For the love of all thats demonic..... what's n... - Thyroid UK

Thyroid UK

141,244 members166,489 posts

For the love of all thats demonic..... what's next??!!!

ChemicalAngel profile image
18 Replies

For the last couple of days, my left foot has felt a bit weird. It is now decidingly numb under the heel. It is tingling as I have just hobbled to the kitchen and back for a cuppa!!

Now is this something else thats connected, or is it because of the osteochondrial lesion od the talus that I have on that foot??

dont wanna ask the quack, I go on the 13th Feb for the results of the wrist xrays.

Getting fed up with one thing after another giving up!!

Ann xx

Written by
ChemicalAngel profile image
ChemicalAngel
To view profiles and participate in discussions please or .
18 Replies
PinkNinja profile image
PinkNinja

Don't give up :( It is horrible when there's just one thing after another. Perhaps it is because of the lesion. It's in the ankle, yes? If it is, it could be responsible for the numbness. A bit like carpal tunnel syndrome perhaps.

I hope you get to the bottom of it soon.

I feel a bit like Mrs Potato Head at times too! Wouldn't it be great if we could just swap out the offending body part ;)

Take care and definitely don't give up!

Carolyn x

ChemicalAngel profile image
ChemicalAngel in reply toPinkNinja

Hi Carolyn, the talus is the big bone in your foot, that the ankle bones sit on top. My podiatrist and the orthopaedic surgeon she sent me to had never seen that damage in the bone before. In layman terms, I have took a big chunk out of the enamel surface of the bone, and it was a severe injury as it has damaged the cartilage too.

Yeah, hopefully Doc will have gone through my results, he said he would, for the appt in feb. Hoping he will see things my way and maybe agree to a trial of thyroxine.

I thought though, that once you were on thyroxine, you cannot ever stop it. Is that right??

Ann xx

PinkNinja profile image
PinkNinja in reply toChemicalAngel

Ouch!

I'm not sure if that is true about never being able to stop thyroxine. It might take a while for your own production of thyroid hormone to resume though. People with post-partum hypothyroidism often reverses after 18 months - 2 years. I would presume then that these patients can stop taking thyroxine, else how would they know it had reverse? Just a thought. I don't know for sure.

If you are borderline hypo, you could have some swelling as a result. This could be aggravating your injury and trapping a nerve, like with carpal tunnel syndrome that is so often a symptom of hypothyroidism.

I hope your doctor sees things your way too. It's about time you caught a break!

Carolyn x

henrykeats profile image
henrykeats in reply toChemicalAngel

I had 90% removed 20 years ago.. my thyroxine administration has been appauling for 20 years.. I don't take them anymore.. I meditate.. I'm fine.. the human mind is very powerful is used correctly.. maybe my remaining 10 % is functioning .. I don't know. I won't let the pharmasuitical industry poision my body.. never take any tablets.. never realy been I'll.. never had the flu..

PaulB profile image
PaulB

Hi

If it is worse or painful in mornings, then it could be start of plantar fasciitis.

My GP diagnosed me with this a couple of years ago. GP advises it can be linked to thyroid.

In me, my plantar fasciitis is a belweather for my thyroid treatment, ranging from perfectly normal to sleeping with feet up against the wall to kill the discomfort.

Worth asking about.

Paul

ChemicalAngel profile image
ChemicalAngel in reply toPaulB

Hi Paul, it is worse in the mornings, and we have got a fair decent amount of snow here. We got a good 6 inches last night, and am not that far from the M6 that had a foot of snow!! Now it is persisting it down! lol

Will mention to the quack if it is still the same

Ann xx

PaulB profile image
PaulB in reply toChemicalAngel

Ann

Took me 2.5 hrs to do 35 miles on Friday night. Snow tyres got me to village but had to use chains to get up the last hill, so was frozen by time got home.

Is it me or has thyroxine got to be variable at moment, some batches seem really strong, others seem to be as strong as a sugar lump? Playing havock with energy levels and work.

Paul

PaulB profile image
PaulB

Interesting link

northcoastfootcareblog.com/...

thedoghouse profile image
thedoghouse

I found that when I started taking Selenium the pain disappeared, almost overnight. It was most probably just a coincidence but it could be worth a try if you don't take it already. I have read that selenium can help convert T4 to T3 so that is what I am basing my hypothesis on. I hope it will get better soon, it is so wearing and tiring. x

