Guest guest Posted February 29, 2000 Report Share Posted February 29, 2000 In a message dated 2/29/00 3:06:43 AM US Eastern Standard Time, onelist writes: << Can anyone provide me with ideas for other ways to fall asleep and > stay asleep? > > Thanks, > Bekah >> Dear Bekah, I was taking trazadone 50 mg. 2 tabs at bedtime for about a year; along with .25 xanax. The trazadone stuffs up your nose, so I would take a decongestant. In the last month I am only taking one trazadone and .25 xanax. NO stuffy nose with just one! I hope this helps. The trazadone must be pretty safe, my son's Dr. is going to put all three of them on it. Actually I have already started my boys on .50 mg and it really works for them. I gave them mine, and their Dr. knows. But she wanted to check with other Drs. before she wrote a prescription for them. They weren't sleeping at all! It also stop all nightmares. They really like the trazadone. They have been kidding me and saying I am addicted Mom. This drug is not addictive. Good Luck! In God's love & mine, ) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 29, 2000 Report Share Posted February 29, 2000 In a message dated 2/29/00 3:06:43 AM US Eastern Standard Time, onelist writes: << Antibiotic uptake and immune responses may be inhibited by > some drugs, and antidepressants (sertaline [Zoloft], > fluoxetine [Prozac], amitriptyline [Elavil], maprotiline > [Ludiomil], desipramine [Norpramin], clomipramine > [Anafranil], nortriptyline [Pamelor], bupropion > [Wellbutrin]), muscle relaxants (cyclobenzaprine > [Flexeril]), opiate agonists, anticonvulsives or certain > analgesics (oxycodone [Percodan], carbamazepine [Tegretol], > acetaminophen/hydrocodone [Vicodin]), narcotics (codeine > w/Penergan, propoxyphene [Darvon], morphine), antacids, > antidiarrheas among others should not be taken, if possible, > or gradually decreased during therapy. Some drugs (certain > antibiotics, antidepressants, analgesics, narcotics, etc.) > may inhibit immune responses and interfere with therapy. > from: > CONSIDERATIONS WHEN UNDERGOING > TREATMENT FOR GULF WAR ILLNESS/CHRONIC > FATIGUE SYNDROME, FIBROMYALGIA > SYNDROME, RHEUMATOID ARTHRITIS AND > OTHER AUTOIMMUNE ILLNESSES > > by Prof. Garth L. Nicolson > > The Institute for Molecular Medicine, 15162 Triton Lane, > Huntington Beach, California 92649-1041 > > Tel: (714) 903-2900 Fax: (714) 379-2082 E-mail: > gnicimm@... Website: www.immed.org > >>I feel this Dr. is way off. My children aren't taking any med's like the above. And they are getting sicker. I finally ask the Dr. today if we could get something stronger. She said we would try a few Tylenol 3's just to help the body rest. When you go to the E.R. with severe pain it can raise your blood pressure. The first thing they do is give you shots of pain killers to help the body relax and allow the blood pressure to drop. Maybe some CFIDers can get away without taking some of these med's, but some of us can't. He can't take away our med's unless he has a cure. And he can't have a cure until he knows what the case is. We all have so many symptoms that are alike, but at the same time we also have many symptoms that are different. I will not be his guinea pig. Every drug he has named are the ones we take, so we can function to some degree. Come up with a cure Dr! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 17, 2001 Report Share Posted March 17, 2001 What does yeast in stools look like? Thanks. Darrell ===== Carpe Noctem! (Seize the Night!) __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 18, 2001 Report Share Posted March 18, 2001 On 17 Mar 2001, at 18:58, darrellblackandblue wrote: > What does yeast in stools look like? Thanks. Darrell I've never had it myself, but people describe it as a whitish coating, either fluffy-looking or oily. Ann ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ http://www.willow-web.net Quality Web Design ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 18, 2001 Report Share Posted March 18, 2001 The Ducolax tablets are very small, just a strong laxative. Can really cramp you up. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 18, 2001 Report Share Posted March 18, 2001 I have the professional model C-1 Hydro-San Plus colon therapy equipment. I took the training, and have given colonics to a few friends and my wife. Do a good through cleaning once a week, plus using some fiber supplements to keep things open and moving. Subscription email: mailto:bowel cleanse-subscribeegroups Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 29, 2002 Report Share Posted May 29, 2002 Hi G, What a heart-warming story about Tanner!! It always amazes me when I read these success stories! I have to say, from a moms opinion as I have 3 beautiful children who are all a gift and each have many gifts and talents, that the little things some parents take for granted (without realizing it of course) we find simply miraculous!! It gives me great hope for my children who are Apraxic, that they are destined for great things. I pray for them daily and for all of us for strength and wisdom!! H mom to 3 great kids! 15 (driving) Micheal 14 Apraxia (almost driving)non-progressive muscle weakness, 9 Apraxia VERY independent!