Myasthenia Gravis (MG) Support Forum, Page 2, : Special Forum View. Complete messages are Expanded, and threads are ordered by the Date of the First (Topic) Message (classic old view).

Combining breathing normalization https://normalb... Medicineman9 15 m 317 † C †

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Combining breathing normalization https://normalbreathing.com with the so called oil-protein-diet by Dr. Johanna Budwig http://www.healingcancernaturally.com/index-budwig.html should (perhaps!) ...

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Combining breathing normalization
https://normalbreathing.com
with the so called oil-protein-diet by Dr. Johanna Budwig
http://www.healingcancernaturally.com/index-budwig.html
should also work for the ailment discussed here!
https://www.curezone.org/forums/fm.asp?i=2458906#i

For some subforums the following is an additional important information, switch to squatting see https://naturesplatform.com immediately!! (if you are obese, never climb on a regular toilet with your full weight, the porcellain MIGHT BREAK (!!!) and this can cause massive injury!!)
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digestacure???? peachteach 10 y 7,537 † C †

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digestacure????

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Has anyone used and would share reviews of a product called DIGESTACURE?

I have something going on with me that can take many autoimmune disease shapes. Mostly it takes the shape of Myasthenia Gravis but all of the tests have concluded I don't have MG yet I have a lot of the MG symptoms.
Anyway, Dr's are confused and stumped with what I have and I tired of dealing with this. I found out about Digestacure and was wondering if anyone had any experience with it. If I try it I was planning on trying it for 6 months with nothing else supplemental. PLEASE RESPOND TO THIS POST ASAP. THANK :)

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- ”The symptoms of myasthenia gravis may include eye... grizz 10 y 7,021
  
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  This is a reply to # 2,183,151
  
  ”The symptoms of myasthenia gravis may include eye muscle weakness, eyelid drooping (ptosis), blurry or double vision (diplopia),unstable gait, a change in facial expression, difficulty in swallow ....
  
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  "The symptoms of myasthenia gravis may include eye muscle weakness, eyelid drooping (ptosis), blurry or double vision (diplopia),unstable gait, a change in facial expression, difficulty in swallowing, shortness of breath, impaired speech, and weakness in the arms, hands, fingers, legs, and neck...."
  
  You defined your problems perfectly..."I have something going on with me that can take many autoimmune disease shapes"
  
  Just look at the INSANE list of symptoms from Candida and the 5 stages of Candida here:
  http://tinyurl.com/Iodine-Candida
  
  Then see my answer that I just posted a few minutes ago here:
  //www.curezone.org/forums/fm.asp?i=2183202#i
  
  I hope this helps,
  Grizz
  
  View all messages by grizz on this forum, all forums.
  
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- I don’t know what Digestacure is, but I believe th... omo 10 y 6,790
  
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  This is a reply to # 2,183,151
  
  I don’t know what Digestacure is, but I believe that bad digestion is a central problem to probably a number of illnesses, quite probably ”Adrenal Fatigue”. I believe that digestion problems can ....
  
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  I don't know what Digestacure is, but I believe that bad digestion is a central problem to probably a number of illnesses, quite probably "Adrenal Fatigue". I believe that digestion problems can result in autoimmune disorder-like symptoms, if not actually lead to full-blown autoimmune disorders. The problems in digestion seem like they might be an imbalance in bacteria and intestinal permeability, but these are just guesses. From what I can tell, supplementing with yogurt or kefir, maybe kombucha and other probiotic foods seems to help. I'm testing this out now. Also, I'm paying closer attention to what peppermint and ginger can do.
  
  If you want to try a commercial product aimed at helping digestion, I say you stand a fair chance at benefit. But this could be a long battle, so you might want to look more closely at the details so you can learn from your trials.
  
  View all messages by omo on this forum, all forums.
  
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  - I’m using digester care I try to trial bottle coup... Thedoodr 10 y 6,266
    
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    This is a reply to # 2,185,060
    
    I’m using digester care I try to trial bottle couple minutes ago and it started working five days on Kindia eczema leaky gut. I just got the regular size bottle because it’s expensive I couldn’t a ....
    
