Here is my brief story outlined in a list! I would love to hear what others may have experienced
OCtober 2009 - Son born
DEcember 2009 - IUD place
2/1/2010 - Woke with one sided facial numbness which over the next 3 months turned into
1. Muscle fasciculations (twitching) in legs mailny calves
2. Perceived Weakness
4. Facial tingling and a feeling of facial numbness
5. Tingling in legs and arms
6. Weakness in one hand
7. Adies pupil and blurry vision
8. Feeling of heaviness in legs
9. dizzy at times and feeling almost drunk when walkings
10. Weight gain, especially after weening, literally 7 lbs in a week and I run 9 miles a day
I have had 1. Brain MRI 2. Spinal MRI 3. Optic Nerve MRI 4. Opthomologist visit 5. Evoked potentials and 3 neurological exams 6. Blood work. Everything is 100% normal. I am so scared it is something else but NONE of this started happening until Mirena. I just got Mirena out on Friday and hjave to say I am feeling better
Wow. I've struggled with #1-9 at various times over the last year since I've had the Mirena removed. I started having problems after it had been in for 1 1/2 years. I had it placed when my baby was 10 months old, however, so a little later than you. I had a brain and optic nerve MRI. Both normal. I feel better after a year since having it out, but still struggling mostly with tremors, weakness in my arms and legs (worse on the rt. side), heavy legs, vision distortio, slight dizziness (it was vertigo at first so this much better and doesn't bother me too much), occasional twitching (most recently my eye lid twitching horribly for a month. Now it has stopped.
Get the IUD out and start recovering! Glad you've joined us!
I hope you are doing ok and have continued to feel better. Thank you for sharing you symptoms.
I had mine in for 4 years
only leg pain
Arrived at complete loss of posture
Began to have sudden weakness
upper back pain
Emotionally like I was pregnant
Lack of coordination of legs and hips
Flu like symptoms
Loss of appetite
extreme pain in various places
Numbness in half of face and slight damage to vision on that side
pain in knees
loss of walking
feeling like nothing is supporting my insides
See sick felling
exhausten all the way through
obbsessive thoughts about suicide
7 weeks post
Have regained walking
Weakness has improved
No more anxiety
Feel that my body tissues are damaged but don't know what to do about it.
Still some pain
horrible feelings in body
extreme body odour
Auto immune tests
have all come back clear, but I know something is still wrong.
Having nerve and muscle tests on the 15th
Thats my Mirena story told a concisely as I can and i have probably missed some symptoms. This site is amazing and you will find it an absolute godsend through your recovery. Take it easy on yourself. This can be a slow process, so give yourself time.
November 2009 -son is born
January 2010- IUD inserted
end of OCt. 2010 when I started weaning my son I noticed a numb spot would come off and on in the middle of my back, like someone had applied icy hot. I also had a day of vertigo.
since then, I have experienced the following:
1. facial numbness and tingling, more on the right side around the ear, but also other parts of my face and lip.
2. legs numb and tingly especially calves. More on the right side also.
3. restless leg feeling, especially at night. My leg feels tight and like it wants to twitch, but it doesn't
4. My body kind of jerks as I am falling asleep, like I am scaring awake.
5. stiffness in knees, particularly when I take a bath.
6. Numbness and tingling in arms and hands
7. dizziness and nausea -I feel like when I am pregnant or motion sick.(I am NOT pregnant)
8. throbbing/aching in legs, more in right leg
9. anxiety -probably due to the fear of having MS
I have had an MRI- it showed tiny spots, but the neurologist wasn't sure if they were normal for my brain or due to something else. The report said not diagnostic of MS, but early ms could not be excluded completely.
Blood work was all normal. I had a spinal tap, but the results will not be back until later this week. I am praying it is all normal and I do not have to head over to the MS forum. I have not had my Mirena out yet, but if this test is normal, I will.
Hope this helps you!
I am so thankful to have found you all. I have had so much anxiety that even thought ALL tests point to this not being MS it could be. But now that I know that others are out there with the same problems I feel so relieved. Trisha, I will be eager to hear what spinal says; I am confident it will say nothing!
