Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 hi lesley, sorry to hear of your poor baby's reaction--i pray there will be no more " side effects " that show up later on. it's unfortunate, but most parents are unaware of the risks associated with vax until they experience them & then it may be too late for their little one. congratulations on your upcoming birth and i don't mean to pressure you, but, you need to get going asap, preparing yourself and making decisions for this baby's birth--DO NOT just hope that you will find another understanding dr.--the one you found was a rarity--believe me!!!! you need to make a serious commitment (your husband too) about what you will and will not allow to be done to your child when it is born. do not think that you can just casually mention to your delivering ob and nurse, that you don't want anything " done " to your newborn--because they'll do it all anyway. you need to be extremely specific and asserative in your stance. i don't know what state you're in, or if they will attempt the hep b vax at birth, but call hospital and inquire now(or talk to your ob--don't think this one talk will suiffice for a final decision either--you'll need to up on EVERYTHEING that is done to the baby as soon as it comes out). anyway, i'm just trying to get you to prepare yourself before it is too late--ask here on this list for advice, direction etc, they are lots of knowledgeable/experienced people here who will help you. good luck and again, welcome!!! brigit Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 Hi and welcome! Just a side note first of all........I didn't even notice you wrote midol instead of motrin until you corrected yourself! I guess with us women, those things can easily get interchanged! LOL Anyway.......I first want to say that I think it's awesome how the emergency room doctor handled your situation! That is awesome! I think you should write him a thank you or something! I wish I could find a doctor that would respect me as an ADULT PARENT!!!! As for your second child, I wanted to suggest to you something........talk with your OB about writing up a birth plan and what you want or don't want. I'd probably make a big deal to them about what happened to your daughter..........they don't need to know all the details........just tell them that your daughter had a reaction to her vaccines that was proven by your doctor, and therefore you and your husband have decided to delay your newborn's vaccinations awhile. Therefore, you DO NOT want them done at birth. They don't have to know that you aren't planning to have them done at all......just tell them you're going to delay them, due to the reaction your first child had! The least amount you tell them, the better. Plus, write up a birth plan that would tell your desires and wishes. You sign it, your husband signs it, and your doctor signs it. The only way they can go against that is if there is an emergency! Friends of mine did this and were glad they did! Another thing I would suggest is....do not let that baby out of your sight while you are in the hospital. This isn't to scare you and you don't need to be paranoid; however, I would suggest that whereever that baby goes......your husband goes. The baby should be able to stay in your room the whole time if you want (atleast that's how it is here in Iowa). The only reason our son was taken out of the room was for a bath and picture, and there's no reason your husband shouldn't be able to go with the child! I pray you have a safe and uncomplicated delivery and are able to enjoy the birth of your newest little one! Debi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 Once in there I saw first the triage nurse who gave her some midol, Duh I meant Motrin not midol...lol ===== Lesley Married to my high school sweetheart: Todd 4/18/98 Mommie 2: Kaylie 2/23/99 Audrina Marie due to arrive 7/14/00 __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 --- beebemcel@... wrote: i don't know what state you're in, > or if they will attempt > the hep b vax at birth, Hi Brigit- We live in PA where when my dd was born they told me AFTERWARDS that she had the hep b shot. Never once did they ask me or my dh for permission, they just gave it to her, so I guess you're right I need to take charge now and straighten out everyone before my baby is born. Thanks ===== Lesley Married to my high school sweetheart: Todd 4/18/98 Mommie 2: Kaylie 2/23/99 Audrina Marie due to arrive 7/14/00 __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 In a message dated 6/12/00 6:21:39 AM Pacific Daylight Time, clewell821@... writes: << doesn't administer any shots without my knowledge. Any ideas on how to handle this? >> Lesley - Hi, and welcome to the group!! I'm glad everything worked out well with your daughter. As far as your upcoming birth, you have the right to deny the Hep B shot, the eye salve and the