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2002 Report Share Posted August 1, 2002 Hello Carol, Since my husband has lost sooooo much weight, I been trying to cook extra rich just to keep a few lbs. on his bones. (Even with taking the pred. he will not gain any weight.) Well, he does not gain a pound, I do all of that for him. Gained 40lbs in 18 months. Now I got to loose it because my health is in serious danger. ( I got AOD) I am feeling sluggish and tired all the time, on top of getting depressed and have killer migraines. for some time now I been looking for an address for this weightloss thing, and I finally found it. My friend in Pa used it a few years ago and had terrific results, and I finally got the address. Got it just today and will send it off tomorrow. It is a food program where the combination of the foods you eat will make you loose body fat. To order, just send your name and address, a 30 day postdated check for $9.95 to Janet McBarron, M.D., c/o Green Tree Press, Inc., Dept 555, 3603 West 12th Street, Erie, Pa., 16505 They will send your check back if you do not start loosing weight within a couple of weeks. That's why they ask to postdate your check for 30 days, and even if you are not happy with the program 6 months down the road, they still send you a full refund. This program has been around for a while now, and like I said, my friend in Pa lost a lot of weight in the first 6 months of using it. I think it was something like 80 pounds. Maybe that will help, and the best part of it is that there are no extra chemicals to take, just good wholesome food. I hope I could be of some help. Jenaka Message: 6 Date: Thu, 1 Aug 2002 11:16:21 EDT From: worcspubl@... Subject: new still's problems Hi Loop, I have been very fortunate. I know that. I had been feeling really good for the most part and it lasted pretty long. But all good things seem to pass, don't they. I got my MRI and nerve test back and apparently the neurologist said my back is a mess. I had back problems occasionally in my 20's and 30's when I was into running and not stretching properly. But lately my back hasn't hurt at all. Just having numbness in my toes and feet. Well, according to the tests, I have two smashed discs and one's sitting directly on my psyiatica (spelling?). He sounded like it could be from the stills. But he didn't really know much about stills, so who knows. My husband who is a firm believer in chiropractors asked about their services and the Doc said that could paralzye me, so I guess I won't be going that route. Well, I'm supposed to go see a neuro-surgeon now. I really don't want surgery. He said I need to lose 30 pounds by the next time I see him (3 months). (I've been in OA, unsuccessfully). For some reason, in the back of my mind, I just don't feel like I'd make it thru surgery. Just a hunch but I've been kind of psychic at various times in my life, so I have to take hunches seriously. So, then I call my rhuemy because the nerve test seemed to kick off fevers. Well, she's very concerned as I had a " cold " last month that I never seemed to get rid of and now I have the same type of cough I had when I first got sick. So she wants me to get more blood tests (even though I see her on 8/9) and a chest xray and worst of all - increase my pred from 1/2mg every other day to 10mg per day!!!!! Boy, I have become a beligerent patient in my old age - <grin> I really didn't plan on increasing my pred. But when I told my hubby, he insisted. My hubby is from the school, " better living thru chemistry! " and always thinks drugs are the answer. So this morning I took 10mgs of pred. But I was kicking and fighting. You know it's funny. People will sometimes tell you that when you want to do something you shouldn't be doing or don't want to be doing something you should, remember it's important to follow the instructions of someone who knows better than you. They always use the example, " if you were a diabetic, you'd take the required insulin, wouldn't you? " Well, my problem is that I really fight about taking the advice of anyone!!!!! And I probably wouldn't take the insulin! But I'm taking the pred now, so there <pouting like a three year old>. Anyway, I was really mad yesterday and now I need to lose 30 pounds while being on a higher dose of pred. Just my luck. But I can't continue to take cough med with codeine and try to work and drive like that. Not a good idea. So I guess I'll do what I'm told - for a change. Anyone else in there feel like a defiant brat today. Boy I sure do. Thank goodness I at least trust this doctor a lot. Hope you all are doing very well. Love Carole Humankind has not woven the web of life. We are but one thread within it. Whatever we do to the web, we do to ourselves. All things are bound together. All things connect. ... Chief Seattle Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 11, 2002 Report Share Posted September 11, 2002 I am also happy to help with any registration problems nne Digest Number 720 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 13, 2003 Report Share Posted November 13, 2003 Evel, Try to ask the surgeon how many operations he has done. It helps to know how many operations at a hospital but you will want to know who the surgeons are and how many operations they have done. One surgeon could do only ten implants while the other do much more. You never know. Where I got implanted, at least two surgeons do 100 to 125 operations a year. I didn't know this at the