My report said exactly the same thing...two tiny spots not diagnostic of MS, but early ms could not be excluded completely.
I am scheduled for an MRA tomorrow because I have an unusually large blood vessel in my head and I guess they are worried about aneurism (sp?).
Funny thing is, my facial numbness has disappeared in the couple of weeks that I have been making trips to the neurologist. Now, I spent Friday night in the ER having chest pain, for them to tell me it wasn't my heart, but my chest wall muscles spasming.
Gotta love Mirena!
What did your neurologist say about your MRI report? Did he think it could be normal for your brain? Did he encourage you to have a lumbar puncture (spinal tap)? I am so happy to hear someone else had something show on their MRI, but still not MS. I have been thinking I was doomed because mine showed something and everyone elses was clean. I am praying this is just the Mirena. There is a good chance I will have spinal tap results tomorrow. I will let you all know. PLease keep praying for normal results! I want this chapter in my life over!
My brain MRI said I have 15-20 tiny lesions on each side of my brain. My follow up with the neuro is Wed. The report said the pattern is not the usual for MS, but it can't be excluded. Could also be blood vessel problems. I think they will do more tests. . .I am 15 months post but Mirena was outside the womb so I got a 10x dose of progestin (according to the 1 medical journal I found on the subject-)Good luck on your results, fabteach, and welcome ashymae.
I haven't gone back for the revisit since the MRI since my doctor has cancelled out on me TWICE. I went to the hospital and picked up my own report. I'm supposed to go in next Wed. to see what the doc. says.
Hi- I know this is an old post- any updates on your results? How are you feeling now?? I am about 3 months post removal and still have symptoms. This has been the worst year ever. Any updates would be helpful. Xo allie
The side effects that everyone is experiencing, that they think is or is like MS, is not MS it is a bad side effect of levonorgestrel, a harmon that they use in your IUD/Mirena. If you are having these side effects, you should have it removed as soon as possible by a ob/gyn, not yourself, and do not let anyone talk you out of doing it, unless you want to have worst problems. You can look at the list of side effects caused by levonorgestrel on, http://www.drugs.com,
and put levonorgestrel in the search engine.
I just got my IUD out on friday and already feel much much better. It is almost like a year from absolute hell that is finally over. I cannot believe all of the MRI's and other tests I went through were,most likely, due to mirena
I am from Poland, and- any way, first sorry for all my mistakes and missunderstundies ;)- but I'm reading this forum and I start to scare! I have Mirena since 3 months and I feel worse and worse :( I saw many doctors- and nobody see anything bad, but I feel sick! Do you really think that there is a problem with MIrena?
In Poland all of doctors whom I know (gin) say that it is the best way and the most saftly from the other??
I will be really very happy when you will answer me!
All I know is that I never had visited an online health forum in my entire life until my health fell apart while I had the Mirena in. I am slowly getting better now that the Mirena is out. My Dr. also said the Mirena couldn't do this. Just about every one on this forum had a Dr. who said the Mirena could not to do this. But they are obviously wrong (the Drs.). Just keep reading, and you will start to see the truth.
I'm reading these posts and literally feeling like there might be hope in the future for me. I am having my Mirena out next Friday. My doctor says "It's been lost in your vagaina". Great.
I had my IUD put in in 2009 with very little side effects. I was thrilled that my periods were so light. I bragged about how great it was.
This summer has been living hell. I woke in the middle of the night to painless muscle twitching in my legs. Annoying, but I didn't think much of it. Now, in October, I have muscle twitching over my entire body, my leg and arm muscles are so weak I can barely walk or hold my hairdryer. I have had MRI's, xrays, bloodwork enough to fill the blood bank, Lyme disease testing, nerve testing, and seen 5 different doctors. I cry ALL the time. A mother of 2 (3 if you count my husband) I don't want to slow down, and this has literally immobilized me. At one point I thought I was having a seizure because the "buzzing" wouldn't stop. My joints are inflammed, and I hurt everywhere. I sleep, but wake up as if I haven't slept in days.
