mms 4 ms 
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Hello everyone ;) I was wondering, has anyone had any positive results with MMS for MS?- Re: mms 4 ms Willow753
15 y
4,750
MoreThis is a reply to # 1,453,228I took it about a year and a half ago. Stress is bad for MS as you probably know and I had a lot of stress while taking it. My husband was in the hospital and almost died. When he finally got to come home he was on the strongest Antibiotic available and it was intravaeous twice a day. So me with MS had to do evrything and take care of him as he couldn't take care of himself. Well with taking the Miracle-Mineral-Supplement at the same time, I never had an attack which normally I would of because of the stress.
Do you have any almagam fillings? Have you looked at mercury poisoning at all? We didn't have MS 75-100 years ago and now people are getting it all over the place. It isn't just one or two its a lot of people. Something is wrong. I am looking into getting my almagam fillings out by a biological dentist and then doing the detox. It has cured people of MS, so I am hopefull.
Best wishes,
DebbieAdvertisement
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- Re: mms 4 ms space
15 y
4,288
MoreThis is a reply to # 1,453,266Debbie thanks for answering ;) well I took the mms today and had no nausea or any other symptoms, ill go up to 3 drops later this pm, re amalgams, I kno I have fillings, im just not sure what their made off, how do u find out? many thanks ;)
- Re: mms 4 ms Willow753
15 y
4,358
This is a reply to # 1,453,705Are they silverish in color? If so, then they are 50% mercury.
Debbie- Re: mms 4 ms space
15 y
4,172
This is a reply to # 1,453,712Oh wow mine are dark silver, they were put in the 70's so I bet its the BAD stuff.......Im definitely going to look into this, thank you so much for bringing it up, as I had heard the rumour but never knew that people with MS that had them taken out got better afterwards ;) please keep me posted on how yours go Bruce ;)
- Re: mms 4 ms Willow753
15 y
4,326
This is a reply to # 1,453,923I will do that. Yes mine were put in a long time ago also so they are the bad ones. The new ones are white and are a coposite material. I am just waiting for my husbands settlement to come and then i am off and on my way to get them gone.
Best wishes to you.
Debbie- Re: mms 4 ms space
15 y
4,188
This is a reply to # 1,453,984Advertisement
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Your very welcome, and thanks to you I spoke last night with a wonderful gentelman named Leo who works at DAMS at 1- 651-644-4572 he was immensely, knowledgeable on the subject and is sending by mail all the info pertinent to the removal, apparently one of the founding members of the association (shes has now passed away) was a MS patient and she improved so much after removing the amalgan that she became a huge activist.......well this gives us renewed hope!.....my feet get worse by the day, today their like cement boots and I havent been able to wiggle my left foot toes for 2 weeks ;(
Oh I did 3 drops of mms this morning and have been gargling some more as I have an absesed tooth thats bothering quite a bit apart from this life is great ;)
ttly
Bruce
- Re: mms 4 ms Willow753
15 y
4,460
This is a reply to # 1,454,375Bruce:
Yes Leo was very helpful, he sent me all of the information as well. I am so glad you called so quickly. There is a lot of information in there, plus it gives you the local Biological Dentist in your area and natropath doctor as well. You will be amazed, I was.
Yes the acutal founder was Louise Beckham (I think not positive on the last name) and she did have MS. She got better after the almagams were removed (so hopefully we do too), then after detox which I think is 3 months later she was totally cured (which hopefully we are too).
i know what you mean about the feet. I cannot feel anything. Just a couple of cement bricks I stumble around on. I haven't been able to move my toes on my right foot for years. If you wrap your leg in 3" of wet cement and then let it dry and try and walk, well that is what my right leg feels like. But at least I can still walk there are others who are far worse than I.
I am very hopeful this almagam removal gets rid of all of this. Have to have hope without it all is lost.
We shall HOPE and PRAY!!!
Belssings,
Debbie
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- Re: mms 4 ms space
15 y
4,170
This is a reply to # 1,454,675Advertisement
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Dear Debbie, Hi and thats great that you also spoke to Leo, he was so nice and helpful ;) Im looking forward to receiving all the info on the amalgams.
Im so sorry, I had no idea you were going thru the same issues with your feet, thats exactly how both of mine feel, but thank God i can still wiggle my right toes! ;) but the worse part is the tightness, its as if I had 2 x 300lb muscle guys grabbing at mty feet and constricting them 24/7, do you also have the constricting and tightness I just described? or only the numbness and the cement heaviness? btw, how long ago were you diagnosed?