Vitamin K shot if you so chose. My best advice is include it in your birth plan with your ob/gyn ASAP. Also, as soon as you arrive at the hospital (or before...whenever you fill out the paperwork for your hospital) inform them of your wishes, especially pertaining to the Hep B shot. MAKE SURE that they give you something to sign saying that you do not want the shot. If you don't sign anything, chances are good that they may still do it and say 'we forgot'. (They could still do it with a signature, but you have a better chance.) The best thing we did was that my husband was in charge of making sure our wishes were followed so I could focus on delivery. And the second thing...unless an emergency occurs, do not let your baby out of your sight. Most hospitals do rooming in now, so that she can stay with you at all times. When they take her to the nursery for weighing, have your husband go with you. Always being there is the only way to make sure that they don't do anything outside of your wishes. Good luck, and congratulations on your upcoming arrival!! Teri and (6/4/99) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 >I am currently expecting another baby in July. I can >only pray the hospital I go to has a doctor as >understanding as this one was and doesn't administer >any shots without my knowledge. Any ideas on how to >handle this? Thanks for any advice in advance and for >listening. Hi Lesley, If it were me I'd do everything I could to get those toxins out of her body. I don't want to scare you, but your daughter may not be out of the woods yet. If you knew how many times your same story has happened...... Homeopathy works well with that, often. If it were me I'd see a quality classical homeopath right away. If you are interested, email me as to where you live. See article I wrote on how homeopathy works http://www.nccn.net/~wwithin/homeo.htm 2nd - PLEASE fill out a VAERS form - Vaccine reaction form. Your doctor by law should fill one out but it doesn't sound like he would, so you should. This is the only way we can track what goes on and get something done about it and also you are covered for the future. Call National Vaccine Information Center 1-800-909-shot for details. 3rd - Glad you are on the list. Now is when you need to research everything you can so you know that you don't want anymore vaccines - know the risks of the diseases and the risks of the vaccines. I personally don't think any vaccines are necessary, but you need to come to this conclusion yourself. 4th Know your states exemptions from vaccines. Sheri -------------------------------------------------------- Sheri Nakken, R.N., MA wwithin@... Well Within's Earth Mysteries & Sacred Site Tours http://www.nccn.net/~wwithin Bookstore - http://www.nccn.net/~wwithin/bookstor.htm International Tours, Homestudy Courses, ANTHRAX & OTHER Vaccine Dangers Education, Homeopathic Education KVMR Broadcaster/Programmer/Investigative Reporter, Nevada City CA CEU's for nurses, Books & Multi-Pure Water Filters Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 sign papers saying you don't want them. have someone totally separate from your family with you who will be designated to stay with the baby and make sure nothing is done that you don't want done until you are ready to be with it and take over. my dil is due 7/17. once the baby is born it is mine to watch over. we also have someone else to be there. that way my son can watch over the other children and his wife and neither one has to be concerned about what is being done to the newborn. Hello I'm new >Hi everyone. I'm new here. Alison recommened this list >to me and I'm glad > >I guess I should begin by saying " it happened to me " . >I was always one of those parents who just accepted >whatever the doctor told me, did whatever they said, >got my daughter whatever shots she needed, never said >a word. After this past round of vaccines I see things >very differently. > >Alison posted a messages that I put on our Feb 99 list >so you may know a little of my story already. I have a >beautiful 15 month daughter named Kaylie . Up >till now Kaylie has always received vaccines and never >had a problem with them. On June 1st she went for her >15 month appointment and was given the HIB, dpt, >polio, and MMR. She's had them all before except the >MMR. The next day I did not recognize my own daughter. > >She was hysterical, screaming, crying, falling over, >inconsolable. She wasn't running a fever, but she was >miserable. I called her pediatrician who tried to tell >me it more of the stress of moving into a new place >than a reaction to the shot. We'd been living here a >week already....funny how she was perfectly fine till >she got the shot. The next day wasn't much better but >by Monday she seemed fully recovered and was herself >again. > >Saturday night while getting her ready for bed, I >noticed she was very hot. Upon taking