Hi all.
my father was diagnosed with lung cancer 2 weeks ago- found out since biopsy it’s adenocarcinoma in 1 lung and lymph nodes.
wondering if you could share your diagnosis journey (it’s hard to know when things are taking too long? Or moving fast? Do we go private or stay NHS?) still waiting on bio marker results to tell us treatment plan. What questions should we be asking?
wondering if you could also share any medications or remedies for the cough. Luckily it eases when he lies down but it’s v irritating him in daytime. Did this ease with treatment?
thanks for any help.
Of course , I had 6 weeks combined chemo and radiotherapy so chemo once a week and radiotherapy every day Mon -Friday … I had some issues week 2-3 when I had a reaction to one of the chemo drugs it was sorted pretty quickly though …, side effects chemo , days 3-5 each week some nausea and generally unwell and radiotherapy fine first 3 weeks then some burnt skin on chest and back remedied with creams , sore windpipe and fatigue which has continue after treatment but I’m only 2 weeks out of treatment so to be expected … I was told 4/6 weeks before I started to feel any improvement and perhaps longer for the fatigue to ease … it’s a tough regime but doable …. I get an initial scan on Friday …hope this helps … but remember treatment plans and side effects are very different for everyone… . Elly x
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