Hello

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Hi all, I've just joined up so I thought I best post a message here first.

My lovely wife is going through a tricky patch at the moment and we're currently in the position of waiting on CT results.

Flu like symptoms started began around march this year - a cough, very tired and she struggled to breath. She recently started working for the NHS so we put it down to her catching various bugs from the wards.

3rd of may I had to take her to a&e as she more of less collapsed after a shift on her ward. She couldn't get up a flight of stairs. They listened to her heart, checked her bloods and sent us on our way saying she was anaemic but the rest checked out fine. No infection was identified. The next day we visited the GP who prescribed iron tablets and pain killers. 

Shortly after this incident she started having pain in all her joints, unable to walk upstairs. Back to the GP who eventually prescribed codeine, did further blood tests (lupus and RA I think). 

They initially put the cough down to remnants of the flu but 1 June the GP referred her on for an x-ray of her lungs and a spittoon (not sure if thats right name). He did say he wasn't expecting anything to come back. 

Whilst on holiday we received a call from the GPS receptionist to say she did have an infection which was called haemophilia influenza? We managed to get hold of antibiotics in Spain and this was a bit of a relief as we thought that would sort everything out. The following day the GP rang again and said the x-ray had come back and had showed very large lymph nodes and I think he said nodules on the image. I can't remember if he said very suspect but it wasn't something we were really prepared for. 

Annurgent CT scan was made and she attended this yesterday (the day after we arrived home). 

So here we are, as many of you will know - full of anxiety and worry not knowing what is going on. My wife has been complaining of chest pain and stabbing pains in her lymph nodes. We're hoping it's just a nasty infection but have to be realistic. 

It is a struggle to hold composure for her as I do tear up when I stop. My wife is only 31 and we have 2 children under 7.

Ayway, writing this has helped me somewhat already but I just don't know how long we will have to wait now. I know they have Dr striking at the moment so I'd imagine it may take longer. 

Thanks for reading 

  • Hello Mnts3

    I am sorry to read about your wife being unwell and having to have all these tests. I can understand how worrying it is and how the waiting to find out what is causing her symptoms is. Naturally you are concerned as you are parents to young children. 

    I hope that she does not have to wait too long for the results of the CT scan that was done yesterday. Hopefully it will give a clearer picture.

    I know what you mean by writing down your worries helps in some way- I felt the same during my cancer treatments. 

    Please let us know how you both get on and we are here if you need any support. You just need to ask.

    If you feel chatting to someone would help then may I suggest giving the Support Line a call. They are lovely on there.

    Jane

           

    Macmillan Support Line - 0808 808 00 00, 7 days a week between 8am-8pm

  • Hi,

    I hope you get the results back very soon. I do find the waiting so hard.

    My husband had a CT scan and MRI scan and we waited about a week for the results.

    Unfortunately we had the news last week that he had baowel cancer and we are now waiting for the referral appointment which seems to be taking forever.

    How are you both? Try to keep as busy as possible (although it is hard not to think about it)

    We have a 14 year old who is a very big distraction!!

    Good luck and keep us posted.

    Kell x

  • Sorry to hear that kell and I hope the appointment comes through sooner for you both so you can focus on the treatment. 

    You are right, kids are a great distraction so there is that. We're doing ok thanks - just playing the waiting game now. For me it's the uncertainty that is the most difficult.

    I think I've very quickly tried to come to terms with what could be. I'll make sure to use places like this for support when needed and like everyone has to, deal with whatever it is by helping my wife. 

  • So we spent most of the day in a&e today. My wife had a few new symptoms last night so took her straight to the hospital. This was a good thing as it's meant we have fast tracked the CT analysis of her lungs.

    They've told us it's either sarcidosis or lymphoma. So we're seeing lung Dr on Monday to arrange a plan and discuss the CT scan. She been made a opthalmology appointment for Tuesday to have a look at other visual issues.

    At least the diagnostic is moving fairly quickly now but hoping for good news. 

  • Hi  I am Mike and I help out around our Lymphoma groups. I just noticed your post so If it is a type of Lymphoma your wife has we have a number of groups available for you and your wife to get support.

    There are over 60 types and sub-types of Lymphoma so we can’t have a group for every type but these are our main Lymphoma groups below.

    Hodgkin's Lymphoma

    General Non Hodgkin's Lymphoma

    Follicular Lymphoma

    Diffuse Large B-Cell Lymphoma

    Mantel Cell Lymphoma

    T-cell lymphomas

    CLL, SLL, HCL

    These are safe places to talk to others with a similar diagnosis, treatment experience, to ask questions and get support.

    I was diagnosed way back in 1999 at 43 with a rare, incurable but treatable type of Low Grade Non Hodgkin’s Lymphoma eventually reaching Stage 4a in late 2013 so I do appreciate the challenges of the journey rather well but I will say that my last treatment was back in 2015 and I turns 67 last Nov and am living a great life.

    Mike (Thehighlander)

    It always seems impossible until its done - Nelson Mandela

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