Hey all. Been on a very steep decline for the last year and do t have any clue what to do. Last year I took methylfolate, methyl b12, p5p, riboflavin and vitamin E together to try and get my energy levels and muscle gains up (have had some thyroid issues for years despite normal testing). A few weeks in and I feel like I have a bad flu, after a gym session I took my nitric oxide and had some weird dopamine rush I've never experienced before, so I stopped everything cold turkey. In January 2017 I took vitamin K2 for 2 weeks due to borderline high blood calcium, and after 2 weeks I had a "crash" that has left me in a downward spiral this whole year. My symptoms incude: worsening thyroid symptoms like colder body temp, very thin skin, pale skin, tired all the time, not very good sleep, dry skin, body hair loss, weight gain (50 lbs this year)...other issues like digestion problems, slow growing hair/nails, smooth stretchy skin, gum line recession (very bad), brain fog through the roof, there's several more but the worst of all is the connective tissue disintegration I'm having. I've developed hypermobile joints in some body parts, and ALL my connective tissue seems to be disappearing including tendons and ligaments. Everywhere on my body clicks/pops/cracks including my spine and neck. My neck is very loose and feel I'll need spinal and neck reconstructive surgery to fix it when this problem becomes worse (which it will......it has NOT slowed down a bit since January). I've seen some doctors at UCSF medical center and they say it's not EDS, but I'm not so sure. I had an appointment with a private wellness coach named Sean Bean and he is very intelligent, he believes I could have Lyme due to taking the methylated vitamins.....he said taking those is an open door for Lyme that's been dormant. I can't afford the testing out of pocket and can't have another appointment with him for the near future due to money issues (I'm broke as hell). I really feel this will kill me and don't know what to do. Does this sound like Lyme? Are hypermobile joints and total collagen loss normal signs of Lyme? Am I scaring myself thinking that eventually I'll dislocate my spine or neck? Any help or advice would be very appreciated.