Guest guest Posted July 5, 2012 Report Share Posted July 5, 2012 Hi Susie I have been to a neuro,ent,octo neuro,have had all the ear testing all fine.My brain mris are showing many white spots have had 3 lumbars and ms was ruled out.. This is completly devastating my balance as well is off.Also my lyme westernblot the igm bands 23 and 41 are positive but all my igg bands ar negative,I just dont know anymore and the fatigue i have is unbearable.. Subject: Re: lighteadednessTo: Lyme_and_Rife Date: Thursday, July 5, 2012, 11:47 AM Terry,I have big problems with dizziness, lightheadedness & faintness. I don't know if it's what other people refer to as "brain fog". A few years ago I had extensive testing on my ears because I thought that was what causing it, but it didn't turn out to be that. I also suffer from panic disorder for over 30 years now & found out last year I could have had Lyme since I was a child. Throw in mercury poisoning, old root canals & chronic sinusitis & there's no way to tell what's causing the dizziness. It's a process of elimination trying to find the culprit(s). It's not an easy or short process, but you are not alone. I hope you find the answer to your problem.Susie>> Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> Thank You> Terry> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2012 Report Share Posted July 5, 2012 Hi Terry,I don’t have those symptoms all the time but I do get dizzy quite often and my balance has been off for years. I have just gotten over months of that really awful fatigue. Have you tried MMS? That was helpful for me with the fatigue.Take care,Jeff From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of T.BSent: Thursday, July 05, 2012 12:03 PMTo: Lyme_and_Rife Subject: Re: Re: lighteadedness Hi SusieI have been to a neuro,ent,octo neuro,have had all the ear testing all fine.My brain mris are showing many white spots have had 3 lumbars and ms was ruled out..This is completly devastating my balance as well is off.Also my lyme westernblot the igm bands 23 and 41 are positive but all my igg bands ar negative,I just dont know anymore and the fatigue i have is unbearable..Subject: Re: lighteadednessTo: Lyme_and_Rife Date: Thursday, July 5, 2012, 11:47 AM Terry,I have big problems with dizziness, lightheadedness & faintness. I don't know if it's what other people refer to as " brain fog " . A few years ago I had extensive testing on my ears because I thought that was what causing it, but it didn't turn out to be that. I also suffer from panic disorder for over 30 years now & found out last year I could have had Lyme since I was a child. Throw in mercury poisoning, old root canals & chronic sinusitis & there's no way to tell what's causing the dizziness. It's a process of elimination trying to find the culprit(s). It's not an easy or short process, but you are not alone. I hope you find the answer to your problem.Susie>> Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> Thank You> Terry> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2012 Report Share Posted July 5, 2012 Not yet Jeff i ordered it but i havent received it yet..Thank you for replying its geatly appreciated Subject: Re: lighteadednessTo: Lyme_and_Rife Date: Thursday, July 5, 2012, 11:47 AM Terry,I have big problems with dizziness, lightheadedness & faintness. I don't know if it's what other people refer to as "brain fog". A few years ago I had extensive testing on my ears because I thought that was what causing it, but it didn't turn out to be that. I also suffer from panic disorder for over 30 years now & found out last year I could have had Lyme since I was a child. Throw in mercury poisoning, old root canals & chronic sinusitis & there's no way to tell what's causing the dizziness. It's a process of elimination trying to find the culprit(s). It's not an easy or short process, but you are not alone. I hope you find the answer to your problem.Susie>> Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> Thank You> Terry> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2012 Report Share Posted July 5, 2012 Terry,I don’t have enough experience or knowledge about Lyme or Rife to contribute much, but have more than enough of both when talking about symptoms and am always glad to chime in. I’ve learned so much from the members of this group and am so appreciative that I try to pass on what I can. I hope the MMS helps you as it’s helped myself and many others. I still have some fatigue but it’s more like the normal everyday fatigue that I’ve had for over 22 years, not the totally disabling kind that I was struggling with and I think you mean. Take care,Jeff From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of T.BSent: Thursday, July 05, 2012 12:15 PMTo: Lyme_and_Rife Subject: RE: Re: lighteadedness Not yet Jeff i ordered it but i havent received it yet..Thank you for replying its geatly appreciatedSubject: Re: lighteadednessTo: Lyme_and_Rife Date: Thursday, July 5, 2012, 11:47 AM Terry,I have big problems with dizziness, lightheadedness & faintness. I don't know if it's what other people refer to as " brain fog " . A few years ago I had extensive testing on my ears because I thought