@drgreghealth: Here are the first signs of an autoimmune disorder, long before anybody gives it a name. I've been a functional medicine doctor for more than 25 years, and this is the stretch that gets missed for years. Autoimmunity does not begin the day you get a diagnosis. The antibodies are usually present long before the damage is. Sign one: Fatigue that sleep does not fix. Not tired. Wiped out, after a full night, for weeks at a stretch. Sign two: Symptoms that come and go. A joint that aches for ten days and then stops. A rash that appears and disappears. Low grade fevers nobody can explain. Flares are the signature. Things that leave on their own are the easiest things in the world to dismiss. Sign three: Your labs get called normal while you clearly are not. Standard panels are built to find damage that has already happened. Early autoimmunity is an attack still in progress. If several of these are stacking up in the same body, that is worth a real workup, not another year of being told it is stress. Which one of these has been going on the longest for you? Find the root. Heal the whole.

Dr. Greg
Dr. Greg
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Monday 05 October 2026 15:07:17 GMT
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erickahelmer
Ericka | Jesus.Wife.Momma :
I hit perimenopause about 3 years ago after a partial hysterectomy (they left my ovaries to not be thrown into peri..surprise surprise). My entire system has been in a horrible storm ever since, I was diagnosed with hashimotos during perimenopause but doctors will not treat me, just said, come back and test once a month basically until your thyroid is already damaged. They will not treat me (including en endocrinologist) until my thyroid already shows damage, left me to suffer, both doctors. I suffer with the worst thyroid symptoms. My quality of life has diminished and just keeps getting worse. I’ve been on all the hormones in all the different forms, and I get no relief, the ONLY symptoms I get relief from out of the long list are hot flashes and night sweats, that’s it, that’s all. How is it that I’m on all the hormones yet I may as well be taking a placebo or sugar pill? No one can help me and has helped me. I have no answers. The only things that o ever get told is, this is just perimenopause and have to deal with it, you only have so many options, and just eat better and exercise more. That’s it. I’ve had pellets, patches, cream, pills, injections…I get absolutely nothing from them. It feels like something is severely wrong with my body yet no one is catching it. Perimenopause has ruined my entire existence, but no one to help me or give me answers…
2026-10-09 16:50:54
0
osidecrib
Herart local :
What’s happening? You’re not talking on your last two posts? 🫪
2026-10-05 15:25:26
1
darlavann2
Darla Vann :
The sun is his trigger !
2026-10-07 01:40:05
0
tam.gallagher.86
tam.gallagher.86 :
Yup that's been my life since I was 14, I'm 40 in a few weeks
2026-10-05 19:58:12
0
parrgirl1974
user9751512755583 :
Mouth ulcers, GERD, joint pain, flu like feeling, and exhaustion was the first signs then came muscle pain, Raynauld’s, livedo, muscle weakness, dry eye, Automic nervous system dysfunction, tendon pain, swelling in fingers, and so much more.
2026-10-07 00:33:11
1
user7g4qfuyfld
Taylor Harms :
I started feeling exhausted when I got together with my wife I was 27 at the time, out of the blue I just felt more tired, when I was trying to find the root of the issue it, only found out that my liver enzymes were elevated and they kept being elevated for a time, I also been dealing with headaches just got diagnosed with cluster headaches this year took maybe 20 years to that figured out, but as each year goes by I keep getting neuropathy pain at random spots, my hands start developing dead skin it okay at first just a couple of patches but it spread pretty much, almost two years ago my right foot would feel sore on the outer right side, and noticed it's been cracking more and more as months has past. The end of last year, my foot has gotten worse to were it hurts to walk, it gets swollen or numb, do physical therapy for about three months to get stuff done, here I am today still dealing with foot pain and now it's spread occasionally to the top of my Midfoot and difficulty to bend my toes, I have been to a podiatrist, rheumatologist, orthopedic and now pain clinic, a few X-rays and one mri, they found bursitis at the end of last year, treated it and my foot would still cause issues even getting injections only took a week for the pain to come back, podiatrist has said my bones are changing pretty much my toe is already developing bunions at the age of 32 and my toes are going more up, in July of this year I had tmj out of the blue, both podiatrist and pain doctor started me on Lyrica and my body can't tolerate with things that effect my brain or tired, so Lyrica and gabapentin is a definite no, just tried cymbalta and this med basically reawaken the pain I used to have and had a steady burning aching pain in my bottom right quadrant of my back, and still not much but I had to stop cymbalta because it caused me too many side effects and plus meds don't do good on my
2026-10-07 00:19:44
0
heidigustin363
heidigustin363 :
I need a functional doctor
2026-10-07 11:57:40
0
austinssketchbook
austinsart :
yeah I just continue getting told that my labs are fine despite positive ANA and CK at 650 multiple times plus constant symptoms, face rash in the sun, petechiae and purpura all over my legs, non stop headaches, unreal joint pain and muscle pain, the list goes on lol.
2026-10-06 05:42:53
0
cnw6721310
Carissa :
This sounds like me rn going through perimenopause 😳
2026-10-05 21:55:00
0
marcella.riojas
Marcella Riojas :
Walk
2026-10-05 23:55:17
0
silverfoxy74
Ange :
What are the links of oral facial granulomatosis to facial paralysis with sarcoidosis? I've had 2 facial paralysis in the past 5 months...I've been diagnosed with oral facial granulomatosis but it's mutating like symptoms of a stroke?
2026-10-06 11:23:29
0
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