Hormone Therapy

I guess that is good that it is not the drugs causing your sore feet as that means you can stay on them. But I have had Plantar Fasciitis and it is an annoying problem in itself. Hopefully they will get better now you have a diagnosis & know what to do to help them.

I have investigated the settings on my profile and found where to change them so I get notified of replies.

I guess that is good that it is not the drugs causing your sore feet as that means you can stay on them. But I have had Plantar Fasciitis and it is an annoying problem in itself. Hopefully they will get better now you have a diagnosis & know what to do to help them.

I have investigated the settings on my profile and found where to change them so I get notified of replies.

Hi Allicat,

 

No they didn't say how Triptorelin could make your feet sore.  My Oncologist just said that he didn't think Triptorelin would do it but that he couldn't really rule it out.  I have since had a diagnoses made and they have said it is Plantar Fasciitis so good news it is not the drugs. 

Sorry to hear about your headaches I used to have them early on but after a few months they went away, so hopefully yours will too.

 

Hi Blissy

Sorry I haven't replied until now. I thought I would get email notification if there were replies to comments I made but I guess not.

You still have such frequent Hot Flushes - that sounds really annoying. I have been on triptorelin for 7 months and tamoxifen for 2 months. I got mild hot flushes when I started on the triptorelin which had mainly faded but then started again with the tamoxifen.

I am not getting them as frequently now as I was a just few weeks ago, or as badly. They make me feel panicked/unable to cope as well as too warm and they often seem to be brought on by stress or thinking negative thoughts. I usually have just a few a day.

The only other definite side effect I have is a headache which I have had most of the time since starting the tamoxifen.

My feet are somewhat sore but only the same as they were back before I was diagnosed with cancer. I am a runner & tend to have a lot of issues with my feet. I feel a bit nervous about these being made worse. Did they say how exactly the triptorelin could make your feet sore?

Hi Blissy

Sorry I haven't replied until now. I thought I would get email notification if there were replies to comments I made but I guess not.

You still have such frequent Hot Flushes - that sounds really annoying. I have been on triptorelin for 7 months and tamoxifen for 2 months. I got mild hot flushes when I started on the triptorelin which had mainly faded but then started again with the tamoxifen.

I am not getting them as frequently now as I was a just few weeks ago, or as badly. They make me feel panicked/unable to cope as well as too warm and they often seem to be brought on by stress or thinking negative thoughts. I usually have just a few a day.

The only other definite side effect I have is a headache which I have had most of the time since starting the tamoxifen.

My feet are somewhat sore but only the same as they were back before I was diagnosed with cancer. I am a runner & tend to have a lot of issues with my feet. I feel a bit nervous about these being made worse. Did they say how exactly the triptorelin could make your feet sore?

Hi,

Sorry I haven't replied before this but have been really busy with work and getting home late. Yes it is good to find someone else who is on it. I will have been on the Tamoxifen and Triptorelin for 2 years in October. I have really bad Hot Flushes every 40 minutes and night sweats every night. What I would give to be able to have just one good nights sleep!!! I have also in the last 6 months ended up having really bad calf muscle cramps at night although they have improved a fair bit since taking Magnesium. The other weird one is that my feet are really painful to walk on it is like they are permanently cramped my Oncolgist put me on Lyrica to see if that helped resolve the problem which it hasn't so he is thinking we might have to take me off the Triptorelin to see if it is it causing it. How have you been going with side effects so far?

Can you let me know if you egt this as I sent it awhile ago but am not sure it went to you

Hi,

Sorry I haven't replied before this but have been really busy with work and getting home late. Yes it is good to find someone else who is on it.  I will have been on the Tamoxifen and Triptorelin for 2 years in October.  I have  really bad Hot Flushes every 40 minutes and night sweats every night.  What I would give to be able to have just one good nights sleep!!!  I have also in the last 6 months ended up having really bad calf muscle cramps at night although they have improved a fair bit since taking Magnesium.  The other weird one is that my feet are really painful to walk on it is like they are permanently cramped my Oncolgist put me on Lyrica to see if that helped resolve the problem which it hasn't so he is thinking we might have to take me off the Triptorelin to see if it is it causing it.  How have you been going with side effects so far? 

 

Hi,

Sorry I haven't replied before this but have been really busy with work and getting home late. Yes it is good to find someone else who is on it.  I will have been on the Tamoxifen and Triptorelin for 2 years in October.  I have  really bad Hot Flushes every 40 minutes and night sweats every night.  What I would give to be able to have just one good nights sleep!!!  I have also in the last 6 months ended up having really bad calf muscle cramps at night although they have improved a fair bit since taking Magnesium.  The other weird one is that my feet are really painful to walk on it is like they are permanently cramped my Oncolgist put me on Lyrica to see if that helped resolve the problem which it hasn't so he is thinking we might have to take me off the Triptorelin to see if it is it causing it.  How have you been going with side effects so far?