★★★★★
I have scleroderma. My hands were sore, stiff and swelling. Getting digital ulcers every couple of mths. The borax protocol seem to help the symptoms plus was feeling better in general. I also take colloidal silver msm in green juice, water kefir, probiotics, colostrum plus some other supplements and essential oils. Autoimmune disease is epidemic and yet you hear very little about it. It effects each person individually. Drs just want to give us drugs to suppress the symptoms instead of attacking the root cause of the disease and seems like the research doesn't do anything to prevent the disease. It all starts with leaky gut syndrome. When we can't absorb essential nutrients then our bodies cannot fight off invaders or heal itself. Most AI patients are deficient in Vit. D3, boron and K2. If the body does not have theses essential components then you develop disease such as cancer or AI. They say 1 in 200 people have these diseases and most do not know it. So bringing awareness to people is critical to getting a cure and methods of prevention.
I find the Borax is effective. So when someone worries about the "safety" of this, I always tell them the drugs that are prescribed for my illness are far more "dangerous" than this. LOL.
Borax
Borax
Airborne Pathogens and Idiopathic Diseases
Airborne Pathogens and Idiopathic Diseases
Borax and Liposomal Glutathione
Borax
High Intracellular Calcium Levels for Myosititis
Avoid High Histamine Levels
Autoimmune Paleo Protocol
Avoid High Histamine Levels
★★★★★
Check out 7 Surprising Factors that Can Increase Histamine Levels (And How to Deal With Them):
I couldn't find your post on any TMA forum. I am very much interested in your research.
In February of this year, I was hit with a viral infection that started out as a sore throat quickly followed by terribly achy legs for 3 weeks. I tested negative for COVID, but I don't know the reliability of that test. I have had mild leg muscle aches almost every day since that time. But worse than that is I have a super easy tendency to upper extremity muscle strain, tendon and ligament tears where I'll injure myself just lifting/washing pots and pans or doing anything repetitively like rolling dough.
I plan to have some bloodwork done, including a creatine kinase level and am considering getting a muscle biopsy done. Hopefully, starting today, I will work on lowering the inflammatory foods in my diet. I already take fish oil, cod liver oil and turmeric as well as a multimineral, B complex, and vitamins C, D and E amongst other supplements.
Your recommendations would be super appreciated.
High Intracellular Calcium Levels for Myosititis
High Intracellular Calcium Levels for Myosititis
Scleroderma
Https://www.cancure.org/12-links-page/43-artemesia
"Additionally, Dr. Rowen stated that he adds cod liver oil (for its omega-S and vitamin D) and conjugated linoleic acid (CLA) to this therapy. He says that, with the exception of patients very near death, taking artemisinin or derivatives have stabilized, improved, or remitted every cancer patient he has followed. Medical literature also seems to suggest that oxygenating the system might make the products effective."
You have to avoid any food with iron when taking artemisinin. Pre-load iron beforehand.
High Intracellular Calcium Levels for Myosititis
I am sorry that I never noticed or responded to your query. I don't even recall leaving this post and hadn't received anything in my mail.
I knew absolutely nothing about myositis when I was first diagnosed with it so realised that I needed to find someone who had a preference for natural treatments for disease and who was much further advanced in their research than myself. I annoyed people on a forum by posting pieces on what I did know regarding simple treatments for arthritis and the like.
When I did find the nurse, whose husband suffers from IBM and necrotizing myositis, she introduced me to the issue of defective ion channels and genetic defects. As her own research had stalled, I was able to provide the momentum to take things much further. If you have a combination of the ACTN3XX gene variant and MLCK variant it results in enormous losses of creatinine kinase from your muscles when they get damaged by anything. Researchers have been generally avoiding looking into this despite a Mexican study finding that almost all myositis patients in their test group all had the ACTN3XX gene. Researchers seem fixated upon the idea that the immune response is somehow, magically, kicking out the CK. You can basically guess at whether you have the two genes by whether you were an incredible athlete in your youth. If you weren't then there's a good chance that you do.
