Those of you sensitive to Codeine I'm wondering if you've tried half dose Co-codomol & adding 2nd half of the dose an hour or so later??
I ask as I too have problems with codiene - weirdly less problems the with morphine I have on repeat, though I don't like really it & do find it can make headaches worse, though again I found taking half dose worked better for me, some pain relief & able to cope as not as woozy etc, though still gives me a temporary headache
I had a fall last Oct, cracked a couple of ribs - @ the damned hospital of all places
- A&E gave me co-codomol 500s for it, which was a Godsend at the time & weirdly I realised they actually help with my migraine too :) - nothing else i can tolerate does, but did leave me spaced out, but not so bad as the other drugs I have - I've now found splitting the dose as above gets passed the side effects & still gets me pain relief for general aches, & some nerve pain & migraine
Diazepam works best for me on muscle spasms & takes the edge of the TOS & other neuro pain too
I too am not keen on taking drugs, especially as I've already damaged kidneys, so manage as naturally as possible & keep drugs as a back up for when I want to get out & about & do stuff, takes the edge off so I can be more active - I do rely on Ibruprofen on a morning though :( not keen on that, but sinus swelling leaves me with real groggy tender head which again feels swollen as do my arms etc & effects my balance, vision etc, so I have to take a couple early in order to be in any state to even manage the short school run
I do find things like clary sage aroma oil, Epsom Salt & black pepper & ginger baths, paingone pen for localised pain, oxygen for cluster headache, tens machine for back pain, magnesium & riboflavin(vitB?) for migraine, & MLD massage & PMA can all help me cope as naturally as possible,
I now realise my old attitude of desperately trying NOT to take any drugs was a mistake, Pain itself is a stressor & stress in my case causes BIG flare ups
(shite for an ex adrenolin junky like me, but c'est la vie
)
& helibea I had to laugh at your comment as regards your Kids - when I was first ill & not knowing what or how to deal with it & dealing with a lot of stress, DD was vey young - I lost my voice almost completely for over 6 months
M.E. still badly affects my throat/throat muscles in a flare up
- I was shocked that DD EVER learnt to talk - let alone be a very early talker
- she did a lot of finger wagging & scowling though - as that was the only way I could keep her in line & let her know something wasn't allowed/dangerous etc - she still wags her finger if she's telling anyone off now - & she's 8!! ...LOL