
Originally Posted by
GlamourRouge
Welcome to my fucking life. Silicone lip injections about 5 years ago and 3 years ago bedridden with lupus. I still want to get implants, but I'm opting for saline if I go through with it. I'm TERRIFIED it will make things worse as well.
My symptoms ~ 1.5yrs after injections (no shell/casing) were: joint popping/stiffness, feeling like I am getting the flu non-stop (like a throbbing electric ache and extreme fatigue), brain fog, sleeping a MINIMUM of 9-12 hours a night or I physically cannot get out of bed (if I need to get up early, I have to not sleep for like 24 hours), hair loss (its grown back now), ANA+, a lot of internal inflammation, acid reflux/GERD, ulcers, gluten intolerance, dairy sensitive (I can have a little and be ok though), frequent bronchitis/colds/pneumonia, voice loss lasting for months (now only lasting for a couple days at best thank god), swollen lymph nodes, I'm sure there's more.
Silicone triggers an immune response in those who are prone to autoimmune disorders. In my case, I've had psoriasis since like toddler age, now psoriatic arthritis (thank GOD it didnt end up being rheumatoid!) + lupus.
Saline grows black mold because its water-based.
You just can't win lol. But you can get them changed/replaced/taken out.
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