putting one foot in front of the other

2 minute read time.

i've had a bad week , health wise. on monday i had the gp out to discuss problems i had with the hospital and she also put me on new slow release pain killers ( oxycontin ).the problems  i had with the hospital are

1 why have they delayed treatment until mid october , this would be 11 weeks from diagnosis

2 how on earth can they expect me to sit in a chair , even a recliner, for 7 1/2 hours for chemo once a week. i can't even sit in a chair for an hour at home

3. why have i been given 3 different desisions on treatment plan from the 3 consultants.

the gp gp got back to me on friday , and said she had contacted the ocologist and was told

1.  they are delaying treatment as it is a fairly complex radiotherapy and it takes this long to set up

2 the chemo is actually an hour long the other 6 1/2 hours is spent giving me saline.

3. the difference in treatment plan is because they all disagree! lol

none of the answers reassure me , not in the slightest . 7 weeks ago today it was my son's birthday and we went bowling , walked along the seafront and had a meal out. today i tried to walk to the end of the road , my little bit of independance going to get a paper. i just about managed to get to the shop , my legs wobbling as i stood to pay . i just kept think of how stupid i would look if my legs went from under me . then i had to try and get home , literally at the end of the road. i never realised how difficult it could be to put one foot in front of the other, i just thought to myself  ' just one more step and i'll be home'.

i made it ..just i think i fell through the door . my partner got me up to bed and i've been here all day. so here i am 9 weeks after i was diagnosed , a long time after i thought they might help me , and i'm struggling to put one foot in front of the other. and the icing on the cake .. i have another 2 weeks to wait before they even start treatment . i feel like they've just left me . i saw my 15 year old daughter today for the first time in a week and even though i tried really hard to look normal , i could see the fear and confusion in her eyes . i look far from normal.

i tried the new painkillers for a while but they just made me more dizzy and wobbly on my feet so i'm just sticking to oramorph and paracetimol. i've asked my partner not to call the doctor , partly because i'm afraid they will rush me in , but i think if i get any worse he will take that desision out of me hands . i can honestly say i've never felt so helpless.

 

 

Anonymous
  • FormerMember
    FormerMember

    hi sammie ,

    sorry you are having such an awful time its just so annoying to hear how these drs leave ppl hanging on a string not knowing whats happening or why ,its a total disgrace they would act so differently if it was their loved ones suffering .......makes me so mad ,to them we may just be a name or number on a list but we are all human with feelings and loved ones and families that need us ....

    i'm thinking of you and hope things improve soon

    big hugs trudy xxx

  • FormerMember
    FormerMember

    Sending you love and hugs, Sammie xxx

  • FormerMember
    FormerMember

    Sammie, if you went into hospital then

    thy would have to do something,you have been fighting this battle for a long time, dont these doctors realise the stress thy

    are putting you and your family through.

    Please dont let them stop you from

    fighting, kick up a stink its your life you

    are fighting for. i really feel for you and

    i wished i could help you but you know

    you have my support and all your friends

    here will be rooting for you.

    Much love Lucylee. xxxx

  • FormerMember
    FormerMember

    Sending love and hugs.

    A xxx

  • FormerMember
    FormerMember

    HI Sammie

    Sorry its all crap at the moment, hang in their I know you are not convinced by the reason for the delay in RT, but the reasons probably right.  It took them 3 weeks to plan mine and that was jus tto my chest.  I can't imagine how hard it must be to plan yours and hit the right spot without causing damage elsewhere.

    Keep your chin, as Sharry says we are all here for you.  Take inspiration from Kezzer

    Love and Hugs

    Carol xx