Guest guest Posted June 29, 2008 Report Share Posted June 29, 2008 Hi, Rosemary. We've already met. I'm glad you're doing so well. I've heard that it can be beneficial to take an occasional break from MMS. If you decide to do that, sometime, you might find a course of colloidal silver good at clearing up stubborn skin problems. I have to alternate the two, as they work on different areas of my body. MMS is better for almost everything, but one particular "hot spot" needs CS... Wishing you continued improvement, Gaele Maat, in Qld. [ ] Lump on head. Hi Gang,I have Lyme 29 years and believed I contracted it sexually from my ex-husband. I got sick as soon as I married him and he had a classic bull's-eye rash in his armpit. I was misdiagnosed for 22 years. When I got sick I developed a hard, painful, itchy lump on the top of my scalp. I thought it was due to a hair perm at the time and it has driven me crazy with itching and burning all these years. I have tried various medicated shampoos, cortisone cream, etc, but nothing helped much. It has even been too painful to comb the hair at times and occasionally becomes infected right in the centre. The itching and burning would radiate out from the centre to about 6 inches in diameter. My scalp was not itchy anywhere else. The doc said it is just a sebaceous gland and my pharmacist friend couldn't see anything wrong, so I learned to live with it. Often it would feel like the skin was crawling & I wondered if there was some kind of "critter" in it. I have been on salt & C for 3 years with slow, but steady improvement. I introduced MMS, 8 months ago and guess what? My itchy lump is almost gone!!!!!! I am beginning to think it may have been a tick bite. Perhaps my ex and I both got bitten. I may never know, but I do know for sure that MMS is getting rid of whatever it is.oo!Rosemary.------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 11, 2008 Report Share Posted July 11, 2008 > > Hi Gang, > I have Lyme 29 years and believed I contracted it sexually from my ex- > husband. I got sick as soon as I married him and he had a classic > bull's-eye rash in his armpit. I was misdiagnosed for 22 years. > When I got sick I developed a hard, painful, itchy lump on the top of > my scalp. I thought it was due to a hair perm at the time and it has > driven me crazy with itching and burning all these years. I have > tried various medicated shampoos, cortisone cream, etc, but nothing > helped much. It has even been too painful to comb the hair at times > and occasionally becomes infected right in the centre. The itching > and burning would radiate out from the centre to about 6 inches in > diameter. My scalp was not itchy anywhere else. The doc said it is > just a sebaceous gland and my pharmacist friend couldn't see anything > wrong, so I learned to live with it. Often it would feel like the > skin was crawling & I wondered if there was some kind of " critter " in > it. > I have been on salt & C for 3 years with slow, but steady > improvement. I introduced MMS, 8 months ago and guess what? My > itchy lump is almost gone!!!!!! I am beginning to think it may have > been a tick bite. Perhaps my ex and I both got bitten. I may never > know, but I do know for sure that MMS is getting rid of whatever it > is. > oo! > Rosemary. > Dear Rosemary, What other Lyme symptoms do you have? I have had Lyme for 5 years and just started using MMS. Do you know of anyone who has seen marked overall improvement from Lyme with MMS? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 11, 2008 Report Share Posted July 11, 2008 Have you tried a clay pack? www.aboutclay.com -- [ ] Re: Lump on head. >> Hi Gang,> I have Lyme 29 years and believed I contracted it sexually from my ex-> husband. I got sick as soon as I married him and he had a classic > bull's-eye rash in his armpit. I was misdiagnosed for 22 years. > When I got sick I developed a hard, painful, itchy lump on the top of > my scalp. I thought it was due to a hair perm at the time and it has > driven me crazy with itching and burning all these years. I have > tried various medicated shampoos, cortisone cream, etc, but nothing > helped much. It has even been too painful to comb the hair at times > and occasionally becomes infected right in the centre. The itching > and burning would radiate out from the centre to about 6 inches in > diameter. My scalp was not itchy anywhere else. The doc said it is > just a sebaceous gland and my pharmacist friend couldn't see anything > wrong, so I learned to live with it. Often it would feel like the > skin was crawling & I wondered if there was some kind of "critter" in > it. > I have been on salt & C for 3 years with slow, but steady > improvement. I introduced MMS, 8 months ago and guess what? My > itchy lump is almost gone!!!!!! I am beginning to think it may have > been a tick bite. Perhaps my ex and I both got bitten. I may never > know, but I do know for sure that MMS is getting rid of whatever it > is.> oo!> Rosemary.>Dear Rosemary,What other Lyme symptoms do you have? I have had Lyme for 5 years and just started using MMS. Do you know of anyone who has seen marked overall improvement from Lyme with MMS? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 15, 2008 Report Share Posted July 15, 2008 > > Have you tried a clay pack? > > www.aboutclay.com Hi Esther, Thanks for the idea. I feel the MMS has almost cured this problem. That is what is so exciting. I have been on it 8 1/2 months and having many great improvments. Regards, Rosemary. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 15, 2008 Report Share Posted July 15, 2008 >> Dear Rosemary, > > What other Lyme symptoms do you have? I have had Lyme for 5 years > and just started using MMS. Do you know of anyone who has seen > marked overall improvement from Lyme with MMS? > > Hi , I have Lyme 29 years and so many symptoms, I haven't got time to list now as I am traveling again thanks to 3 years of salt & C www.Lymephotos.com and 8 months of MMS www.miraclems.com . I was very disabled for many years, using a wheelchair at times and a walking frame for years. I was dizzy, had chronic migraine, Bell's Palsy, numbness, depression, anxiety, etc. 3 years of salt & C brought temendous improvements which enabled me to go from mostly housebound and dying, to traveling overseas! I feel that MMS is killing something that salt & C had not. Perhaps a virus or just more Lyme & co. It is powerful stuff and I really think it may be a cure for Lyme. You just need to listen to your body and detox when you are herxing. It can be gruelling and frustrating, but most definately worth it and much better than anti-biotics, in my opinion. My husband has chronic food mal-absorption for over 30 years. We believe he has a chronic bowel infection. He has tried Flagyl, Parex, Tri-plex, probiotics, enzymes, etc, etc. Nothing worked. Finally, since being on MMS he is having formed stools, looks and feels much better. This stuff is awesome! Rosemary. Quote Link to comment Share on other sites More sharing options...
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