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6/21/2016 10:23:35 PM | Hi Siani, This is also my first post. I've got a quick question for you. Are you from the UK? Reason I ask, is because I've read that a particular, much sought after doctor in the UK has prescribed Dermol 500 and Betacap for morgellons, but I wasn't aware that he prescribed an anti-psychotic drug as well; DP indeed. I'm not going to name the doctor, since I have a long awaited first appointment with him towards the end of October this year (waiting since March 2016). I know that this doctor works alongside a chartered clinical psychologist, since they opt for a holistic approach to this condition. I have the pin pricks, tingling, stinging and the fibres. I've meticulously pictured and labelled a whole swathe of fibres etc from when I've first realised that I have morgellons and I bought an USB Microscope. If you are from the UK, I'm dreading that you've seen the doctor that I am anxiously awaiting to see, and he might be like the other dermatologist I saw, who instantly said that it was 'all in my head'. Perhaps I should start from the beginning. I got bitten at the back of my head around December 2015, from something contained within a drop of green water falling off a mouldy building, I happened to be standing under. Within a few days, I had symptoms of scabies burrows/bites etc. I know the signs since, I've had scabies around 12 years ago, and it was a nightmare to both live with; and get rid of. I went through 4 courses of permithrin and 3 of Malathion, by the time I saw the first Dermatologist (March 2016). Without inspecting me, well she started looking at the webs between my fingers for 5 seconds, and as soon as I mentioned that I have a crawling sensation in my scalp, she instantly dismissed me, saying that it's all in my head, and that I've never had scabies. This was before I've even heard of Morgellons, so I basically told her that, OK, perhaps it's not scabies, since I've had 7 treatments for it, but there is something tangible, 'biting' me, seemingly, crawling all over me. She gave me a topical steroid and Balneum cream and told me that this will fix my condition. Discouraged, I got my GP to refer me to another dermatologist for a second opinion, and someone who will take blood samples and test me skin a bit/lot more throughly. My next appointment was a week ago (June 2016). This dermatologist has worked with the Dr I wanted to see, so was aware of some of the protocols he followed, she saw the 100 plus carefully labelled microscope images and has me booked to see my preferred Dr at the end of October 2016. Blood tests were taken for microbial reasons, throid health, borrelia bacterium and another bottle for perhaps white blood cells count – not sure, but at least tests were done. From January to March 2016, I went overboard with chemicals from reading a whole heap of misinformed stuff on the internet. This definitely put a huge payload on my liver, and even though I used to get 'a' good nights sleep, even this was too much for my body to bear, and now I've stopped everything that is harmful to my body. All I use now is a tree tree oil shampoo, neem soap and pure virgin coconut oil. Supplements I take are MSM (Methylsulphonylmethane) 1000mg, CoEnzyme Q10 100mg, Starflower Oil with B6 1000mg, Candida Support with Black Walnut Hull and wormwood, Alfalfa 600mg and a multi-vitamin tablet. I'm not sure I can buy the Logos supplement from the UK, not sure about ingesting Silver and have heard a lot of negatives about the MMS, but will re-read up about it. Are there any alternatives for the Logos supplement that can be bought from within the UK. Whenever a website advocates a cure and then panders it's own wares it makes me suspicious. In all honesty, I do have slight doubts about this site, whilst trying not to be offensive about it, since I do need any help I can be afforded. Some websites appear to be bogus, especially the Michael guy selling magnetic resonance machines. Any website that comes over as a portal for conspiracy theorists turns me off. Any mention of nanotechnology and chemtrails turns me off. One strange thing that is happening to me now; that I've not heard anyone else mention, are pressure headaches and a feeling that the whole world is spinning. Stranger still, is that it happens around 5pm give or take half-an-hour almost daily. I hope I've been quite comprehensive in describing my problems, I'm at wits end; have 4 kids and a wife I'm absolutely scared to death that I might infect. Whenever anyone scratches in the family, it makes me tearful. I used to steam everything, everyday, now I'm just so sick and tired of it all. I sleep on the leather settee, and every morning I thoroughly vacuum it, and spray it down with disinfectant. I really can not afford to buy expensive supplements, since I'm the sole breadwinner, feeding a family of 6. Any help that anyone can afford me will be much appreciated. If anyone can tell me with any conviction, that this illness is NOT contagious, will have my heart-felt gratitude. I'm really beating myself up over this – this wasn't supposed to happen, was it? |
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