her temperature >it was 100.4. Not real high and I thought well it >could be due to teething. I gave her some tylenol and >didn't think much more about it. Since the incident >the following week, we've been co-sleeping and I woke >during the night to feel her burning up agaisnt me. I >took her temp again and it was 102. Sunday morning I >again called the ped who once again strongly denied >that it could be from the shot, and went through this >list a mile long asking question after question trying >to find another answer. I got nowhere and hung up >extremly frustrated. > >By mid-afternoon her temperature soared to 104 >rectally. I took her to the ER. Once in there I saw >first the triage nurse who gave her some midol, and >sent me into another waiting room. A nurse checked her >in there. Both the triage nurse and nurse in the ER >didn't believe this came from the shot, again dashing >around it. By the time she was FIANLLY seen by the ER >doctor my poor baby was a mess. She was screaming >uncontrollably(having being forced to wait 2 hours to >be seen) and she just didn't want to be there another >second. I again went throught the speech about the mmr >shot figuring I was probably wasting my time since no >one seemed to want to hear it. The ER doctor asked >when she had the shot, and for the first time someone >AGREED with me!!!! I was so happy I could've kissed >the doctor..lol. He gave me a bunch of information >that pointed to a reaction and said this was the time >she would get the fever. Her recommened a different >pediatricain for me, and also told me to purchase the >book " A shot in the Dark " . He said lots of people are >in denial of these things becasue no one wants to >ADMIT it!!! I was soooooooooooooo mad, I thought about >suing the ped!! All I can say is Kaylie will NEVER get >another vaccination!!!! > >After examining her with a complete physical he >determined nothing was wrong other than the fever. He >said I should watch for a rash, or other symptoms, but >that the worst was over. Of course he also told me >there could be long-term things that I might not know >about for a while, but for now everything looks >normal. SO all I can do is pray she'll be ok. This >was the scariest thing that ever happened to me, you >never know what's going to happen. So no more for >her!!! > >I am currently expecting another baby in July. I can >only pray the hospital I go to has a doctor as >understanding as this one was and doesn't administer >any shots without my knowledge. Any ideas on how to >handle this? Thanks for any advice in advance and for >listening. > > > >===== >Lesley >Married to my high school sweetheart: >Todd 4/18/98 >Mommie 2: >Kaylie 2/23/99 >Audrina Marie due to arrive 7/14/00 > >__________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 Lesley, Welcome to the list and congrats on the impending birth.I hope that Kaylie will be okay.I agree with Brigit in that you need to get moving on those newborn procedures.Best advice is NEVER EVER let your newborn out of your sight.Insist that she stay in the room with you.Everything like NB checks can(and should ) be done at bedside with both parents present.Mother provides better warmth than those bun burners.I know how hospitals can be,but it is your right and obligation to do what you feel is appropriate for your child.If you opt for the vitK injection check the bottle before they draw out the dose(it is a bottle no?).Never know if it could be a hepB vaccine instead! Wishing you a wonderful birth.And I am sure others would agree that a homeopath would be a good idea for Kaylie. Welcome! I am a feb 99 mum too! Sara-mom to Nimet born at home UC 2-9-99 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 Also you may want to give your daughter Vitamin A. In Africa they give it along with MMR. Why not here? Here is research by Megson, MD at Autism/MMR conference. Its a little complicated but you'll get the drift...She is treating children with vaccine damage from MMR with Vitamin A - she has found their vitamin A stores to be depleted totally by the vaccine.. Sheri If you would like the full article, email me. Excerpts.... April 6, 2000 Mr. Chairman, Honorable Dan Burton and members of the committee; My name is Norfleet Megson. I am a board-certified pediatrician, Fellowship trained in Child Development, a member of the American Academy of Pediatrics and Assistant Professor of Pediatrics at Medical College of Virginia. I have practiced pediatrics for twenty-two years, the last fifteen years seeing only children with Developmental Disabilities, which include learning disabilities, attention deficit hyperactivity disorder, cerebral palsy, mental retardation and autism. Excerpted.... I am using natural lipid soluble concentrated cis form of Vitamin A in cod liver oil to bypass blocked G protein pathways and turn on these central retinoid receptors. In a few days, most