Guest guest Posted March 15, 2001 Report Share Posted March 15, 2001 , ever look into mercury toxicity? > My overriding symptom is a feeling of toxicity and having a > bad " buzz " . It starts when I wake up in the morning and basically > lasts all day. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 9, 2003 Report Share Posted April 9, 2003 >>>no changes and then we turned to Enzym Complete with PPDIV. > I think this is better for him, he seems happier, more " present " but when I try to reach the serving dose of 2 caps my son is more hyper screaming, and I have to return to one cap. It is common for people with phenol sensitivities to react poorly to the Complete maybe because of all the fruity enzymes it contains. If your son doesn't get better in a week or so, consider a different product without so much papain, bromelain, or actinidin (kiwi). The kiwi enzymes are a really big problem for some. Does he have any problem with fruits in general? . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 16, 2004 Report Share Posted February 16, 2004 , I live in NC, also and have heard the same thing. It's not true. That was the last lie that they told me. They will bully you and give you a lot of inaccurate information to talk you into vaccinating your children. If I can be of any help email me. in Wilmington, NC > I live in NC and I was told that all children that are in daycare have to be up to date on their shots. Which is not a problem for us since I am a SAHM. Here comes the but. But I was also told that all school age children have to have all their vaccinations before entering school. Is this true? > > May God bless you and yours. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2008 Report Share Posted March 4, 2008 Hi , I have the same thing happen to me. I'm always telling my family that my hands just don't work like they used to. I still haven't been diagnosed but during testing a Rehumatolgist sent me to a hand specialist. They did testing and my hand strength is 20% of a normal woman my age (49). I will start trying to document when this happens and what my other symptoms are before during and after and see if I come up with anything. Joni Jordan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 4, 2008 Report Share Posted March 4, 2008 Hi , I have the same thing happen to me. I'm always telling my family that my hands just don't work like they used to. I still haven't been diagnosed but during testing a Rehumatolgist sent me to a hand specialist. They did testing and my hand strength is 20% of a normal woman my age (49). I will start trying to document when this happens and what my other symptoms are before during and after and see if I come up with anything. Joni Jordan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 9, 2010 Report Share Posted September 9, 2010 Hi..sorry bout the confusion. No problems with this group on groups...the one I was mentioning is a forum on the web related to scoliosis: http://www.scoliosis.org/forum/index.php It's the National Scoliosis Foundation Forum...I was just wondering if anyone else was on it or if they had problems getting on it. There were several references to restrictive lung disease and scoliosis and was wanting to sorta ask questions of those that had posted on that forum. I had sent e-mails to whoever runs the forum to find out why the final step wasn't allowing me to post....I sign into it and it lets me read but says I can't reply or post new threads. Thanks for responding.. > > I allowed this through to see if there was any hang ups and there doesn't appear to be. So welcome to the group. > > > > BTW I never got any emails. Quote Link to comment Share on other sites More sharing options...
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