My doctor's response "You must have a virus". Thank you all for posting and making me feel as though there is hope on the way. I will keep you posted on my status after they rip this thing out of me!
What makes you think that your meat can not be roast?
You play with the fire? Why are you surprised that the fire will burn? All the places are painful have a correspondence with a pocket with a purse or with a place in which hold for a very long time a cell phone in operation.
See the leaves from the top of the tree? The same happens to our cells next to the cell phone. Do you still keep the cell phone next to Your brain? Now you know the cause of all the problems your health?
Do you think that option is your highness? Do you think that is only your problem? You are wrong. Is the problem of all. A cell phone affect the environment into a sphere with a radius of 5000 m. A router affect the environment into a sphere with a radius of 250 m. There is nothing to stop the propagation of them. This problem is the problem of all.
Please help me! It started off with a slight sensation of wormlike creatures (really just general crawling sensations) underneath my scrotum and the skin between the scrotum and the anus. I just went about my day and thought nothing of it. Then they progressively got worse. I felt wormlike creatures crawling around in my legs at a steady crontrolled pace, the creatures being of all different sizes but the same shape. Note I have not actually seen anything just felt. And I am not on drugs and am not making this up. Okay so back to the point here, they traveled down to my feet and at this time they were only in that area there was nothing in my torso neck and head. In the morning I would feel an intense sensation like they would go into my penis and start pushing outward as if trying to escape and then give up and go into the thigh. I felt one go into an area in my leg and the area went cold and felt as it a liquid dripped down my thigh on the inside and traveled down the thigh and into the calve and when it hit the foot area it was gone. Over the next couple of days I felt worm like creatures travel up into my arms and I was slurring my speech really badly and was off balance, I had horrible brain fog and I felt these things crawling like crazy. So I was admitted to the emergency room with a blood pressure of 150/90 and all the people there thought I was nuts. I finally got out with my blood pressure back at normal and I went home. Well the feelings didnt go away their now worse then ever. They have entered my torso and I feel pins and needles in my stomach. A few days ago there was absolutely no crawling sensations in my head. I then felt something travel up my neck into my head and the next morning I felt a HUGE worm like creature crawl across my brain on the outside and stop. When I wiggle my head or grind my teeth it retracts or moves. I now feel like theres something in my eyes. And it feels like there is a whole host of worms in my brain and my face and my lip all the time. Ill feel a bunch of random symptoms such as it feels like theres a hole in my lungs and it hurts really bad when I breathe in all the way (could a parasite have swum through the tissue?) and then within half an hour the sensation was gone. I woke up with my jaw hurting alot. Im tired absolutely all the time. I get intense headaches in a very specific spot and it soon clears up (could this be a worm digging into my brain?) The symptoms are getting worse. My doctor gave me a stool sample and said it was clear. He says I have no parasites and that these symptoms are all in my head. He says that it isnt possible to feel worms moving around inside you. I got a bloodtest and it turns out that my vitamin b6 level is around 56mg which is considered an overdose amount. Some of the symptoms are neurological symptoms and parasitosis. But their just taking about tingling sensations in the arms and legs not things moving around inside you. So im here to ask all of your opinions. Do you think I have some kind of serious parasitic infection or is it deffinitely all in my head and being caused by the vitamin b6? Thank you all.
Well we worm our cats, dogs, horses, livestock etc... if they all have worms what would make us so special that we wouldn't have them? We do. I personally use Humaworm (its on curezone has its own forum). I have visibly seen white worms and liver flukes and other stuff. The doctors do not want to admit that they could or do exist in us. Hence why I found Humnaworm which works great. The first time the die off was awful but since then I haven't really experienced anything to horrendous. I intend to continue using Humaworm probably for the rest of my life, it works and it works ALL over the entire body.
I have a fair amount of knowledge about parasites due to my own situation.
