Guest guest Posted February 20, 2006 Report Share Posted February 20, 2006 Kathy & , thank you so much for replying. I will add the supplements and try harder to stick to the yeast free diet. Did you definetely notice a difference in health when you got your yeast in check? I hate to say the word candida (sounds like a woman thing ) keith --- low dose naltrexone wrote: > There are 18 messages in this issue. > > Topics in this digest: > > 1. Re: Increased Myoclonus > From: " maryebe " <eberlein@...> > 2. Re: LDN - UK National Institute for > Neurology - > From: " " <pomsaregreat@...> > 3. Re: LDN - UK National Institute for > Neurology - > From: " Aletha Wittmann " > <Aletha@...> > 4. Re: Digest Number 1863 > From: foxhillers@... > 5. Re: LDN for cancer > From: " jsgarvin " <jsgarvin@...> > 6. Re: Off topic/ Noni juice > From: " Aletha Wittmann " > <Aletha@...> > 7. Re: LDN for cancer > From: " Bren " <b63powell@...> > 8. Re: Re: LDN for cancer > From: " jsgarvin " <jsgarvin@...> > 9. Re: Re: LDN for cancer > From: " Aletha Wittmann " > <Aletha@...> > 10. LDN Side Effects? > From: " Beth " <bethdebrook@...> > 11. Re: Re: LDN as treatment for hairloss? > From: nutrimedent@... > 12. OT: This is a test, pls delete > From: " LarryGC " <larrygc@...> > 13. Re: LDN Side Effects? > From: C <covo@...> > 14. Re: yeast test > From: " Kathy " <kathyhaworth@...> > 15. Re: Off topic/ Noni juice > From: chris bowes > <sens4life2002@...> > 16. Re: yeast test > From: " Bren " <b63powell@...> > 17. Boston College Research Participation > Request for Gay Men > From: " cjhamilton72 " > <cjhamilton72@...> > 18. Re: yeast remedy from threelac > From: keith kowalis <wescokk@...> > > > ________________________________________________________________________ > ________________________________________________________________________ > > Message: 1 > Date: Mon, 20 Feb 2006 01:07:17 -0000 > From: " maryebe " <eberlein@...> > Subject: Re: Increased Myoclonus > > It seems to me I read somewhere an article about > valtrex and > myoclonus. Not sure though - maybe worth a google > though. Valtrex has > been very effective against my CFS. > > > > > > YES. THE BAR OF SOAP WORKS. HAVE NO RHYM OR > REASON, BUT I USE IT > IN MY > > BED AT HOME AND IN MY RV WHEN WE GO PLACES. > WOULDN'T BE WITHOUT IT. > DR. > > GOTT WROTE AN ARTICLE IN OUR FRESNO BEE IN FRESNO, > CA. ABOUT THE > SOAP REMEDY > > WORKING. NOTHING TO LOSE BY TRYING. GOOD LUCK. > GOD BLESS. > > > > -- Re: [low dose naltrexone] Increased > Myoclonus > > > > Hi " Pushcrash " , > > > > I looked up Myolonus on the net and my > understanding is that it > means mussel > > > > twitching, is that right? > > One strange thing that seems to be working for > many people for pain and > > spasms has been to put a bar of soap in bed with > you near the areas > that are > > > > affected. Don't use Dove or Dial. But apparently > all other soaps > work. So > > > > many people have said they have been surprised but > really it worked. > > > > is right that it seems that it takes longer > for LDN to work > in most > > people that have been taking opiates. So just > hang in there. You > have made > > > > a good choice to give LDN a try. > > > > If you would like, I can send you a copy of the > " welcome e-mail " for > LDN. > > It is mainly geared for MS, but you might find > some helpful info in > there > > for your condition. > > > > Take care, and we are all here with you. > > > > Keep us posted > > Aletha > > > > > > > > [low dose naltrexone] Increased Myoclonus > > > > > > > Doc and I decided to try LDN for mycotoxicosis > (looks, acts like, and > > > is CFS - except that we know the cause in my > case). I was on darvoset > > > for a long time, but had started to develop > tolerance for it. I've > > > been on LDN at 4.5 mg for a week now. Pain > control is incomplete even > > > with celebrex, and myoclonus is downright scary. > What used to be legs > > > jumping at sleep time, or legs jerking when > calves along shin were > > > touched has turned into crawly, itching skin and > myoclonus of the > > > trunk strong enough to nearly put me right out > of my chair. Limbs > > > jerk enough when asleep that it wakes me right > up. > > > > > > I get that the darvon is a pretty ordinary > treatment for both > > > myoclonus and pain, but now I'm without it. I > wouldn't be bothered if > > > the symptoms were only mild. I could live with > that. And I liked the > > > idea of not taking any mind or mood-altering > drugs at all. But the > > > symptoms are worse than they ever were before. > I'm not necessarily > > > blaming the LDN, but I've got to be able to get > some effective pain > > > control and treatment for the myoclonus back in > place - and by all > > > reports, the LDN is actually going to be in my > way, since the darvon > > > is a mild opiate. Absolutely can't do any ergot > alkyloids. > > > > > > So. There it is. I need to do something, and > quickly. Any > > > suggestions? > > > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 20, 2006 Report Share Posted February 20, 2006 I definitely felt better and I had to go on antibiotics this past year and guess what? I had a white tongue and started feeling sluggish. Now after cleansing and doing several things for my colon I am back on track. The trick for me has been to spend a couple years being very diligent about my health in general. your immune system becomes so strong that you can cheat and do things like " regular People " whatever that means, hee hee but get right back on track . That way I don't feel like I'm in a bubble . Best wishes, Kathy [low dose naltrexone] Increased Myoclonus >> > >> > >> > > Doc and I decided to try LDN for mycotoxicosis >> (looks, acts like, and >> > > is CFS - except that we know the cause in my >> case). I was on darvoset >> > > for a long time, but had started to develop >> tolerance for it. I've >> > > been on LDN at 4.5 mg for a week now. Pain >> control is incomplete even >> > > with celebrex, and myoclonus is downright scary. >> What used to be legs >> > > jumping at sleep time, or legs jerking when >> calves along shin were >> > > touched has turned into crawly, itching skin and >> myoclonus of the >> > > trunk strong enough to nearly put me right out >> of my chair. Limbs >> > > jerk enough when asleep that it wakes me right >> up. >> > > >> > > I get that the darvon is a pretty ordinary >> treatment for both >> > > myoclonus and pain, but now I'm without it. I >> wouldn't be bothered if >> > > the symptoms were only mild. I could live with >> that. And I liked the >> > > idea of not taking any mind or mood-altering >> drugs at all. But the >> > > symptoms are worse than they ever were before. >> I'm not necessarily >> > > blaming the LDN, but I've got to be able to get >> some effective pain >> > > control and treatment for the myoclonus back in >> place - and by all >> > > reports, the LDN is actually going to be in my >> way, since the darvon >> > > is a mild opiate. Absolutely can't do any ergot >> alkyloids. >> > > >> > > So. There it is. I need to do something, and >> quickly. Any >> > > suggestions? >> > > >> > > >> > > >> > > >> > > >> > > >> > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2009 Report Share Posted May 25, 2009 > > Hi Bee, > I have mentioned before that my #1 symptom is a vaginal yeast infection. Mainly itchiness more than anything. I know you mentioned before this is the die-off if I had yeast infections in the past. To give you a little background...about 6 years ago I woke up with a yeast infection. Since then...it has never gone away. I am now on your program fully and even experience more vaginal itchiness. Have you ever heard of other women going through this? The more I read others posts it doesn't seem like many people have vaginal yeast infections so severe. I have been to medical doctors and have been tested for everything...even had a biopsy and everything has always came back negative. I guess I just want your input on this. Is this common with candida to have vaginal itchiness everyday non-stop for the last 6 years? +++Hi . Yes it is normal to have vaginal itchiness every day non-stop. I had vaginal problems for over 25 years, and it was the last thing to improve on my candida program. Some people don't have vaginal yeast, but their bodies perfer to detoxify through their vagina which causes the symptoms you describe. In that case it's the toxins that are causing the symptoms. I recommend you douche with clear non-chlorinated water every 4 days. Bee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2009 Report Share Posted May 25, 2009 Thanks Bee. It is good to know that I am not the only one that has gone through these symptoms. One other question about coconut oil. Typically mine is always hard because my house is usually around 70 degrees. When I measure it...I just use a tablespoon and eat that. Is that too much because I'm measuring it hard? Should I be using a heaping teaspoon rather to get the right amount? > > Hi Bee, > I have mentioned before that my #1 symptom is a vaginal yeast infection. Mainly itchiness more than anything. I know you mentioned before this is the die-off if I had yeast infections in the past. To give you a little background.. ..about 6 years ago I woke up with a yeast infection. Since then...it has never gone away. I am now on your program fully and even experience more vaginal itchiness. Have you ever heard of other women going through this? The more I read others posts it doesn't seem like many people have vaginal yeast infections so severe. I have been to medical doctors and have been tested for everything.. ..even had a biopsy and everything has always came back negative. I guess I just want your input on this. Is this common with candida to have vaginal itchiness everyday non-stop for the last 6 years? +++Hi . Yes it is normal to have vaginal itchiness every day non-stop. I had vaginal problems for over 25 years, and it was