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    I'm using digester care I try to trial bottle couple minutes ago and it started working five days on Kindia eczema leaky gut. I just got the regular size bottle because it's expensive I couldn't afford it for a while I'm on day three I am getting a hexing effect which is not too bad. The first to make sure I did it start to clear my skin within a few days so I do feel it does work it's anything to help me so far my diet is clean I need a lot of plant-based foods no grains no gluten no dairy,no sugar. I juice once a day. Hope this helps. I love digestaqure
    
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    - Re: digestacure???? Thedoodr 10 y 6,164
      
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      This is a reply to # 2,194,792
      
      Re: digestacure????
      *digestaqure
      
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    - I’m sorry for all the typos. My phone typed it out Thedoodr 10 y 6,232
      
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      This is a reply to # 2,194,792
      
      I’m sorry for all the typos. My phone typed it out
      I'm sorry for all the typos. My phone typed it out
      
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    - Hi there, I have been on digestacure for about ... peachteach 9 y 5,702
      
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      This is a reply to # 2,194,792
      
      Hi there, I have been on digestacure for about 7months now. I did buy the 6 bottle pack first and when that ran out I bought another 6 bottle pack. The first pack took approx. 60% of my sympt ....
      
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      Hi there,
      
      I have been on digestacure for about 7months now. I did buy the 6 bottle pack first and when that ran out I bought another 6 bottle pack. The first pack took approx. 60% of my symptoms away so they said probably another 4 bottles and the the other 2 would be for maintanence. I have increased my daily dosage to the 12/day and man am I detoxing. I am vegan/plant based diet.....actually raw till 4pm. I agree that it seems quite pricey but I stopped taking other supplements except for D3 and living oils.....so minusing my other supplements has made the cost that bad.
      
      Are you still on this? I'm sorry I haven't replied to you sooner....I haven't been on curezone recently.
      
      I hope things are going well your way.
      
      View all messages by peachteach on this forum, all forums.
      
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  - take ashwagondha to get rid of the acetylcholinest... william gick 10 y 6,505
    
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    This is a reply to # 2,185,060
    
    take ashwagondha to get rid of the acetylcholinesterase that is robbing you of acetyl radicles that you can get in N ACETYL CYSTEINE...NAC
    take ashwagondha to get rid of the acetylcholinesterase that is robbing you of acetyl radicles that you can get in N ACETYL CYSTEINE...NAC
    
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  - thank you! Digestacure (supplement that cures aut... peachteach 9 y 6,257
    
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    This is a reply to # 2,185,060
    
    thank you! Digestacure (supplement that cures auto immune disorders) has helped me greatly.....so far 65% of my symptoms are gone....I’m On it till all are gone. Raw till 4 plant based diet ....
    
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    thank you! Digestacure (supplement that cures auto immune disorders) has helped me greatly.....so far 65% of my symptoms are gone....I'm On it till all are gone.
    
    Raw till 4 plant based diet has helped greatly too......
    
    Thanks again
    
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some have cured myastenia gravis with the iodine p... knowledge seeker 10 y 2,207

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some have cured myastenia gravis with the iodine protecol

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as found in the book the Iodine crisis

I saw this mentioned in an interview she did here

http://www.cheeseslave.com/interview-with-lynne-farrow-author-of-the-iodine-c...

One doctor said 90% of the patients he tested were Iodine deficient, so even if it does not help thew myastenia gravis, it may still help with a number of other problems

This the high doses taken with the associated nutrients etc as laid out in the above book by Lynn Farrow

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Please tell me the name of any powerful adjunct me... #182849 10 y 2,548

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Please tell me the name of any powerful adjunct medicine (supplementary medicine) for myasthenia gravis ?

