Swollen lymph nodes in neck

Hello, 

 

I've been following these forums for a while, but this is my first time posting. I found a swollen cervival lymph node approximately 6 months ago, on the left side of my neck. I kept an eye on it but I was too scared to go to the doctors, which I know is ridiculous, but I have anxiety and I suppose I just wanted to block it out. It's about the size of a pea at its biggest. It hasn't got any bigger, if anything it sometimes feels smaller and fluctuates in size, however a few more small one's have now popped up. Also the lymph nodes under my jaw are now quite swollen and tender. I did have covid about a month ago, and I've only noticed these new ones since then, however they are still there and now I'm worried sick. 

 

I've just seen the doctor, who had a feel and has referred me for an ultrasound and also a chest X-ray as a precaution. I knew he was going to do this, from reading all of your posts on here, however as soon as he did I broke down, as it made it feel so real. I know that's the only way to find out, but I have convinced myself that it's something serious and I can't ignore it anymore. I'm just so scared. I don't know what I'm looking for really, but I know many people on here have had similar experiences. If anyone would like to share their experience or if you're going through the same right now, then maybe we can support eachother. Thanks for reading. 

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  • Just an update in case anyone comes across this post. I will keep updating, as I know this forum has helped me so much and its always good to hear the final outcome, either way. 

    So, I called the hospital and I'm booked in for a chest x-ray in a few weeks. However, the ultrasound of my neck is going to be at least 16 weeks! So I have called a private hospital and I'm going to have my scan done there to speed things up. 

    I checked my notes from the GP on my online records and the GP is concerned and put the referral through as URGENT. However, there is also a comment stating 'doesn't appear to meet the 2ww criteria.' So although this is a good sign that the GP hasn't put it through as the two week referral, during my appointment he was concerned and said he wanted it done urgently. So on the one hand I'm thinking I should just wait as the GP can't be that concerned, but on the other hand, there is no way I can wait 16 weeks with this worry. So the cost of the scan will be worth it, even if just to save me 16 weeks of worry and give me some answers. Apparently I'll get the scan results there and then. X 

  • Hi, I am also playing the waiting game for a swollen lymph node diagnoses. My lump is in the right side of my neck and has been present for around 6/7 moths but getting bigger.

    I had a GP referral (non urgent) for an ultrasound which happened just over a week ago. The Dr took two biopsies and said that my results would be fastracked and the the hospital would be taking over my care. 

    I have an appointment with the haematology consultant on the 24th and the wait is really starting to get me down. I'm trying to stay busy and distract myself but it's tricky at times.

    Sending you strength and support xxx

  • Hi Rose, 

    Hope you don't mind me messaging! I just wanted to say your positivity is truly amazing! I just know you are going to smash your treatment! 

    Did you receive your final staging/ treatment plan?  Onwards and upwards from here!

    I did want to ask how quickly your node grew/ was it a massive jump? I'm sure mine has gotten bigger over 7 months but not drastically. 

    All the best, Chloe 

  • Hi Chloe, not at all! Thank you xx

    It was a steady growth but it wasn't me that saw it really as I suppose you don't always notice these things yourself! It was my sister and my best friend who noticed the changes between gaps in seeing them who noticed it growing.

    I did get my plan! Chemotherapy starts Monday for 2 months (ABVD) and after a clear PET scan I'll move on to radiotherapy for 2 weeks. Nothing compared to others but, in the words of my consultant, aggressive treatment for a shorter time span works best for my type of cancer.

    I hope that helps but please shout up if not!

    Xxxx

  • Best of luck for Monday, Rose. Will be thinking of you. Hope it all goes well. Thanks again for sharing everything. You're so helpful.xxx 

     

    I have my scan at 8:30 tomorrow. Saw the consultant today who thinks they are reactive nodes. Scan will hopefully confirm this. Xx

  • Thanks for thinking of me xx

    Good luck for your scan tomorrow. I have a new found love and respect for radiologists and radiographers! :grin: 

  • Thank you so much. Getting anxious tonight xx

  • I know it's a stressful. You could try your favourite film or box set this evening? Something comforting that you can half focus on while you try to relax?