Since only one or two percent of genes have been researched, it's a fair bet that there are even more genes which are involved in all of this and I could already speculate on some but don't want to complicate things.
As for the autoimmune aspect itself, I am now aware that this relates to the spleen. It caught my attention that a study done in Georgia in the US proved that baking soda can reset the immune response, temporarily stopping the autoimmune reaction.
Since then, I found out much more about my own condition, which was induced by a paralysed diaphragm (though we are still trying to work out why that occurred), and my attention is now on carbon dioxide. Where cells have lots of mechanisms for detecting low levels of oxygen, and various mechanisms to try to increase those levels, the spleen responds to low levels of carbon dioxide. Essentially this means that the less oxygen your cells are using in metabolism, the less carbon dioxide they are producing. The spleen reads these low levels as being evidence of disease and triggers the immune system to go on high alert. Whatever is causing a particular individuals myositis then draws the attention of the immune systems T cells to the damaged, or compromised (infection), muscle cells and you have what is misinterpreted as an autoimmune reaction.
High Intracellular Calcium Levels for Myosititis
Thank you. Claudia from Sheboygan, Wisconsin
High Intracellular Calcium Levels for Myosititis
★★★★★
If you want to know more about our research feel free to contact me though I already have it posted on an obscure natural treatment thread on the myositis TMA forum.
Your condition is a bit vague, but I suspect a general recommendation could do you a world of good:
Aloe vera Turmeric fresh raw Bok choy Cabbage Fennel Pineapple Beets Ginger fresh raw Lemon juice fresh Colloidal silver Activated charcoal Psyllium husk Oxygenated magnesium bowel cleanser Diatomaceous earth *food grade* Ashwaganda Ginseng Goldenseal Green tea Look into these. I would start with the aloe, turmeric, bok choy, and ginger. Make a smoothie or juice from them for example. It should be quite soothing.
Consider taking vitamin e in generous doses, too. Maybe get some sun. You might want to avoid acetaminophen and nsaids for a while. https://articles.mercola.com/sites/articles/archive/2014/03/26/acetaminophen-overdose.aspx And consider going grainfree and organic to avoid noxious chemicals.
Borax and Liposomal Glutathione
Borax and Liposomal Glutathione
Borax and Liposomal Glutathione
★★★★☆
Recently I started taking liposomal glutathione and have been feeling much better. I recommend this. - I have mild autoimmune issues. I have been taking the “maintenance dose” of borax, only one to two teaspoons of the concentrate a day. It has given me some results I am happy about.
I only take OTC supplements at this point. My doctor has not prescribed me any meds at this point. - Recently my “alt” test is slightly high, 36. I have stopped the borax and the curcumin I have been taking wondering if they are part of the problem. Could or should I switch to boron or fructoborate tablets? I have taken curcumin but not much, only when I felt some pain or neuropathy. - I am having stomach issues and wondered if my stomach issues were also related to the borax or curcumin?
If so, what do you do about it? - There is blue coloring under my fingernails near the lunula. I understand this is sign of low blood oxygen. Could this raise enzymes? Would sleeping with oxygen help me with low blood oxygen? - Autoimmune issues seem to have multiple causes. They could be from fungus, bacteria, viruses or triggered by something like a drug. Borax works against fungus. If you cannot take borax what would be the next best options to take? What would be the best thing to fight viruses and bacteria? Were my physician to give me prescription drugs can you take the boron or borax with them? Is it possible to treat the autoimmune antibodies? I thought about a cleanse but I don't want to damage my organs. What would be a gentle option that works even if it takes longer?
★★★★★
Autoimmune Disease and Vitamin A Toxicity
Viral Link to Autoimmunity
Oh, I hope that the Children's hospital will find the missing link for what will help your grandson!
That is sobering about the possible long term effect of pitocin on children. So many unintended consequences of drugs...
Perhaps the stuttering is related to stress? Many years ago we had an extended family member living with us and it caused a very stressful time in our life. My son who was 5 at the time began to stutter. The stuttering completely ended when that family member moved on. I hope it is also short term for your little guy.