First of all western med docs are poorly trained in parasitology even infectious disease doctors. testing is highly unreliable, even the inf disease doctor I saw admitted that. the proper lab to test is MetaMetrix GI Effects Stool test, the reason this is the best is that they use PCR testing which can find a needle in a haystack. If you are having gastrointestinal issues (which would indicate a possibility of parasites) then this test will find them. If you do the test do not do the complete profile but opt for the parasite/bacteria panel.
It is possible for parasites to disseminate which means they can leave the gastrointestinal tract and migrate to other body organs (although this appears to be rare).
If this is the case (dissemination), alternative treatments (herbal formulas) are not going to be that effective but rather prescriptive meds would be the choice (agents like Albendazole).
There is a parasite forum and a parasite drug forum here on curezone, although I would warn you that some of the information is misleading. You need to seek expert advice and not from amatuer parasitologists although some can have beneficial information.
kill tapeworms. Zymex II kills (digests) them. I just bought it for $14.00 for a 30 day supply. Doc Sutter says you should repeat the process two times. I would give you the same advice I'm following...even if you don't know what parasites you have, take it, it's cheap and worth it just in case. If I were in your shoes, I'd take them both (and I am) and call the companies and ask if they could overnight them to you due to your extreme situation. Here's the link http://www.standardprocess.com/display/StandardProcessCatalog.spi?ID=163
Hi I too have the same exact symptoms. I had had these worms like things in my body for 3 years. your right the doctors do say I'm crazy . but the worms are in my thighs and move to my anus to my crotch area even in my penis. they seem to come up to anus and i can hear them breathing . but they go everywhere and anywhere. I have been looking for a solution for quite a long time. the skin on my thighs have gone dead as they feel like they are eating my fleash from the inside. if you find a cure or a doctor please let me know and if i find a cure or a doctor i will let you know. thanks alot. nice to know that i'm not alone in this. ps. ever since i had these worms i have been aneimic. that ought to tell the doc but the don't care.
thank you all on your imput. glad to know im not crazy lol and ill be sure and let you know if I find a solution poster above me. Well to give you all an update ive pretty much plateaud ive been to a neurologist to rule out the posibility of nerve damage because my left foot has partial numbness and i get random pains such as burning sensations in my fingers when i run them under water. And ive been off balance and still have the brain fog. I used to get goose bumps constantly even in a warm room. and my neck has been crackling when i twist it and that never used to happen before. my jaw also builds up something inside it that makes a very loud cracking sound at first when i move my jaw from left to right and then a squishing sound. maybe a cyst? there are some days when im jittery and others where im very tired. Ive also noticed an increase in floaters. anyway ive been rambling so sorry for that lol. The neurologist says that the symptoms are not related to my nerves...which means it must be real right? ive also been noticing really foamy pee lately if that means anything. Im gonna order some humaworm to see if it does anything. Ill post afterwards to let you all know. Thank you all for posting! God Bless.
I am happy to come accross this site. Pls, I need any one's advise that will help. I took a worm expeller more than 10 years ago and since then I have been feeling plenty worms moving around my body. They went to the head first. As i took more worm expeller to kill them, they went to other parts of my body (eye, my chest, back,leg, joint, all over). The worm expellers are not able to kill them and the medical Doctors cannot help.
It has even gone worst at the moment. Once I eat any food presently they will start moving. It is really painful and furstrating as they move in my body.
Someone should please advice, particularly if you had a similar case and you were able to resolve it.
I am writin from West africa, can I get help closer to me here since I don't stay in US to acquire the products mentioned earlier in this site.
Hoping to get some response soon.
Thks in advance.
From Mr. Daniel Ade
I can see you wrote this post long time ago in 2009 and I just found it today 03/03/2016.
I has been trying for years to find someone else that could feel the same symptoms because I am not crazy and now I see I am not alone with this.
I has been feeling wormlike moving around inside my body since 2007, I already visit different kind of doctors: Neurologist, infection deseas specialist, gastroenterologist, rheumatologist; and nothing change, all of them do not accept that there are parasites in USA, they always asked me if I traveled to another country and I didn't. They think that only a person who traveled out of the country MAY have the possibility to have parasites (their mind is closed with that), they don't keep their mind open to any possibility and that is why they are not trained on this.
