Thyroid :: Synthroid And Foot Cramps


Sep 7, 2015

Well, after a year and a half on Erfa Thyroid, I had to switch back to Synthroid because the heart pounding at night on the Erfa just kept getting worse and worse.

Of course, with the Synthroid I'm now back to having severe foot cramps all night; by that I mean that my foot twists around on the ankle and I have to stand up and push my foot down to get it to go back into position. Sometimes it's both feet at once. Try sleeping with that going on!

Not sure which side effect is worse, and I feel as though I can't win, since neither medication allows me to sleep.

My doctor doesn't believe that switching back to Synthroid would result in foot cramps and won't offer any help. When I was on Synthroid previously my old GP game me quinine sulphate, which keep the cramps down to once or twice a week, but this one won't prescribe it.

Has anyone else had this problem and found a solution? I take lots of calcium, magnesium, Vitamin D, and B vitamins, so I should be okay on that score.

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Thyroid Disorders :: Leg Foot And Toe Cramps

i have my lab results, and the same goes for me my dr. changed my prescription from .5 to .75, i think .75 is to strong for me so i talked him into me alternating .5 one day and .75 the next. i did this for 60 days and felt pretty good, i had leg cramps but not as severe as now. i am back up to .75 because  of my lab test showing me to have very high numbers. its pretty much just my right leg cramping , you can actually see the muscle tighten up starting at my lower calve and climb right up yo my knee. my foot contorts and stays like that  for a few minutes , its unbelievably painful. what should i change, I'm willing to do anything .

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Meds recently changed from armour to these. Am I supposed to take them both first thing in am, or take cytomel later?

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Thyroid :: Acne From Synthroid And Cytomel?

Overall, I am doing MUCH better - still have tweaking to do but this has by far been the best year for me since getting diagnosed. Things like my cycle becoming regular again, to even some weight loss (over the summer and it came back but it was nice to see my body responding for once...hopeful that once I am in my new job, my stress will be much better and Ill have time to be active again but I digress).

I had previously been on Armour and spent over 2 years never really feeling better (my body didn't tolerate it at all it seemed), so I switched to synthroid plus cytomel I had some side affects so switched again to tirosint plus cytomel.

That was when I noticed I was making progress - except for TWO annoying side affects. Zombie head that never went away over 8 months (even tried taking it at night instead which helped but getting out of bed in the morning was an act of god) and acne. Seriously, I feel like I'm going through puberty all over again. I should note, that I think the progress was due to finally increasing meds (anytime i increased armour I would be in pain so I avoided it)

I finally made a switch back to Natural Thyroid - I take the Acela NP thyroid which I tolerate much better than Armour. The good side effects have stayed and my zombie head is gone. My skin is a BIT better but not much.

Has anyone experienced this? I have read stories of people with Hashi's having skin issues due to low thyroid but that was never my problem. I have to say that my skin was maybe my one source of pride (even when my hair was falling out, i gained weight, my skin stayed clear and smooth).

Before I clearly wasn't on enough thyroid. I was on 1.5 grains Armour before switching to about 118 synthetic (it changed a few times but it was around that). When I switched to NO Thyroid (no more cytomel),I was one 2.5 grains and have now worked my way up to 3.5 grains. Increasing to 3.5 actually didn't make me worse skin wise - it was a bit better than it was on 2.5 so I can't quite figure out what the deal is.

Just looking to hear if anyone else has experience this, what they did and if it eventually went away? Would trying another version of NDT be worth a shot you think?

I am THISCLOSE to looking into accutane. I need help! I have tried every skin care product under the sun. It seems to be an internal problem and not a result of what I am putting on my face.

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Thyroid Disorders :: Synthroid To Nature-throid

Had my thyroid removed 2001 and was on Synthroid for 11 years.  Felt awful the entire time, was always very tired, gained lots of weight, dry skin and hair, the whole bunch of symptoms so finally I dug my heels in and did not take anything for 3 months.  Very dangerous but was tired of being so confused could not find my way home when I was a block from home.  So the doctor put me on Armour and then I switched doctors and the new one put me on Nature-throid.  I'm still very tired and sleep a lot, my neck hurts where the thyroid was removed 11 years ago, drainage from that area.  Any suggestions for a different med that actually works without exacerbating my symptoms?

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Thyroid :: Can't Tolerate - Synthroid, Armour And Cytomel

2 1/2 years ago my hypothyroid meds (90 mcg synthroid) started to make me feel extremely hyper, but my blood tests came back looking good. I was finally diagnosed as having Adrenal Fatigue (after seeing 13 doctors and 18 months later) and was taken off my thyroid meds totally for a about 6+ months to heal my adrenals.

My saliva test says my adrenals are much better (still not 100%). I tried to then go on Armour, but continued with anxiety, neck pain, headache all day on right side, depression…the usual.

I am now chopping up the meds and take small doses of 12.5 Synthroid and 1.25 Cytomel twice a day - morning and afternoon - for about 3 weeks but I still feel hyper…and tired and anxious, depressed. If I take more T3 I start to get really anxious.

I went on the above combination after I first tried just Cytomel alone at 1.25 and went through the roof after about 3 days, so I stopped.

We are trying the above combination thinking the Armour we tried earlier was the wrong ratio of T4/T3 (75/25%). According an online chart, my current med routine of synthroid/cytomel = a ratio of 90/10%.