that was what causing it, but it didn't turn out to be that. I also suffer from panic disorder for over 30 years now & found out last year I could have had Lyme since I was a child. Throw in mercury poisoning, old root canals & chronic sinusitis & there's no way to tell what's causing the dizziness. It's a process of elimination trying to find the culprit(s). It's not an easy or short process, but you are not alone. I hope you find the answer to your problem.Susie>> Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> Thank You> Terry> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2012 Report Share Posted July 5, 2012 Thank you Jeff This is so overwelming i have literally been all over the USA at hospitals i am scheduled to go to Hopkins in Sept other than the Hospital and the Mayo i have been everywhere with no answers..Everyday i feel as if death is knocking on my door here.To think 2 years ago my life was so different... Again i thank you for responding here Subject: Re: lighteadednessTo: Lyme_and_Rife Date: Thursday, July 5, 2012, 11:47 AM Terry,I have big problems with dizziness, lightheadedness & faintness. I don't know if it's what other people refer to as "brain fog". A few years ago I had extensive testing on my ears because I thought that was what causing it, but it didn't turn out to be that. I also suffer from panic disorder for over 30 years now & found out last year I could have had Lyme since I was a child. Throw in mercury poisoning, old root canals & chronic sinusitis & there's no way to tell what's causing the dizziness. It's a process of elimination trying to find the culprit(s). It's not an easy or short process, but you are not alone. I hope you find the answer to your problem.Susie>> Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> Thank You> Terry> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 5, 2012 Report Share Posted July 5, 2012 Hi The neuros i have seen which have been quite a few from all over the US just say theres something wrong but we dont know what it is.I have had 3 lumbars all were normal the lyme serum was indeterminate in the spinal.The thing is i had only a few white spots was put on iv rocephin did very poorly on it had a mri after i did 22 days and now my brain is full of spots...No one has answers to this. Subject: Re: lighteadednessTo: Lyme_and_Rife Date: Thursday, July 5, 2012, 4:41 PM Terry,I had a brain MRI a long long time ago for headaches but nothing was determined wrong. Did the doctor tell you what the white spots mean? On my Igenex western blot, the igm bands 34, 58 & 83-93 are pos & bands 31 & 41 are indeterminate. On my igg bands, only 41 was pos but you need at least 2 to be really pos. Bands 31 & 39 were indeterminate. It's all very confusing plus I tested neg for co-infections, but later testing by Electro Dermal Screening said I also had Babesia & Ehrlichia. My balance is off too. Sometimes I think I'm alright & then I'll turn around or look down & bingo, it's right there. What I have been using for a few weeks now is Burbur & Pinella by Nutramedix. It seems to help sometimes but I might not be using enough of it yet (today I took 25 drops of each). Others have reported using over 100 drops before they get some relief. Burbur is for detox & Pinella is for brain-nerve cleanse. Maybe you could try them to see if they might help somewhat. Hang in there.Susie > >> > Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> > Thank You> > Terry> >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2012 Report Share Posted July 6, 2012 Hi Jeff I Terry , this story of biofilm give sme imagination if there are biofilm over there in the ears it will impair th ebalance with the little air gued by the biofilm the bee venon melting biofilm on contact I experienced it I would try this ointment venex on my neck vein area if it would be me . Kindly Marie To: Lyme_and_Rife Sent: Thursday, July 5, 2012 12:11 PMSubject: RE: Re: lighteadedness Hi Terry, I don’t have those symptoms all the time but I do get dizzy quite often and my balance has been off for years. I have just gotten over months of that really awful fatigue. Have you tried MMS? That was helpful for me with the fatigue. Take care, Jeff From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of T.BSent: Thursday, July 05, 2012 12:03 PMTo: Lyme_and_Rife Subject: Re: Re: lighteadedness Hi Susie I have been to a neuro,ent,octo neuro,have had all the ear testing all fine.My brain mris are showing many white spots have had 3 lumbars and ms was ruled out.. This is completly devastating my balance as well is off.Also my lyme westernblot the igm bands 23 and 41 are positive but all my igg bands ar negative,I just dont know anymore and the fatigue i have is unbearable.. Subject: Re: lighteadednessTo: Lyme_and_Rife Date: Thursday, July 5, 2012, 11:47 AM Terry,I have big problems with dizziness, lightheadedness & faintness. I don't know if it's what other people refer to as "brain fog". A few years ago I had extensive testing on my ears because I thought that was what causing it, but it didn't turn out to be that. I also suffer from panic disorder for over 30 years now & found out last year I could