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Firstofall, I thank you for spending your valuable time in reading this email.
I am unmarried woman aged 33 years. I am suffering from congenital myasthenic syndrome or CMS and taking treatment from NIMHANS, Bangalore.
My symptoms of congenital myasthenic syndrome are as fallows:-
1. Drooping of both eyelids. no movement of both the eyeballs.
2. No Respiratory problem, can breath easily.
3. Little bit of swallowing and chewing problem.
4. weakness in whole body
5. No Double vision.
6. Can see clearly.

No one in my family has CMS or myasthenia gravis or no history in my family had CMS or myasthenia gravis.

Now, I am taking Pyridostigmine bromide 60mg daily 5 tabs.
From 2002, I was taking Corticosteriods 30mg daily for about 3-4 yrs. With Doctor’s advice, from 2005, I tapperdown Corticosteriods and with God’s Grace, now I completely stopped taking Corticosteriods.

Three years back,for some days, I took Cellcept tabs and now, I stopped it completely. At present, in addition to Pyridostigmine bromide tablets, I will take Meganeuron OD Plus and Antoxyl Forte and Potklor syrup and Gravitor SR tabs. This four medicines I will take (as and when required) whenever I go outside or when there is more work or when there is more weakness.

At present, I am having moderate weakness.

We are non-resident of Bangalore. Suddenly, my sister's marriage has been fixed and there is no time to go to Bangalore and consult my doctor and also ask for any more powerful adjunct medicine (powerful medicine/general medicine) other than the above four mentioned by me. I don't have any other diseases other than myasthenia gravis.

Please tell me the name of any powerful adjunct medicine (supplementary medicine) other than the above four mentioned by me, so that I will be very grateful to you.

Waiting for your early reply
thanking you

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- Gluten??? 32771 10 y 2,075
  
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  This is a reply to # 2,161,441
  
  Gluten???
  
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  In a Google search of the terms: myasthenia gravis gluten Lancet on a single line, this is some of what came up. They want $36 for a reprint and refused that offer. But what it shows me is that the medical community KNEW over 35 yr ago of a gluten connection.
  
  http://www.ncbi.nlm.nih.gov/pubmed/49641
  Lancet. 1975 Jul 5;2(7923):41.
  Letter: Gluten and myasthenia gravis.
  Edwards JH.
  
  http://image.thelancet.com/journals/lancet/article/PIIS0140-6736(75)92992-X/f...
  The Lancet, Volume 306, Issue 7923, Page 41, 5 July 1975
  GLUTEN AND MYASTHENIA GRAVIS
  Original Text
  J.H. Edwards
  
  Is it too much to ask that you do a trial of 2 months gluten-free?
  Although modern wheat is the greatest offender, my MD says even a little gluten in foods can do a lot of harm. Gluten sensitivity if far more common than most realize. See some of my previous posts below.
  
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Sudden Severe Joint Pain/Muscle Pain Everywhere, T... LaurelC 10 y 4,723 † C †

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Sudden Severe Joint Pain/Muscle Pain Everywhere, Then Disappears as quickly as it came.

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I don't know if this condition fits this forum, but I am selecting various forums that someone on those forums MIGHT know or have heard of this condition:

--------------

I have a friend who has a condition that comes on suddenly where he goes into severe pain all over his body. He then is down on the floor, cannot move.. not even one joint. Every joint in his body is in severe pain and is rigid.

The hospital put him on HUGE dose of muscle relaxers, which did not work. They also tried traction.. that did not work either. They told him it is like he is in rigor mortis.

At one point, he fell asleep and when he awoke, he was then perfectly fine.

This was not the first episode of this he has had.

Has anyone ever heard of such a condition?

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- Re: Sudden Severe Joint PainMuscle Pain Everywhere... DaoYin 10 y 3,608
  
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  This is a reply to # 2,143,375
  
  Re: Sudden Severe Joint PainMuscle Pain Everywhere, Then Disappears as quickly as it came.
  
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  I'll base my response on the assumption that the hospital has ruled out a brain tumor or other sever neurological disorders via imagery and diagnostic testing, if not, he needs to see a neurologist ASAP.
  
