PEG Nasal tube

FormerMember
FormerMember
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Hi newly diagnosed base of tongue and large lump in lympnode have been told after MDM will be having chemo and radiotherapy do all head and neck patients have a peg or nasal tube I reall don't no what to expect any advice thanks.

  • Hi Bradlou,

    i have had both an NGT and a PEG. I don't know about everyone else but I would go with a PEG any day. It is certainly better if you end up needing it for a longer period.

    good luck.

    Clive

  • Hi this is Hazsl I am 11 month post radiotherapy for Ron’s I’ll cancer with affected lymph nodes I had the naaal tube fitted week 3. I have a blog detailing my experiences 

    www.radioactiveraz.wordpress.com

    have had a lot of people comment how much it has helped them just remember we are all differently in Hiw we react.

    keep in touch

    Hazel 

    Hazel aka RadioactiveRaz 

    My blog is www.radioactiveraz.wordpress.com  HPV 16+ tonsil cancer Now  6 years  post treatment. 35 radiotherapy 2 chemo T2N2NM.Happily getting on with living always happy to help

    2 videos I’ve been involved with raising awareness of HNC and HPV cancers 

    https://www.instagram.com/merckhealthcare/reel/DBs8Y0niJ8N/

  • FormerMember
    FormerMember in reply to Clive_r

    I think it depends on the exact location of the cancer and the location of the radiotherapy.

    My OH had left tonsil cancer and spread to left lymph node... nearly five weeks through radiotherapy and he is still swallowing ok, he has not had a PEG fitted.  I think also it will often come down to where you are treated and their treatment protocols.

  • Excuse typos should say tonsil cancer oops 

    Hazel aka RadioactiveRaz 

    My blog is www.radioactiveraz.wordpress.com  HPV 16+ tonsil cancer Now  6 years  post treatment. 35 radiotherapy 2 chemo T2N2NM.Happily getting on with living always happy to help

    2 videos I’ve been involved with raising awareness of HNC and HPV cancers 

    https://www.instagram.com/merckhealthcare/reel/DBs8Y0niJ8N/

  • FormerMember
    FormerMember in reply to Clive_r

    Thank you for reply Clive r

  • Hello Bradlou , I have never had a NG tube but have had a PEG for a few years now , I think the peg is more discreet and easier to use and once its in it will not come out where as the NG tube can get caught and restrict you movement . Some people do not get offered a PEG so it is worth discussing it with your consultant before the treatment has started as they don't normally fit one half way through ,this is where the NG  is normally put in as its quicker and no minor surgery is needed . The amount of people who have regretted not having a PEG  fitted is quite common so I think its a decision between you and your consultant  but don't leave until the last minute . Please re-post if you have anymore concerns or worries during treatment , take care and best wishes .

                                                                                                          Chris 

    Its sometimes not easy but its worth it ! 

    Community Champion Badge

  • FormerMember
    FormerMember in reply to RadioactiveRaz

    Thank you hazel for reply .

  • FormerMember
    FormerMember in reply to chris2012

    Thank you Chris.