I think all this symptoms are new and strange for them and that makes me think this parasite is an undiscovered yet.
When my anus has been itchy I collected something that look like eggs and I show them to some doctors and they didn't pay attention, WHAAAT!, they are idiots or what because the answer is in front of them.
I just need to find a real profesional that is not only interested to get money from the insurance, someone who can run the extra mile and investigate or refer me to a research crew. BUT THAT LOOK IS IMPOSSIBLE!!
I hope one day we could fight together and show them that they were wrong making us to have a nightmare life with these symptoms and don't get the appropriate treatment.
I hope to get an update from you. Tell me if you found the cure or a good doctor.
No matter how long and confusing is the list of symptoms a person has, from chronic fatigue to infertility to mental problems, I am sure to find only two things wrong: they have in them pollutants and/or parasites. I never find lack of exercise, vitamin deficiencies, hormone levels or anything else to be a primary causative factor." 'Cure for all Diseases' page 2.
So----get her book (free download here), do her parasite cleanse WITH zapper, and then start detoxing. It worked for me. :) And you don't feel parasites; you're feeling toxins causing your blood vessels or nerves to spasm.
Everything you mentioned is what I am experiencing and more. They seem to bite! Travel very fast throughout when I am perfectly relaxed or lying down to rest. Starts with my thigh, tremors, like a stampede of things moving around rapidly then to areas once did traveled. The nose, ears, down my arms back, butt eyes. I too feel my mobility is effected, sometimes light vertigo, and I feel like some of my memory is affected. Lots of testing resulting in no parasites present. Must be in my head! Now I believe it is literally IN my head. Where can we get help!
I have (4) german homeopathic remedy treatment packs for free if interested. each pack is a (10-week) protocol. Product cannot be purchased in the U.S. and is only made in Germany. Product expires 12/09 but is obviously still good for use. I spent very good money for them and you will never see these again I can assure you. Product can be taken orally or injected itramuscularly (like vitamin B-12) and is not a controlled substance. I'd be willing to send (1) pack per person to those who would like to try this if interested, I only ask that you pay shipping and handling for Priority Mail $5.25(2-3 days). You can also view a video on these rare remedies if also interested on youtube. Just enter: TheRemedyman into serch engine for viewing if interested. Thanks and take care! chiropractor31 ( S$H payment of $5.25 has to be sent via PayPal account).
I am researching people who have claimed to be cured by MS or atleast in complete remission so I can build a presentation for my family in the event of gaining support for helping to put my mother on a thorough cleansing program.
So far I have manage to compile a list people I have found online.
Debra D Kaiser - remove Amalgam fillings + chelation + ozone therapy symptom free 2 years
Jacque C. Rigg - diet + supplements + mind power
Nancy Delise - Colloidal Silver symptom free 2 years
Gina Kopera - fasting + diet + exercise + cayenne symptom free 4 years
Lisa Cochran - remove Amalgam fillings symptom free after 10 days
Dale Humpherys - diet + supplements + injections symptom free 2 years
Roger mcdougall - diet + supplements condition improve after 4 years treatment
Jean-Pierre Bély - Grotto of Lourdes 1 day miracle cure
Donna Carver - water fast cleanse 3 weeks 93% symptom free
Ken Presner - remove Amalgam fillings
Dermott Oconner - remove amalgam fillings, diet, supplement, positive mind training - 1 year
Linda Brocato - remove amalgam fillings MS symptom free
Robert Cartland - Symptoms improved
If anybody else knows of anyone, please add to this list. It will help to encourage others to consider any of these treatments.
I know Ken Presner was. He swears by his Ultimate Zapper. I can't say about the rest, but believe me this names were hard to find. If you do a google search for them + Muliple sclerosis you might be able to find out.
Thank you very much for the information you provided in the list. I have a friend who just diagnosed for MS. His right leg started to get numb and stopped working in three days. Today is his fourth day in the hospital.
