Guest guest Posted August 19, 2008 Report Share Posted August 19, 2008 ummm...yeah....it was just an observation, I'm not freaking out about it. In a message dated 8/19/2008 8:54:45 P.M. Eastern Daylight Time, butterfliesrfree309@... writes: JEN THAT'S A POSSIBILITY. OR MAYBE NOT. WHEN IN NOVEMBER IS YOUR SISTER GETTING MARRIED? IF THE INSURANCE CO. APPROVES YOU SOON, AND THE SURGEON CAN PUT YOU ON THE SCHEDULE QUICKLY, YOU MIGHT BE ALMOST FULLY RECUPPED. IT DOESN'T PAY TO MAKE YOURSELF CRAZY UNTIL YOU KNOW WHEN THE INSURANCE CO APPROVES YOU. THEN YOU HAVE TO SEE HOW QUICKLY THEY CAN GET AN OR.. TAKE ONE STEP AT A TIME. DON'T WASTE ENERGY ON THINGS YOU CAN'T CONTROL SUE C MODERATOR. From: _UCJAM1977aol (DOT) UCJ_ (mailto:UCJAM1977@From: _UCJ<_UCJAM1977@_UCJAM1977@<WB (mailto:UCJAM1977@(mailto:UC> Subject: Re: Hi _Stimulator@ groStimula_ (mailto:Stimulator@_Stimulator@ Date: Tuesday, August 19, 2008, 2:32 PM It has been so quiet that I thought everyone was just busy. I am praying for our entire group and I am still here if anyone needs anything. Sunday night I went to stand up off the floor and ripped the lead cord out of the stimulator box. My husband put it back in and I was okay. Then the paper tape (I can't use plastic because I get an awful rash) started eating away at my skin and had to come off. All this messing with the stim caused there to be a short in the lead and my Medtronic rep said to disconnect it all and then see my doc at the regularly scheduled appointment, which is tomorrow and tape the lead down on my back until then. Within about a half hour, the pain returned and I was pretty sad to not have the relief of my stim anymore. Now, I have to wait for insurance approval. I knew it was going to have to come out, but I really hoped it would be tomorrow and I would have it for the whole week. Anyway, I am here. I just haven't written because I was a little bummed. I am praying for everyone and hope that warm wishes find each of you. In a message dated 8/19/2008 10:00:34 A.M. Eastern Daylight Time, butterfliesrfree309 @ writes: Good morning everyone. I wrote back to Larry last night and told him that I, as well as the group, wish Kathy a speedy recovery, as she will be in our thoughts and prayers. I hope Mike is OK with his back and Kathy G's dad is home from the hospital..I hope everyone else is having a good day. I am here for anyone who wants to talk, vent, has any questions, etc. Hope everyone has a nice day. Sue C Moderator [Non-text portions of this message have been removed] ************ **It's only a deal if it's where you want to go. Find your travel deal here. (__http://information._ (http://information./) _ (_http://information._ (http://information./) /) travel.aol. com/deals? ncid=aoltrv00050 000000047) [Non-text portions of this message have been removed] [Non-text portions of this message have been removed] ************ **It's only a deal if it's where you want to go. Find your travel deal here. (_http://information._ (http://information./) travel.aol. com/deals? ncid=aoltrv00050 000000047) [Non-text portions of this message have been removed] [Non-text portions of this message have been removed] **************It's only a deal if it's where you want to go. Find your travel deal here. (http://information.travel.aol.com/deals?ncid=aoltrv00050000000047) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 19, 2008 Report Share Posted August 19, 2008 JEN THAT'S A POSSIBILITY. OR MAYBE NOT. WHEN IN NOVEMBER IS YOUR SISTER GETTING MARRIED? IF THE INSURANCE CO. APPROVES YOU SOON, AND THE SURGEON CAN PUT YOU ON THE SCHEDULE QUICKLY, YOU MIGHT BE ALMOST FULLY RECUPPED. IT DOESN'T PAY TO MAKE YOURSELF CRAZY UNTIL YOU KNOW WHEN THE INSURANCE CO APPROVES YOU. THEN YOU HAVE TO SEE HOW QUICKLY THEY CAN GET AN OR.. TAKE ONE STEP AT A TIME. DON'T WASTE ENERGY ON THINGS YOU CAN'T CONTROL SUE C MODERATOR. From: _UCJAM1977aol (DOT) UCJ_ (mailto:UCJAM1977aol (DOT) com) <_UCJAM1977aol (DOT) UCJ_ (mailto:UCJAM1977aol (DOT) com) > Subject: Re: Hi _Stimulator@ groStimula_ (mailto:Stimulator@gro ups.com) Date: Tuesday, August 19, 2008, 2:32 PM It has been so quiet that I thought everyone was just busy. I am praying for our entire group and I am still here if anyone needs anything. Sunday night I went to stand up off the floor and ripped the lead cord out of the stimulator box. My husband put it back in and I was okay. Then the paper tape (I can't use plastic because I get an awful rash) started eating away at my skin and had to come off. All