Thyroid Meds To Treat Fibromyalgia?
Nov 23, 2013
I went to a new rheumy who specializes in fibro. He spent an hour with me my first visit. I really like him. He typically treats many people with synthroid for fibro because he feels we really have a hypothyroid even though our numbers are good. i do have many symptoms of thyroid, always cold, used to have constipation, dry skin and eyes, heavy periods, etc
He called in a script for synthroid name brand for me, I haven't picked it up yet I guess I am nervous to try it.
He did do my bloodwork, TSh was in guidelines, free T 4 and T3 were in range but at 50% of the range.
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I am dealing with an intolerance to Thyroid meds. Having been diagnosed with Hashimoto's Thyroiditis 5 years ago my family doc has prescribed every Thyroid med she could think of and various strengths. Side effects were thick itchy rashes, shakiness, massive headaches and tremors. I stopped taking the Thyroid Meds for 2 years and believe me it was no picnic. I had no strength, terrible digestion, heat and cold intolerance, memory loss and on and on and on. I am now on a very low dosage.025mg. My last t3 & t4 test indicates that my levels are very low but because of all the negative side effects I have experienced my doc is terrified to increase the dosage. Along with Fibro,Celiac,Diverticulosis and Hashimoto's life is a bowl of cherries . I would like to hear from someone who is also iodine intolerant and is there a different path I could take..
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I had a complete thyroidectomy four years ago (removed thyroid, two parathyroids and two lymph nodes) and have been taking my meds (112mcg) regularly until I lost my insurance 6 months ago. I can't afford insurance and can't get help with insurance anywhere! I'm now back to work and my health is RAPIDLY declining. I'm retaining fluid like crazy, tired constantly, headaches, severe body cramps, lymph nodes in my neck are so enlarged other people are noticing them, constipated, blurry vision, deep and severe spine pain, ect. I can't afford to pay out of pocket to see a doctor so they can renew my thyroid meds for me! The appointment will cost me around $400 for visit and bloodwork. Are all of these symptoms from being off of my thyroid meds? This has never happened before but I've always been very strict with taking my thyroid meds until now. Btw I'm only 27 years old.
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This post is simply me sharing my story so other people may not make the same mistake as I did. I am a 27 y/o male. I first noticed hemorrhoid issues when I was 20, just an occasional flare up for a week or 2 out of the year, no big deal. Each year it continued to flare up more and more. Until for the past year or so every time I would have a bowel movement there would be bleeding sometimes just a couple drops in the water sometimes blood sprayed all over. Still I did not seek treatment besides trying not to strain. Then an unrelated health issue sent me to my Doc, in the course of this he did all the blood tests known to man I think. My consistent bleeding for over a year had made me anemic with a hemoglobin of only 8.3, two weeks later hemoglobin of 8.0 and an extremely low testosterone level as well which was caused by the chronic anemia. The hematologist had me immediately scheduled for an appointment with a surgeon. Endoscopy, Colonoscopy, and a Banding. The banding at first didn't seem to bad, luckily I was knocked out for the colonoscopy so I wasn't awake for the banding. However, the next week was constant pain, and the first two days were nearly unbearable. I've never had a problem with hemorrhoids that seem to remain outside the body until after this procedure not sure if the banding or colonoscopy could have worsened that condition. However 2 weeks after the banding I still have hemorrhoids and the symptoms were worse than ever: pain, itching, burning. Well I had already decided unless the bleeding was extreme again I WOULD NOT go back for another dr visit. I tried sitz bath (which for me over the years have always seemed to provide quick relief BUT then cause worse inflammation in a few hours). I tried ACV on cotton balls, painful and after a week didn't notice any improvement. During this entire time I had also converted to a high fiber diet. After the ACV I continued high fiber diet, using a stacker to put my feet on when I'm having a bowel movement, and using tucks witch hazel in the morning and before bed. With those I finally am symptom free. However, I am going to keep doing these thing forever because it seems to me that hemorrhoids, once they get out of control, will never go away completely. You just have to treat them and manage them and you will remain symptom free but if you go back to the same old habits. They will come back same as before. I am still on an iron supplement and taking testosterone shots as well.
