Welcome, Guest
Username: Password: Remember me

TOPIC: MCS and Dental work.

MCS and Dental work. 1 month 6 days ago #1

  • tamie
  • tamie's Avatar
  • EiR Newbie
  • Posts: 6
  • Karma: 1
Hi everyone :)

I have seen so many doctors over the years i have lost count, and i have spent a small fortune.

I hardly know where to begin, but here goes, my problems mostly began after the birth of my second child, I had several different antibiotics, to control an infection, the infection cleared, but I was ill for a couple of months after and never felt 100% again, didn’t blame the antibiotics at this stage.

A few years later I took Minocycline for 11 months, for acne. I remember the whites of my eyes been yellow on and off, and I had pale stools, I stupidly didn’t see my GP. Then I began feeling extremely dizzy, had constant nausea, flushing, so weak, jelly legs, weight fell from 81/2 stone to under 6 (fast) even though I was forcing myself to eat at this stage, I had arrhythmia's, diarrhea, severe hair loss, flashing lights in my eyes and pressure on my brain, the list was endless. I was so ill my family thought I wouldn’t make it. It took a year after stopping Minocycline just to start to feel better. I was given topical Dalacin for acne, I applied it to my neck, and straight way the head pressure returned, I stopped it immediately.

About seven years later I took Amoxycillin for what I thought was cystitis, thinking i would be okay with an Antibiotic from a different group, but I felt slightly weak and fatigued for about a month after the course. The cystitis came returned, I was prescribed Amoxicillin again, after completing the course my health nosedived, I was nauseated all the time, severe weight loss again many of the symptoms I had with the Minocin, only this time, I developed allergies to just about everything I came into contact with, I was left eating potatoes, chicken and some green veggies. My cystitis turned out to be interstitial cystitis, not bacterial, if I eat bacon I will get it, it is the nitrates! So I didn’t need the Amoxycillin after all, I now use D Manosse at the first sign.

I saw many environmental doctors, spent a fortune, had lots of treatments including EPD. I FELT SO ILL.

I just about lived in my IR sauna for a year. I also had a tooth extracted with mercury under a nickel crown, and all my mercury fillings replaced with composite. My dental problems where ongoing, and my holistic dentist at the time wasn’t as knowledgeable as he claimed in his marketing, I trusted him completely, travelling thousands if miles, and spending a lot of money.

I never fully recovered from antibiotics and was always ultra sensitive to life, wash powder, shampoos, petrol, plastic, perfume, newspapers, new furniture etc list is endless.

I had composite bonding placed by a new dentist, on my upper front teeth, soon afterwards I had excess saliva all the time, I slept with a towel on my pillow. My dentist replaced the material with Admira thinking it was more inert. Same thing happened, chronic cough, pounding headache, sore peeling throat etc. He drilled it off, my symptoms went away. I ordered Diamond Lite from USA, after placement the symptoms returned, plus numbness/pins and needles around my top lip. I had it drilled of and now my teeth are a mess.

I did testing with Cliffords lab, the results where that almost every composite and every adhesive are unsuitable for me. Implants where suitable, but I assume that is because I haven’t had exposure.

I did do follow up testing some time later with Cliffords lab, after doing lots of saunas and detox regimes, and oddly enough, they found some materials that had been unsuitable for me on my last test where now siutable. I have lost confidence in trying anymore filling materials, but i have missing teeth and the rest are cracking, I feel I must do something.

Has anyone with MCS tried implants?
Last Edit: 1 month 6 days ago by tamie.
The administrator has disabled public write access.




Related Articles:


Time to create page: 0.168 seconds