this messing with the stim caused there to be a short in the lead and my Medtronic rep said to disconnect it all and then see my doc at the regularly scheduled appointment, which is tomorrow and tape the lead down on my back until then. Within about a half hour, the pain returned and I was pretty sad to not have the relief of my stim anymore. Now, I have to wait for insurance approval. I knew it was going to have to come out, but I really hoped it would be tomorrow and I would have it for the whole week. Anyway, I am here. I just haven't written because I was a little bummed. I am praying for everyone and hope that warm wishes find each of you. In a message dated 8/19/2008 10:00:34 A.M. Eastern Daylight Time, butterfliesrfree309 @ writes: Good morning everyone. I wrote back to Larry last night and told him that I, as well as the group, wish Kathy a speedy recovery, as she will be in our thoughts and prayers. I hope Mike is OK with his back and Kathy G's dad is home from the hospital..I hope everyone else is having a good day. I am here for anyone who wants to talk, vent, has any questions, etc. Hope everyone has a nice day. Sue C Moderator Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 6, 2008 Report Share Posted October 6, 2008 On Mon, Oct 6, 2008 at 10:24 AM, kiran ovalkar <k_ovalkar@...> wrote: send me mail KIRAN OVALKAR PROSPERITY CONSULTANT TRANSFORM YOUR LIFE-FOREVER ovalkar@... 09821283709 - 09324573178 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 7, 2008 Report Share Posted October 7, 2008 hi send me mail KIRAN OVALKAR PROSPERITY CONSULTANT TRANSFORM YOUR LIFE-FOREVER ovalkargmail (DOT) com 09821283709 - 09324573178 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 8, 2008 Report Share Posted October 8, 2008 hi hi...AMOL JADAV <amoljadav30@...> wrote: On Mon, Oct 6, 2008 at 10:24 AM, kiran ovalkar <k_ovalkar > wrote: send me mail KIRAN OVALKAR PROSPERITY CONSULTANT TRANSFORM YOUR LIFE-FOREVER ovalkargmail 09821283709 - 09324573178 Add more friends to your messenger and enjoy! Invite them now. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2008 Report Share Posted November 4, 2008 Hi Bhargava, Please give your continue time to your meditation, This is very important like other works it gives energy to our soul..........Meditation very close to GOD, so we can understand wat we are and wat is part in the world......... actually we all are playing different type of roles so when we play this role with all these funcation we have to remeber GOD and meditation is the very important part of this life. Sagar From: bhar gava <bhargav_surya@...>Subject: hi Date: Tuesday, 4 November, 2008, 5:40 PM Nice to meet u It is good see ur message i am new to this group i have joined this group for some suggestions and some help which help for my growth in positive thinking i do meditation for some period but now iam not doing its another issue,there is no time for me for doing that about me i am engineer doing job in private firm, and i am just 22 Add more friends to your messenger and enjoy! Invite them now. Add more friends to your messenger and enjoy! Invite them now. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2008 Report Share Posted November 4, 2008 hi , KIRAN OVALKAR PROSPERITY CONSULTANT TRANSFORM YOUR LIFE-FOREVER ovalkar@... 09821283709 - 09324573178 From: bhar gava <bhargav_surya@...>Subject: hi Date: Tuesday, November 4, 2008, 5:40 PM Nice to meet u It is good see ur message i am new to this group i have joined this group for some suggestions and some help which help for my growth in positive thinking i do meditation for some period but now iam not doing its another issue,there is no time for me for doing that about me i am engineer doing job in private firm, and i am just 22 Add more friends to your messenger and enjoy! Invite them now. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2009 Report Share Posted January 23, 2009 hello Im 35 now but I have this since I was 22 ,, my surgeries didn't work I have multiples dilations and even a perforation in the stomach but still hanging in there I learn to live like this but right now I'm doing better I don't if is resignation what I have ,, my DR want to take my E out because he said will be easy ,, easy for him that way the endoscopies will not take long ,, is hard to live with the pain and vomit and stuff but hang in there you will learn ,, I hate hospitals too,, specially when you don't look sick and people don't understand that you are really sick I learn how to eat normal in small amounts and drinks lots of liquids to flush it down , good DR's are hard to find , but find one that make yu feel good and understand Frances 35 WA From: m.naulty <m.naulty@...