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What are the best supplements to treat hemorrhoids? I have a few suggestions I am willing to compare.
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It has brought so many problems.
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How can you treat pinworms in first trimester , I'm 6 weeks now ? Also I have never had any vaginal infection before , it doesn't smell but I am itchy and irritated , I have a white thick discharge that gathers in the folds of my vaginal and clit area! :( I am very hygienic and bath and wash regularly, so I don't know how I would get either of these :( can someone help me as to what treatments are possible ? And and these harmful to my unborn baby ? Or my husband ?
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I'm 29 weeks, and just failed my glucose test. According to my sono the baby is almost 4lbs already. Is that high? And what is the likely hood that I have gestational diabetes? If it turns out that I do have it how will they treat it?
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I was just rubbing my girlfriend down there, and my hands weren't probably completely clean (I haven't really done anything like this before). I was mainly stimulating the clitoris, at times using her wetness to lube her up. She didn't seem to mind and at that time, she wasn't in pain or anything, in fact according to her she was enjoying it. After going back home though, she felt that the area around her clit became really sore and that it hurts horribly while trying to pee. It also itched when soap touched the area while trying to take a shower. It feels uncomfortable in general, and aches when trying to move. Most importantly, she says she has discovered some sort of a 'hole' beside her clitoris, which does not look like a scar, but is red. This has freaked us out both, and although I haven't seen the condition myself, I can't describe it more precisely. She says it's like the type of 'fold' we get when we apply pressure on our skin with the nails, except that it's round, tiny and deeper. She is also having pain in her tummy (in fact this happens when she masturbates too much) which makes it all the more worse. She is really mad at me and I know I have done something careless (especially when it is the first time we have been doing something like this), and I probably don't even deserve to be her boyfriend, but I feel really guilty and I want to help her in every way possible but I don't really know what to do about it. She hasn't spoken to anyone about it yet although she is suffering and all I care about now is that this condition goes away as soon as possible. She is not ready to go the gynecologist because she is too ashamed to talk about it as she is from a conservative family.
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I saw my doctor last week and she said she had just been to a menopause seminar where the continual use of vagifem was discussed to treat VA. She said that there have not been any long term effects and that patients could use it twice a week for an indefinite time.
She also said that if a patient stopped taking it the recurrence of VA could be severe and much harder to treat going forward.
I asked about the Mona Lisa laser treatment but she had not heard of this.
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I'm a 53 year old male in good health except for the fairly recent onset of Nocturia. My need to urinate pretty much every hour during the night began suddenly around 3 months ago. At the time of writing this, the resulting fatigue/frustration due to sleep deprivation is having a massive impact on every aspect of my life and I'm at the point of giving up any hope of a restful nights sleep in spite of being totally exhausted.
After several visits to see my GP for blood and urine tests plus a DRE (after which the Dr told me my prostate felt okay) I was referred to a urologist 2 weeks ago. After a second DRE (again told my prostate felt okay) and a urine flow test, the urologist explained my PSA level was slightly high for my age at 4.5. He offered me two options, either have an immediate prostate biopsy or wait 3 months and retest my PSA level... I elected to wait. Unbeknown to me, the urologist also instructed my GP to prescribe Tamsulosin 400micrograms (Diffundox). I only found out 10 days later having made yet another appointment to beg for help with getting some sleep.
My annoyance with the GP was cancelled out by the immense relief at finally being prescribed something that might help, but any relief was very short lived... After taking the Tamsulosin for the past 3 days, I can't face taking them again today due to the side effects!... I know it may sound trivial to some, but the side effects are compounded by the fact the medication is having zero effect on the nocturia and my being exhausted. I was still waking almost every hour by the urge to urinate, but thanks to the Tamsulosin my throat and mouth were so dry I didn't even have any saliva to swallow, a persistent dry cough, pounding headaches and disturbing nightmares impaired what little sleep I had been getting, chronic diarrhoea began the morning after taking the first capsule, while the headache and hoarse voice persisted throughout each of the 3 torturous days... On the only positive note, I did notice a slight increase in my urine flow rate, but as I'd never considered the pre-tamsulosin flow a problem it was nothing to be excited about.
