Aching Lymph nodes

FormerMember
FormerMember
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Hi, this is all new to me but does anyone ever experience lymph nodes that ache or have sharp twinges that only last a few seconds? The mild pain/sensation also moves around. The only node the doc could feel last week was a small node by my collar bone. The nodes started to be slightly painful just after the Lymph node biopsy in my neck. Before that I never had any pains.

Adam

  • FormerMember
    FormerMember

    Hi Adam

    I have enlarged nodes in my groin which twinge and twitch from time to time but I had a biopsy of an enlarged node in my armpit and that is quite painful all the time. I also developed pains that I was sure hadn't been there before my diagnosis.... I did become super aware of aches generally.

    How are you feeling Adam, apart from the node pains? Actually, that's a huge question, I realise. I guess your emotions are still all over the place.

    hugs

    sparkler x 

  • FormerMember
    FormerMember in reply to FormerMember

    Thanks for getting back sparkler. Today is the first day that I haven't cried, so that's a positive thing for me. It's just such an enormous thing to adjust to and all I want is to go back to normal but i can't. I suppose that I just have to wait until living with CLL becomes the norm. I just can't believe this has happened to me x

  • FormerMember
    FormerMember in reply to FormerMember

    You're very welcome Adam and now that you've posted here, others will find you too. It is a huge thing to take in and just takes time. Nick (hairbear) says it's a case of adjusting to a "new normal" and that's exactly what it is really. At first though, it's a massive shock and just a struggle to get through each day. I felt like the ground was shifting hourly. 

    That you've not cried today is progress, even if you cry later or tomorrow; I think between us here, we could fill an ocean with our tears. It is something that you don't ever think will happen to you.

    Have you been told anything about the stage you are at?

    Please feel free to ask anything here, or use this place as a safe haven, where you can let out any feelings you want, no matter how bad. Often, just writing down how you feel can be really helpful. I read your profile and it's great that you have such good support but we're all here for you too.

    hugs

    sparkler x

  • FormerMember
    FormerMember in reply to FormerMember
    Hi Adam, I've just read your profile and want to welcome you to the club we never wanted to join but by doing so have found friends, supporters and people who genuinely understand. I was diagnosed at the end of May this year so coming up to 4 months and can remember the first devastating weeks trying to make some sense of all this. I too have CLL, am on W & W, stage A and am battling the paranoia that comes with this condition that every single thing must be because of IT. But I'm so pleased you have a supportive partner and good people around you. I've stopped seeing the CLL as a separate entity. It's me, my immune system and I've never given up on myself before so I won't now. There are people who have lived for decades with this and masses of impressive work and research being undertaken. It's not just empty belief. And like they say, the only thing stronger than fear is hope. I hope you'll have more and more days without tears. Lots of great support on here Adam. Take care, hugs, Jue xx
  • FormerMember
    FormerMember in reply to FormerMember

    Lovely to meet you Ju, and thank you for your calming words. I think I'll find out what stage I'm at when I next see the consultant on 30th Oct. Until then, I have a bone marrow biopsy and full CT scan arranged. So, on top of not knowing what the stage is yet, the only thing I can keep hold of is that my blood results came back good. So fingers crossed! 

    I used to enjoy a glass of wine or two each evening, but some things I have read on websites say to avoid alcohol if you have CLL. I gave up smoking 12 years ago, not wine too!

    Adamx

  • FormerMember
    FormerMember in reply to FormerMember
    Give up alcohol altogether! Shriek! Glad I missed that piece of advice Adam. Of course you must be guided by medical advice Adam but I take the view that the anxiety reducing qualities of a moderate tipple far outweigh other considerations for me. At the moment. I obviously wouldn't drink during the treatment phase. I'm off out tonight and will be enjoying a few voddies. What are others views on this? Are we all on the wagon now (honestly?). Good luck for the tests Adam, keep us informed. Love, Jue x
  • FormerMember
    FormerMember

    Hi Adam, Glad you've found this group, you'll find lots of support and hopefully some info that will help you in the future. I've been diagnosed for nearly 2 years and on watch and wait. I have a lot of smallish nodes in my neck and find that they do ache a lot at times. I find the wind and cold really makes them worse - so a scarf is a new accessory to my wardrobe. I've not had a biopsy on any of my nodes so can't comment if that makes them painful. My consultants don't seem to be to concerned when I've previously mentioned them hurting - maybe if you're worried you could ring your doctor or nurse - some times a little re-assurance from them goes a long way. Take care Louise

  • FormerMember
    FormerMember in reply to FormerMember

    Forgot to say - I still enjoy a nice glass of wine - not planning of going tee-total yet! Louise

  • FormerMember
    FormerMember in reply to FormerMember

    Oh please please someone tell me I don't have to give up my glass of wine each evening - I absolutely look forward to it and wine is one of the lovely things in life. Haven't heard of this before but must admit to not reading all the do's and don'ts.

    Best wishes to all - has anyone else got the heating on? xx

  • Hi Adam,

    I see you've had a nice warm welcome from our Sparky and Jue and I add my own.

    You will, in time, come to terms with the diagnosis and it will become the 'norm'. I don't think much about it in between hospital appointments. I have a few enlarged nodes but they don't bother me.

    I had a bone marrow biopsy 2 1/2 years ago and it really is nothing to worry about, a bit like having a tooth out, you can feel a bit of 'digging about' but no pain!

    I had been a blood donor for over 30 years before I was diagnosed and very fit and, like many, couldn't believe that I could have leukaemia. I have since diagnosis completed the Great South Run twice and try to keep up with the exercise and as much as possible, an alkaline diet.

    I do still drink red wine but no other alcohol (which is 'acid').

    My haemo doesn't even check me for enlarged nodes, she goes purely by the blood results and how I feel in myself,  which is fine by me.

    As you have heard, there's lots going on in the way of research which you can read about here and at CLLTopics and other sites. CLL Topics is a good place to start and to get to 'know your enemy'.

    I hope, having found this place, you will feel a part of this 'extended family'.

    Best Wishes,

    Mikey