The doctors first guess was a brain stroke but then after two or three MRIs they are now confident he has MS.
Your list provided a very useful information for me. I will try some of those things the patients in your list used and then will share the results with you. I think he might have a 50% chance to get cured or get better. Let us pray for all those who have MS or any other disease. Insha'Allah they will all get cured!
I hope everyone who knows someone who had MS and got cured will add to this list. It might help.
i had thought for a long time that Colloidal Silver would be effective but never got a confirmation on that till now. this is good, because CS doubles for Iodine in the body by performing many of iodine's extrathyroid functions like immune system enhancement and tissue repair.
i am not surpised about diet. i think the Iodine protocol and eating, wearing, and swishing some quality oils is all it would take. avoidance of mercury and fluoride is essential as well.
I have found noone claiming cure by use of iodine. Whats more, Max Gerson who cured cancer in 50+ patient suffered from Iodine overdose. I would just recommend being wary about using excess iodine. Hulda Clark inclines all diseases are a combination of pollution and parasites. It would make sense, since all these cases claiming cures have used remedies that would kill parasites in the body. All except for the Lourdes miracle cure.
Thanks for asking. Of course this has been a big experiment for me (as most people) but I have been on different forms of Iodine since Feb. I started out with what was available to me at the time and that was Atomidine. I started with one drop a day in water for a week with weekends off. Each week I would up the dosage by one drop. I did detox even on one drop, so it was good I took it very slow. I then tried the correct protocol of Lugol's brand iodine. At first I detoxed just like before and then it stopped. Like before I started with one drop and worked up with weekends off. I later had one side effect (apparently not a common one) of edema, I'm not sure if it was the Lugol's or the salt water part of the protocol so I stopped using Lugol's and moved on to detoxified iodine. I am currently doing great at 4 drops in a glass of water in the morning with weekends off. Detoxified Iodine is made with Asian Kelp in an alcohol base.
I hope that answers your questions. I'm still experimenting and learning. 48124
I failed to mention one of the strange side effects of taking the detoxified iodine. The first 2-3 days I had vibrational type of sensation in my legs, feet and hands. I'm not sure why because none of the others affected me that way. Perhaps one day we will understand all of this but until then I will be happy just feeling good and having energy. 48124
My friend Mark has been taking a glyconutrient called G*********n for a year and a half and his brain lesions are disappearing. His Doctor thought it was the new meds but he quit taking them a long time ago. He has had MS for 30 years and was in a wheel chair but now can get out of it. He says for a person in as serious condition as he was in try it for 3 months before you give up. At 3 months he stopped wetting himself and was able to get out of the wheelchair. The link is http://www.G*********n.com
If you email me I can see if Mark wouldn't mind personally emailing you or phoning you.
I agree. This looks good. Another great ingredient in this product is the arabinogalactin. It is an immune modulator. You don't want to boost your immune system when you have MS as it seems to be an auto immune disorder. I know people who just take the arabino... but I like the combination of these ingredients.
One of the readers in the forum asked to contact my friend. I thought I would post what Mark wrote.
This is Mark T...... I have been diagnosed with MS for a little over 18 years and am thrilled to help You. Unlike most of the rest of the folks out there, trying to make money on folks who really need help, I just do it because I know how devastating the effects of MS can really be. I feel as if, in 16 years I went from being "Hero" to "Zero" to my family and friends. I simply wish I had met someone like me 10 years ago. In just 1½ years of using the "G*********n", I have gone from a crippled old man in a wheelchair, with "ED" and optic neuritis so bad I couldn't use the computer, to a real man again that is now running his own company that, by the way has nothing to do with MS or Glyconutrients.
I will forward You about 10 E-Mails, some with Links in them, that I found very helpful and encouraging.