    And a nice warm drink always helps me xxx

  • Thank you for being so kind and thoughtful, Rose. I really do appreciate you taking the time to reply. Decided to watch The Apprentice tonight ️ Xx

  • Hiya, 

     

    Im in a similar boat to you all. On Sunday noticed a large (golf ball sized) lump behind my collarbone, and subsequently found about 3 more smaller pea-sized lumps in the area. All are very hard, not sore and sligthly moveable/wiggle-able. No sore throat etc or any other signs of infection.

    Went to the doctor on Tuesday, had bloods taken that day and was referred for 2WW. 

    Got my letter today saying I've an appointment at the hospital ENT department on the 7th - does anyone have any idea what to expect from this appointment? Will they likely take a biopsy? I haven't had ultrasound etc done as the doc wanted me to be seen ASAP. I've also had itchy legs for the past month and occasional infrequent night sweats so I am quite worried it might be lymphoma. The next 10 days waiting is going to be extremely hard :( 

  • Hi All

    Quick history - all my life I've had tonsillitis twice a year. The doctor refused to take them out when I was a kid and told my mother they were doing what they were designed to do and would save me from other illnesses. 
    Fast Track to 2020, aged 50 and after the last bout of tonsillitis my glands don't go down like they used to. I just put it down to Covid anxiety and carry on - even letting friends touch them as a party piece!! In spring 2021 my doctor rushed me in for a CT scan as she feared a blood clot after the Covid vaccine (all clear). When I went back to see her afterwards she just asked if there was anything else worrying me and I mentioned the lump in my neck. Within 4 days I had the camera investigation, then an ultrasound and needle biopsy on what was actually 2 large lumps, and then nothing for over 3 weeks until a phone call telling me I had an appointment 3 days later. After that it was a whirlwind of scans, blood tests and biopsies,  after which I was told I had Stage 2 cancer in the base of my tonsil (under tongue) and in 2 lymph glands. Surgery not an option so within 3 weeks I went into 7 weeks of daily radio + 2 blasts of chemo. I finished formal treatment at the end of October and now it's doing what it needs to do in my body until the end of February. 

    My Oncologist told me she was confident of a cure but there would be side effects of treatment. As it stands the worst side effects have been loss of taste and inability to eat/drink certain foods due to low saliva levels. I am also experiencing slight lymphedema swelling in my neck which I need to manage by massage, diet and exercise. Overall I've been nothing but blown away by how clued up the specialists are on all things throat and lymph related and that has been very reassuring.  If your results show that you need their help, then I can assure you that you will be in safe hands.  

    I know I'm very lucky that the medical teams involved with my case were super efficient, and if I'm honest I haven't really had the time to think about everything - until now. The worry I am going through now is for the end of treatment PET scan. Only then will I know if it worked. 
    I'm obviously not sharing this worry with the family who have already been through enough. 

    I am naturally quite control freaky, but made the decision at the outset that I had to step back and trust the specialists - and keep away from Dr Google. My exact words to the Oncolgist were that I would give her 80% of myself to complete the science bit, but the last 20% I would reserve for myself to fight along the way. She corrected me by saying that the numbers needed to be reversed, and in fact 80% of my recovery chances were down to me, my determination and how I looked after my physical & mental health. 

    It's been hard at times because the anxiety tried to sneak in, but I would put some music on and have a boogie, go for a walk or something else that made me happy, and that seemed to help push it backwards.  

    In all honesty the anxiety will never go away, whether it be the testing, treatment or recovery phases, but it can be managed so it doesn't take over your life. The most important bit to remember is that you are still YOU. Whilst you are Patient Ref X to the medical teams, it doesn't take anything away from the person you have always been. Try and enjoy the usual things as much as you can, and this might help alleviate the anxiety a bit. 

    Best of luck to everyone in their tests and treatment. Trust the science, but most importantly have faith in yourself and your strength to beat whatever is put in front of you. You will be amazed at how strong you really are and it will genuinely change your life. 

    xx  

  • Hiya, just wanted to see how your ultrasound went? Hope it has reassured you? Xx

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