OMG!
i had my thyroid removed in september last year,
found out in dec i was pg and had a mmc two weeks later(@ 8+3wks), after my op i was on calcium for a 6wks but was told to come off it as bloods were fine.
i had the numbness in my feet/legs and part of my face,
it just makes you think that they should test bloods more often to rule out these things.
sendingto you and hope we get a
really soon xx
Mrs JD I hope all goes well for you...however a big slap on the hand for searching the net it is a bad source for information. Can I recommend to you in future that you go to a search engine called INTUTE to get any medical information as it is all from approved sources and you won't get any of the junk of fear in there. I hope that all goes well for you in the future and I will keep my fingers and toes crossed for you.
Mrs JD I hope all goes well for you...however a big slap on the hand for searching the net it is a bad source for information. Can I recommend to you in future that you go to a search engine called INTUTE to get any medical information as it is all from approved sources and you won't get any of the junk of fear in there. I hope that all goes well for you in the future and I will keep my fingers and toes crossed for you.
I knowdesperate times means desperate measures....Internet research is bad, bad, bad I know I should just
it.....
But in my defence it was the National Thryoid page that the info was posted on.
Thanks for the info hun, I will be a doctor by the end of all this
XXXXX
Mrs JD I hope all goes well for you...however a big slap on the hand for searching the net it is a bad source for information. Can I recommend to you in future that you go to a search engine called INTUTE to get any medical information as it is all from approved sources and you won't get any of the junk of fear in there. I hope that all goes well for you in the future and I will keep my fingers and toes crossed for you.
I knowdesperate times means desperate measures....Internet research is bad, bad, bad I know I should just
it.....
But in my defence it was the National Thryoid page that the info was posted on.
Thanks for the info hun, I will be a doctor by the end of all this
XXXXX
I 100% know how you feel, I think we will both be doctors lol!! I am a terror for googling stuff however cause I am a student nurse we get directed to the good search engines - I would like to say I practice what I preach but.....
Anyhoo Mrs I really really am holding my breath for you and hope that all your dreams come ture - good luck xxx
im pleased that they are doing further tests, im due to see my GP in a couple of weeks so will be asking some questions while im there.
just goes to show, if you don't read the stuff on the net then the doctors can just fob you off.
xx
Im with you on this one, hun, you know i am. As a qualified research whore, yes i did say that, lol, i believe that if you are a reasonably rational person you can be your own best advocate, and i think you have proven this. Im well impressed!
Now, lets hope you get those answers you so deserve!!
Im absolutely on tenterhooks and am steadying myself with some vino for tomorrow, lol!
My biggest fear is that it wont show up- ive got every marker and im SURE that the blood clotting issue is the problem..but of course that dosent mean it'll show up..oh god..groan! LOL!!
Very chuffed for you honey, its great having someone taking you seriuously- after all this info wouldnt be out there was it not for it actually being an issue for some people.
Anywhoo...hope you get what you're looking for and baby to boot- here, here!!
Hugs, OMi xxx