Bad feet

Hi

I've been on tamoxifen for the last 6 months and have noticed this week that my hands ache, mainly my finger joints. I'm also on prostap injection.

Does anyone else's feet ache? Mine feel like I've been running every day, last time I ran was in February. They feel bruised, the only word I can describe the sensation.Too scared to go running in case I fall over.

Any help or just to know I'm not on my own in this XXX 

 

  • Hello Love_Life, 

    A big welcome to our forum! I am sorry to hear that you have suffered these side effects and that your hands and feet are aching at the moment. I hope that you will hear from others on the forum who have experienced this before. We have information on our website on Tamoxifen side effects which you can find on this page and you can also find out more here about side effects which may be linked to the Prostap injection. But to determine which one of these drugs may be affecting your hands and feet and giving you pain in your joints, it would be a good idea to ring your doctor and discussing it with your GP or specialist. They will be able to tell you more about this and hopefully to tell you whether there is anything they could suggest that could help you with these pains. Do mention to your doctor that this is having an impact on your ability to go for a run. 

    I hope you feel better soon and that you can get back to running soon!

    Best wishes, 

    Lucie, Cancer Chat Moderator

     

     

  • Hello Love-Life,

                          one of the downside effects of chemo can be neuropathy of hands and feet.For most it is temporary and will go after treatment ceases,but for a few(1-2%) the nerve endings are permanantly damaged leaving lack of sensation and pain behind.l realise that statement sounds contradictory,but you cannot get initial feeling of touch,so tripping ,stumbling and a general unawareness of where your foot actually is,combines with a painful tired foot, that yes like you say feels bruised and sore.

                                                                                As has been suggested by Lucie,make sure you raise your issues and fairly strongly with your treatment team,as the drugs can have a culmalative impact and it might be possible to modify your treatment level to counter those effects.After my treatment l have since read that certain people are predisposed to this and a test has been developed to identify those at higher risk of permanant damage,which may not have been available at my time,or the option for modifying my treatment was just not there.

                                                                               In my case l just have to get on with it and hope for soft landings when l fall,and after 5 years l can manage a laboured trundle for 50 metres at a time Given the alternative l was facing, a price paid that l cannot really complain about,although really better to avoided if at all possible,

                                                                   Hope this helps and it gets better for you