> Subject: hi achalasia Date: Friday, January 23, 2009, 3:54 PM whats up everyone.ive had achalasia since i was 21 years old.im now 28.ive had botox injections 3 times when i was 22.unsuccful. then lost insurance and when i got insurance again i was 26.i went through test saved money to take time off work for surgry,had the surgury and still did not help.in the mist i lost my soon to be wife and new born baby girl.abbie and lexi.were and still are the love of my lifebut abbie had dealt with my condition for serveral years.we split got back togather then split again.now the doctors want to do surgry again to redo basicaly what she already did.the doctor will call me act concernd say see will call me back and i dont hear anything.o yea i also had ballon strech.but im upset becauce i hate hospitals took a long time let them do first operation now anther one, im mad and upset with this.im a male 28.is there any members that are around same age that has had simialer problems Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 23, 2009 Report Share Posted January 23, 2009 Hi, I am sorry to hear that you still have problem after surgery. I am 29 and have a similar story but I didn't had botox and dialations. I was diagnosed last year, had a failed first surgery then went for second surgery after 5 months. My second surgery was performed by Dr.Rice in Cleveland Clinic. I am two months post surgery and doing great. If you could tell us where you are located people in this board might help you in locating a good surgeon. Ayondeep > > whats up everyone.ive had achalasia since i was 21 years old.im now > 28.ive had botox injections 3 times when i was 22.unsuccful.then lost > insurance and when i got insurance again i was 26.i went through test > saved money to take time off work for surgry,had the surgury and still > did not help.in the mist i lost my soon to be wife and new born baby > girl.abbie and lexi.were and still are the love of my lifebut abbie had > dealt with my condition for serveral years.we split got back togather > then split again.now the doctors want to do surgry again to redo > basicaly what she already did.the doctor will call me act concernd say > see will call me back and i dont hear anything.o yea i also had ballon > strech.but im upset becauce i hate hospitals took a long time let them > do first operation now anther one, im mad and upset with this.im a male > 28.is there any members that are around same age that has had simialer > problems > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 17, 2009 Report Share Posted April 17, 2009 Hi Holly, I had a CSF leak and my pain management doctor did something call a Blood Patch were he took some of my own blood and injected it into my spine or the durma space. It stopped the leak the headaches everything it was all gone as soon as he was done. Has your doctor tried that yet? I don't know if yours is the is the same kind of leak, But that's an idea I have. Keep On Smiling Kathy Sweet Group Moderator > > Hi Everyone my doctor put me on a medication to reduce the csf fluid that is a leak from surgery back in August. It makes me throw up and sick every time I take it. I am not sure what I should do at this point. I started taking it Tuesday I wonder if I should give it more time it makes it so I can't eat anything really at all. But I want to give it a try as well. If anyone has idea's please let me know thanks for your support. > Holly > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 25, 2009 Report Share Posted April 25, 2009 , Hi Welcome to the group.. I'm glad your stem is helping.. I wonder why they would say your using it to much... weird... My rep always tells me I use alot of power but has never told me to lower it... Well I hope you have good recovery.. Please take it easy,, don't over do it.. It is so easy to do when you start feeling better.. Got to give yourself time to heal... I'm so glad you have found us.. We are here if you have any concerns or anything.... Good luck and hope to hear from ya Soft hugs T group moderator lisa From: denisefive5 <denisefive5@...> Subject: Hi Stimulator Date: Saturday, April 25, 2009, 5:05 PM Hi everyone my name is Sharron but I go by and I just got my spinal cord stimulator put in on the 14th of April. Went back for my first md check and he said I was " using it to much " for someone who just got it and to cut back....it's just like telling someone who has an addiction to cigarettes or alcohol to just all of a sudden to cut back....I just love it!