God bless you and your grandson.
~Mama to Many~
Viral Link to Autoimmunity
Viral Link to Autoimmunity
I know our experience with mono has been that it does reoccur! Perhaps that is the reason for those monthly fevers - at the least his immune system is overtaxed.
Are you using coconut oil? It has been the very best thing we have found for mono. It has to be the cold-pressed kind that isn't processed. Unfortunately it isn't everyone's favorite taste. For my adult children, they would take 3 T. a day. Even now, my 19 year old will take coconut oil for viruses since he sees how well it has helped him in the past.
For a little guy though, 1/4-1/2 teaspoon three times a day is likely sufficient. Some people experience digestive distress with coconut oil; my family never has though.
I have also probably mentioned that nettle has been huge for us for immune strengthening. I use nettle leaf capsules but tea and tincture work as well. Tincture is easily hidden in anything. A dose of it would be 5 drops a couple of times a day.
I know that you are concerned about the steroids. I don't like them either. But I know you may not have the final say about whether are not they are used. If they are, be encouraged that they may be a help to get over a health hump. We have used them a few times with children over the years in desperate poison ivy situations. Recently we did this for one of my sons. But he continues to mow and get into poison ivy. At first he was still breaking out some (though not nearly as bad.) even after the steroids. But I have been giving him nettle daily for maybe 6 weeks and he is currently poison ivy free, though I am sure he still gets exposed here and there.
I am so glad that your grandson has you on his side. You have done so much for him.
I hope you find just the solution for him.
~Mama to Many~
Viral Link to Autoimmunity
Airborne Pathogens and Idiopathic Diseases
★★★★★
Hello,
I can't remember if I already contacted you but this common but overlooked airborne pathogen is known to cause rheumatological syndromes (during a large outbreak of over 100,000 victims in Indianapolis) and this type of microorganism has been suspected for decades to cause gout:
https://pdfs.semanticscholar.org/f1b7/6b287b9595328716016b6815473714e3e532.pdf
Some online documents state this cancer-causing, mental illness-inducing airborne pathogen that can cause so many idiopathic diseases/conditions/symptoms is not zoonotic. That's wrong! It's carried by bats and shed in their feces. The bats even evolved to deal with the photophobia and tinnitus the pathogen causes by hunting at night by echolocation.
My coworkers and I, all immunocompetent, got Disseminated Histoplasmosis from roosting bats, that shed the fungus in their feces. The doctors said we couldn't possibly have it, since we all had intact immune systems. The doctors were wrong.
This underdiagnosed airborne infectious disease mimics the flu and can cause hematological malignancies, precancerous conditions, rheumatological diseases, connective tissue diseases, heart disease, autoimmune symptoms, inflammation, adrenal insufficiency, seizures, migraines, hydrocephalus, hallucinations, etc., etc. etc. and is often undiagnosed/misdiagnosed in immunocompetent people.
More than 100 outbreaks have occurred in the U.S. since 1938, and those are just the ones that were figured out, since people go to different doctors. One outbreak was over 100,000 victims in Indianapolis. 80-90+% of people in some areas have been infected, and it can lay dormant for up to 40 years in the lungs and/or adrenals.
It's known to cause hematological malignancies, and some doctors claim their leukemia patients go into remission when given antifungal. My friend in another state who died from lupus lived across the street from a bat colony. An acquaintance with alopecia universalis and whose mother had degenerative brain disorder has bat houses on their property.
Researchers claim the subacute type is more common than believed and that many children in California have the subacute form. It's known to at least “mimic” autoimmune diseases and cancer and known to give false-positives in PET scans. But no one diagnosed with an autoimmune disease or cancer is screened for it. In fact, at least one NIH paper states explicitly that all patients diagnosed with sarcoidosis be tested for it, but most, if not all, are not. Other doctors are claiming sarcoidosis IS disseminated histoplasmosis.
What if this infection, that made us so ill, isn't rare in immunocompetent people? What if just the diagnosis is rare, since most doctors ignore it?