have had Lyme since I was a child. Throw in mercury poisoning, old root canals & chronic sinusitis & there's no way to tell what's causing the dizziness. It's a process of elimination trying to find the culprit(s). It's not an easy or short process, but you are not alone. I hope you find the answer to your problem.Susie>> Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> Thank You> Terry> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2012 Report Share Posted July 8, 2012 I find a spoon of Barley grass (I use morlife) in Oj regularly helps with extreme fatigue, but I don’t know why.I also find sarsaparilla helps me too with balance probs. Cheers From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of ScharffSent: Friday, 6 July 2012 2:11 AMTo: Lyme_and_Rife Subject: RE: Re: lighteadedness Hi Terry,I don’t have those symptoms all the time but I do get dizzy quite often and my balance has been off for years. I have just gotten over months of that really awful fatigue. Have you tried MMS? That was helpful for me with the fatigue.Take care,Jeff From: Lyme_and_Rife@yah oogroups.com [mailto:Lyme_and_Rife ] On Behalf Of T.BSent: Thursday, July 05, 2012 12:03 PMTo: Lyme_and_Rife Subject: Re: Re: lighteadedness Hi SusieI have been to a neuro,ent,octo neuro,have had all the ear testing all fine.My brain mris are showing many white spots have had 3 lumbars and ms was ruled out..This is completly devastating my balance as well is off.Also my lyme westernblot the igm bands 23 and 41 are positive but all my igg bands ar negative,I just dont know anymore and the fatigue i have is unbearable..Subject: Re: lighteadednessTo: Lyme_and_Rife Date: Thursday, July 5, 2012, 11:47 AM Terry,I have big problems with dizziness, lightheadedness & faintness. I don't know if it's what other people refer to as " brain fog " . A few years ago I had extensive testing on my ears because I thought that was what causing it, but it didn't turn out to be that. I also suffer from panic disorder for over 30 years now & found out last year I could have had Lyme s ince I was a child. Throw in mercury poisoning, old root canals & chronic sinusitis & there's no way to tell what's causing the dizziness. It's a process of elimination trying to find the culprit(s). It's not an easy or short process, but you are not alone. I hope you find the answer to your problem.Susie>> Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> Thank You> Terry> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2012 Report Share Posted July 8, 2012 Hi Terry, I had the disabling kind of fatigue and could not stand up without passing out. Best of luck. From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of ScharffSent: Friday, 6 July 2012 2:27 AMTo: Lyme_and_Rife Subject: RE: Re: lighteadedness Terry,I don’t have enough experience or knowledge about Lyme or Rife to contribute much, but have more than enough of both when talking about symptoms and am always glad to chime in. I’ve learned so much from the members of this group and am so appreciative that I try to pass on what I can. I hope the MMS helps you as it’s helped myself and many others. I still have some fatigue but it’s more like the normal everyday fatigue that I’ve had for over 22 years, not the totally disabling kind that I was struggling with and I think you mean. Take care,Jeff From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of T.BSent: Thursday, July 05, 2012 12:15 PMTo: Lyme_and_Rife Subject: RE: Re: lighteadedness Not yet Jeff i ordered it but i havent received it yet..Thank you for replying its geatly appreciatedSubject: Re: lighteadednessTo: Lyme_and_Rife Date: Thursday, July 5, 2012, 11:47 AM Terry,I have big problems with dizziness, lightheadedness & faintness. I don't know if it's what other people refer to as " brain fog " . A few years ago I had extensive testing on my ears because I thought that was what causing it, but it didn't turn out to be that. I also suffer from panic disorder for over 30 years now & found out last year I could have had Lyme since I was a child. Throw in mercury poisoning, old root canals & chronic sinusitis & there's no way to tell what's causing the dizziness. It's a process of elimination trying to find the culprit(s). It's not an easy or short process, but you are not alone. I hope you find the answer to your problem.Susie>> Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> Thank You> Terry> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2012 Report Share Posted July 8, 2012 how did you do please Thanks Marie To: Lyme_and_Rife Sent: Saturday, July 7, 2012 7:53 PMSubject: RE: Re: lighteadedness Hi Terry, I had the disabling kind of fatigue and could not stand up without passing out. Best of luck. From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of ScharffSent: Friday, 6 July 2012 2:27 AMTo: Lyme_and_Rife Subject: RE: Re: lighteadedness Terry, I don’t have enough experience or knowledge about Lyme or Rife to contribute much, but have more than enough of both when talking about symptoms and am always glad to chime in. I’ve learned so much from the members of this group and am so appreciative that I try to pass on what I can. I hope the MMS helps you as it’s helped myself and many others. I still have some fatigue but it’s more like the normal everyday fatigue that I’ve had for over 22 years, not the totally disabling kind that I was struggling with and I think you mean. Take care, Jeff From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of T.BSent: Thursday, July 05, 2012 12:15 PMTo: Lyme_and_Rife Subject: RE: Re: lighteadedness Not yet Jeff i ordered it but i havent received it yet..Thank you for replying its geatly appreciated From: tim2buk <http://us.mc845.mail.yahoo.com/mc/compose?to=tim2buk@...