Recovering from Mercury Toxicity

 So this time last year I had been given the herbs for my 3.073 ppm of mercury hair test by a naturopath, and I was getting worse and worse. I wish so badly that I kept a journal this time last year but from what I remember this is when my “crashes” began to creep up on me. I was beginning to feel spacier and spacier. I had done 1 art lesson October 28th ish and I was too sick todo another one. I remember because I was talking about Halloween.  I was scared to have another art lesson cause one second it would be ok ish and then bam the spaciness would hit me, then out be out for like a day. I also remember trying to put an art easel together and it was like the hardest thing in the world.  Another memory is getting so spacey I went to the ER I think in the beginning of November ish. Then in December I actually stopped herbs altogether. Another is I used to be able to take my dog for a long walk but the herbs only allowed me to take my dog to the park and straight home. I ...

 So today is the last day of round 30, OFF day. Tomorrow will be round 31 and I’m going todo DMPS 2.5 mg, 1.5mg ALA as that was what I did for the latest round.  I am better then the last time I posted. I had a bad dip for about a week. Just felt altogether worse. I need to remember that when I am having a dip that it won’t last forever. But it’s hard to at the time.  I have noticed that when I do have a bad dip my symptoms just become more extreme and I also gain head pressure and weird sensations in my brain. But then the weird sensations/head pressure lessen when I’m not so bad.  I am looking at supporting my adrenals. I am wondering if they are contributing to my symptoms and why I feel worse at some periods of the day. I have started to take Ashwaganda in the morning (capsule) and one teaspoon on licorice morning and evening. I am going to read up more on adrenals. I find that I go down around 11am, 3pm and sometimes in the evenings. One way to describe my sympt...

 So I am currently on round 28, 13 combo rounds with ALA. I have increased my ALA dose by 0.5, so I am taking 1.5mg for the last 2 rounds.  Things are going okay. So I am currently taking 2.5mg DMPS & 1.5 mg ALA.  I had some blood results back recently and my Dr told me my liver results are improving. But I am a little low on Zinc, copper, selenium and Iodine.  I have had really really sore eyes since I took a drug called roaccutane in 2017 but in September 2020 (7 months since being sick)  I took an antibiotic for my gut (SIBO) and since then they have been wayyy worse. Being sick in general has made them worse. Like it’s hard to focus my eyes on things. Went to an eye specialist the other day and they told me I have blepharitis.  “  An inflammation of the eyelid that affects the eyelashes or tear production. Blepharitis commonly occurs when the tiny oil glands of the inner eyelid become inflamed. It often occurs along with other skin conditions o...

So today is six months from my major major crash. Where I believe the dump hit (10.2.2022). Currently on round 23, 9 rounds ALA.  Funnily enough I got hit with food poisoning this morning, so I am feeling awful.  But I’m just glad to hit this milestone. In the 6 months since that crash I haven’t had another one like it. So that is a positive (:  Currently on round 23 (2.5mg DMPS + 1mg ALA). Before this round I wasn’t sure if I was going to be able todo ALA but I just went ahead. I’m pretty sure after 3 rounds of ALA continuous I begin to feel worse neurologically. It must build up.  On a boat sensation, head sensation, nauseous, haven’t eaten for 12 hours now, upset stomach. Pretty sick. Gritting my teeth to get through the day. If I had to rate how I feel I would be 3.5.1 (1 being good, 5 being dying).  I’ve been having pretty sore eyes lately; things I’ve been doing: Warm eye compresses, Nulids eye treatment. I’m going to try taking flaxseed oil and taping my ...

 Thus far I have done:  4 rounds 12.5 mg DMSA  10 rounds  2.5 DMPS  7 rounds 2.5 mg DMPS+ 1mg ALA (so in total 21 rounds).  I am planning on doing another combo round tomorrow for round 22.  I am not finding ALA too hard now. I think I’m going to be able todo ALA every week (hopefully). But overall I don’t feel any better, but not any worse either.  I have noticed that I usually feel worse on the third and fourth OFF day and worse after 11am and in the evenings. Today I actually went with my mum to a garden center but I went back to sit in the car after walking around a little. I’m not feeling any better exactly, but I’m not feeling any worse and I’m not “crashing” like I was before (which I’m really happy about.) My eyes however are quite sore. I’m really hoping that as chelation progresses the dryness, light sensitivity and soreness goes away. I’m trying to stay off my phone and looking at far objects to help my eyes. Also my face is very sensit...

This is what I look like at round 17. Skin is pretty bad   So I am on the last day of round 17.  Thus far I have done 4 rounds of 12.5 DMSA then crashed HARD and then the dump hit HARD (10.2.2022).  9 rounds just 2.5mg DMPS. 4 rounds 2.5mg DMPS + 1mg ALA. So I’m currently sitting at round 17. (still no major crashes like before).  The ALA I believe is increasing my symptoms. It’s just a bit harder getting through each day. Every round is slightly different I have noticed. For round 18 I am just going todo 2.5mg DMPS. I think no ALA for awhile, maybe too early to add it in yet. I don’t think I can handle getting much worse then I already am. I am thinking of doing alternative rounds such as DMPS only, then ALA/DMPS every other week or so. At the moment I am not able to go for walks. Nor can I have a bath or do anything like that. I am just laying down outside listening to audible books. That’s the only thing that is getting me through the day. I try and walk arou...

This is me   Hi there, This is a blog where I will be sharing my story of how I became sick as a normal, healthy university student (I was 22 when I became sick), how I found out I was poisoned with Chronic Mercury Poisoning, how I found the Andy Cutler Chelation method and my ongoing experience recovering from this awful poison. I’m not going to hold back in my posts, the good, the bad and the ugly! This is going to be a long journey (I suspect 2-3 years) I hope my story can help someone else. I am determined to get better, and I want to help other people! So here it is: My name is Georgia, I am 25 years old from Australia. In 2020 I developed these symptoms. They’re are all mainly things I experience 24/7.  •24/7 Debilitating brain fog (my main symptom)  •Dizziness  •No longer able to drive a car  •Felt like the cells of my body hurt  •Body pains •Fatigue •Weakness  •Difficulty walking sometimes (unbalanced)  •Drunk like feeling  •Weig...