the last thing to improve on my candida program. Some people don't have vaginal yeast, but their bodies perfer to detoxify through their vagina which causes the symptoms you describe. In that case it's the toxins that are causing the symptoms. I recommend you douche with clear non-chlorinated water every 4 days. Bee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2009 Report Share Posted May 25, 2009 > One other question about coconut oil. Typically mine is always hard because my house is usually around 70 degrees. When I measure it...I just use a tablespoon and eat that. Is that too much because I'm measuring it hard? Should I be using a heaping teaspoon rather to get the right amount? > > > Hey . I am not Bee, but I've asked her the same question. You should measure it liquid. When you measure it solid, it is much more than liquid. Marisa Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2009 Report Share Posted May 25, 2009 > > Thanks Bee. It is good to know that I am not the only one that has gone through these symptoms. One other question about coconut oil. Typically mine is always hard because my house is usually around 70 degrees. When I measure it...I just use a tablespoon and eat that. Is that too much because I'm measuring it hard? Should I be using a heaping teaspoon rather to get the right amount? +++Hi . Like Marisa wrote you should measure it in liquid form. It is easy to melt it; just put it in a sink of hot water, or keep it on top of the fridge. If you have a gas stove keep it over the pilot light. The best, Bee Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 21, 2010 Report Share Posted December 21, 2010 I would look much more closely at her environment - specifically the other kids, aids, teachers etc. for clues. Also, in my opinion, unless your child has Celiac or is shown by a doctor to have sensitivity to gluten that requires a change in diet, I would steer clear of gf/cf diet. We all have candida (yeast) in our digestive tract, it occurs naturally. That's not to say she (or any of us) wouldn't be better off with a healthier diet. We discovered that my son burned through calories much faster than we would expect and that his blood sugar drops would coincide with bad behavior. Our solution was to give him more protein and complex carbs (vegetables, whole grains) and cut back on the starchy snacks. That naturally reduces the amount of gluten in his diet (not casein, cheese is one of his protein sources), but gf/cf diets are not ones we'd choose - otherwise there'd be no health market for the diet, we'd already be on it. So before switching to a diet (I'm assuming that's a relatively new thing) that she will perceive as punishment (seriously, unless one has to be on it, one would not choose to be on it), you should see what's going on at school - is there a kid or group of kids who've figured out how to push her buttons? Does she have a new bus driver who screams at kids and upsets her (happened in our case, and would be upset every morning)? Also, your daughter might prefer to be in the room with the aid to herself, especially if there is a student who bothers her. In that case, the school is rewarding her for acting out. It's the same principal as when a kid throws a tantrum to get candy and we give in and give it to them. Next time they want candy and we say no, they start that tantrum where the last one left off - they've learned how to get what they want. Good luck, I know it is difficult to go through these times when you feel like you're going backwards. Ron From: nataliamgomes@... Date: Thu, 16 Dec 2010 10:27:54 -0500 Subject: [ ] yeast problem Hi I hope someone can relate to my problem and has come out with some answers. My child has been in a private school for the last 2 years, last September during an IEP I was told if she continued doing has well as she was doing that she would be able to go to her homeschool, well nothing changed in our life, her diet or at school but she became extremely sensitive to sounds, clearing of the throat, body noises and the wort is showing gum witch the kids are allowed to do in her school, that resulted in her becoming very aggressive after she would ask them to spit the gum out. She has always had problems with constipation and wen we did the stool analisis it comeback that she had yeast in her gut, but she has doing ok until this last September and that's what is very confusing to me. Right now we are doing a yeast treatment with " candigest plus " but we are having a hard time with the diet she's not having any sugar, but she's on GF/CF diet so she eats carbs and refuses to eat vegetables. I'm really scared she went from almost being main steam to be by herself in a separate room with the aid for most of the school day. If anyone has any ideas or suggestions it would be greatly appreciated Thank you Natalia G Quote Link to comment Share on other sites More sharing options...
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