>Subject: Re: lighteadednessTo: http://us.mc845.mail.yahoo.com/mc/compose?to=Lyme_and_Rife Date: Thursday, July 5, 2012, 11:47 AM Terry,I have big problems with dizziness, lightheadedness & faintness. I don't know if it's what other people refer to as "brain fog". A few years ago I had extensive testing on my ears because I thought that was what causing it, but it didn't turn out to be that. I also suffer from panic disorder for over 30 years now & found out last year I could have had Lyme since I was a child. Throw in mercury poisoning, old root canals & chronic sinusitis & there's no way to tell what's causing the dizziness. It's a process of elimination trying to find the culprit(s). It's not an easy or short process, but you are not alone. I hope you find the answer to your problem.Susie>> Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> Thank You> Terry> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2012 Report Share Posted July 8, 2012 Hi Marie, I have done so much that I am not entirely sure which has done what, but I’m happy to share what I’ve done! When I had full blown fatigue, I could not stand up for long and spent most of the day on the couch. It took all of my energy toGet up and get the kids to school, shop, rest all day, pick them up, rest, struggle to make dinner, rest, wide awake until late andExhausted all day. I could not hang up washing as I would drop to the floor if I raised my arms up for more than a few secs. I could Not vacuum the floor and heat made me dizzy. There is more I am sure bloated stomach, weight gain, light sensitivity, cold. I went from doc to doc trying to figure out what was wrong. I finally found a thyroid doc who put me on T3 (as I had rev t3) and low dose steroids s he felt my adrenals were exhausted and needed a rest. (Not sure now whether this was so good asI know I have Lyme, however some Lyme patients with adrenal probs have to have low doses so???) The T3 helped my thyroid probs but I did not get ‘better’ so I tried homeopathy ( to little effect). I began to think I might have cancer and Started apricot kernals 10 to 20 a day with vit c. I then added in colloidal silver and bought a machine to make it as it was so expensive to buy. I tried mmsBut now of us could stand the taste and often vomited and had huge stomach pain. I might yet try it again now that I’m much better, maybe I was wayToo toxic back then? I also took Morlife barley grass twice a day mixed in orange juice for energy. During this period I just gradually got better until I could vac and stand and clean again so I know it was something to do with the above, but which part I am not sure. Despite all of the improvements I however ‘never felt well’ or normal again, just grateful not to be as completely incapacitated. Slowly however I did get worse again. IHave lately wondered a lot about the apricot kernals with vit c and whether I should restart them...but I am doing other things now and getting well in other areas, so Not sure whether to ‘add them in’. Last year, I was able to mow a lawn again, but still felt very sick. I suffered from heat stress, could’t lose weight, depressed, ached all over, horrible memory, difficulty Recognising faces. Trouble getting up and down with sore hips and knees, TMJ, sore glands, sore neck and back etc. I had found a new doc by then and he thought I had lyme but would not treatment as he had too many Lyme patients and had to watch script numbers and did not know me well enough yet.. He watched me for a year . During this year I kept going back and asking for treatment but got off the low dose steroids, got on salt c and cats claw and colodial silver and  mms. I was still sick, (though looking back, some of it might have been die off) and felt I was going nowhere I got desperate enough to pay for and do blood tests which was huge, as money was tight. I had to know one way or the other, especially as now my kids were sick too and my husband had tendon problems and couldn’t work for 6 months. It was horrible. My doc would not fill in forms for Igenex only for Australian Biologics in Sydney which requires you come off all antimicrobials for 8 weeks before you can have the test or it will be neg. I was sicker than I had been in years..by the time I had the test my balance was gone on a daily basis and I had to hold onto walls to stay upright. I lived on stematol daily and after the test ramped up on everything I could as quickly as possible. My doc gave me antibiotics and I started plaquinel and then minocycline and then bacterim. I slowly began to regain what i lost and with the antibiotics.....gain ground. I did antibiotics  with herbs and some chinese meds for one year before I added in Rife. plus clay and seaweed to detox and smilax I felt a real obvious jump in health using antibiotics but it took months to realise this. I did not ‘feel better’ I just started to realise some symptoms I had had for years were gone. Someone on this site said it is really important to write down every symptom, because treatment takes so long it is easy to give up hope and stop treating as you think you are not getting better. The best way to know you are improving is to watch your symptoms are disappearing.  