Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 > > Hi. I am 34 years old and just had a baby four months ago and went in for some routine > blood work and it showed a THS level of 0.04. I went for an ultrasound and it showed 3 > nodules on my thyroid. I am going to see an endocrinologist next week. I wanted to know if > that THS level is bad because I don't really feel that bad. > > I'm just worn out from nursing a baby and caring for an older toddler too, but I thought how I > feel is normal. Also, can nodules go away on their own? Has anyone else out there breastfed > a baby with hyperthyroidism? Should I expect to have medicine started with that kind of THS > level? I have never had a thyroid problem before in my life. Any advice and pointers for > questions to ask my doctor would be appreciated. Thanks! > Hi there, I dont know how much help I will be but firstly did you doctor say anything about medicine when you got your lab work done? And I have never heard anything about nodules. I had hyperthyroid so my thyroid became engorged. I dont think I ever had anything on them... however it sounds more to me like you have Hypothyroid. There is a small difference there. I dont know if you know all the symptoms or not but... slugishness is only one of them. Irratic heart rate...like for instance your sitting on the couch watching tv and all of a sudden your heart starts beating out of your chest, your out of breath...also look for shakey hands...its not an all over shake but just in the hands, look at your eyes...do they look swollen or does one look bigger than the other? Another sign of hypothyroid which is low thyroid is weight gain. Now I understand you just had a new baby...congradulation by the way...but did you gain an exsesive amount during your pregnacy or are you gain weight rapidly now...I am talking new pant sizes within a couple months? As far as medicine goes...my aunt has thyroid problems and shes on Synthroid to keep it maintained....she had a baby a year ago and they gave her her meds in the hospital the same day she had the baby...I dont know about breast feeding because she didnt breast feed...thats a question for your doctor. Also I would find out exactly what you have hyper or hypo...this could really effect you because you have a new born. How do they plan to remove these nodules thingys? Surgical or Radiation? If its radiation I can tell you that you wont be able to be anywhere near your newborn for about 24 hours...because of the radition treatment...now this isnt like kiemo or anything...mine was two small blue pills and there arent any kind of side effects to it...just that you can not go near new borns or the elderly for 24 hours...and they suggest not standing,sitting, or sleeping beside anyone because your radiation and inturn effect the other person. So check with your doctor about it. Thats all I know really. I hope I helped a little however I would research nodules and your ths levels online just to see what you come up with. That will give you a better understanding of what you have and the kinds of questions to ask your doctor. Leanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 28, 2005 Report Share Posted November 28, 2005 Hi, I am 22 months pregnant with hyperthyroid. I have nodules in my thyroid. My tsh level was 1.05 while conceiving after i got pregnant it dropped to 0.01. since i m pregnant i cannot take thyroid throu. I suggest you to read greenlife-herbal.com and ithyroid.com. The tablets prescribed for hyperthyroid will give you just temporary relief and nothing more. Instead of thyroid doing its work the medicine take over the work of thyroid. The tablets stops the production of hormones which may later leave you being hypothyroid for the rest of your life. Start taking action now itself before your symptoms increase. You are your own judge in curing thyroid disease. For time being follow the diet in ithyroid.com and see how you feel bec i bet you will not like taking any medication while breast feeding. Once you stop nursing see if you want to try Thyroid Throu. I m no expert but giving some suggestion on what i know. Hi. I am 34 years old and just had a baby four months ago and went in for some routine blood work and it showed a THS level of 0.04. I went for an ultrasound and it showed 3 nodules on my thyroid. I am going to see an endocrinologist next week. I wanted to know if that THS level is bad because I don't really feel that bad. I'm just worn out from nursing a baby and caring for an older toddler too, but I thought how I feel is normal. Also, can nodules go away on their own? Has anyone else out there breastfed a baby with hyperthyroidism? Should I expect to have medicine started with that kind of THS level? I have never had a thyroid problem before in my life. Any advice and pointers for questions to ask my doctor would be appreciated. Thanks! --------------------------------- Music Unlimited - Access over 1 million songs. Try it free. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 20, 2010 Report Share Posted April 20, 2010 Hello my name is Lorine and I am 62 years old. I was diagnosed with SLE lupus 15 years ago. 13 years ago they said that the lupus was contained and I had fibromyalgia. The last three years my finger start peeling like some one taken a knife and peel my skin from my finger and razor blade cut follow the skin peel. I was diagnosing as having psoriasis of the hand. My condition has gotten worse this last four months. I was going to see a new rheumatologist before he saw me he wanted me to take a bone scan where they inject a nuclear shot to show up more than a MRI would show up. It shows up arthritis in my spinal cord and all of my back and more places. My doctor said today I had psoriatic arthritis and he wants me to take Remicade. I have read some literature on this and the side effect is dangerous. I don't trust doctor fully. I am concern is his diagnosed right? He is order other blood test for me. What should I know? Etc Sometime I have brain fog as well, if I didn't write this right please over look it. lorine Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 20, 2010 Report Share Posted April 20, 2010 After arguing for years with a rheumy who was sure I just had fibromyalgia I got him to diagnose the psoriatic arthritis that runs in my family thanks to a bone scan. That test worked well for me when blood tests and x-rays didn't. Remicade is a TNF inhibitor like the Enbrel I take. It has been a great blessing to me and unlike methotrexate, sulfasalazine and prednisone, I have never experienced a single side effect with Enbrel. Janette Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 20, 2010 Report Share Posted April 20, 2010 Thank you for getting back with me. As I said earlier 15 years ago I was told SLE Lupus, afterward been on disability I was told fibromyalgia. Now this new doctor tell me it psoriatic arthritis. I forgot to tell you that it started in Memphis Tennessee, Hawaii now California. This is a new doctor. That the reason I join this group. I been doing a lots of research. When I though I had lupus I went to the lupus meeting until I learn all I needed to know, same with fibro. My doctor want to give me Methotrexate and Leucovorin and surfasalazine. These two medication is prone to liver damage,except the Leucovorin. Plus give me the Remicade. I am trying to learn as much as I can on these medication. Meanwhile my body is getting worse. It all in my spine area and spinal cord. Other place in my body as well. Once again Mahalo (thank you) for your help Lorine Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 21, 2010 Report Share Posted April 21, 2010 Hi Lorine! I take Remicade and for me it has been a Godsend! I know those side effects the literature lists sound horrid but please understand very few people have those worst ones and many people have no or very mild side effects at first. I was scared too! But by my fourth treatment with all the improvement in my symptoms I was so glad I decided to try it. When I started Remicade my hands and feet looked like raw hamburger all the time. The peeling, splitting and bleeding just like you have. I had to keep them wrapped all the time if I went out in public to avoid being asked if I had AIDS or if I was contagious. My right ankle, left knee and lower back were so bad and painful I walked like a very old woman, hunched over and hobbling. My quality of life was pretty much non existent. Remicade changed all of that. My hands and feet are usually clear or very mild in small patches. I still have joint damage but the swelling and pain are much improved. Like others here will tell you, I am not a doctor. Only you and your doctor can decide what the best treatment will be for you. But if you just don't trust and aren't comfortable with the doctor you have now, then maybe you should check out other rheumies in your area. Your doctor is a very integral part of your ability to deal and live with this disease. Discuss all the alternative treatments, the pros and cons, and what you are comfortable with with your doctor. If need be keep a notebook just for writing questions or concerns in to take to your doctor with you. That notebook can also be used to keep track of any new or worsening symptoms too. As for the brain fog and fatigue, well we all understand that! I know I live with those two things all the time. As many others here do. So you have come to the right place for support and to ask questions. Gentle hugs!! Dalene Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 28, 2010 Report Share Posted April 28, 2010 Just wanted to say that y other rheumy also kept wanting to pin fibromyalgia on me too. I don't know why, because I did not have any of the trigger points. Finally, I am with another doctor and my psoriatic arthritis is being treated and I am getting some good results. Why is it that the doctors are so quick to pin the fibromyalgia on women? I doubt it is the same for men. - Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 28, 2010 Report Share Posted April 28, 2010 I've found that since I was diagnosed with fibromyalgia several years ago and something new comes up, some doctors will slap the name on the new problem as a catch-all diagnosis when they're not sure what it is. I think it's a good lesson that we have to take on the responsibility of staying on top of our health concerns - even more so than the docs. Some are arrogant and can't say " I don't know " . When this happens I assert myself and get a second opinion and I have yet to fail. Fortunately my family doctor is not one of that kind. He works with me and will automatically go for a second opinion when the diagnosis is unclear. The fibro for women does have a higher statistic for some reason, but that's no excuse. Let's make sure our doctors are looking at the problem and not the gender... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2010 Report Share Posted May 1, 2010 I agree. I was diagnosed with fibro and that seems to be a blanket diagnosis for anything else that turns up. Its very frustrating when you feel like you're not being taken seriously. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 2, 2010 Report Share Posted May 2, 2010 Lorine - PA is very difficult to diagnose, so you could very likely have been misdiagnosed for a long time. I had the joint pain long before I had any skin involvement and that is not completely uncommon. I am taking Remicade and it has changed my life - I am not creaky and in pain, I am not sleepy all the time...it can give you your life back, so it is worth trying! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 3, 2010 Report Share Posted May 3, 2010 THANK YOU FOR SAYING THIS.....I START MY TREATMENT THIS MONTH. LORINE Lorine - PA is very difficult to diagnose, so you could very likely have been misdiagnosed for a long time. I had the joint pain long before I had any skin involvement and that is not completely uncommon. I am taking Remicade and it has changed my life - I am not creaky and in pain, I am not sleepy all the time...it can give you your life back, so it is worth trying! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 12, 2011 Report Share Posted October 12, 2011 Hi, Becky - welcome! Sorry you're having trouble. you list a long string of problems, some serious. The " liquids for 24 hours " rule is fine for temporary problems, aimed at resting the stoma while very minor problems and issues heal. It is not a CURE for bigger problems! ** ANY ** time we have problems for more than a day or two, it is essential to see our Band surgeons for an exam and possibly a fluorosopy to look at the stoma and band position. Please see your doc at once - you have waited far too long already. You're correct that the band does not cause immune problems. but those eating poorly and becoming deficient in many of the vits and minerals we need, surely do compromise the imune syatem. Has your doc done vitamin studies? Are you careful about taking a good daily Band vitamin? See the " Vitamin " document in the files here for much more on this issue. Good luck - please let us know how you are. Sandy,RN - group co-owner banded March 2003 pretty much at goal weight since 2004 > > Hi All, > New to the Group and unfortunately I'm here because I need help with some problems. I had my band surgery 11/4/2010 and until about 2 months ago I was doing really well. About 2 months ago I started having a lot of food sticking problems. I hadn't had any issues with food so I kept trying to get food down, sliming, vomiting etc... I finally checked some online resources and was reminded that I needed liquids only for a day. Did the liquid only for 24 hours and went on vacation without any problems. Back from vacation and was fine for a week until we spent the day at a local College Football game. I had a headache after the game; attributed it to sitting crooked at the game. Got home from the game, thought I was hungry and thirsty but about 30 min. after eating I vomited. My headache lessened so I did feel better. I stuck with liquids only for the rest of the night. I did have liquids and snacks at the football game but maybe not enough? In the days after the game I didn't sleep well, didn't exercise and caught a cold. I started drinking milk 1st thing in the AM to get a jump on my blood pressure, stool softener, and anti-depressants thinking that would help me feel better, (if my bp meds were taken before noon) but I started having problems with the pills sticking. They eventually go down after about 20-30 minutes. I have always cut my anti-depressants in half and my bp pills are tiny. I don't take them all at once, 2 or 3 at a time then the rest a couple hours later. Anyway - I've now had the cold, for 2 weeks, with a runny nose mostly down the back of my throat. I took Sudafed for a couple of days which dried me up but obviously didn't get rid of the cold. When the pills started sticking I gave up on the Sudafed because the other drugs are more important to get down. This morning I woke up feeling like crap and drank a small amount of milk about an hour after waking and took ½ my pills and I was fine. About 1.5 hours later I ate a piece of string cheese on the way to the vet with my cat and thought everything was fine, until I was standing in the exam room and I started to slime. I didn't want to run out while my cat was being examined so I swallowed my slime – which I know is bad. I vomited the slime after leaving the office and am on the liquids only for the next day. My apologies for being so gross, but I'm not sure how else to explain what's going on. I wanted to stop at the health food store to find a better way to get rid of this cold and boost my immune system, but being that I was having issues I just came home. I'm getting really frustrated, I'm tired of food getting stuck and I think my cold and the mucous running down the back of my throat is adding to the problem. The last 2 months I've been more tired and sicker longer than anything I remember from the past. I don't believe the band would cause a compromised immune system but I think the way I'm using it may be. Am I just pissing my band off too often and not being delicate enough after a problem? I'm wondering if my band has slipped although my gut tells my probably not. Any suggestions how to boost my immune system, stop this mucous, sleep better etc.??? In the past I used natural remedies from the health food store but I don't think those capsules will fit thru the band. I'm a mess and I'm starting to ramble – so any help would be greatly appreciated. > Becky Disner > Quote Link to comment Share on other sites More sharing options...
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