Guest guest Posted December 9, 2000 Report Share Posted December 9, 2000 Help... I don't know who to address this request to ...I don't know who to complain to but my messages are coming to me with only four spaces of lettering in the right hand corner. As an example: mess age. is dif fi cul t re ad. Please if anyone can direct me to assistance I'd be grateful. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 6, 2001 Report Share Posted March 6, 2001 I heard of a really great ped in Leesburg, VA and one in Shepardstown, WVA. I haven't been to either, but if you'd like their number email me. Jenn Frederick, MD > Subject: for Yahmeema - re: ped in D.C. > > Hi Yahmeema - > > I've lost your e-mail so am writing to the list (sorry everybody else). I > wanted to let you know that I met with the new pediatrician in Ballston and, > while I was impressed with some aspects of her practice (use of meds as last > resort, etc.), I don't foresee a very extensive future with her. She is > *very* pro-vax (which I got before even speaking with her... posters all over > the office) and when I told her of my position, she told me that she can > condone waiting for a while (6 months or so, she said) but if I was > absolutely not going to vaccinate him, then she wouldn't treat him. So... > the search continues > > Amber > Arlington, VA > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2004 Report Share Posted April 18, 2004 In a message dated 4/17/2004 9:52:24 PM Eastern Daylight Time, writes: From: Grace M <foxyfox8@...> Subject: Re: Taurine , That's really interesting becuase I have read several articles on epilepsy and one of the supplements they recommend to take is Taurine. I have heard of a couple of moms who wanted to give it to their children, but I don't know if they ever did or not and how it was working for them. Grace On Fri, 16 Apr 2004 16:47:24 -0000 angel_lts@... writes: > I have just ordered Taurine and just received it in the mail. I was > going to try it for my epilepsy. On the back says, specificly if you > > have epilepsy do not take. Now I am afraid to try it. I sm going to > > ship I back. Someone told me to try it and I have heard a lot of > good things about taurine to be helpful in epilepsy. > I'm curious, Does anyone take Taurine????????? > > .. .. Ladies See Dr Balch's book, Prescriptions for Nutritional Healing, Epilepsy chapter. l-Taurine is recommended. My son gets 500 mg l-Taurine plus it's cofactor three times a day. mjh http://foxhillfarm.us/FireBasil/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2004 Report Share Posted April 18, 2004 In a message dated 4/17/2004 9:52:24 PM Eastern Daylight Time, writes: From: angel_lts@... Subject: Re: Taurine Grace I also have read alot of good things about it. I am going to check it out more. Maybe another company will not say that on the back. Maybe it was just the company I ordered it from??????? .. .. Grace and Do a google search on epilepsy and l-taurine. mjh http://foxhillfarm.us/FireBasil/ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2004 Report Share Posted April 18, 2004 MJH, All I can find at the local GNC is just Taurine, I cannot find L-Taurine, is there a difference? Grace On Sun, 18 Apr 2004 08:47:59 EDT foxhillers@... writes: > In a message dated 4/17/2004 9:52:24 PM Eastern Daylight Time, > writes: > From: angel_lts@... > Subject: Re: Taurine > > Grace I also have read alot of good things about it. I am going to > check it out more. Maybe another company will not say that on the > back. Maybe it was just the company I ordered it from??????? > > . > . > Grace and > > Do a google search on epilepsy and l-taurine. > > > mjh > http://foxhillfarm.us/FireBasil/ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2004 Report Share Posted April 18, 2004 Mjh, I found it. I am still hesitate to use it. I will in time. I have heard alot of goods things about it. > In a message dated 4/17/2004 9:52:24 PM Eastern Daylight Time, > writes: > From: angel_lts@y... > Subject: Re: Taurine > > Grace I also have read alot of good things about it. I am going to > check it out more. Maybe another company will not say that on the > back. Maybe it was just the company I ordered it from??????? > > . > . > Grace and > > Do a google search on epilepsy and l-taurine. > > > mjh > http://foxhillfarm.us/FireBasil/ > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 6, 2004 Report Share Posted July 6, 2004 Hi , I've heard someone on the peg intron treatment say that they had symptoms until they drank the recommended amount of water. I don't know what that is as I've not yet started the treatment. Hope this helps. Lynn Hi, I just joined this group to hopefully get some insight and hints. My kids' Nanny has Hep C and has just started pegatron treatment. She has had 4 injections, and wow, has it been rough! Only 20 more to go though! (Hopefully! She is a genotype 2a, so she has a pretty good chance at coming through this HepC free) She is so flu-y and tired all the time, my husband and I feel pretty helpless some times, standing there, we want to help, but how? Anyway, I may just lurk and listen for a while, but if anyone has any suggestions on what makes them more comfortable (treatment or not) I would welcome them!Thanks, . Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 15, 2005 Report Share Posted August 15, 2005 Hey guys, I don't have migraines, but my hands ache incredibably? Does anyone know what that is about. actually all my joint tend to ache and my thighs throb. I feel like I need to continue to stay as active as I am, so don't let this get the best of me. I am also extremely tired and need to take a nap, but have a very difficult time getting out of be in the morning. does any of this sound familiar to anyone, or am I just going crazy?? Annette There are 2 messages in this issue. Topics in this digest: 1. questions From: " " 2. Re: questions From: AntJoan@... ________________________________________________________________________ ________________________________________________________________________ Message: 1 Date: Sun, 14 Aug 2005 02:49:26 -0000 From: " " Subject: questions Hello all: I am new to the group and also new to hyperthyroidism and am wondering how many have suffered from these symptoms? In the past couple of months I have been having migraine auras without the headache ( never had them before ), I have hot burning swollen feet, am having carpal tunnel symptoms that I didn't have before, I am lucky to sleep for an hour at a stratch and usually wake up drenched and of course I can't handle the heat at all. I am seeing a specialist in September and am hoping that it can be managed. My ultrasound showed the gland to be enlarged and has nodules so who knows what my treatment will be. Anyway I guess my main reason for joining rthis group and writing this post is to see if anyone else has suffered any of my symptoms? Thanks in advance to all who give me some input/ ( Canada ) ________________________________________________________________________ ________________________________________________________________________ Message: 2 Date: Sun, 14 Aug 2005 08:24:39 EDT From: AntJoan@... Subject: Re: questions In a message dated 8/13/2005 10:49:48 PM Eastern Daylight Time, N.HOWE@... writes: In the past couple of months I have been having migraine auras without the headache Dear , I also get migraine auras w/out headaches. However, I got them both before, and after, my Graves Disease. I've often wondered about them, and how common they are. I've also never found out exactly what causes this. I hope you feel better soon. I'm sure there are lots of folks on this list suffering from the other symptoms you described, who can offer help and suggestions. Take care, AntJoan Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 30, 2005 Report Share Posted August 30, 2005 Annette, that sounds much like me when I need to reduce my anti- thyroid meds. I get achy all over, especially in colder environments, and I feel SUPER groggy in the mornings and sluggish/tired/sleepy throughout the day. It's pretty much as though I have hypo- which I technically do when I am taking too much medication. > > Hey guys, > > I don't have migraines, but my hands ache incredibably? Does anyone know what that is about. actually all my joint tend to ache and my thighs throb. I feel like I need to continue to stay as active as I am, so don't let this get the best of me. I am also extremely tired and need to take a nap, but have a very difficult time getting out of be in the morning. does any of this sound familiar to anyone, or am I just going crazy?? > > > Annette > > > > > There are 2 messages in this issue. > > Topics in this digest: > > 1. questions > From: " " > 2. Re: questions > From: AntJoan@a... > > > _____________________________________________________________________ ___ > _____________________________________________________________________ ___ > > Message: 1 > Date: Sun, 14 Aug 2005 02:49:26 -0000 > From: " " > Subject: questions > > Hello all: > > I am new to the group and also new to hyperthyroidism and am wondering > how many have suffered from these symptoms? In the past couple of > months I have been having migraine auras without the headache ( never > had them before ), I have hot burning swollen feet, am having carpal > tunnel symptoms that I didn't have before, I am lucky to sleep for an > hour at a stratch and usually wake up drenched and of course I can't > handle the heat at all. I am seeing a specialist in September and am > hoping that it can be managed. My ultrasound showed the gland to be > enlarged and has nodules so who knows what my treatment will be. Anyway > I guess my main reason for joining rthis group and writing this post is > to see if anyone else has suffered any of my symptoms? > Thanks in advance to all who give me some input/ > > ( Canada ) > > > > > _____________________________________________________________________ ___ > _____________________________________________________________________ ___ > > Message: 2 > Date: Sun, 14 Aug 2005 08:24:39 EDT > From: AntJoan@a... > Subject: Re: questions > > In a message dated 8/13/2005 10:49:48 PM Eastern Daylight Time, > N.HOWE@S... writes: > In the past couple of > months I have been having migraine auras without the headache > > Dear , > > I also get migraine auras w/out headaches. However, I got them both before, > and after, my Graves Disease. I've often wondered about them, and how common > they are. I've also never found out exactly what causes this. > > I hope you feel better soon. I'm sure there are lots of folks on this list > suffering from the other symptoms you described, who can offer help and > suggestions. > > Take care, > AntJoan > > > Quote Link to comment Share on other sites More sharing options...
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