  In Chinese medicine, as you have described it, I would suspect this sort of pain to be an aspect of severe "blood" stasis, where the 'blood" stasis is and its origin would require a proper evaluation. Other things to look for is fascial pain syndromes (myofascial dysfunction, trigger points) and the autonomic phenomena that can come with it, these conditions being western explanations of qi and "blood" stasis and can be be treated effectively by a well trained Chinese medical practitioner with the use of acupuncture, moxibustion, physical manipulation and therapy, and herbal medicine.
  
  Good Luck!
  
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  - Hi.. thanks for your reply. We do have an acupunct... LaurelC 10 y 3,582
    
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    This is a reply to # 2,149,162
    
    Hi.. thanks for your reply. We do have an acupuncturist here who is also a Doctor of Chinese medicine(although the wait to get in is 6 months). I will relay this to the ailed man.
    Hi.. thanks for your reply. We do have an acupuncturist here who is also a Doctor of Chinese medicine(although the wait to get in is 6 months).
    
    I will relay this to the ailed man.
    
    View all messages by LaurelC on this forum, all forums.
How I beat myasthenia gravis and hypothyroidism small wonder 11 y 2,802 † C †

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How I beat myasthenia gravis and hypothyroidism

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Hi I have a proven method for curing myasthenia gravis and hypothyroidism please go here to read my story http://curemyastheniagravis.weebly.com

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Cure for MG small wonder 11 y 1,059 † C †

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Cure for MG

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Hi, everyone I am new here and I just wanted to say that, You guys are awesome and brave to try to help yourself and others by talking about it. I had MG a year ago or less and Hyperthyroid over three years ago but I was living with it for 2 years but know I don't. You can read about my success on my blog curemyastheniagravis.weebly.com

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myastenia gravis and genectic predispostion Karen1991 11 y 4,270 † C †

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myastenia gravis and genectic predispostion

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Hi All,

I am new to your wonderful forum and I am at my wits ends. I am afraid and I am not getting ANY answers except running into a brick wall, what makes it worse, I a RN, I still can't get information. Please any and all comments, information, suggestions are welcome and I guess I am scared and frustrated. I have even asked my mother's neurologist says that she can't talk to me directly regarding myself and my primary doctor doesn't want to investigate further because I am I not suffering any "obvious concerning" MG symptoms and won't authorize a referral to a neurologist/MG specialist. GGGRRRRRRRR......

HISTORY: I am a 39 year old female who has been diagnosed with psorasis, psoractic arthritis and rhuematoid arthritis, all immunological disorders. Lately I have been experiencing increased fatigue and what appears to be a lower immune response to diseases (getting sick WAY MORE, going septic from a strep infection WHILE ON ANTIBIOTICS) and more severe allergic reactions (5 anaphalactic reactions to one dose of 500mg of Keflex)

FAMILY HISTORY: My mother at 78 was diagnosed with Myastenia Gravis via a Myastenia Gravis crisis which involved 8 weeks in the hospital. She too was diagnosed with psorasis, psoractic arthritis and rhuematoid arthritis prior to her MG diagnosis. My mother has been stabilized, discharged home (I live 5 townhouses away), is on 240 mg daily of mestinon, 2000 mg daily of cellcept and monthly IVIG treatments.

My question is: It is obvious that my mother and myself are suffering from various immunological disorders, I am concerned that because I am trending JUST LIKE MY MOTHER, am I at risk for getting MG? I have done research and it seems as though MG is not a genetic linked disorder, but I can't stop the feeling that I am at risk and from my recent history, my immune system is apperantly and obviously wacked out.

Thanks in advance for your help and responses and I apologize for this thread being so long.....

Karen

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- Re: myastenia gravis 32771 11 y 4,663
  
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  This is a reply to # 2,042,654
  
  Re: myastenia gravis
  
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  I have a family friend that has used the Schulze formula listed in the MG post before yours. She saw some improvement but has yet to do what Schulze says to do first, the Incurables Program. In 1998(?) he said: “Obviously, when anybody has any neuromuscular disease, multiple sclerosis, muscular dystrophy, myasthenia gravis or others, it is the Incurables Program. That’s where everybody has to start.” I have the18 page section where this subject is discussed in more but similar detail.
  