I am still feeling extremely tired, anxious, no appetite, no energy, dizzy, feel like I'm not here, and depressed. Was considering changing the T4/T3 ratio to perhaps 50/50%. Anyone ever try this?

NOTE--best week ever: A few months ago, we tried switching from 15 Armour only to 12 Synthroid only for 1 week. Just to try something different. After 1 week of no progress we switched back to about 7.5 Armour for a few days--then upping to 15. And WOW, I had the GREATEST week in the last 2 years ever, then it started to decline again the next week while keeping Armour at about 15.

I was also off Gluten for 3 months with no noticeable improvements.

I keep thinking this has to have something to do with my Adrenals. As I said my saliva test came back much better - the doctor said I was 80% back to normal. I'm thinking that's not close enough?? I need to be 90% before I can tolerate the meds?? 95%?? I don't know!!

Has anyone had experience with this? Were you eventually able to take your thyroid meds again? How were you able to do it?

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I had RAI treatment for Graves 15 years ago. I have only been on Synthroid since. I have ranged form 125 mcg to 200 mcg. I never felt completely well. None of the endos (I have seen them all) in town would prescribe NDT. In November of 2012 I found a wonderful OB/GYN that has a wellness practice. He is very into integrative medicine. Finally, I found someone that will prescribe NDT.

These are my labs while on 175-200 mcg (alternating) of Synthroid.
11-15-2012
Taking 175 200 mcg Synthroid during these test. Not feeling well, fatigued, hair falling out. Switched to 2 grains of Nature Throid after these tests......

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so i went back to 1.5 grain and still had heart pap and felt bad so after a week of trying a grain every other day....

i gave up and went back to 100mcg of synthroid and heart paps stopped.....my hair loss was less the week i started on synthroid....which shocked me....alot less.....

but today i did have some pulling feeling in my neck and a head twitch is what i call it...those symptoms that are not constant but fleeting  when the thyroid is changing

...and wondered has anyone else went from nature throid back to synthroid....

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Cramps :: Leg And Foot Cramps

I've suffered from these for years. When I told the GP he prescribed 200mg quinine sulphate but I still had cramps - albeit fewer. so he prescribed 300mg tablets. I still get the cramps, perhaps not as frequently but it's quite distressing.

Leg cramps can be eased by standing on the leg and stretching it. Foot on the leg and stretching it. Foot cramps are quite different, my foot turns inwards and my toes turn position. Nothing but time can resolve it, my husband watches in amazement, as do I. It's quite painful.

A son says that lack of salt can cause cramps, might this be so? We have very low sodium chloride intake.

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I have severe feet and leg cramps can this be caused from Sjogrens ? I have take muscle relaxers with no relief

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Cramps :: Toes, Foot And Calf Muscle

its great to know i'm not going mad thinking i'm unique in this - i get cramp in my toes every single time i go to bed, if i dont try to nip it in the bud within a few minutes it moves to the rest of my foot and then to my calf muscle, i am wondering if i have a circulation problem, i did have Quinine for this and to be honest i noticed a reduction in the amount of times per week i got it then my husband said try an Aspirin which i did and noticed an aspirin in the morning then one at night reduced it even more than the quinine but, after a month of doing this, my cramps have increased to every night again whether i take aspirin or quinine, i am thin, relatively healthy but i am not a drinker of water so wonder if i should try that one next and maybe get hold of some concentrated Magnesium Citrate, i'll do anything to stop this, i even get it come on when driving and putting my foot on the gas pedal occasionally.

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I am 7 1/2 weeks post of from Flat Foot Surgery and the outside area of foot from where my incision ends from the double calcaneal osteotomy up to my little toe the soft tissue is halfway numb and very painful. Has anyone else experienced this and if so how long did it last.

I am not sure how long it takes the soft tissue to heal to a point where it does not hurt when you are not walking. Or is what I am feeling nerve pain. I started PT this week and am PWB. My doctor thinks I will be in a shoe in 3 weeks and I don't know at this rate how that could be possible. I am icing a majority of the day for sure after I do my PT exercises.

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I had what felt like ovulation cramps last week and tonight have vaginal bleeding, fresh blood not old.

I did this in 2012 after my mom died, was checked pap smear, uterine biopsy and I feel those hurt, it was all good, they thought it might of been stress related because it lasted only one day.

My abnormally normal periods were only 1-3 days, they were one coming in, one day of heavy bleeding, and spotting on third day. But every 28 days like clockwork with no issues there. In my 20's I was told I had endometriosis and when they went to do the ultrasound the cyst had went away. I didn't take it any further than that but never had children and never took birth control. Cramps were always very painful, had to curl up in a ball, always had severe back pain with them as well.

Last week they were like that not quite as bad but nearly.

Is this just a fluke you all think? Even menopause I had no symptoms, when I turned 50 it shut off like a faucet never again until 2012, and now.

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My doctor has put me on 75mg/day synthroid, because his diagnostic is hypothyroidism. However, I understand that hypothyroidism is normally associated with low T4, but high TSH.

Based on what I have read, it seems that a low T4 associated with a normal TSH may be linked to issues with the pituitary gland (and not the thyroid) or issues with binding agents.

Is hypothyroidism and the use of synthroid indicated in my case?

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Has anyone experienced this ? Did it go away on its own? Was there anything that helped this . I am afraid I will not be able to proceed the wt bearing with this continued heel pain.

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