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 25, 2009 Report Share Posted April 25, 2009 I'm curious also. I asked if I had to turn mine off sometimes, and I was told I could use it continuously and never shut it down. And I only turn it off if I'm having a test done; EKG, CT Scan, etc. Take Care, B. in TEXAS Until one has loved an animal, part of their soul remains in darkness ________________________________ From: lisa thompson <bluejeans412003@...> Stimulator Sent: Saturday, April 25, 2009 4:16:07 PM Subject: Re: Hi , Hi Welcome to the group.. I'm glad your stem is helping.. I wonder why they would say your using it to much... weird... My rep always tells me I use alot of power but has never told me to lower it... Well I hope you have good recovery.. Please take it easy,, don't over do it.. It is so easy to do when you start feeling better.. Got to give yourself time to heal... I'm so glad you have found us.. We are here if you have any concerns or anything.... Good luck and hope to hear from ya Soft hugs T group moderator lisa From: denisefive5 <denisefive5@...> Subject: Hi Stimulator Date: Saturday, April 25, 2009, 5:05 PM Hi everyone my name is Sharron but I go by and I just got my spinal cord stimulator put in on the 14th of April. Went back for my first md check and he said I was " using it to much " for someone who just got it and to cut back....it's just like telling someone who has an addiction to cigarettes or alcohol to just all of a sudden to cut back....I just love it!!! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 13, 2009 Report Share Posted July 13, 2009 Hello Himanshu Once your fiancée gets onto the right dose of thyroid hormone replacement that takes away her symptoms, she should be absolutely fine. However, she needs to make sure that there are no associated conditions that go along with being hypothyroid. She can read about these on our web site www.tpa-uk.org.uk under 'Hypothyroidism' and then look on the drop down Menu under 'Associated Conditions' Read about these and understand what problems might arise. The more she learns the more she will be ready with the knowledge of how to deal with these. Number one is that she might find one day for some reason she is unable to convert the mainly inactive hormone thyroxine (T4) to the active hormone triiodothyronine (T3). T3 is needed by every cell in the body and brain to make them function. If people can't convert T4 to T3, they need to add some form of T3, either synthetic, or through the natural thyroid extract (Armour Thyroid). Number two is she might find she has low adrenal reserve which, if she has, will stop her thyroid hormones from being absorbed. She can get a 24 hour salivary adrenal profile done to check out where her cortisol and DHEA levels are at four specific times during the day. This is an expensive test, but worth every penny. They don't supply this test on the NHS. She can get it done through Genova Diagnostics www.gdx.uk.net .. If she does suffer low adrenal reserve, she will need a course of some form of adrenal supplementation. Number three is that she might be suffering with systemic candidiasis - and again, she can get checked to see if she has candida antibodies at the same laboratory as above. Again, this will stop her thyroid hormone from working. Number four - she should ask her GP to check to see if any of the following blood tests are too low in the reference range. These are ferritin, B12, Vitamin D3, copper, zinc and magnesium. If any one of these are low, it will need to be supplemented - because again, any of these low in the reference range will stop her thyroid hormone from being absorbed. All of these she can read about under 'Associated Conditions' on the web site and in the FILES section on this forum Having said all that - her GP will test her thyroid function every 6 weeks to 3 months and increase her dose of levothyroxine appropriately, and if she has a good doctor, this may be all that is necessary. Most people do well on levothyroxine only, and let's hope this is the case for your fiancée. Anybody who has been diagnosed with hypothyroidism, irrespective of the actual cause, has to take thyroxine for the rest of their lives. If you are not making a particular hormone, there is no substitute but to replace that