  You ought to do a Google search for: “Myasthenia gravis + gluten intolerance”. My new Dr is of the “Functional Medicine” variety. First visit put me on a gluten-free diet because I was deemed “gluten intolerant”. Dr’s mother has RA, still does but without the pain. I personally have less pain as a result of the diet. You don’t realize what modern, hybrid wheat has done to us in so many ways since the 60’s and how/why it messes up the adsorption of nutrients that pass thru the small intestine and thus cause illness.
  
  Search YouTube videos “Dr William Davis MD wheat”
  
  Dr Glidden: http://www.youtube.com/watch?v=k4GOLkjbDcc
  
  Dr Tom O’Bryan to Drs about celiac & gluten-free:
  http://www.youtube.com/watch?NR=1&v=DjvKrAvolMQ&feature=endscreen
  Part1 (53min)
  http://www.youtube.com/watch?NR=1&v=9VuZ2tL8KAQ&feature=endscreen
  Part2 (53min)
  http://www.youtube.com/watch?NR=1&v=Z9FYYdydj8U&feature=endscreen
  Part3 (32 min)
  When I watched some of these videos, I was reminded of what one nutritional chiropractor in the Atlanta area said concerning why elderly often die: they die of starvation as a result of poor digestion in later yrs. What’s the difference if our gut is so messed up due to gluten?
  
  When it comes to family genetics, I’ve heard it said: 10% heredity, 90% environment. So, do you eat similar foods as do your parents?
  
  Just take a look at gluten as a possibility. We are all different and there may be other options. Now what Dr O’Bryan says, the next step is to heal the damage. So the heath journey is not over for me.
  
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  - On Nov 11-19, 2013 there was an online Gluten Summ... 32771 11 y 3,187
    
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    This is a reply to # 2,042,819
    
    On Nov 11-19, 2013 there was an online Gluten Summit put on by Dr Tom O’Bryan of www.thedr.com Of the 29 interviews, I watched 18. Several of the researchers/Doctors mentioned MS (a close cousin ....
    
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    On Nov 11-19, 2013 there was an online Gluten Summit put on by Dr Tom O’Bryan of http://www.thedr.com
    
    Of the 29 interviews, I watched 18. Several of the researchers/Doctors mentioned MS (a close cousin to MG???) as a link to gluten sensitivity. I am trying to get the family friend to just do it for a month or two. My problem is that I have converted no one despite them knowing my health has improved this past year. Guess that unless you stumble onto a knowledgeable Dr yourself and pay big $$$...
    I need to quit spiting into the wind.
    
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- Re: myastenia gravis and genectic predispostion fcsteacher 11 y 3,186
  
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  This is a reply to # 2,042,654
  
  Re: myastenia gravis and genectic predispostion
  
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  I too wonder if there is a genetic link to MG. Everything I have read says it is not. My father was recently diagnosed with MG. His mother also had it and died due to complications from it. From what I have researched, there are only about 1 in 5,000 people diagnosed with MG. For a mother & son to both have it seems a little too much of a coincidence for me. Your post is from 8 months ago, and I was wondering if you found any new information?
  
  View all messages by fcsteacher on this forum, all forums.
  - Hi, I was diagnosed at 15. I am now 38 and still h... natsi 11 y 4,127
    
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    This is a reply to # 2,122,696
    
    Hi, I was diagnosed at 15. I am now 38 and still haven’t heard any difference when reading about MG. Does this mean they don’t have many case studies and don’t know much about it? I have never sou ....
    
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    Hi, I was diagnosed at 15. I am now 38 and still haven't heard any difference when reading about MG. Does this mean they don't have many case studies and don't know much about it? I have never sought a support group or chat group so I'm unsure how common it is. However, I have 2 sons 19 and 17, both healthy and symptom free. That's all the advise I can give sorry
    
    View all messages by natsi on this forum, all forums.
Did this Nerve Regen formula work for you? 32771 12 y 1,119

Mercury Detox
Dental work and fillings, not a problem.