My dilemma is... I feel as though I'm back at square one. Where do I go from here? Do I make yet another appointment with a GP and ask for referral back to the urologist?... Will the urologist simply offer me option number 1 again and point at a biopsy needle?... Or is there an alternative medication to Tamsulosin?... Hopefully one that works for frequent night time urination and without the side effects, but with that said, I'd suffer the side effects and hopefully medicate to lessen them if it meant getting even a few hours quality sleep.
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Im 7 1/2 months pregnant and i have a severe cold which the doctor refuses to treat. You can imagine how miserable i am. Apparently i'm a selfish b**** because i didn't cook my husband a 5 star meal today. He has not once asked if there was anything he could do to make me less miserable. Anyone else's husband a complete douche bag even though you are carrying their child?
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Has anyone used Parsley leaf capsules or tea to treat kidney stones and/or low functioning kidneys.
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Just a couple weeks ago I had a bump forming right next to my nostril and directly on my cheek. I've had it for over two weeks and just yesterday I had it checked by my doctor and she prescribed me a topical solution ( smells a lot like alcohol) called Clindamycin Phosphate. I've done everything she had mentioned to me as far as putting a warm compress on my face which I have done the past couple nights and later applying the solution. Well, just a while ago as I was searching for some advice, I twitched my nose then all of a sudden I felt a tingle on my face and was in a way relieved to see that the boil had popped! I washed my hands, took a q-tip and just dabbed all the puss and blood out. Not sure if I'm doing anything incorrectly since I can't seem to get all the puss out of it since the bump is still there. I waited it out a bit before washing my face for the rest of the blood to come out since it was still dripping a bit. I gently washed my face with aveeno and waited for it to dry as I later dabbed the solution on the boil which stung like bloody murder >;) ! I'm very worried that this bump will remain on my face as this is the very first time in my life to experience such a traumatizing experience. If there is any help, please I beg you, how do you treat a boil/pimple after it hasn't completely drained?? Should I just wait it out and continue to use my prescription? My doctor told me I didn't need a follow up for it, but I'm so worried I can't help it! Should I continue to apply a warm compress twice a day? What should I do?
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I was wondering if anyone has had a metal stent placement to treat SOD level one at all. I have posted here in the past as I have gone through 5 ERCP since my gallbladder removal summer of 2013. 3 of the 5 had a single plastic stent placement which all worked until the stent either passed on its own, or was removed by my GI doc. The other 2 times I had multiple stents placed intended to stretch the duct open in hopes of staying that way when these were removed. Obviously it didn't stay open as I relapse into the same set of symptoms that I hope to alleviate......stinging pain where the GB was, bloated all the time, the feeling of a softball lodged into the R abdomen, and pain in the back and R shoulder blade. GI doc (who is well respected here at the Univ. of MN) says that the only options left for me are a botox injection, or metal stent. Any opinions out there? Status quo being stent-less right now is not how I want to live the rest of my life. I am 52 and feel way too young to concede this whole thing.
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Some doctors cured their patients of ulcers in the mid 20th century with cabbage juice. Supposedly they got some relief after 4 days and most of them were cured after 7-10 days.
Here is how to proceed: one has to drink 200 ml of fresh cabbage juice 5 times a day, so every 3 hours. I am going to mix mine with one apple in the morning (if I can take the acidity of the apple), and other vegetables (carrots, spinach, celeri, fennel) the rest of the day to make it more tasty.
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My question is that is there anyone out there that is fighting or cured anxiety without meds?
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I have a 10 year old son who is diagnosed with ADHD, Anxiety, SPD/IPD and rule out of Asperger's/PDD in 2013. Currently, we have him on Methylphenidate ER 30mg per day, but lately we have been noticing issues. Mind you, the school hasn't been very helpful this year with information on how he is doing so I can only go by the vague messages received... the first 6 months, they say he was great! Though I have documents to prove otherwise - lately though, the teacher keeps saying he lacks focus, needs to pay attention and all that jazz. (I say it so flippantly because this teacher has been a pain to work with.
