#Lupus is my #1 health condition. I was diagnosed 12 years ago.
May is
#LupusAwarenessMonth
I am 1 of 1.5M that suffer from the disease in the United States alone. 10% are men.
Lupus may be an invisible Illness but I fight it every single day & unfortunately am in a flare.
I will NEVER GIVE UP!💜
May 6, 2025 23:13RFK jr make a comment about a ‘made up ‘ disease called lupus. My family’s diseases are Sjogrens & lupus
Sending every good wish as you fight bravely on.
My daughter has Lupus! Hope your flare is over soon!
May is also Fibromyalgia Awareness Month. Lupus was one of the diseases that had to be ruled out. I understand your pain. Take care of yourself.
Thank you. I actually have fibromyalgia and Lupus. 🙏💜
Hope your flare settles soon, Peter.
I am so sorry, Sir. I am two years into trying to be diagnosed. It’s starting to look as if it’s going to be Lupus. Just got my first case of shingles…Woohoo!!🎉
As a sufferer of an autoimmune disease (scleroderma), I know how tough some days can be. But you are an inspiration! 🤩 Keep fighting! 💪 And keep sharing. It helps fellow warriors of chronic illnesses to know they're not alone. 🙏❤️
I, too, have lupus. My sympathies. I hope you’ll be kind to yourself as you move forward.
Check out Dr. Brooke Goldner at
goodbyelupus.comGoodbye LupusGoodbye Lupus – Take back your health with super market foods.
It's also myositis month and I was diagnosed in January 1992.
I see you.
I hope the flare passes soon, Peter!❤️🩹
My #1 is systemic sclerosis. Diagnosed 2 years ago.
Flares are physically exhausting & mentally draining.
I hope your flare eases soon💙
Good days and bad days... as long as they are days above ground.
Much love to you from one Lupus haver to another. 💜💜💜
Flares suck hard.
Tomorrow will come … eventually.
Hang tight.
I have never once skeeted about having lupus, and yet this magically shows up on my timeline 2 weeks after I start talking about having it irl. Good to know my phone is listening to me ig.
How long did it take btwn first symptoms and diagnosis? Just curious.
Hypothyroid is my cold cuppa tea - and I've been diagnosed with Lupus too - in other words, we share shonky immune systems - smiles.
💜💜💜💜💜💜💜
I’m currently in the middle of a Scleroderma flare right now. I’m so sorry you are suffering. Praying it passes soon. 🙏🏻❤️
I have a good friend that had a hip transplant due to lupus. She still has flares. It’s real, and nothing to be trifled with.
💜💜💜
As chronic illness sufferer myself, I wish you quick subsidence of your flare
I had a dear friend who had both types of Lupus - SLE and DLE. She lived with both for 30 plus years. Strongest person I ever met. You are so strong, too, Peter!!💙🥰
I stopped my autoimmune liver disease by the gut health approach. If you haven't looked into this, I highly recommend you do.
pmc.ncbi.nlm.nih.gov/articles/PMC...
Leaky Gut As a Danger Signal for Autoimmune Diseases
The intestinal epithelial lining, together with factors secreted from it, forms a barrier that separates the host from the environment. In pathologic conditions, the permeability of the epithelial lin...
Oh no. Flare.
Sorry man that sucks
I have been diagnosednwith Lupus since 1997. Am now 65. It is an invisible illness that impacts every aspect of my life. I appreciate your advocacy for the disabled social security recipients.
🦋🙏
🤗