time I asked my surgeon how many he did prior to my surgery. He did over 800 operations with a very low complication rate. Yes, I asked about that too! Have a great anticipation period! ===== Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2004 Report Share Posted June 2, 2004 , Ferguson's pictures are self-portraits. I do not know how anyone could consider them exploitative. Are you aware of the controversy surrounding scoliosis screening? I commend you for the community work you are doing. Re: Digest Number 720 In a message dated 5/31/2004 10:21:18 AM Eastern Daylight Time, Ka1kpm writes: > I can understand the negative reactions, as they arise from > our legacies of > negative body image and shame. Let me go on the redord here. I've never been ashamed of my body. All my life I've been very confident. I was approached once to be in a photo shoot for some ad about the Navy Family shortly after the birth of #2. Not only did I say no...I said HE** NO! Some might even think I'm conceited, but that's their problem not mine. I know who I am. I just don't believe in using the scoliosis body for financial gain. Unless all proceeds go to benefit scoliosis research. If that were the case I'd hope there would be opportunity for more scoliosis voices to be heard. But that's just me. There are other ways to get scoliosis noticed. I visit schools in my local area and I speak about scoliosis. Thus far I've met 7 young girls who have the disease. One may be a surgical candidate. On June 15th I am visiting a private school to speak about it yet again. It seems everybody knows somebody who has scoliosis. I am also looking at national exposure and am being real cautious. I don't want this disease to be presented in such a way where people think we're a bunch of freaks. But then again, you cannot control what people think or say. I could go on and on expressing my passionate beliefs about how things should or should not be done. But it's just my opinion. My hope is that all of you will make just one telephone call to your local high school or junior high school. Tell them you are an adult with scoliosis who struggled with the disease as a young school person and ask if their school nurse does screening for scoliosis. If the answer is no...tell them they should. You'd be surprised just how many schools have stopped screening for scoliosis. I wish the artist well. But if I ever meet somebody on the street who wants me to hunch over so they can take a pix of my back because they saw an exhibit one time I'm gonna punch 'em. LOL Juuuuust kidding. xoxo's Support for scoliosis-surgery veterans with Harrington Rod Malalignment Syndrome. Not medical advice. Group does not control ads or endorse any advertised products. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2004 Report Share Posted June 2, 2004 Sherry, You make some excellent points. Thank you for your thoughtful post. Re Upcoming Event I really love Ferguson's art. Last year I purchased the Crouching Figure and kindly granted me permission to incorporate the image into a poster presentation I did for an audience of nurses. It was well received, and I actually was asked to present it a second time for a different audience. I can understand the negative reactions, as they arise from our legacies of negative body image and shame. We are all at different points in our lives with this. However, I feel strongly about the worth of the art for a wide range of viewers, and see 's work as bigger than any one of us. I am personally horrified at the messages reality-based TV is sending to young people with shows like The Swan. Art such as 's is a powerful way to counter a very narrow definition of normacy. I could really get on a soapbox about this. I have strong feelings about the value of difference. My own comfort with my body image lags a little behind my more abstract ideals here, but I am always looking to expand my horizons. I would go to the exhibit in a heartbeat. Unfortunately, won't get to DC in June but may have an opportunity in July. Sherry Kahn Support for scoliosis-surgery veterans with Harrington Rod Malalignment Syndrome. Not medical advice. Group does not control ads or endorse any advertised products. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2004 Report Share Posted June 2, 2004 What is the controversy surrounding scoli screening? I am in charge of the commmittee at school next year and would love a heads up. I've never heard that it was controversial here in Alabama, although pretty much everything else is!! > > From: " poetryperson " <poetryperson@...