Older documents state people who spend a lot of time in a building with roosting bats and in caves are known to get Disseminated Histoplasmosis, but the info appears to have been lost, for the most part. And now bat conservationists encourage people to leave bats in buildings/homes. What a terrible mistake they've made.
This pathogen parasitizes the reticuloendothelial system/invades macrophages, can infect and affect the lymphatic system and all tissues/organs, causes inflammation, granulomas, and idiopathic (unknown cause) diseases and conditions, including hematological malignancies, autoimmune symptoms, myelitis, myositis, vasculitis, panniculitis, dysplasia, hyperplasia, etc. It causes hypervascularization, calcifications, sclerosis, fibrosis, necrosis, eosinophilia, leukopenia, anemia, neutrophilia, pancytopenia, thrombocytopenia, hypoglycemia, cysts, abscesses, polyps, stenosis, perforations, GI problems, hepatitis, focal neurologic deficits, etc.
Many diseases it might cause are comorbid with other diseases it might cause, for example depression/anxiety/MS linked to Crohn's. (It's known to “mimic” inflammatory bowel disease.)
The fungus is an Oxygenale and therefore consumes collagen. It's known to cause connective tissue diseases (Myxomatous degeneration?), rheumatological conditions, seizures, and mental illness. Fungal hyphae carry an electrical charge and align under a current. It causes RNA/DNA damage. It's known to cause delusions, wild mood swings (pseudobulbar affect?), and hallucinations. It's most potent in female lactating bats, because the fungus likes sugar (lactose) and nitrogen (amino acids, protein, neurotransmitters?), releasing lactase and proteinases to obtain them. What about female lactating humans…postpartum psychosis (and don't some of these poor women also have trouble swallowing)? The bats give birth late spring/summer, and I noticed suicide rates spike in late spring/early summer. It's known to cause retinal detachment, and retinal detachments are known to peak around June-July/in hot weather. A map of mental distress and some diseases appear to almost perfectly overlay a map of Histoplasmosis. Cancer is known to occur more often near rivers than in mountains or deserts, just like this infection. Johns Hopkins linked autism to an immune response in the womb. Alzheimer's was linked to hypoglycemia, which can be caused by chronic CNS histoplasmosis.
The bats eat moths, which are attracted to blue and white city lights that simulate the moon the moths use to navigate, so diseases in cities would be expected to increase. Bats feed up to 500 feet in the air and six miles away in any direction from their roost, but not when it's raining or when the temperature is less than approximately 56° F. The fungus can grow in bird feces, but birds don't carry it because their body temperature is too high, killing the fungus.
I believe the “side effects” of Haldol (leukopenia and MS symptoms) might not always be side effects but just more symptoms of Disseminated Histoplasmosis, since it causes leukopenia and MS symptoms. What about the unknown reason why beta receptor blockers cause tardive dyskinesia? The tinnitus, photophobia, psychosis “caused” by Cipro? Hypersexuality and leukemia “caused” by Abilify? Humira linked to lymphoma, leukemia and melanoma in children? Disseminated Histoplasmosis is known to cause enteropathy, so could some people thought to have nonsteroidal anti-inflammatory drug enteropathy have it and taking NSAIDs for the pain/inflammation it causes, and the NSAIDs aren't the actual culprit?
From my experience, I learned that NO doctor, at least in DFW, will suspect subacute and/or progressive disseminated histoplasmosis in immunocompetent people. Some doctors, at least the ones I went to, will actually REFUSE to test for it, even when told someone and their coworkers have all the symptoms and spend a lot of time in a building with bats in the ceiling. Victims will be accused of hypochondriasis. (My doctors told me only farmer's or AIDS patients get it, it's only in bird feces, and it always infects the lungs...wrong, wrong, and wrong!) In fact, the first doctor to diagnose me was a pulmonologist, and the only reason he examined me was to try to prove that I didn't have it, when I really did. No doctor I went to realized bats carry the fungus. And NO doctor I went to in DFW, even infectious disease “experts, ” understand the DISSEMINATED form, just the pulmonary form, and the only test that will be done by many doctors before they diagnose people as NOT having it is an X-ray, even though at least 40-70% of victims will have NO sign of it on a lung X-ray. It OFTEN gives false-negatives in lab tests (some people are correctly diagnosed only during an autopsy, if then, after obtaining negative test results) and cultures may not show growth until after 6-12 weeks of incubation (but some labs report results after 2 weeks).