I spoke with the doctor and she wants us to come in next week to discuss his meds, but we have had issues with additives in the past and it's not a route I want to go... to sit and wait. His diet is modified already, we also work with a behavioral therapist and a chiropractic neurologist and he takes Taekwondo.
With all this, I'm wondering if anyone has tried the genetic testing (IE: HarmonyX or Genesight) to see what meds would work best with his specific genetic makeup?
I read all these stories of parents having all these issues and suddenly their kids are on Vyvanse or something else and it's a miracle. I wouldn't mind that... him being able to function better at school (academically and socially) ... he gets bullied (though he can start it up too) - I just wonder, what next?
Here is his medication history:
August 2011 – Vyvanse ??mg (very small amount)
September 2011 – Vyvanse 30mg (adjusted to 30 mg)
May 2012 – Trial samples of Intuniv w/ Vyvanse for two weeks. After two weeks he was out of school and parents decided not to continue the Intuniv.
September 2013 – Intuniv 2mg w/ Vyvanse
September 2013 – Concerta 36mg (removed from Vyvanse and Intuniv because he became over-emotional and violent/aggressive)
December 2013 - Concerta 54mg (Dr. Snyder prescribed)
March 2014 – Methylphenidate 10mg (3 times a day) (March 7th thru March 14th)
Methylphenidate 15mg (3 times a day) (started March 15th)
April 2014 – Methylphenidate 20mg (3 times a day) (started April 14th)
May 2015 – Adderall (adderall) 10mg (3 times a day) (started May 14th)
June 2015 – Adderall (adderall) 15mg (3 times a day) (started June 3rd)
August 2015 – Guanfacine 1/2mg (3 times a day) (started August 21st)
September 2015 – Methylphenidate ER 30mg (once a day) (started September 6th)
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Went to see new neurosurgeon on Monday and she has prescribed Gabapentin to add to the mix of my daily cocktail of drugs. Having looked it up though, it seems to have some pretty worrying side effects. For me, as I work full time, I am concerned about being drowsy, sleepy and generally spaced out at work. Apparently it is all magnified if you are also on opiate based painkillers too. I am also concerned that I may pile on the weight!
Can I ask what adverse reactions others have had to this? Also it says on the box that stopping the meds can cause seizures, but is this only in people that have epilepsy (the main reason the drug is prescribed) or can it cause that in people that have never had a history of epilepsy?
By the way, my meds had not changed since May 2007. Nobody has had the slightest interest in monitoring me, either in terms of if they are still suitable, dosage levels, if I am now addicted, if they are working well or even if they are harming my body. Some of the boxes state that you should have regular blood tests but I have never been offered any. Considering I have had two lumbar operations since last May and numerous problems since, it seems quite odd that this has been allowed to go on for so long with not one of the numerous doctors/surgeons giving a damn. I just order the meds from my GP surgery online and then pick up the prescription. That gives a review date, usually 6 monthly intervals, but nobody actually reviews me, they just put a new review date down on the records.
Apart from back pain my main problem these days is the burning/numbness the whole length of my leg and my locked up toes. Apparently the Gabapentin will help with this. But the worse of the problem is at night, hence the fact that I can function reasonably well during the day. But now if these new tablets are going to knock me out and render me incapable during the day, then I'm tempted just not to bother.
All in all the meeting with the new neurosurgeon went quite well. I will be having another MRI shortly (my 6th in 16 months) and hopefully I'll know more then about what is going to happen going forward. The bad news is that she thinks that a lot of the problems are from the internal scarring from the two operations and nothing can be done about that. Hey, ho, I guess I'll find out in time.
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Has any one every taken detox meds? If so which ones?
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Including, inhalers, ingested, etc.... To say it again, what works for one may or may not work for another person. I don't understand why people ask this or that inhaler or whatever med. worked for them? It, to repeat myself, may work for you but not for me. What I have realized in this whole journey of copd and other chronic diseases that I'm dealing with is that it is up to me to do everything I can to find out about the disease; ie. research, talking to people and pulmonary care. That's about it really.
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