IT is scary i got to have ultrasoubd next week can i ask do you feel like you choke and hard to take breaths in i hope all goes ok yes im getting panic atracks too bless you x

Not for an ultrasound. U will notice slight pressure for ultrasound when they hold the equipment against your neck but shouldnt be choking feeling or hard to breathe.

Hello

I had my appointment today with the consultant, the FNA came back as follicular neoplasia, he said it was abnormal but not definitive, he said the chance of it being cancer was still low.  I'm booked in for a hemithyroidectomy in 2 weeks time, they will send the sample away and I will know 2 weeks later.  

Feels like such a long way away until I find out.

Lorna xxx

Hi had another biopsy of womb over four weeks ago waiting for results my endometris hyoerplasma has got bigger 32mm

Good evening 

This is my first post here. Having read through all the previous posts it has made me feel calmer.

A little history:

End of May I went to the dentist for a check up and he noticed a large lump on the right side of my throat/thyroid.  Referred me to the hospital.  First appointment 2 weeks later. Bloods - came back normal.  Had US and FNA on 21st June. Was told I'd have my results in 2 weeks. Almost 3 weeks and having made numerous calls to the consultants secretary I've still not received my results which tbh I feel quite appalled at. 

I have an ENT appointment on 21sr July which I'm assuming will be my results?  But the waiting is killing me and I'm feeling like I'm being fobbed off.

The not knowing is awful. I have kind of accepted that if it's cancer I'll deal with it but I just wish someone would tell me!

How long did you have to wait for thyroid biopsy results?

Thanks x

Hi Ditzie2009,

I waited about a week or just over it to get my results.

Did u have any symptoms?

No although I'm post menopausal and from what I've read some symptoms can apply to either menopause or thyroid cancer. 

A tricky one. I had no symptoms and mine was cancerous. Every case is different.

I was blindsided with my diagnosis as they kept telling me it's likely benign, but not all cases are cancer so try to distract yourself or listen to calming music. Once you get your result at least you'll know - I felt shocked but much calmer when I knew what I was facing. 

Thanks for your response.  I think the not knowing awful.  At least if I can get my results I can deal with whatever they are. At the moment I feel in limbo.

Sorry to hear your diagnosis.  Did you have surgery?

No problem. Yes I had my left lobe of thyroid removed in Oct 2018 and doing well since. I had a 2.5cm cancerous nodule (papillary type) with no evidence of spread. My bloodwork was normal prior to diagnosis and I had no symptoms. 

I have bloods taken and neck ultrasounds every 6 months. So far I haven't needed any meds and didn't have rai treatment. The right lobe has been picking up the slack so far. 

Hi Hoof1, just wanted to thank you for posting your story and about how your FNA and surgery went as it's been so helpful and reassuring.

Our stories are quite similar (so far) as I found a painless lump in the left side of my thyroid a few months ago, though when I think back I may have been aware of something there for up to a year so I feel so stupid for not getting it checked sooner. For a long time I wasn't certain if it was just how my neck had always been but then in June I realised the lump was larger and obviously growing. I've not had any symptoms from it other than a slightly hoarse voice at times and needing to clear my throat more than usual which didn't ring any alarm bells before.

I was seen by a nurse practitioner who took bloods and referred me for an ultrasound. Bloods came back normal (TSH and CRP fine) and it took nearly a month before I got a date for the ultrasound. I had that on 5th August. As soon as the scan started I could tell the sonographer wasn't happy. She told me I had a 6cm nodule in my left lobe ("a whopper") and that at least half my thyroid would need to be removed. I asked if it could be cancer and she said yes in such a way as to make me think she was sure that's what she was looking at. I felt my stomach drop and honestly thought I was going to cry during the rest of the scan but managed to hold it in and keep composed.

The original nurse practitioner called me a few days later to explain the nodule was suspicious (grade U4). I saw an endocrinologist on 17th August who went through what would happen if it was benign, indeterminate or malignant on the FNA. If malignant, she recommended full removal of the thyroid and RAI treatment. I had the FNA this week on the 25th and am now waiting for the results. I'm convinced it's cancer at this point as am guessing the odds are in favour of that with a U4 grade.

Weirdly what I'm struggling with most isn't even the (likely) cancer at this point, it's the thought of losing my thyroid and having to swallow a radioactive substance. I've had very poor mental health for 20+ years (OCD, anxiety, low mood) and the thought of all this being exacerbated by levothyroxine is horrendous. Plus I'll never stop thinking I've got cancer with every ache, pain or lump, even if it's unlikely.

I'm wondering why the doctors are satisfied with only removing half the thyroid in some cancer cases. My ultrasound showed that the right lobe looked healthy and didn't demonstrate any lymph node involvement, the nodule is well contained in the left lobe. If that remains the case after further investigation, I was hoping to just have my left lobe removed to give me a chance at continuing to make my own hormones. I mentioned this to the consultant but she said that would go against NICE guidelines and that they'd recommend full removal. Is that because my nodule is 6cm? Or perhaps it depends on the exact type of cancer or maybe the age of the patient? I'm 38 (and female).

I know I'm jumping the gun a bit here as don't have my FNA results yet but I'm preparing for the worst as don't think it would be healthy to cling on to the idea of it being benign. If it is benign then that will be an amazing bonus, though I know cancer could still be detected during the full analysis after surgery. Either way I need at least half of my thyroid out and I'm pretty scared.

Anyway, sending love and support to anyone else out there who is going (or has gone) through this. It's hard, especially when you've had no symptoms and feel physically well. Feels impossible to get my head around.

P.S. For anyone worried about the FNA, I was ridiculously anxious during mine to the point where my full body was visibly trembling. But it was absolutely fine. I felt a tiny sting when they administered the local anaesthetic (hardly any pain at all) and then genuinely didn't feel anything at all during the sampling to the point where I was shocked when they told me they'd done the first one! I think having a large nodule helped though as they had a lot of surface area to choose a sampling site from. I was panicking for nothing anyway so to anyone about to have it, just try to relax before and during it. Deep breaths and, like Hoof1 mentioned, concentrate on a fixed point on the ceiling. It will be over quickly.

Hi Ditzie.

Did you get your results through, I fojnd the waiting time tremendously difficult. 

Just wanted to check in.

E. Xx

Hi Ditzie.

Did you get your results through, I fojnd the waiting time tremendously difficult. 

Just wanted to check in.

E. Xx

Hi

Yes got my results on 28th July. They came back indeterminate! It was just a relief to finally have them.

Since then I have had a hemithyroidectomy (right side removed) on 17th August and am doing really well so far. I have my post op check up in 2 weeks and hopefully find out more about my lump!

How are you?

Ditzie

That's great news that you're recovering well - well done! I'm 4 weeks post total thyroidectomy and right neck dissection, 90 lymph nodes out of which about a quarter were positive. Meeting my oncologist in a week and should learn more on RAI timings etc. Its slow improvements but getting there.