One disease of unknown cause that could be caused by Disseminated Histoplasmosis: I suspect, based on my and my coworker's symptoms (during our “rare” infectious disease outbreak) and my research, that interstitial cystitis and its comorbid conditions can be caused by disseminated histoplasmosis, which causes inflammation throughout the body, causes “autoimmune” symptoms, and is not as rare as believed. I read that “interstitial cystitis (IC) is a chronic inflammatory condition of the submucosal and muscular layers of the bladder, and the cause is currently unknown. Some people with IC have been diagnosed with other conditions such as irritable bowel syndrome (IBS), fibromyalgia, chronic fatigue syndrome, allergies, and Sjogren's syndrome, which raises the possibility that interstitial cystitis may be caused by mechanisms that cause these other conditions. In addition, men with IC are frequently diagnosed as having chronic nonbacterial prostatitis, and there is an extensive overlap of symptoms and treatment between the two conditions, leading researchers to posit that the conditions may share the same etiology and pathology.” Sounds like Disseminated Histoplasmosis, doesn't it?
My coworkers and I were always most ill around May, presumably since the Mexican Free-tail bats gave birth in Texas during May (and the fungus was most potent), and late fall/Thanksgiving to December, for some unknown reason (maybe migrating bats from the north?). We had GI problems, liver problems, weird rashes (erythema nodosum, erythema multiforme, erythema marginatum/annulare, etc.), plantar fasciitis, etc., and I had swollen lymph nodes, hives, lesions, abdominal aura, and started getting migraines and plantar fasciitis in the building, and I haven't had them since I left. It gave me temporary fecal incontinence, seizures, dark blood from my intestines, tinnitus, nystagmus, blurry vision/floaters/flashes of light, benign paroxysmal positional vertigo, isolated diastolic hypertension, what felt like burning skin, various aches and pains (some felt like pin pricks and pinches), tingling, tremors, "explosions" like fireworks in my head while sleeping, and temporary blindness. Suddenly I was allergic to Comice pears (latex fruit allergy or oral allergy syndrome?). I had insomnia (presumably from the fungus acidifying the blood, releasing adrenaline) and parasomnias. It felt like strong bursts of electrical shocks or steady electrical currents in my body, which now feel like low electrical currents at times, mostly at night. I was always worse at night (because bats are feeding? Or maybe because fungus follows a circadian rhythm?).
I suddenly had symptoms of several inflammatory/autoimmune diseases, including Fibromyalgia, Sarcoidosis, ALS, MS, Sjogren's syndrome, etc. that have disappeared since leaving the area and taking nothing but Itraconazole antifungal. No one, including doctors (we all went to different ones), could figure out what was wrong with us, and I was being killed by my doctor, who mistakenly refused to believe I had it and gave me progressively higher and higher doses of Prednisone (2 years after I already had Disseminated Histoplasmosis) after a positive ANA titer, until I miraculously remembered that a visiting man once told my elementary school class that bats CARRY histoplasmosis. There's a lot more. I wrote a book about my experience with Disseminated Histoplasmosis called “Batsh#t Crazy, ” (now you know where that term, “bats in the attic/belfry, ” and “going batty” came from) because bats shed the fungus in their feces and it causes delusions and hallucinations, I suspect by the sclerotia fungal mycelia can form emitting hallucinogens (like psilocybin and dimethyltryptamine) along with inflammation in the CNS. (Schizophrenics have 2X of a chemical associated with yeast, part of the fungal life cycle.)
Thank you for your time,
Susan McIntyre
P.S. Doesn't this infection share all the same symptoms with Gulf War Syndrome?
