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What are the latest advances in Multiple Chemical Sensitivity?
Here you can see the latest advances and discoveries made regarding Multiple Chemical Sensitivity.
I have not seen any new advances in the treatment of MCS. Because most of the treatment is happening outside of the medical institution, the independent nature of the holistic community doesn't allow for the culmination of data for scientific scrutiny, nor can double-blind studies be done on any patients with MCS because of the nature of the disease..
Posted Oct 26, 2017 by Paul 3000
Acceptance as a physical disease is still slow in the Allopathic Medical field. The chemically hypersensitive can't take drugs. Since pharmaceutical companies are chemical manufacturers, no money is diverted to research that doesn't increase their bottom line.
That being said there are treatments that are working. First and foremost, avoidance of all toxins. Foid, environment, everything. Next get a biometric test for environmental toxins and nutritional deficiencies. Work with an integrated Environmental Illness practitioner to remediate those . Have your genomes mapped and have someone like Dr. Amy Yasko interpret it for you. Access her books online for free. Brilliant woman! Work with your EI on any variance issues you may have.
IV glutathione and IV Bs 5&6 with magnesium and C have helped many sufferers. As has hyperbaric oxygen. I have not had the latter. My condition was so severe I couldn't access it.
I've found certain homeopathics helpful, like Nux Vomica, and Lymphamyasote. I've also found acupuncture, shiatsu massage and IR sauna helpful.
That being said there are treatments that are working. First and foremost, avoidance of all toxins. Foid, environment, everything. Next get a biometric test for environmental toxins and nutritional deficiencies. Work with an integrated Environmental Illness practitioner to remediate those . Have your genomes mapped and have someone like Dr. Amy Yasko interpret it for you. Access her books online for free. Brilliant woman! Work with your EI on any variance issues you may have.
IV glutathione and IV Bs 5&6 with magnesium and C have helped many sufferers. As has hyperbaric oxygen. I have not had the latter. My condition was so severe I couldn't access it.
I've found certain homeopathics helpful, like Nux Vomica, and Lymphamyasote. I've also found acupuncture, shiatsu massage and IR sauna helpful.
Posted Oct 27, 2017 by JLMcK 5550
Annie Hopper is partnering with other professionals to examine the neuro-modulation causative aspects of MCS.
Posted Oct 28, 2017 by Katya 1042
It has finally been recognized by some as an actual physical reaction.
Posted Jan 6, 2019 by Cindi 3050
Certain hospitals have taken it on board abroad. The only hospital in the UK is the former Homeopathic Hospital in Queen Square London.
Posted Apr 1, 2019 by Susan 2500
I don't know if there are any advances being made. We need to clean up our world, get back to basics, the good life.
Posted Jun 4, 2019 by Heather 3000
I’ve heard of rumours of ‘Allergy housing’ and ‘Allergy communities’ but I’ve yet to see it! In the 20 years I’ve had my conditions and reactions I’ve yet to see an advancement, with the state of the NHS health service in the UK, I’ve only experienced a deterioration in my condition and the care provided, is your country any different? Do you pay for your care? How did you acquire insurance because in the UK you can’t get any kind of insurance or a mortgage with a debilitating illness! How do you pay for your care? I don’t work, do you? I also don’t get state disability payments, I don’t claim any social security benefits as I don’t meet the criteria to claim, how do you fair in your country?
Posted Aug 22, 2019 by Carmen Rosemarie 2550
There are links to Electrical sensitivities - I keep up with Anne Steinemann's research and pass it to my doctors.
Posted Nov 18, 2019 by Angie P. 5000
If you want to learn more, please look for my forthcoming book, Silent Winter, and visit my Facebook page: https://www.facebook.com/ChemicalsAndChronicIllness
Posted Dec 12, 2019 by Joanna 6200
In South Africa ... NONE! They do not even know that MSC exist and we a 3rd world country so basic thing come first like water and electricity. You need to fend for yourself and the care options are NONE
Posted Jan 30, 2020 by Noeleen 2500
Just tell. More people just make corporations understand
Posted Mar 8, 2020 by MCSzombie 6220
Most of the advancements related to MCS are advancements in coping with the illness.
Best updates come from people who are living with it.
Recommend joining a group with other people who have MCS.
Facebook is a great place to find community.
Best updates come from people who are living with it.
Recommend joining a group with other people who have MCS.
Facebook is a great place to find community.
Posted Sep 27, 2020 by Rebecca St. Martin 3570
They re really just starting to study mcs. They are slowly learning more about it, but until our govt is willing to make necessary changes, it will be difficult to help us
Posted Nov 12, 2020 by shelley 3650
Many are using the brain retraining techniques
Posted Jul 24, 2021 by Serenity 2500
UCLA did a study last year on MCS.
Posted Nov 11, 2021 by kola05 2620
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SINCE 2014 IT IS RECOGNIZED IN SPAIN WITHIN THE NATIONAL HEALTH SYSTEM AS A SYNDROME.
Posted May 16, 2017 by Emilio 2070
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for now I do not know but that the treatments with vaccines and minerals
Posted Jun 11, 2017 by Esther 1950
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I think that there is a clinic carisima in dallas Usa which I am not.I peemitir. But if that could be the governments habiliata areas white for us to have a quality of life.
Posted Sep 9, 2017 by Karma 1900
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It seems that every time he goes giving more awareness among the medical staff, but there is a long way. I hope that some day all the doctors to know the disease, even if only in name...
Posted Sep 10, 2017 by Pilar 2000
