Following my blood test on 21/6/2019 to see if I am Hypothyroid the results have come back normal again.
I have asked for a printout of them only too be told I can if I pay £20 for them.Im still waiting for a date for the ultrasound of my thyroid, apparently as my gp put routine, I have up to a 6 week wait .The feeling of a lump in my throat is getting worse and I’m having more trouble swallowing food
.
I’m constantly clearing my throat and have an annoying tickling in my throat that makes me cough a lot.
My Gp said that my remaining bit of thyroid was bulkier than usual.But he couldn’t feel any nodules .He thinks the swelling is at the back of my thyroid. I’m just about to give up because its not worth perusing anymore
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Dizzydoris
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Whatever you do, don't give up! You may be offered advice here which enables you to push for a diagnosis/treatment from an amgle you may not yet have exhausted.
Firstly, who told you your results were normal and did they verbally tell you what your results were?
Secondly, who told you you have to pay to access your test results? On the NHS you are entitled to view your results online (you may need to request further access, but this is quick and easy to do). Health professionals have a legal requirement to allow you to see your results (more info here: nhs.uk/using-the-nhs/about-...
Edit: I see on your previous post you were already given advice about accessing your results. Did you act on any of that advice and then were still denied?
I would recommend speaking to the practice or patient service manager and explain you are legally entitled to a copy of your test results and they can not legally charge you. Put in writing if need be so your 'complaint/dissatisfaction' is officially lodged. Once you have those results you can post here and the more experienced forum members can advise you on your results.
Never take notice of someone who works in a surgery.
Even GPs don't quite know how to interpret blood test results.
Always ask for a print-out of your results with the ranges. We are entitled by LAW to receive them. Some surgeries charge a nominal sum for paper/ink.
If the cost is too high, tell receptionist to let you copy from her computer.
£20 is ridiculous and it should be a 'nominal sum' to cover paper/ink. I get mine for nothing. If she still refuses say you will be speaking to your MP as you know many get a print-out for nothing.
It annoys me so much that we who are ill and have an autoimmune disease, through no fault of our own are then denied a copy of our own blood tests with the ranges. We have to battle to get diagnosed (I had to diagnose myself): then we have to battle to get an optimum dose of hormones: have to battle to request a T4/T3 combination. T3 then withdrawn. It is too exhausting.
I will do Thankyou, I think they see me a neurotic female who won’t accept that nothing is wrong. It’s so frustrating, 4 years ago I had an endoscopy because of the same problem. It showed I had swellling at the back of my throat but nothing was done.
2 years previous to that and having the same problems although not as bad as they are now , an ultrasound showed a blood filled cyst on my remaining bit of thyroid.
I was scheduled for a fna and was provided with diazepam to calm me down .
When I got in the room to have it done the dr told me he wasn’t going to do it after all and I could leave.
I spoke to the ultrasound department of my local hospital today and was told my gp had emailed asking for an appointment for me . He headed the email “anyone that deals with necks” which I think is disgusting ! I now have between a 6 and 9 week wait for an appointment.
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