hormone with the same hormone, synthetic or natural. luv - Sheila I just stumbled upon this group, and thought that I might find some long term survivors of Thyroid cancer on this group. I just want to know from them that what is the quality of life that the normal survivors lead ? Are they always troubled with various kinds of health problems related to thyroid, throughout their lives ? Her doctors said that she would just have to take the thyroxine tablets everyday in the morning and that's it and she would even forget, in few years, that she ever had thyroid cancer. How true is it? I know that it would vary from person to person, but just wanted to know what happens for the majority. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 13, 2009 Report Share Posted July 13, 2009 MODERATED TO DELETE MESSAGES PREVIOUSLY READ. PLEASE CHECK THAT YOU HAVE DONE THIS BEFORE CLICKING SEND. LUV - SHEILA _________________________________________________________________ Thanks a lot Sheila. I went through the website provided by you. it is really helpful. I just wanted to ask that how debilitating these conditions generally are.. if some body does suffer from an adrenal problem or candidiasis.. are these really difficult to control and lead a normal life ? Also do you have idea about the general lifespan of pappilary thyroid cancer patients.. whether they suffer from any other specific problems.. ? Regards, Himanshu > > Anybody who has been diagnosed with hypothyroidism, irrespective of the > actual cause, has to take thyroxine for the rest of their lives. If you are > not making a particular hormone, there is no substitute but to replace that > hormone with the same hormone, synthetic or natural. > > > > luv - Sheila > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 14, 2009 Report Share Posted July 14, 2009 Hello Himanshu Hypothyroidism can be debilitating if the correct therapy is not being prescribed for the patient. Low adrenal reserve can be a problem because it stops the thyroid hormones from being absorbed, so you get a double whammy. The first thing that should be treated is the adrenals to make sure they can cope, as every hormone gland in the body depends on well functioning adrenals. This is why we recommend the 24 hour salivary adrenal profile that you can get from www.gdex.uk.net .. Is there any possibility that she could see Dr Peatfield at one of h is metabolic clinics that he holds throughout the UK. See our web site www.tpa-uk.org.uk and check in the right hand column to see where he holds these. He is a very knowledgeable man and knows about the problems caused through low adrenal reserve and systemic candidiasis. All of these are treatable, and will make such a difference to her thyroid hormone replacement therapy once these have been boosted. The general lifespan of anybody suffering these condition is good if these conditions are the problem and have been treated. Some of us live VERY healthy and long lives. Prognosis, fortunately in most cases, for people with cancer of the thyroid are usually treated very successfully. Papillary cancer of the thyroid is not associated with a high degree of progression, so many sufferers maintain a normal life expectancy if diagnosis is made early. Luv - Sheila Thanks a lot Sheila. I went through the website provided by you. it is really helpful. I just wanted to ask that how debilitating these conditions generally are.. if some body does suffer from an adrenal problem or candidiasis.. are these really difficult to control and lead a normal life ? Also do you have idea about the general lifespan of pappilary thyroid cancer patients.. whether they suffer from any other specific problems.. ? Regards, Himanshu Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 14, 2009 Report Share Posted July 14, 2009 Sorry, the link to the Genova Diagnostics laboratory should read www.gdx.uk.net Luv - Sheila This is why we recommend the 24 hour salivary adrenal profile that you can get from www.gdex.uk.net . Is there any possibility that she could see Dr Peatfield at one of h is metabolic clinics that he holds throughout the UK. See our web site www.tpa-uk.org.uk and check in the right hand column to see where he holds these. He is a very knowledgeable man and knows about the problems caused through low adrenal reserve and systemic candidiasis. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 14, 2009 Report Share Posted July 14, 2009 Thanks a lot Sheila. We are currently in India, so it might not be possible for us to visit Genova Diagnostics. We would try to find out from her doctors about where in India, we can get these tests conducted. Thyroid problems being common everywhere I am sure, it should be possible to get them done here too. Thanks again for so much help, Best Wishes, Himanshu > > Sorry, the link to the Genova Diagnostics laboratory should read > www.gdx.uk.net > > Luv - Sheila > > > > This is why we recommend the 24 hour salivary adrenal profile that you can > get from <http://www.gdex.uk.net> www.gdex.uk.net . Is there any > possibility that she could see Dr Peatfield at one of h is metabolic clinics > that he holds throughout the UK. See our web site > <http://www.tpa-uk.org.uk> www.tpa-uk.org.uk and check in the right hand > column to see where he holds these. He is a very knowledgeable man and knows > about the problems caused through low adrenal reserve and systemic > candidiasis. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 22, 2009 Report Share Posted September 22, 2009 , I am so tired so won't write so much but just had to let you know that I enjoyed the personal email and about part of your family. I am not sure what we can do on this group but personally I like to hear these kind of things along with help on the stimulator but we don't always have something to say about it. Up until yesterday my days and nights were horrible but I had a really good night last night. I have been busy for two days taking one fifteen year old granddaughter to get her glasses. There wasn't any school yesterday so it was a good time to do it. 'She usually wears contacts but wanted both. I will try to get started earlier tomorrow night. I saw so many that I wanted to reply to. It sounds like you are doing well which I am so grateful for. I am back to normal pain today so hope it is going to continue. Best wishes to you and thanks for the hugs. Lois PS I hope to remember to tell you the story about meeting Dutch relatives from the Netherlands on the internet in 2002 and what has happened since. Must go now. On 9/22/09, <radiant.salubrity@...> wrote: > Hi Lois, > > I'm really pleased to hear your family is so supportive. Friends are > wonderful, support groups understand you, but family is just such a > treasured commodity in so many ways. Even when we have days that we are > down, it only takes a phone call from one of the grandies to tell us about > their day and seems to perk you right back up again. > > I'm always telling my kids I love them. I don't care if they hear 100 times > a day. My eldest grandson is 9. He thinks he is over kisses and hugs. I told > him the other day, as long as Nanna is alive, I will always have a kiss and > a hug with him. It's in the Nanna / grandson contract. He believes me for > now - lol. > > My daughter rang me the other day, I went visiting to her house. Her little > one has just turned one. I had been playing with him before she put him down > for a sleep. I left about 15 mins later. When he woke up, he was walking all > through the house crying yelling Nan Nan Nan .... I just thought that was > beautiful. My daughter didn't think so, it was driving her nuts!! > > I suppose it's the little things like that, that help take our mind of > ourselves now and then. > > I know the family try and understand what we are going through. But it is > hard to explain what it's like. I consider myself lucky too. I think I have > 2 families now. My family that surrounds me here in West Oz and my network > of people I have met on here as well. > > I do hope your feeling a little better about things. I wish I could visit > and have a cuppa with you, give you a big hug, and listen to lots of things > you must have to share. > > Thinking of you always > > > > > > > -- Lois Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2010 Report Share Posted January 2, 2010 Hi My advice would be Iodine! Either Iodoral tablets or Lugols (which is cheaper). Whichever you chose, 50mg per day. Here's some info : https://www.drbrownstein.com/bookstore_Iodine.php If you are near London, Dr Brownstein is in UK 23rd Jan 2010 : http://www.nleducation.co.uk/seminars/david-brownstein-md-thyroid-health\ -and-iodine Lugols : http://bobbys-healthy-shop.co.uk/show-product-details.php?ID=51 Iodoral : http://www.nutrivitaldirect.com/iodoral-p-89.html (I think this is the cheapest UK price. Typically, the US users pay less than half!!) Good luck!!! Ian > > Hi, I am new to this group so just want to say hello. I have been diagnosed with hypothyroidism for about nine years and am currently on a prescription of 175mcg levothyroxine. I have been back to the doctors many times, my most significant symptoms are low mood, irritability, weight gain and tiredness. However, all my tests come back normal and I stay on the same medication. Any advice as to what to do next would be greatly appreciated. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2010 Report Share Posted January 2, 2010 Hello and welcome to our happy little bunch of Thyroidians - I hope you will find all the help and support you need here. Many people seem to do quite well on levothyroxine for quite some time, years even, and then suddenly, it doesn't work anymore. There are many associated conditions that go along with being hypothyroidism that stop the thyroid hormone from getting into the cells, and you need to go through a process of elimination to find out why it is not working for you. One of the most obvious reasons is that the thyroxine (which is only one hormone and a mainly inactive hormone) is not converting through the liver, kidneys and other thyroid hormone receptors into the active hormone triiodothyronine (T3), T3 is needed by every cell in your body and brain to make them function. Are you taking 200mcgs Selenium daily, as this is needed to help with conversion. Two other reasons are that you could be suffering with low adrenal reserve or systemic candidiasis. If you are suffering with either, again, the thyroid hormone cannot get into y our cells and you need to boost your adrenals and treat the candida. Read about this in our web site www.tpa-uk.org.uk under hypothyroidism, and then in the drop down Menu under 'Associated Conditions'. You can get tests done through Genova Diagnostics (you can get a discount through TPA-UK for both of these), but before spending any money, go to our FILES section of this Forum (from the Home Page) and scroll down the list until you come to 'Medical Questionnaires' and do the Candida Questionnaire, the Adrenal Questionnaire and the Questionnaire to see whether you might be suffering with reverse T3 (rT3) and see how you score. Next, ask your GP to test your blood to see whether any of the following are low in the reference range: ferritin (stored iron), B12, vitamin D3, magnesium, folate, zinc and copper. Once more, if any of these are low in the range, you will need to supplement and build up the level and then your thyroid hormone could well start working again. Will you get your last thyroid function test results from your GP together with the reference range for each of the tests and post them here so we can have a look. You also need to know whether you have antibodies to your thyroid, so ask your GP to check this unless he has already done so. Antibodies see your thyroid tissue as public enemy number one and set about its complete destruction. Treatment is the same as for any other cause of hypothyroidism, but you may well need a combination of synthetic T3/T4 or T3 alone or natural thyroid extract. Do you have other members in your family with a thyroid or autoimmune disease? Luv - Sheila Hi, I am new to this group so just want to say hello. I have been diagnosed with hypothyroidism for about nine years and am currently on a prescription of 175mcg levothyroxine. I have been back to the doctors many times, my most significant symptoms are low mood, irritability, weight gain and tiredness. However, all my tests come back normal and I stay on the same medication. Any advice as to what to do next would be greatly appreciated. No virus found in this incoming message. Checked by AVG - www.avg.com Version: 8.5.431 / Virus Database: 270.14.123/2595 - Release Date: 01/01/10 09:20:00 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2010 Report Share Posted January 2, 2010 Hi Ian - we never 'advise' anybody on this forum, simply because we are not medically qualified and we don't know whether is suffering from Hashimoto's disease or not. Advising anybody to take anything can get us into trouble if anything goes wrong - so we need to keep our noses clean. There could be many and varied reasons why is suffering with the problems she is, and we need to go through a process of elimination. She might be short of iodine, she might not be, so let's wait and see, and then give her the appropriate recommendations of where she can buy supplements if she does need iodine. I wish I was near to London though, I would very much like to hear what Dr Brownstein has to say. Luv - Sheila Hi