FYI, I was having some back pain the other day so I tried something new and went to a neurosurgeon, and didnt tell them I had been diagnosed w/ MS, they had me take MRI's, and they came to the conclusion that I needed a micro-disectomy due to a herniated disk with an extrusion!
On the other hand my neuros have been trying to get me on tysabri for quite sometime, and point at my back pain a regular MS symptom.
Anyway I just found a very good Holistic Biological Dentist about 40 minutes away, and hopefully tommorrow Ill call and get the inside scoop as to price, and which composite I should have them replaced with. Ill keep you posted, in the meantime have a Happy Sunday!
Many Blessings
Bruce ;)
- Re: mms 4 ms Johny Apple Bomb
15 y
4,217
This is a reply to # 1,454,866I've had my Amalgams removed with no regret. The worst thing is I had to have 2 new crowns on the bottom jaw molars due to Amalgam damage.
The safest, most complete way I know of to remove mercury and other heavy metals is Chelorex.
http://www.scienceformulas.com/
- Re: mms 4 ms Willow753
15 y
4,333
This is a reply to # 1,454,936Do you take the Chelorex after the almagam has been removed or before and after removal?
Thanks for the info!
Debbie
- Re: mms 4 ms Willow753
15 y
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- Re: mms 4 ms Willow753
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This is a reply to # 1,454,866Hi Bruce:
I was diagnosed on April 17th, 2001 at 3:15pm. I call it "D" day, Lol. I do have the consticting and tightness that you speak of. I just recently started taking a magnesium citrate for it and it seems to be helping. I haven't woken up with charlie horses since I started taking it.
i do not have any back pain at all. The doctors, neuroligist in my opinion are all just guessing. They truly do not know how to really help us. I think they want to they just don't know how so they try this and that but nothing works.
I was on Copaxone (haven't taken a shot in a year). they tried Rebif (Thank God I was allerigic so that failed), they then wanted me to go to the University of Minnesota for the Tysabri. I said no. How come my neuro asked and I said people die from that and he said "they are watching it really closely now". I said they can watch someone else die but it is not going to be me. Tysabri can be dangerous, people have died I for one will NOT try it. I do no drugs from them now and I feel a lot better. Yeah I am stiff like cement, walk like a dork, have dead feet, but I am awake I don't sleep 18 hours a day anymore and I am pretty happy so all is good. Plus I am on this side of the dirt.
That is great you have a Biological dentist nearby. I do too which made me very happy. I was LMAO at that other doctor telling you that you had micro-disectomy due to a herniated disk with an extrusion. Perhaps you should show the MS docotr this. They just don't know. They have found spirochete's in dead MS patients brains. That is a Lyme disease bug. The doctors truly don't know. Perhaps when they leave us sitting in the room all by ourselves they are in there office with a dart board that has different diseases on each section, then they throw a dart and wherever it lands well then they come back in the room and tell you that you have "this" disease. Just a thought.
Maybe I think to much...hee hee.
Have a Blessed day!
DebbieAdvertisement
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- Re: mms 4 ms - love your attitude! CdnFarmgirl
15 y
4,571
This is a reply to # 1,454,976Just an aside from reading your posts re: Miracle-Mineral-Supplement and MS. We have a family friend who was diagnosed with MS a year and a half ago. My in-laws sent her Jim Humble's book to read, we told her parents about the success stories with Miracle-Mineral-Supplement , mercury-removal, etc., but unfortunately, she has made up her mind to obey her doctors blindly, and has accepted to get progressively worse with the disease's onset. My husband and I were grateful that we have never been in such a state of health, but we both agreed that we would be kicking and screaming all the way, looking for alternative remedies.
I just love reading your above posts, Debbie, and know that you are a fighter! It's great that through this blog, many can be encouraged to know that there is hope out there for them, that they do not need to suffer alone, and that they alone need to take responsibility for their health.
Best wishes as you all recover from your MS!!
Julie
- Re: mms 4 ms space
15 y
4,060
This is a reply to # 1,454,976Debbie Hi
Oh wow so you have the constricting too, well your the first person Ive met with my same symptoms, is it in both feet? and did it start on your soles and progressivley advance to the tops of your feet as well?
Great that you have no back pain, actually mine was never been that bad, the thing is that I noticed that everytime I would work on my Mac straight for 3 or more hours the numbing in my feet would get much worse and I felt a little pain when getting up, nothing bad, but it was there, and thats when I decided to go to the neurosurgeon, and were I got my new diagnosis of a herniated disk and were the Dr.explained that the disk herniation was reponsible for the numbing on both my feet.