Borax
Bicarbonate of Soda
★★★★★
The study was on rodents but some healthy student volunteers were also followed for 2 weeks in a small human study. After taking 0.5 tsp bicarb dissolved in water every day for that time their immunity was pronounced to be improved. I can report that following this regime for 4 weeks has produced no noticeable effect. Symptoms are unchanged. As ever, one wonders whether those humans studied had a healthy diet/lifestyle to begin; otherwise the bicarb could simply be countering an acid diet.
Gluten Free Diet for Polymyositis
★★★★★
My son was diagnosed with an autoimmune disease that I had never before heard of. It's called polymyositis. This disease caused the protein in his blood to rise to 11000. The norm for men is 200. He developed all type of symptoms, swollen joints, dry eyes, rashes all over his body, liver infection, water in his lungs and around his heart. He was hospitalized for a while and was treated with high doses of steriods. He did better after the steriods but I had concerns about the side effects of the steriods. I prayed to God every day to help me to help my son.
One day out of the blue an email about autoimmune diseases and gluten pop up in my email. That was the answer. My son has been gluten for 4 months and he is doing fine. No more steriods. If he accidentally eat something that contained gluten, he knows within half an hour.
Scleroderma
Borax
★★★★★
In one day, my hoarse voice (thyroid symptom) of years returned to normal and my stomach feels relaxed. I'll continue with this low dose as long as it's effective but I personally know two severely arthritic people (with other AI problems) who take the large therapeutic dose with incredible success. I'm looking fwd to more symptoms disappearing, and plan to report back soon.
Steroids
Your response is important to me because my mom has a Pemphigus Vulgaris and using 8 mg prednol and 150 mg immuran daily.
Ganoderma lucidum is a option to cure this ill? If it reinforces the immun system, it could empower the illness also. I need a solution that modulates the immune system to discreminate antigens.
Autoimmune Paleo Protocol
Dehydration is the reason the body creates histamine. Dehydration is not just cured with water but minerals in balance with water
Rashes can be caused by histamine
I learned all this the HARD WAY.
Autoimmune Paleo Protocol
Steroids
Dapsone costs AUS$103.00 for 100 tablets, however I do get them for very little (about AU$6.00 on our national health scheme.)
If you do Google Dapsone and its side effects, don't get frightened off because to my mind the alternative drugs that are on offer I consider to be worse than the disease itself. All drugs have side effects, you just have to weigh up the pros and cons.
If you want to chat further away from here, I can give you my email address. All the best and good luck.
Pemphigus Foliaceus Remedies
Steroids
I'm curious did you have any symptoms of high blood sugars while taking these meds?
My mom now has diabetes from all the prednisone usage due to her pemphigus foliaceus, and her doctor is trying to wean her off of it.
Are the drugs you're using very expensive?
Looking for alternatives in Oregon,
~Melissa
Dietary Changes
LDN
★★★★★
Dietary Changes
Antiphospholipid Syndrome Remedies
Turmeric
Turmeric
Antiphospholipid Syndrome Remedies
Turmeric
This earthclinic.com has been a wonderful site for me and am a regular reader since last 10 years. I am sure all your feedback and comments have helped tremendous people with their conditions including me. I am a big fan of this website.
I wanted to know if anyone can share the benefits of using Turmeric for Auto Immune Diseases like Crohn's, IBD or Lupus. I have read on earth clinic and multiple other sides the benefits of turmeric.
I have been giving turmeric to my 10 year old DD who has been diagnosed with some Auto Immune Disease but doctors are not 100% sure whether it is Crohn's, Lupus, IBD or Arthritis. I take 1 teaspoon of turmeric powder and put some black pepper in it and feed her with water. She gulps it down easily but haven't noticed any benefit in her health so far. On the request of doctor we have been doing blood test every 2 weeks but her
Her diet has been pretty healthy and mostly vegetarian food. She is not eating any sugar, no wheat, no soy, no milk and no potatoes . She eats lot of homemade yogurt, all vegetables, fruits, rice and some pulses.