Did this Nerve Regen formula work for you?

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Was wondering if anyone had good results for their MG using this Schulze formula no longer available from him. May try to find the basic ingredients to make the tincture myself for a friend if reports are favorable.

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View all messages by 32771 on this forum, all forums.
Expand this whole thread (2 messages)

Anybody get severe itchy palms etc. from mestinon peachteach 13 y 3,048

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Anybody get severe itchy palms etc. from mestinon

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I have had to take more mestinon in the past couple of months than I ever have had to take before and my palms, feet and other areas on my body are EXTREMELY ITCHY. Anybody have this issue? I am not taking it for the next several days to see if the itchiness goes away. Any ideas on how to relieve the itch other than benadryl?

View all messages by peachteach on this forum, all forums.
- any ideas? liver flushing and colon cleansing.(... chirontherainbowbridge 12 y 2,299
  
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  This is a reply to # 1,869,737
  
  any ideas? liver flushing and colon cleansing.(only via natural means, with herbs as whole foods and self-administered flushes) read ”The amazing liver and gallbladder flush” C
  any ideas?
  
  Liver Flushing and colon cleansing.(only via natural means, with herbs as whole foods and self-administered flushes)
  
  read "The amazing liver and gallbladder flush"
  
  C
  
  View all messages by chirontherainbowbridge on this forum, all forums.
Expand this whole thread (5 messages)

Person with MG doing Master Cleanse peachteach 13 y 3,595

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Person with MG doing Master Cleanse
Anyone with MG do a Master Cleanse and if so how did it make them feel?

View all messages by peachteach on this forum, all forums.
- I wanted to let everyone know that I did complete ... peachteach 13 y 2,878
  
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  This is a reply to # 1,818,386
  
  I wanted to let everyone know that I did complete a 10 day cleanse however my weakness was intensified. I know I should do another one (and I will) but I don’t know when. Will you keep you posted....
  I wanted to let everyone know that I did complete a 10 day cleanse however my weakness was intensified. I know I should do another one (and I will) but I don't know when. Will you keep you posted.
  
  View all messages by peachteach on this forum, all forums.
  - I was crusing forums using keywords, Lyme and Myas... beams 10 y 2,243
    
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    This is a reply to # 1,869,738
    
    I was crusing forums using keywords, Lyme and Myasthenia Gravis. I found your post of 3 years ago. I’m curious to know if in the long run you had MG or Lymes or both? I suspect I have chronic L ....
    
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    I was crusing forums using keywords, Lyme and Myasthenia Gravis. I found your post of 3 years ago. I'm curious to know if in the long run you had MG or Lymes or both? I suspect I have chronic Lyme and have symptoms of MG and feel the Lyme set me up for it. Just curous how you made out. Thanks if you can reply , I'd appreciate it.
    
    View all messages by beams on this forum, all forums.
    - I’m so sorry it has taken me this long to reply...... peachteach 9 y 2,095
      
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      This is a reply to # 2,183,905
      
      I’m so sorry it has taken me this long to reply.....I haven’t been on curezone recently. I’m still on my health journey. I am currently on Digestacure (supplent that cures autoimmune disorders) ....
      
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      I'm so sorry it has taken me this long to reply.....I haven't been on curezone recently. I'm still on my health journey. I am currently on Digestacure (supplent that cures autoimmune disorders) and I purchased the 6 bottle pack which lasted me 6 months and got me to 65% symptom free. I purchased another pack of 6 and that should take me to the end plus some leftover for maintanence. This supplement and a plant based diet (raw till 4) has worked wonders on me. I am detoxing quite a bit but minimal weakness so yeah!!!!!
      
      Check it out......it is out of Florida.
      
      Stay in touch too.....I'm gonna try to be on here more.
      
      View all messages by peachteach on this forum, all forums.
      
