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

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!!!
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 😷 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💜💜💜
Dating and courting is difficult. However, when you date with your brain it will decide when to give access to your 💜 heart.
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 🥰 in love.
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.
Would I ever…..????????fill in the blank.