She has been loosing weight and we are very much concerned. I would really appreciate if someone can throw more light on turmeric and how to use it and has it benefitted someone with these conditions. She is on prescribed medications since last 6 months but we haven't seen much progress in her. Overall she does not have any issues related to Crohns or Lupus or IBD or Arthritis . She is not gaining any weight or height.
I would really appreciate for your help and reply. Thank you.
Please help.
Allopathic medicine, though it has its place, only offers band aid solutions with toxic drugs. I would encourage you to seek out if possible an Integrative physician if you can afford it. It isn't cheap but sometimes if the doctor really wants to help, they will work with you financially. I sincerely wish you the best in your quest for health.
Antiphospholipid Syndrome Remedies
Supplements
Scleroderma
★★★★★
She takes 4 mgs at bedtime daily. I read that she has to take it between the hours of 9:00 PM and 3 AM (it works in conjunction with serotonin), but she hasn't been doing that as she often gets to bed around 2:00 AM. We're working on her getting to bed earlier as she hasn't been noticing any changes with it controlling pustules and itching. Timing is everything, I guess.
It's a S-L-O-W acting drug as we're told it could take a long time before it finally works.
Her doctor said she's working with another patient who is taking low-dose naltrexone, and it's taken 4 years for it to finally calm her patient's immune system down.
A lot of doctors don't like prescribing it, because they see it as only being implicated for substance abuse patients withdrawing from the effects of alcohol. As a result, most insurance co.'s won't cover it because it's not FDA approved.
However, there have been studies done that show its effectiveness in patients with pemphigus foliaceus. I'd recommend searching for "naltrexone and autoimmune diseases" or "pemphigus foliaceus" in Google to find the specific studies. They're out there!
I hope this helps and good luck!
Dietary Changes
★☆☆☆☆
Steroids
This being said, I thought back to when this issue started. It started not too long after I started working at a California UC Hospital. In order to work there you must be up to date with Vaccines. I had MMR, TDP, TB tests and I want to say there was one more. I never get the Flu shot and I never take antibiotics. I'm started to wonder if this could be a contributing factor to my scenario......
Vaccine Adjuvants
Your doctor tells you it is all in your head, you are just a hypochondriac imagining you have such severe problems. Maybe you just want attention. Maybe you are depressed and feel like wasting your doctors valuable time to treat a disease that does not exist. Perhaps you should go home take your antidepressants and speak to a psychiatrist
Or maybe you have an autoimmune disease.
Where did it come from? how did I get it? The answers may shock you.
A Glimpse into the Scary World of Vaccine Adjuvants - Http://vaccinechoicecanada.com/vaccine-ingredients/a-glimpse-into-vaccine-adjuvants/.
Pemphigus Foliaceus Remedies
LDN and Medicinal Mushrooms
The company that was used by the person with MS for the Lion's Mane is here:
http://mushroommatrix.com/store/mi/nrg-matrix-ingredients
This product is offered on many other health store sites as well as this one. Best wishes.
LDN and Medicinal Mushrooms
Dietary Changes
Viral Link to Autoimmunity
Viral Link to Autoimmunity
In answer to your question about how to drink CS...
I make my own and dilute to about 30 to 40 parts per million. I drink that as is, without more dilution.
Viral Link to Autoimmunity
Antiphospholipid Syndrome Remedies
Get the word out to others who are suffering.
Antiphospholipid Syndrome Remedies
Dietary Changes
Auto-Immune Disease is another name for Vitamin Deficiency Disease and makes the immune system is incapable of defending us from parasites, diseases and toxins.
Most spices are very nutritional and many are medicinal. Makes very interesting research.
Quote, Dr F R Klenner, " white blood cell without adequate vitamin 'C' is like soldiers without bullets". dez...
Dietary Changes
Antiphospholipid Syndrome Remedies
Good Luck, James
Scleroderma
I've read recently that DMSO was very helpful for this. A lady gave an account in senate about DMSO reversing it. This isn't a first hand account though but worth researching more I'd say. Good luck!
General Feedback
N-Acetyl Glucosamine
★★★★☆