of these children regain eye contact and some say their “box” of clear vision grows. After two months on Vitamin A treatment some of these children, when given a single dose of bethanechol to stimulate pathways in the parasympathetic system in the gut, focus, laugh, concentrate, show a sense of humor, and talk after 30 minutes as if reconnected.20 This improves cognition, but they are still physically ill. When these children get the MMR vaccine, their Vitamin A stores are depleted; they can not compensate for blocked pathways. Lack of Vitamin A which has been called “the anti-infective agent,” leaves them immuno-suppressed. They lack cell-mediated immunity. T cell activation, important for long term immune memory, requires 14-hydroxy retro-retinol. On cod liver oil, the only natural source of this natural substance, the children get well. The parasympathetic nervous system is blocked by the second G protein defect. These children are unable to relax, focus and digest their food. Instead, they are in sympathetic overdrive with a constant outpouring of adrenaline and stress hormones. They are anxious, pace, have dilated pupils, high blood pressure and heart rate. These and other symptoms of attention deficit hyperactivity disorder are part of this constant “fright or flight” response. These symptoms improve on bethanechol. excerpted... Megson, MD -------------------------------------------------------- Sheri Nakken, R.N., MA wwithin@... Well Within's Earth Mysteries & Sacred Site Tours http://www.nccn.net/~wwithin Bookstore - http://www.nccn.net/~wwithin/bookstor.htm International Tours, Homestudy Courses, ANTHRAX & OTHER Vaccine Dangers Education, Homeopathic Education KVMR Broadcaster/Programmer/Investigative Reporter, Nevada City CA CEU's for nurses, Books & Multi-Pure Water Filters Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 Just a side note. I had mentioned awhile ago about how we were concerned that our daughter might be colorblind. I attended the 4/6/00 hearing and spoke with Dr. Megson afterward and asked her if it were a possibility. I figured if a vaccine such as MMR could rob the body or deplete the body of certain vitamins, including vit. A that maybe Hep B could do the same thing. She said it was a possibility and that she had heard of such things. I asked her if the cod liver oil could help and she thought it could possibly and at worst it would not hurt. So I ordered the brand that she uses by Kirkman Laboratories which makes one that is certified to be mercury free. (This is a big issue if you have seen the recent posts about fish, specifically tuna, due to dangerous levels of mercury.) I keep it in a refrigerator to keep it fresher. After an initial challenge, my daughter bit into one of the capsules:(, our daughter started taking the cod liver capsules. In less than 2 months (about 6 weeks) we have seen a difference in her response to colors. She very clearly is still having some challenge with certain shades of blue but it appears that she is being able to 'see' the other colors. She is responding when we ask her to bring specific items by color. This has been a blessing. We are continuing to give the cod liver oil in the hopes that any damage can hopefully be corrected. Of course, proving that a correction took place would be difficult since she was never diagnosed as color blind. It was based strictly on what we have witnessed. At the same time, I am unwilling to wait 2 more years for a diagnosis and take the chance that any damage can not be helped. Thought you all might find this interesting. Sheri Nakken wrote: > > Also you may want to give your daughter Vitamin A. In Africa they give it > along with MMR. Why not here? > > Here is research by Megson, MD at Autism/MMR conference. Its a little > complicated but you'll get the drift...She is treating children with > vaccine damage from MMR with Vitamin A - she has found their vitamin A > stores to be depleted totally by the vaccine.. > Sheri > > If you would like the full article, email me. > > Excerpts.... > > April 6, 2000 > > Mr. Chairman, Honorable Dan Burton and members of the committee; > > My name is Norfleet Megson. I am a board-certified pediatrician, > Fellowship trained in Child Development, a member of the American Academy > of Pediatrics and Assistant Professor of Pediatrics at Medical College of > Virginia. I have practiced pediatrics for twenty-two years, the last > fifteen years seeing only children with Developmental Disabilities, which > include learning disabilities, attention deficit hyperactivity disorder, > cerebral palsy, mental retardation and autism. > > Excerpted.... > > I am using natural lipid soluble concentrated cis form of Vitamin A in cod > liver oil to bypass blocked G protein pathways and turn on these central > retinoid receptors. In a few days, most of these children regain eye > contact and some say their “box” of