However I was still scared as I did not feel my neuro symptoms were improving as fast as the rest of me and although my kids were definitely improving on antibiotics, was not happy with neuro for them or my husband either....scared we weren’t doing enough. I also realised we all had bad bartonella and probably babesia and more did not know how to fully treat for  these and wondered how many herbs we could all take and for how long and how much? My friend has these and the treatment was over $20 000 per year for 1 person. We are 5 people plus my mum and her husband.....so we bought a doug coil. I herx obviously from the rife as do my kids especially the one with the most neuro symptoms. It is such a reassuring way of treatment as you finally feel like you have some control over your treatment and how hard each individual can ‘stand to go and when’ . Also I can target co-infections and areas we are struggling with and know symptoms are die off and not reactions to ‘toxins of treatment’. The greatest relief is the help I have had with my head.. I truly feel obviously better..I can think more clearly. When my neck or head hurts I do a treatment and feel better for it. I do herx, but make sure I aim for times I can sit around more like the old days while I go through it and take barley grass, diatomeous earth etc. So it doesn’t completely destroy my ability to look after my family. I know you are not supposed to treat with antibiotics and herbs and rife and long term I will have to come off them, but now I AM IMPROVING! Yahoo. If it means I treat for longer so be it. I also am too scared to come off antibiotics yet. I will also stay on my cyst buster herbs and antibiotics while rifing when I come off the others. The other thing I am now on which I feel has helped me dramatically is serrapeptase strength 40 000 and nattokinase. I chose doctors best brand. I am up to 3 capsules serraptase am and 1 pm. 2 x natto a day. My circulation has improved my veins in my legs don’t ache and I just feel ‘fresher’ more alive, it is a strange feeling. It took about a month to feel better. I thought it was supposed to take a year? Can’t wait for the rest of the improvements so am increasing as fast as I can! Anyhow an epic I know Good luck and chow for now From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of Marie BenoitSent: Sunday, 8 July 2012 2:27 PMTo: Lyme_and_Rife Subject: Re: Re: lighteadednessti how did you do please Thanks Marie To: Lyme_and_Rife Sent: Saturday, July 7, 2012 7:53 PMSubject: RE: Re: lighteadedness Hi Terry, I had the disabling kind of fatigue and could not stand up without passing out. Best of luck. From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of ScharffSent: Friday, 6 July 2012 2:27 AMTo: Lyme_and_Rife Subject: RE: Re: lighteadedness Terry,I don’t have enough experience or knowledge about Lyme or Rife to contribute much, but have more than enough of both when talking about symptoms and am always glad to chime in. I’ve learned so much from the members of this group and am so appreciative that I try to pass on what I can. I hope the MMS helps you as it’s helped myself and many others. I still have some fatigue but it’s more like the normal everyday fatigue that I’ve had for over 22 years, not the totally disabling kind that I was struggling with and I think you mean. Take care,Jeff From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of T.BSent: Thursday, July 05, 2012 12:15 PMTo: Lyme_and_Rife Subject: RE: Re: lighteadedness Not yet Jeff i ordered it but i havent received it yet..Thank you for replying its geatly appreciatedFrom: tim2buk <http://us.mc845.mail.yahoo.com/mc/compose?to=tim2buk@...>Subject: Re: lighteadednessTo: http://us.mc845.mail.yahoo.com/mc/compose?to=Lyme_and_Rife Date: Thursday, July 5, 2012, 11:47 AM Terry,I have big problems with dizziness, lightheadedness & faintness. I don't know if it's what other people refer to as " brain fog " . A few years ago I had extensive testing on my ears because I thought that was what causing it, but it didn't turn out to be that. I also suffer from panic disorder for over 30 years now & found out last year I could have had Lyme since I was a child. Throw in mercury poisoning, old root canals & chronic sinusitis & there's no way to tell what's causing the dizziness. It's a process of elimination trying to find the culprit(s). It's not an easy or short process, but you are not alone. I hope you find the answer to your problem.Susie>> Is anyone besides myself lightheaded ,feeling like there gonna faint 24-7?