Im not trying to be anti establishment but the Avonex was horrible for me and I never felt well during my short time with it, and Ive heard the same thing about all the other crab drugs, btw after I quit the Avonex I didnt get another exacerbation for 8 years, I was riding 10 miles a day in south beach swiming in the beach, pools etc with no problems, it was when I moved up north from south florida, that my sister convinced me to go with her to some sun tanning saloon b4 a wedding of one of our friends, that was when it all came back, up to today i still believe that that triggered my attack, and quite a few people have exacerbated after using these machines, please read what i pasted below, btw b4 I went there I had never read anything like this but I felt so weird and queasy, that I knew something was not right.
PLEASE READ=> Tanning at the salon is dangerous. 2,8 Artificial UVR exposure has been repeatedly identified as a factor that contributes to acute health effects such as erythema, sunburn, skin dryness, pruritus, nausea, photodrug reactions, (((((disease exacerbation)))) (eg, systemic lupus erythematosis), and disease induction (eg, polymorphous light eruption). Long-term health effects include skin aging, effects on the eye.
SO STAY AWAY FROM TANNING SALOONS! ;)
Anyway Im NOT doing their tysabri nor any of the other crab drugs. I want regenarating drugs! the ones that heal by building healthy cells and NOT the ones that kill and suppress our immune systems. Oh and Im not taking their suggestion of buying a wheel chair only for "my bad days" as they put it, the minute I do this Im giving up, not to mention the effect on my muscles, plus Ive perfectioned my my fake limp instead of my normal dorking numbed feet walking, no one ever knows I have MS and exactly like you Im happy everyday and smile alot, why? I have no idea, but its an amazing blessing and I know it will stay with me forever and ever ;)
Early this morning I called and setup my appointment with the Biological Dentist, the earliest they could take me was on July 29, but they sounded wonderful and I really liked their website as well and they follow the right protocal for removing the mercury, dental dams, oxygen, vacuuming of vapors, cold lazer, ionizer etc etc.
BTW since the first time you mentioned this whole thing about the Amalgams last friday, I have read huge amounts of information on the subject, and its amazing that they havent outlawed this stuff like they have in Germany, Holland and a few other places, the statistical information is incredible; and the before and afters are amazing!.....I still cant believe that non of my neuros ever told me anything about this from day one! I sincerely thank you from the bottom of my heart, btw, I have since spoken to a lady with MS who has made made great advances after removal. I pray it resolves some of my symptoms with time, but no matter what happenes their going out, their a toxic time bomb!
Big hugz
Bruce ;)
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- Re: mms 4 ms Willow753
15 y
4,355
This is a reply to # 1,455,525Very happy for you Bruce! You will have yours out b4 me-hee hee. I have to wait for the $$$. You know this is still earth so $$$ talks.
The numbness on my feet is only on the bottoms. It has never spread to the tops, Thank GOD! They do feel so cold though sometimes like blocks of ice. So I wear footsie things even in the summer.:-)
I do have a nice suntan but I get it by hardwork. Laying in the natural sun and when I get hot I spray myself with the hose. :-) Years ago I did use one of those sun tanning bed for about a month or two. I am claustrophobic so I don't know how I did it but I did. Not for me anymore I like natural.
Don't forget to set up an appointment with a natropath doctor as well. This is VERY important as she/he will help you with the detoxing and getting your body ready for the removal. Minerals etc. you may be lacking in. At least that is what Leo told me. You need the mercury that has leaked into your body to be removed. This can be very hard on you (the detox) but there are things the natropath/doctors can give you so it isn't so severe and hard on you.
As far as neuros telling us about this...shoot I don't think they want us to know about it. You have to remember big pharmacy $$$ here are at stakes. Our shots cost $1800.00 a month x 12 months a year x how many years = keep them in the dark so we can make big $$$. That is just my opinion. The ADA still won't admit that almagam is dangerous. Read the info from Leo. They can't, think of the lawsuits. Its all about the almighty buck once again.
Glad to hear about that lady who had MS...gives me hope! I hope and pray this is the case for ALL MS sufferers. Wouldn't that be awesome!
Well glad to hear you are going so quickly, hopefully I can to soon. Wellness here we come!
Hugs & tons of blessings!
Debbie
- Re: mms 4 ms space
15 y
4,136
This is a reply to # 1,455,627Your a vey lucky girl Debbie, numbing in the soles "only" is a great thing, the all over cement boot sucks bigtime
Im from South Florida and beaches are were I go to be under the sun, but we had moved north and my sister insisted I go with her b4 this wedding we were all going too, it was 40F outside and I said yes after a while of her pushing me to go with her ;(
Re. Natropath Dr. non close to me, but im sure the Biological Dentist wont start removing without prior detox plans, and preping me for all this, Ive read about various chelating agents, anyway Im going to ask him all this in my initial visit, as this is in stages, they never remove all at once.