clear vision grows. After two months on > Vitamin A treatment some of these children, when given a single dose of > bethanechol to stimulate pathways in the parasympathetic system in the gut, > focus, laugh, concentrate, show a sense of humor, and talk after 30 minutes > as if reconnected.20 > > This improves cognition, but they are still physically ill. When these > children get the MMR vaccine, their Vitamin A stores are depleted; they can > not compensate for blocked pathways. Lack of Vitamin A which has been > called “the anti-infective agent,” leaves them immuno-suppressed. They lack > cell-mediated immunity. T cell activation, important for long term immune > memory, requires 14-hydroxy retro-retinol. On cod liver oil, the only > natural source of this natural substance, the children get well. The > parasympathetic nervous system is blocked by the second G protein defect. > These children are unable to relax, focus and digest their food. Instead, > they are in sympathetic overdrive with a constant outpouring of adrenaline > and stress hormones. They are anxious, pace, have dilated pupils, high > blood pressure and heart rate. These and other symptoms of attention > deficit hyperactivity disorder are part of this constant “fright or flight” > response. These symptoms improve on bethanechol. > > excerpted... > > Megson, MD > > -------------------------------------------------------- > Sheri Nakken, R.N., MA wwithin@... > Well Within's Earth Mysteries & Sacred Site Tours > http://www.nccn.net/~wwithin > Bookstore - http://www.nccn.net/~wwithin/bookstor.htm > International Tours, Homestudy Courses, ANTHRAX & OTHER Vaccine Dangers > Education, Homeopathic Education > KVMR Broadcaster/Programmer/Investigative Reporter, Nevada City CA > CEU's for nurses, Books & Multi-Pure Water Filters > > ------------------------------------------------------------------------ > Free @Backup service! Click here for your free trial of @Backup. > @Backup is the most convenient way to securely protect and access > your files online. Try it now and receive 300 MyPoints. > 1/4935/7/_/489317/_/960844646/ > ------------------------------------------------------------------------ -- @... *************************************************************** Any information obtained here is not to be construed as medical OR legal advice. The decision to vaccinate and how you implement that decision is yours and yours alone. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2000 Report Share Posted June 12, 2000 Sheri.. could you please send me the whole article? Thanx! :-) ________________________________________________________________________ Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2000 Report Share Posted June 15, 2000 amen to that!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 15, 2000 Report Share Posted June 15, 2000 Lesley, Assuming that you do not have a high risk pregnancy, the best way to avoid doctors who just don't understand and unwanted medical treatment for you and your baby is to have a home birth. Check out what's available in your state: there may be direct entry midwives or nurse midwives who will deliver your baby at home. Good luck. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 20, 2004 Report Share Posted June 20, 2004 Tamara, Heidi, who writes on the www.dadamo.com list is in New York City also, if I remember rightly. hello I'm new > Hello type O's > > I'm new to this list. I live in New York City. I am going to start a > social group for blood type diets in New York, so let me know if you > are anywhere nearby... > > I'm an ex-vegetarian. Most of my friends are vegetarians and a bit > flipped out by my conversion! > > I always had trouble digesting beans when I was a vegetarian, I would > get cramps. I adjusted to eating meat fairly quickly. > > - Tamara Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2005 Report Share Posted March 12, 2005 --I am extremely angry. I miss out on so much of life. I am a waiting my 2nd trial on April 19th. I have become a zombie on the duragesic patches and all I want to do is lie in bed and watch TV lately. Don't give up, I hope that the stimulator will give us some semblance of our lives back and make us more functional. I was also told that what goes around on the boards is a good amount of negativity because the people who do well with no complications don't need the boards or a place to chat. They mostly go on with their lifes so I was told to take these boards with a grain of salt. Welcome and let us know how your trial goes. Karel, NY - In Stimulator , " wildbluerosie " <wildbluerosie@y...