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    - Hi there.... I am so sorry for such the late re... peachteach 9 y 2,650
      
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      This is a reply to # 2,183,905
      
      Hi there.... I am so sorry for such the late reply. I just saw your response. I am not on curezone.com very much because of what I am dealing with. It doesn’t seem to be discussed much on th ....
      
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      Hi there....
      
      I am so sorry for such the late reply. I just saw your response. I am not on curezone.com very much because of what I am dealing with. It doesn't seem to be discussed much on the site.
      
      I was inconclusively diagnosed with Myasthenia Gravis in 2002 at a well known hospital after enduring painful muscle testing. Just recently I requested from that hospital the medical records from those visits and tests. I found out that I DO NOT have Myasthenia Gravis. The tests were not inconclusive but VERY negative for the disease. Thank goodness I followed my gut during that time and did not have my Thymus removed (which was what the dr. wanted me to do at that time)
      
      I have had NMD, ND, ODM, etc. do multiple views of my blood during my weak times etc. and NONE OF THEM can figure out what is going on with me.
      
      What I experience is MAJOR muscle weakness at times. Stress, Heat, Exercise, Hormones etc. can be triggers but not always.
      
      The one thing that seemed abnormal is a lyme test I had done that displayed an inconclusive tests. The MD I was working with at the time stated in his opinion I have chronic Lymes. I have been trying to deal with my illness through a plant based diet, supplements and digestacure.
      
      This is all I have found that I can go on so I am trying to figure this out. It is extremely frustrating.
      
      I don['t know if it is working for me....I am detoxing quite a lot and one of my major symptoms of detoxing seems to be muscle weakness. This is just so very frustrating. I feel like a 80 year old when I am half that age.
      
      Talk with you soon hopefuily
      
      View all messages by peachteach on this forum, all forums.
      
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Expand this whole thread (2 messages)

Myasthenia Gravis fustratedsandie 13 y 2,778

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Myasthenia Gravis

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I have been suffering with this complain since 1989 i have been through so much ,even in Intensive Care. I am presently on medication,mestinon 60mg. Sometimes I get so fed up and frustrated I wish that there is something I can take to help with these dreaded symptoms,anyone can help?

View all messages by fustratedsandie on this forum, all forums.
- I have a close friend that had MG and is now compl... Musiker 11 y 1,940
  
  Bio Cleanse Detox Kit
  ”I have recommended it to family and friends already and am sure...
  
  This is a reply to # 1,805,109
  
  I have a close friend that had MG and is now completely cured. She does not speak English and has asked me to tell her story to as many MG sufferers that I can reach. I know how much she has suffe ....
  
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  I have a close friend that had MG and is now completely cured. She does not speak English and has asked me to tell her story to as many MG sufferers that I can reach. I know how much she has suffered because I was with her every step of the way. I hope this can help others.
  
  I met my friend ten years ago in Europe where I was living at the time. She took music lessons with me but was often unable to hold up the instrument. I realized as I got to know her that she was living in a horrible, hateful family situation (I will be happy to go into details if anyone is interested) and felt trapped. Her doctors at a university clinic told her that her life expectancy would be age 35, which was how old she was when I met her. The disease began in her childhood.
  Our friendship grew very slowly but became very intense. Most of the time, I told her how she had to get out of the house she was in, away from her parents and the influence of her ex-husband. She couldn’t see how sick the situation was because she was in the middle of it. She did not have a good job or partner, and she had two teenage girls that were not easy to raise. Everything about her life was pathetic and negative in my eyes. Plus, she was ill. She had the thymus scar, was taking serious meds. She had migraines and mood swings. Her life seemed hopeless.
  
  She slowly but immediately began making changes in her life.... Over ten years time, she moved, she put her kids in other schools, she stopped dating losers, she joined a new band. She began seeing herself as she really was, rather than the way her non-caring parents saw her. Due to MG, she was disabled and received a pension---now she is learning a new profession as a therapist. She lives with a man who treats her with respect. She shed many tears, and we had hours and hours of talks….and as life got better and better for her and she was able to let go of all of her past, she is now completely cured of MG. It is a miracle but it is the truth and it is all documented by her doctors. She takes no meds at all now. She has become a positive person.
  So I guess her message is: change your life and change your health!
  
