤️

Why you should never say this....people batteling illnesses are sponges.

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.

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.

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.

It was like any other day until I fell and that's when my mind started

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!!!

Update on my cryolesion removal from my face

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

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.

I can tell now when my body is off and going into a flare. We must pay attention to our bodies.

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 love ❤️ to the Luppie Warriors impacted by the storms in Texas.

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

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

I sound so upbeat however, it's not easy to live with being Chronically

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

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 Lymphedema and Lipedema.

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

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

Let's talk about it.

Dating sites how do you feel about them. Are you lucky

I understand that life is a struggle however; check on those strong friends. Sick or not just check.

Yup it's flare time for me. New symptoms or worsening old symptoms.

Lupus and Covid are not friends. My one lung has distress from Covid.

I decided to go back on Chemo for my Lupus /Ra/Fibromyalgia let's see the pros and cons.

My team of Doctors and I have decided that this is needed at this juncture. So Chemo it is. The drug is called methroxate and I know I will have great benefit from it. All will be well.

Become friends with women who don't mirror you.

So much tea on the first day of Lupus awareness month. Eye exam, BP 70/60 lord lord lord what a day.