> wrote: > > > Hi everyone. I'm 31 years old and started going thru. the process for > the trial. I have DDD and my insurance doesn't pay for meds. So I > have had three surgeries and many epi. shots. All of these have not > worked. Next week I have an appointment to get the shrink clearance. > I wish my shrink could do this. I almost never sleep at night > anymore. My doctor calls it sundowning. Honestly it gets to the > point sometimes that I don't want to live but, hopefully with groups > like this it will help. My room mate wants me to get a wheelchair so > that I will feel that I have some freedom again. As you see I live in > a big city and could get around a lot easier but I don't know how I > feel about it I mean after all I'm only 31. Also does anyone have > problems with your disability and anger. > > Thanks so much any advice is greatly needed. > ~Stacey Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2005 Report Share Posted March 13, 2005 , I can relate to what you said. I am only 38 years old and have had two back surgeries. I am waiting to have the stimulator trial in May. It is very frustrating not being able to do what you could before. A lot of people do not understand the emotional side of back issues. Depression, anger, loneliness, social isolation, lack of motivation, sleepless etc. It all wears on us. I am here if you need to talk to someone who is dealing with the same things you are. Chin up and keep on smiling! Hello I'm new Hi everyone. I'm 31 years old and started going thru. the process for the trial. I have DDD and my insurance doesn't pay for meds. So I have had three surgeries and many epi. shots. All of these have not worked. Next week I have an appointment to get the shrink clearance. I wish my shrink could do this. I almost never sleep at night anymore. My doctor calls it sundowning. Honestly it gets to the point sometimes that I don't want to live but, hopefully with groups like this it will help. My room mate wants me to get a wheelchair so that I will feel that I have some freedom again. As you see I live in a big city and could get around a lot easier but I don't know how I feel about it I mean after all I'm only 31. Also does anyone have problems with your disability and anger. Thanks so much any advice is greatly needed. ~Stacey Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2005 Report Share Posted March 13, 2005 Well said Karel! Re: Hello I'm new --I am extremely angry. I miss out on so much of life. I am a waiting my 2nd trial on April 19th. I have become a zombie on the duragesic patches and all I want to do is lie in bed and watch TV lately. Don't give up, I hope that the stimulator will give us some semblance of our lives back and make us more functional. I was also told that what goes around on the boards is a good amount of negativity because the people who do well with no complications don't need the boards or a place to chat. They mostly go on with their lifes so I was told to take these boards with a grain of salt. Welcome and let us know how your trial goes. Karel, NY - In Stimulator , " wildbluerosie " <wildbluerosie@y...> wrote: > > > Hi everyone. I'm 31 years old and started going thru. the process for > the trial. I have DDD and my insurance doesn't pay for meds. So I > have had three surgeries and many epi. shots. All of these have not > worked. Next week I have an appointment to get the shrink clearance. > I wish my shrink could do this. I almost never sleep at night > anymore. My doctor calls it sundowning. Honestly it gets to the > point sometimes that I don't want to live but, hopefully with groups > like this it will help. My room mate wants me to get a wheelchair so > that I will feel that I have some freedom again. As you see I live in > a big city and could get around a lot easier but I don't know how I > feel about it I mean after all I'm only 31. Also does anyone have > problems with your disability and anger. > > Thanks so much any advice is greatly needed. > ~Stacey Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2008 Report Share Posted April 7, 2008 Hi all, this is my first post and I've been prompted to join after googling lots of info regarding underactive thyroids because I feel both my mother and I (and possibly my dear departed Grandmother) have health issues that may be explained by hypothyroidism, although we have both had " normal " blood tests results. However she was also tested for s disease due to anomalies in her results, which came back negative. Mum has arthritis (since pregnant with me 39 years ago) and I have recently developed permanently painful feet (Doc says give up high heels)sacroiliac joint dysfunction,(could be related to being pregnant - but that was 13 years ago and the pain only started about four years ago)and my hands are starting to ache also. I have put on three stone in the last ten years despite trying to control my weight through diet and exercise, and sometimes put on weight while dieting and exercising! My periods are erratic, I have frequent breast cysts, my hands suffer from Reynauds, I am frequently very tired and feel very heavy and sluggish and lethargic. I have had a fair amount