  View all messages by Musiker on this forum, all forums.
  
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Combining breathing normalization https://normalbreathing.com with the so called oil-protein-diet by Dr. Johanna Budwig http://www.healingcancernaturally.com/index-budwig.html should (perhaps!) ...

digestacure????

”The symptoms of myasthenia gravis may include eye muscle weakness, eyelid drooping (ptosis), blurry or double vision (diplopia),unstable gait, a change in facial expression, difficulty in swallow ....

I don’t know what Digestacure is, but I believe that bad digestion is a central problem to probably a number of illnesses, quite probably ”Adrenal Fatigue”. I believe that digestion problems can ....

I’m using digester care I try to trial bottle couple minutes ago and it started working five days on Kindia eczema leaky gut. I just got the regular size bottle because it’s expensive I couldn’t a ....

Re: digestacure????

I’m sorry for all the typos. My phone typed it out

Hi there, I have been on digestacure for about 7months now. I did buy the 6 bottle pack first and when that ran out I bought another 6 bottle pack. The first pack took approx. 60% of my sympt ....

take ashwagondha to get rid of the acetylcholinesterase that is robbing you of acetyl radicles that you can get in N ACETYL CYSTEINE...NAC

thank you! Digestacure (supplement that cures auto immune disorders) has helped me greatly.....so far 65% of my symptoms are gone....I’m On it till all are gone. Raw till 4 plant based diet ....

some have cured myastenia gravis with the iodine protecol

Please tell me the name of any powerful adjunct medicine (supplementary medicine) for myasthenia gravis ?

Gluten???

Sudden Severe Joint Pain/Muscle Pain Everywhere, Then Disappears as quickly as it came.

Re: Sudden Severe Joint PainMuscle Pain Everywhere, Then Disappears as quickly as it came.

Hi.. thanks for your reply. We do have an acupuncturist here who is also a Doctor of Chinese medicine(although the wait to get in is 6 months). I will relay this to the ailed man.

How I beat myasthenia gravis and hypothyroidism

Cure for MG

myastenia gravis and genectic predispostion

Re: myastenia gravis

On Nov 11-19, 2013 there was an online Gluten Summit put on by Dr Tom O’Bryan of www.thedr.com Of the 29 interviews, I watched 18. Several of the researchers/Doctors mentioned MS (a close cousin ....

Re: myastenia gravis and genectic predispostion

Hi, I was diagnosed at 15. I am now 38 and still haven’t heard any difference when reading about MG. Does this mean they don’t have many case studies and don’t know much about it? I have never sou ....

Did this Nerve Regen formula work for you?

Anybody get severe itchy palms etc. from mestinon

any ideas? liver flushing and colon cleansing.(only via natural means, with herbs as whole foods and self-administered flushes) read ”The amazing liver and gallbladder flush” C

Person with MG doing Master Cleanse

I wanted to let everyone know that I did complete a 10 day cleanse however my weakness was intensified. I know I should do another one (and I will) but I don’t know when. Will you keep you posted....

I was crusing forums using keywords, Lyme and Myasthenia Gravis. I found your post of 3 years ago. I’m curious to know if in the long run you had MG or Lymes or both? I suspect I have chronic L ....

I’m so sorry it has taken me this long to reply.....I haven’t been on curezone recently. I’m still on my health journey. I am currently on Digestacure (supplent that cures autoimmune disorders) ....

Hi there.... I am so sorry for such the late reply. I just saw your response. I am not on curezone.com very much because of what I am dealing with. It doesn’t seem to be discussed much on th ....

Myasthenia Gravis

I have a close friend that had MG and is now completely cured. She does not speak English and has asked me to tell her story to as many MG sufferers that I can reach. I know how much she has suffe ....