> > Date: 2004/06/02 Wed AM 02:10:55 EDT > < > > Subject: Re: Digest Number 720 > > , > > Ferguson's pictures are self-portraits. I do not know how anyone could consider them exploitative. > > Are you aware of the controversy surrounding scoliosis screening? > > I commend you for the community work you are doing. > > > Re: Digest Number 720 > > > In a message dated 5/31/2004 10:21:18 AM Eastern Daylight Time, Ka1kpm writes: > > > I can understand the negative reactions, as they arise from > > our legacies of > > negative body image and shame. > > Let me go on the redord here. I've never been ashamed of my body. All my life I've been very confident. I was approached once to be in a photo shoot for some ad about the Navy Family shortly after the birth of #2. Not only did I say no...I said HE** NO! > Some might even think I'm conceited, but that's their problem not mine. I know who I am. > > I just don't believe in using the scoliosis body for financial gain. Unless all proceeds go to benefit scoliosis research. If that were the case I'd hope there would be opportunity for more scoliosis voices to be heard. But that's just me. > There are other ways to get scoliosis noticed. I visit schools in my local area and I speak about scoliosis. Thus far I've met 7 young girls who have the disease. One may be a surgical candidate. On June 15th I am visiting a private school to speak about it yet again. It seems everybody knows somebody who has scoliosis. > I am also looking at national exposure and am being real cautious. I don't want this disease to be presented in such a way where people think we're a bunch of freaks. But then again, you cannot control what people think or say. > I could go on and on expressing my passionate beliefs about how things should or should not be done. But it's just my opinion. > My hope is that all of you will make just one telephone call to your local high school or junior high school. Tell them you are an adult with scoliosis who struggled with the disease as a young school person and ask if their school nurse does screening for scoliosis. If the answer is no...tell them they should. You'd be surprised just how many schools have stopped screening for scoliosis. > > I wish the artist well. But if I ever meet somebody on the street who wants me to hunch over so they can take a pix of my back because they saw an exhibit one time I'm gonna punch 'em. LOL Juuuuust kidding. > > xoxo's > > > > > Support for scoliosis-surgery veterans with Harrington Rod Malalignment Syndrome. Not medical advice. Group does not control ads or endorse any advertised products. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2004 Report Share Posted June 2, 2004 I'm just going to put the topic of Ms. Ferguson's choice of artwork to rest on my part. I voiced my opinion and certainly understand communications get 'messed up' when one reads words as opposed to hears them. Text interpretation lacks the luxury of immediate questioning of intent. A reader may go hours believing an individual posted harsh words when in fact intention was otherwise on the part of the writer. I openly stated my opinion because I believe artists love compliments, controversy, and all other points of view regarding their works. Artists are passionate individuals whom I do hold a great deal of respect for. I'm certain there are different controversial issues regarding school screenings in different areas. I've certainly encountered different schools of thought on topic as we've journeyed up and down this east coast as a military family. Having said that, I attempt at making it all too clear in the belief a school nurse merely opens the door with a positive screening. Some school nurses recognize girls go through puberty at an even younger age nowadays and encourage contacting the board of education to screen in elementary schools. Somebody questioned whether scoliosis was a disease. The team of 12 army doctors who performed my original surgery when I was 11 years of age explained scoliosis is a bone deformation. Further concurring such a deformity is often times referred to as a disease. I've also met many more docs over the years refer to it that way. Personally, I prefer it to be titled a disease as opposed to a deformity. But then again, that's just my opinion, my viewpoint, and the way I like it. Diane, I'm sorry you're leaving. This is a support group and a darn good one. We all go through ups and downs as we approach the next doctor visit, the next MRI, and/or the revision surgery. I don't see this group as being that much different than my quilt guild. Different people...different likes and dislikes. This group is strong in knowledge. Eleanor Roosevelt is famous for this quote; " Nobody can make you feel a certain way without your permission. " I'm hoping this isn't a good bye. I hope it's just a little break. When one or more people agree or disagree on a topic, I don't view it as 'ganging up' or an 'implied club.' I view it as discussion. Let's face it, if we cannot share our thoughts, then what's the point of this forum? Diane, I voiced my concerns about my visit with Dr. Rand, went through a roller coaster of emotions, finally leading my mind to a nice peaceful calm as to my next step. Somehow back then you felt a need to clarify you weren't " in the club " of bashing Dr. Rand. I then explained I didn't lump you in to anything because it was my own experience not anybody else's. The same goes with my thoughts on how the scoliosis body should or should not be displayed. I have further found out Dr. Rand has missed my 6 degree progression of my curve. Getting second even third opinions is something I learned from this group. So to everybody I reiterate advice given me from members of this group...get multiple opinions. I saw Rand who made no mention of my curvature progression. I saw doctor #2 who did mention it. I then saw doctor #3 who saw the progression as well. Do I think Rand is a bad doctor...no I do not. I believe him to be a skilled surgeon. xoxo's Quote Link to comment Share on other sites More sharing options...
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