PinkNinja profile image
PinkNinja in reply tothedoghouse

That is very interesting. I had a lot of joint pain and stiffness when I was on levo. When I switched to NDT the pain reduced significantly, almost overnight. I believed that was due to the reduction of T4 in my system. What you suggest about selenium may well have been having the same effect. If the T4 was building up in your system it may have been causing your pain. Once it was able to be converted, the level of T4 reduced and so did your pain. Makes a lot of sense to me and fits in with my theory of T4 build-up causing pain :)

snowstorm profile image
snowstorm

Hello everyone,

It is my belief that any form of hormone medication can play havoc on our systems. This "havoc" does not always rear it's ugly head immediately. It can take, in some cases, several years and by this time the body has simply had enough (also by this time much damage can have been done) and can't cope with what is going on. This in turn has upset the adrenal glands (these are NEVER supported as they should be) so stress levels remain high and most likely increase. This, of course, just makes matters worse. If an injury has been or is involved the situation intensifies. It is a vicious circle. But how can we get off the circle. Know idea. Perhaps as consumers of thyroid meds we can learn to listen/feel what we need --- take it when we feel we need it or perhaps even giving our systems a complete rest form these dreadful meds (they are not dreadful for everyone on course). People can come off them. Some because they are well again and some just become so intolerant to one type as it makes them so ill --- as in my case.

There is too much readiness/keeness to put people on these medications without doing proper checks. A symptom is treated rather than the whole person. This will never work.

powderpuff profile image
powderpuff

Ann, I would keep a very close eye on this & waste no time in getting a Rheumatologist referral if it worsens. In my experiance, your problems could well be due to not having your Thyroid issues addressed & treated.

For years I had a nipped Sciatic nerve which eventually extended down my leg into my foot causing 'foot drop'. It was the Rheumatologist who suggested my Thyroid meds should be reviewed & possibly increased which is exactly what Dr Skinner did. Gradually the problem improved & is now completely healed.

In your position I really wouldn't hang on expecting the NHS to eventually help you. The longer time goes on more & more symptoms/effects emerge which just become all the more harder to overcome.

PP

auldreekie profile image
auldreekie

I developed plantar fasciitis when on too low dose of NDT (T4 was in low end of the range).

My dog's physio (yes dog!) said get someone strong to press down on your heel with the ball of their hand (husband used his thumb ) and push forward with the same pressure to the ball of the foot (has to be someone strong and you can't do it yourself). We tried with cream but better without, better friction. Physio said it would imporove osmosis. It does help.(me at least).

beanyjeany profile image
beanyjeany

Hi ChemicalAngel. I had plantar faciitis for four years approx. (Self diagnosed) but compared symptoms with folk at work who had the same thing. THEN I was diagnosed with Hashimotos and within a week of starting to take thyroxine, the pain disappeared. Now, that could be coincidence couldn't it, but after four years.... Now I have a frozen shoulder which can apparently be something to do with underactive thyroid too!! It just never ends..... xx

Zoeblu profile image
Zoeblu

Hi all I've been reading your messages with interest. I was diagnosed with an underactive thyroid 8 years ago and was quite happy taking Levo. After the birth of my son 5 years ago I seemed symptomatic all the time but had normal results. Last year I was diagnosed with hashimotos and lupus!

I'm told my lupus is in remission and my thyroid within normal levels (was 17.1 in may last year). However my feet was sooooo painful, the joints of my fingers hurt and my shoulders are always aching! I've tried to get my GP to refer me to a endo but they seem to think all my symptoms are lupus whereas my rhemuy feel he has it under control!

Two diseases that show the same symptoms is leaving me always questioning why I am feeling this way and what is causing what!

Hey hoo!

ChemicalAngel profile image
ChemicalAngel in reply toZoeblu

I put my aching shoulders down to the need of industrial 'over shoulder boulder holders!!'

Zoeblu profile image
Zoeblu

Having just been through the humiliation of a bra fitting, I was told that the underband should take 80% of the strain while the shoulder straps just 20%! Have to admit its a lot more comfortable! ;)

ChemicalAngel profile image
ChemicalAngel in reply toZoeblu

Hi Zoeblu, I was 'measured' at good old marks and spencers, tried on what was supposedly my size, and I had more hanging out underneath and over the top of the cups, than in the bloomin thing!!

Trying on various sizes got me into the bras I am comfortable with, and know the band takes most of the strain, but I need a GG cup size!!!

Not what you're looking for?

You may also like...

What's the next step?

My latest test results have all gone in the wrong direction. 🤦‍♀️ but it at least vindicates why I...

What's the prognosis for Hashmitos....?

Hi everyone, I am new to this board, so please bear with me! I am just curious what the prognosis...
Mandi1987 profile image

Carbimizole not working what's next

Hi I've got hyperthyroidism I was re-diagnosed beginning of December 2018. My levels t3 12.9 my...

What's next?

So hi again. I think I've got the balance right on 150 mcg levothyroxine supplimented with B12 D3...
bardak profile image

Picking your brains/ next step for improved health.

Hi, I'm on 125 levothyroxine. I've got three children and went into the menopause after the third...
Skiski profile image

Moderation team

See all
Jaydee1507 profile image
Jaydee1507Administrator
PurpleNails profile image
PurpleNailsAdministrator
SlowDragon profile image
SlowDragonAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.