Who uses private blood tests and where / how do you do them?
I am under a consultant endo for hyper / graves but my bloods are only done every 12 weeks or so. I have been on 40mg carbimazole for nearly a year and finally my latest test apparently I’m hypo. This was found out the day I had my second RAI treatment.
I now have 1 more week of no carbimazole but then they want me to restart on 20mg a day and not have a blood test until 6 weeks.
I’m wondering about doing bloods privately. Before I moved my fab GP would do bloods every 5 weeks and discuss it all with me. Now getting info is really hard, all I ever get is “it’s still up” or “now yoh have gone the other way” they never give me the levels, it’s always rushed phone calls,
I’m just not feeling in control, also started to feel anxious, palpitations back and my memory is shot, but I though palpitations and anxiety where a result of hyper… so I’m a bit consumed and just want to feel more in control.
dreading it if the RAI works this time and I’m already hypo from over medication.
Thank you!
Written by
MadM24
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You are legally entitled to printed copies of your blood test results and ranges.
The best way to get access to current and historic blood test results is to register for online access to your medical record and blood test results
UK GP practices are supposed to offer everyone online access for blood test results. Ring and ask if this is available and apply to do so if possible, if it is you may need "enhanced access" to see blood results.
Not much to add to what i wrote a year ago but just remember with Graves Disease the TSH once primary hypothyroid is not a reliable measure of anything and you must be dosed and monitored of your Free T3 and Free T4 readings :
Hi both, thanks for your replies. I’m still battling to get visibility of my results. It turns out my GP don’t actually have them either without logging in to a hospital network.
Request now with Endos secretary to send printed copies.
Tomorrow I start my first Levo dose and handily I have an endo apt 21st nov.
So my plan is to get theses flipping results for the last 18mths, particularly the last 3 which cover the switch from hyper to hypo and to do a private test with full vitamins etc and run it past you all ahead of that appointment.
Currently feeling very unwell, don’t have the energy to eat my evening meal, leg, hip arm pain like I have not had since hiking the 3 peaks in 24hrs, plus yesterday I just randomly fell over while walking. Took 5 calls to the GP to get the Levo prescription that they confirmed they did receive a letter about 3 weeks ago.
Shall update on a new post once I have the results.
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