> Thank You> Terry> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2012 Report Share Posted July 8, 2012 Hi , I understand instantly what you have been throught . Thank you for your thorought description and sharing of what a struggle it has been . You are an emblem of beautifull motherhood .I am amazed on how a mother can find the strenghe for love of her familly . My story is as challenging as yours but I am too tyred to write it now forgive me not for doing it .paralysis of the worse kind and all the swing that goes with this desease being let apart medically socially affectively financially and then being helped by grace of God throught all this mist . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 8, 2012 Report Share Posted July 8, 2012 Hi Marie Lovely to hear from you, I have some idea of what you’ve been through as I read your posts! By the way the strength of serraptase I use is 40 000 but at 3 cap am the amount I am on is 120 000 am and I am building to this at night. I felt nothing much at lower doses. Cheers From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of Marie BenoitSent: Monday, 9 July 2012 4:49 AMTo: Lyme_and_Rife Subject: Re: Re: lighteadedness Hi ,I understand instantly what you have been throught .Thank you for your thorought description and sharing of what a struggle it has been . You are an emblem of beautifull motherhood .I am amazed on how a mother can find the strenghe for love of her familly . My story is as challenging as yours but I am too tyred to write it now forgive me not for doing it .paralysis of the worse kind and all the swing that goes with this desease being let apart medically socially affectively financially and then being helped by grace of God throught all this mist . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 12, 2012 Report Share Posted July 12, 2012 Hi , Thank you for you cheerfull answer. I tryed this long ago but at a too low dosage . I had read in Mexico someone healed from paralysis with serrapetase with 80 000 so I did it several month with no success probabley it was not enought . Kindly Marie To: Lyme_and_Rife Sent: Sunday, July 8, 2012 5:22 PMSubject: RE: Re: lighteadedness Hi Marie Lovely to hear from you, I have some idea of what you’ve been through as I read your posts! By the way the strength of serraptase I use is 40 000 but at 3 cap am the amount I am on is 120 000 am and I am building to this at night. I felt nothing much at lower doses. Cheers From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of Marie BenoitSent: Monday, 9 July 2012 4:49 AMTo: Lyme_and_Rife Subject: Re: Re: lighteadedness Hi , I understand instantly what you have been throught . Thank you for your thorought description and sharing of what a struggle it has been . You are an emblem of beautifull motherhood .I am amazed on how a mother can find the strenghe for love of her familly . My story is as challenging as yours but I am too tyred to write it now forgive me not for doing it .paralysis of the worse kind and all the swing that goes with this desease being let apart medically socially affectively financially and then being helped by grace of God throught all this mist . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 12, 2012 Report Share Posted July 12, 2012 Hi Marie, I’m now up to 40 000 x 3 capsules serraptase am and 3 pm plus 2 capsules natto daily..I feel good, my circulation feels better, but the patch of skin on my neck and upper back which has been numb for years is now returning to sensation and driving me crazy with itching....also going to toilet more often. ??? Cheers From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of Marie BenoitSent: Thursday, 12 July 2012 2:11 PMTo: Lyme_and_Rife Subject: Re: Re: lighteadedness Hi ,Thank you for you cheerfull answer.I tryed this long ago but at a too low dosage . I had read in Mexico someone healed from paralysis with serrapetase with 80 000so I did it several month with no success probabley it was not enought .Kindly Marie To: Lyme_and_Rife Sent: Sunday, July 8, 2012 5:22 PMSubject: RE: Re: lighteadedness Hi Marie Lovely to hear from you, I have some idea of what you’ve been through as I read your posts! By the way the strength of serraptase I use is 40 000 but at 3 cap am the amount I am on is 120 000 am and I am building to this at night. I felt nothing much at lower doses. Cheers From: Lyme_and_Rife [mailto:Lyme_and_Rife ] On Behalf Of Marie BenoitSent: Monday, 9 July 2012 4:49 AMTo: Lyme_and_Rife Subject: Re: Re: lighteadedness Hi ,I understand instantly what you have been throught .Thank you for your thorought description and sharing of what a struggle it has been . You are an emblem of beautifull motherhood .I am amazed on how a mother can find the strenghe for love of her familly . My story is as challenging as yours but I am too tyred to write it now forgive me not for doing it .paralysis of the worse kind and all the swing that goes with this desease being let apart medically socially affectively financially and then being helped by grace of God throught all this mist . Quote Link to comment Share on other sites More sharing options...
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