My advice would be Iodine! Either Iodoral tablets or Lugols (which is cheaper). Whichever you chose, 50mg per day. Here's some info : https://www.drbrownstein.com/bookstore_Iodine.php If you are near London, Dr Brownstein is in UK 23rd Jan 2010 : http://www.nleducation.co.uk/seminars/david-brownstein-md-thyroid-health\ -and-iodine Lugols : http://bobbys-healthy-shop.co.uk/show-product-details.php?ID=51 Iodoral : http://www.nutrivitaldirect.com/iodoral-p-89.html (I think this is the cheapest UK price. Typically, the US users pay less than half!!) Good luck!!! Ian > > Hi, I am new to this group so just want to say hello. I have been diagnosed with hypothyroidism for about nine years and am currently on a prescription of 175mcg levothyroxine. I have been back to the doctors many times, my most significant symptoms are low mood, irritability, weight gain and tiredness. However, all my tests come back normal and I stay on the same medication. Any advice as to what to do next would be greatly appreciated. > No virus found in this incoming message. Checked by AVG - www.avg.com Version: 8.5.431 / Virus Database: 270.14.123/2595 - Release Date: 01/01/10 09:20:00 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2010 Report Share Posted January 2, 2010 MODERATED TO REMOVE MOST OF MESSAGE ALREADY READ. PLEASE DELETE THESE MESSAGES AND LEAVE JUST A PORTION OF WHAT YOU ARE RESPONDING TO. LUV - SHEILA _______________________________________________________________ Thank you for all your advice. I shall certainly read all the other information you have signposted me to. I shall ask my Doctor for my last results. I also forgot to mention earlier that I am also on Citalopram (suffered a very close bereavement) although as I mentioned earlier have suffered with low mood/irritability prior to this. > > Hello and welcome to our happy little bunch of Thyroidians - I hope > you will find all the help and support you need here. Many people seem to do > quite well on levothyroxine for quite some time, years even, and then > suddenly, it doesn't work anymore. There are many associated conditions that > go along with being hypothyroidism that stop the thyroid hormone from > getting into the cells, and you need to go through a process of elimination > to find out why it is not working for you. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 29, 2010 Report Share Posted January 29, 2010 Hi Khalid Well,I think first of all you should believe in yourself.England need of Highly qualified workers.(I know that Dentists there is no longer shortage of Dentists in England theoretically...but practically ...lots of advertisement(job) for Dentists.) Yes ,sure GDC doesn't provide the job for Dentists,but there are many sources where you can get the job once you registered with GDC. We shouldn't expect to be given the job by GDC after passing the ORE,we should search for it and find better place for ourselves. Sincerely Lyuda From: Khalid Saleh <kforfaly@...>Subject: hi Date: Friday, 29 January, 2010, 15:39 hi all i wanted to ask u all about the job in UK,it was stated in the gdc site that general practitioners are not in the UK shortage occupations i am not frustrating any1 but y should i go for the ore and i cant guarantee a job offer there.Hope any1 could answer my question,bye Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 29, 2010 Report Share Posted January 29, 2010 hi lyudmyla,yeah that's right!let's all keep away from all these negativities and keep believing! From: Khalid Saleh <kforfaly (DOT) com>Subject: hiDate: Friday, 29 January, 2010, 15:39 hi all i wanted to ask u all about the job in UK,it was stated in the gdc site that general practitioners are not in the UK shortage occupations i am not frustrating any1 but y should i go for the ore and i cant guarantee a job offer there.Hope any1 could answer my question,bye New Email names for you! Get the Email name you've always wanted on the new @ymail and @rocketmail. Hurry before someone else does! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 12, 2010 Report Share Posted February 12, 2010 hi therethere is a list of books on GDC website.u need pink book,blue book,master dentistry vol1 and 2On Fri, Feb 12, 2010 at 2:17 PM, kanthanlagu <kanthanlagu@...> wrote: am going to sit for my ore part1 in sept can anyone tell me where to start or which books i should concentrate in reading? tnx... Quote Link to comment Share on other sites More sharing options...
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