My first neuros biggest concern was to get me on avonex asap and for as long as posible, he was visibly upset when I quit, and like you said its all about the money, lets not forget he also works for that drug company, it pays for his Benz's, his home's, boats, trips etc. I could never do that to another human being, thats just horrible ;(
Well thanks to you ive found new hope in this Amalgam removal, many thanks and Ill keep you posted ;)
Hugz and Blessings to you as well
Bruce ;)
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- Re: mms 4 ms space
15 y
4,136
- Re: mms 4 ms Willow753
15 y
4,355
- Re: mms 4 ms - love your attitude! CdnFarmgirl
15 y
4,571
- Re: mms 4 ms Johny Apple Bomb
15 y
4,217
- Re: mms 4 ms space
15 y
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- Re: mms 4 ms princessjade
15 y
4,376
This is a reply to # 1,454,375I spoke with Leo from DAMS about 5 years ago... I think his name is Leo Cashman... he is local to me in the twin cities area.
It was because of that conversation and the information he sent me, that I went and got my Amalgams out. I had been using my detox foot pads, and had just started selling them myself -- so I had a lot on hand. When I went in to get mine done, (I did it in 4 steps -- one quadrant at a time) I put 3 foot pads on each foot -- the most important area is your toes (the undersides of your toes). I also megadosed with vitamin C, and chlorella.
I went to a biological dentist in Hopkins, MN. They also provided ozone treatment -- ozone therapy. It was interesting. Unfortunately they don't accept insurance so I had to pay cash. Many biological dentists won't accept insurance.
Well, I still have metal in my mouth because I have 2 root canals (one of the new fillings that they put in was too close to my root and became so sensitive that it killed the tooth, hence a root canal -- so there are some side effects to getting any filling replaced in your mouth... another filling / tooth is so sensitive still to this day, and I cannot drink cold or hot on that side of the mouth. And I have an implant where I have a titanium screw in my jaw... at least it isn't mercury but still... wish I didn't have metal in my mouth. Otherwise if you took a look at my mouth all you see is white (composite) and regular teeth -- it is nice to have a mouth like that! hehe.
Here is another option for you... if you happen to go to a regular dentist -- because of financial reasons -- it is better than nothing, but please insist that they use a rubber dam, especially when drilling out the mercury fillings -- the dust can settle all throughout your mouth and be absorbed sublingually. So be sure to have a mask on and a rubber dam. That is the most important part.
Good luck!
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- Re: mms 4 ms Willow753
15 y
4,227
This is a reply to # 1,457,280Wow a regular dentist can do it as long as I wear a mask and they use a rubber dam? I did not know that. Now I am hopeful it may not cost a fortune.
I did have a large on drilled out without any protection right before the MS sympltons (about 6 months after) started. the dentist the refilled it with new almagam. Must of been so i would get a fresh supply of mercury even though it stays in there forever.
The root canals are dangerous also. Yes his name is Leo Chapman, really nice guy. Might want to dig in further on them for more information.
Blessings,
DebbieAdvertisement
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- Re: mms 4 ms space
15 y
4,252
This is a reply to # 1,457,329Debbie, I just read your post, funny but my firstever MS symptoms first started right around when I had my first wisdom tooth pulled out, I remember clearly that b4 they pulled it out, I could feel it pushing against my molar which is full of almagam, back then (10yrs ago) I had very slight numbing on my left leg.......all this is pretty much the same exact thing thats happening to me right now with my other wisdom tooth that wants to come out, the difference being that my symptoms are really hardcore now, as the numbing got much worse and even reached the top of both my feet, a month ago all I had were the soles numb, I would like to add that I have no leg numbing like the 1st time only on both feet.
FYI, I initially came into this mms chat because I thought it very strange that my symptoms got worse because of a slight fever which I got due to my wisdom tooth pushing against my molar, I thought it was because of the infection thus my interest in mms.....I hadnt realized untill you put 2+2=4 that it could be my silver fillings! btw its amazing the amount of neuropathies that are due to mercury poisoning that I found on google!
all the best and many blessings
Bruce- Re: mms 4 ms Willow753
15 y
4,297
This is a reply to # 1,457,894Best Wishes for you at the Biological Dentist tomorrow Bruce! Keep us posted on how it goes please!
Onward to being "normal" again...
Debbie
- Re: mms 4 ms Willow753
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- Re: mms 4 ms Willow753
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- Re: mms 4 ms Willow753
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