Due to the dynamic nature of MS be sure to follow up on these claims. I read a very inspiring story of a woman who claimed to "Cure" MS in her book. I was so excited I called her to find out how she was doing (this was 4 years after the book was published) She stated in her book she was not using any disease modifying drugs traditionally used by neurologists. She was using chelation from amalgrams, Cleansing the bowel,liver and kidneys. she tried Bee Venom Therapy with some results and diet and nutrition. All great ideas and great health practices. After I called her she disclosed that because of the findings on an MRI and worsening symptoms after her book was published she is now using a disease modifyimg drug. I was pretty heartbroken to hear that and I was also pretty pissed as an MS Patient that this "Cure" was published without merit. How many other hopless MS patients have read this with a belief that this will cure MS. There are so many factors to consider with this very complicated illness. I will not point you her way however I did just read a book by Ann Boroch called Healing Multiple Sclerosis I have yet to check her out but it might help your mother God bless
thanks for the information Just out of interest what was the book called so I know not to make too much a deal of it? I am open to possibilities but not niaive that a claim is automatically a cure. However, I have come across a significant number of claims coming from chelation / parasite cleansing, and strict diet control therapies. This could be something and then again it might not. But the amount is overwhelming. I have seen no other remedies to be claimed as much to be as affective, and believe me I researched for years. Either way, whether these processes are cures or not, there is enough proof to suggest removing Amalgam fillings and root canals is certainly a necessity in order to reach optimum health.
This list I have produced could all be bogus as I have not actually met any of these people. I have emailed with several in order to get confirmation of atleast their existence.I would love someone to step forward and offer a visit and I will personally go to visit them, even if they live on the opposite side of the world.
Hi thats perfectly ok. thanks again for the post. I think I once browsed that book in a book shop and didn't pay it much mind. I think its because it gives an idea about the right kind of therapies but doesn't go into scientific detail with encouraging testimonials, tests and results for more than one person like some other books on the subject do. It seems it doesn't have such good reviews in Amazon. Still I admire her efforts. To be broken down into some petty critics about it being BS is just below human intellect.
I have been travelling and don't have all my books with me but here are some I know off by heart due to their quality of content.
NUTRITION AND DIGESTION
Our Earth, Our Cure by Raymond Dextreit
The Natural Remedy Bible by John Lust and Michael Tierra
Optimum Nutrition Bible by Patrick Holford
Good Gut Healing: The No-Nonsense Guide to Bowel and Digestive Disorders by Kathryn Marsden
A Cancer Therapy: Results of Fifty Cases and the Cure of Advanced Cancer by Max Gerson
Guess What Came to Dinner: Parasites and Your Health
The Clay Cure
Cures That Work - Jane Pleshette
Hi im so excited. I thought i'd type in has anybody else cured MS and this website came up. I thought i'd let you people know that I think that I am number 11!
I completely changed my lifestyle dietry wise because my previous diet was a shocker! All of that has changed. No more rubbish very limited sugar,no preservitives/colours,no processed food and also a bowl or more of salad everyday and supplements.
Fixed my gut.I had leaky gut and candida of the gut.
I have never taken any MS medications. Now try and tell me that it is a coincedence that I have had no syptoms in over 3 and a half years. My nueroligist gave me a clean bill of health 3 months ago. Only long term time will tell but I think I have done it!
I have had MS for almost 10 years. I grew up with a mother afflicted by ms, heavily handicaped, and thought life wasn't worth living after my diagnosis. The first few years were the hardest (so far ) with relapses every 10 months or so. I always felt almost normal in between execpt that I was always dizzie. I was able to work and take care of my children ( by myself ) but always felt tired . I then started seing a homeopath every 6 weeks for about 14 months. It felt like I was in a psycotherapy session ! We discussed everything that affected my life and health and went as far back as I could remember. I had told her that I did not beleive in homeopathy and she said that it was perfect because se said that that it was not a grey zone. When it works , its obvious and when the treatment does not work , it's also obvious. We then try something else. I am happy to say that I have not had any symptoms of ms in almost 7 years. I ran my first 1/2 marathon last fall and keep up the running. I eat well but nothing special. My neurologist told me that I had perfect results in the different tests he performed on me. I will have an MRI at the end of the month and can'T wait for the results !