of stress and trauma in my life, so am in psychotherapy which is helping me address issues, but while I concede that some of my mental problems could well be environmental, the fact that I am constantly trying to improve things yet still feel foggy and hopeless and tearful suggests that it's not so simple. I am beginning to think that if I could see a private doctor I might be looked at as a human being from a holistic point of view rather than being treated as though I am simply getting older and a hypochondriac. I do not enjoy feeling under the weather, and try so hard not to let it get in the way of things, but it's getting to the point where I feel hopeless. I would very much appreciate any advice you can give me with regards to convincing my GP that there is something wrong with me physically rather than just psychologically! Many thanks in advance. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2008 Report Share Posted April 7, 2008 Hi there And welcome from me . A lot of what you mention in your symptoms are my symptoms also. I have been hypo for years but only just taking my own health into hand. Even the Sacro Illiac joint pain is the same. I read somewhere that that might have something to do with adrenal fatigue but as I have no idea where I read it and I am not medically qualified please don't quote me on that. Anyway, once again welcome and I am sure you will get the same great support from this forum as I have benifitted from. God bless Dawn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 Hi vicci, Welcome to the group! First thing is to read up on the website and print out the symptoms list and tick as relevant, it's amazing what hypo can cause, but not surprising as it controls our whole metabolism all you describe can be attributable to hypo- I've suffered most myself in the past. And yes it is possible to have hypothyroidism and have a 'normal' TSH- what was yours? The Ranges have changed recently and not to the patients benefit- the USA and Germany have much tighter, lower ranges. Adrenal problems also go hand in hand with low thyroid states, but can cause problems before it gets as low as s disease. Subject: Hello I'm New Hi all, this is my first post and I've been prompted to join after googling lots of info regarding underactive thyroids because I feel both my mother and I (and possibly my dear departed Grandmother) have health issues that may be explained by hypothyroidism, although we have both had " normal " blood tests results. However she was also tested for s disease due to anomalies in her results, which came back negative. Mum has arthritis (since pregnant with me 39 years ago) and I have recently developed permanently painful feet (Doc says give up high heels)sacroiliac joint dysfunction,(could be related to being pregnant - but that was 13 years ago and the pain only started about four years ago)and my hands are starting to ache also. I have put on three stone in the last ten years despite trying to control my weight through diet and exercise, and sometimes put on weight while dieting and exercising! My periods are erratic, I have frequent breast cysts, my hands suffer from Reynauds, I am frequently very tired and feel very heavy and sluggish and lethargic. I have had a fair amount of stress and trauma in my life, so am in psychotherapy which is helping me address issues, but while I concede that some of my mental problems could well be environmental, the fact that I am constantly trying to improve things yet still feel foggy and hopeless and tearful suggests that it's not so simple. I am beginning to think that if I could see a private doctor I might be looked at as a human being from a holistic point of view rather than being treated as though I am simply getting older and a hypochondriac. I do not enjoy feeling under the weather, and try so hard not to let it get in the way of things, but it's getting to the point where I feel hopeless. I would very much appreciate any advice you can give me with regards to convincing my GP that there is something wrong with me physically rather than just psychologically! Many thanks in advance. ------------------------------------ Messages are not a substitute for professional medical advice. Always consult with a suitably qualified practitioner before changing medication. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 8, 2008 Report Share Posted April 8, 2008 Hi there toxic kitten, your best bet is to ask your doctor for some antibodie tests.to start with (TPOab) and maybe thyroglobulin, (TBab/TSBab and ATA.AMA.there are seven to see if you have hashimoto`s disease.these are blood tests but some labs do urine one`s to.if you think you may have arthritis then (ANA) might be useful. angel. for Good helps you make a difference Quote Link to comment Share on other sites More sharing options...
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