Forum Discussion
ellen
14 years agoMember
Arimidex
I have been reading through the blogs about Arimidex and found them very interesting. I have been on Arimidex for 6 months and up until 4 weeks ago, "side affects free" - until now that is.
I now have what appears to be the usual aches and pains in the legs and numbness in the hands, tiredness and headaches, so I guess I didn't escape at all I am just like all my other Arimidex sisters.
I will have to mention this to my oc next visit, but as so many others have said before at least I am here reading the experiences of others. It does help.
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244 Replies
- Bella314Member
thank you so much finita! and I apologise for not replying sooner; I find it a bit confusing to work out which messages I have replied to. I am very grateful to be here, and just enjoy every single day. xx
Sign in to react to this post - Bella314Member
Phew! thank goodness it was just a lipoma; but it shows just how it's never far from the back of our minds that every ache, bump, pain etc .. might mean "it's back". take care, bella x
Sign in to react to this post - Bella314Member
it doesn't hurt :) turning 60 that is...
Sign in to react to this post - Bella314Member
Hi Ruth, thank you for your emails and offer of contact, I really appreciate it. I figure I have a bit of time to make up my mind re the masectomy, - hopefully being on Femara will provide some form of protection. I know it would be a relief, but to be honest, I'm just not quite ready to make that decision; I need to talk to some people re their experiences; and I'm hoping to do that at our local support group. I also apologise for not replying sooner; I find the messages I get from the BCNA website a bit confusing, and I think I've replied to everyone, and then find out I haven't! Sorry. I hadn't heard of Lynch syndrome until you mentioned it; you've certainly copped it. I am concerned about passing the gene to my sons, they haven't decided about being tested yet, and I respect their decision, whatever it is. We have a huge history of prostate cancer (which is linked to BRCA1 and 2); so I am worried; but try not to let it overtake. Off to spend a weekend with my cousins, so probably won't be near a computer until Monday. Take care, love, bella x
Sign in to react to this post - Bella314Member
Hi Ruth, thank you for your emails and offer of contact, I really appreciate it. I figure I have a bit of time to make up my mind re the masectomy, - hopefully being on Femara will provide some form of protection. I know it would be a relief, but to be honest, I'm just not quite ready to make that decision; I need to talk to some people re their experiences; and I'm hoping to do that at our local support group. I also apologise for not replying sooner; I find the messages I get from the BCNA website a bit confusing, and I think I've replied to everyone, and then find out I haven't! Sorry. I hadn't heard of Lynch syndrome until you mentioned it; you've certainly copped it. I am concerned about passing the gene to my sons, they haven't decided about being tested yet, and I respect their decision, whatever it is. We have a huge history of prostate cancer (which is linked to BRCA1 and 2); so I am worried; but try not to let it overtake. Off to spend a weekend with my cousins, so probably won't be near a computer until Monday. Take care, love, bella x
Sign in to react to this post - finitaMember
Bella,
don't pay attention to anyone that doesn't understand your happiness or gratefulness , I turned 62 last February and although I never celebrate or even worry about it, it is always good ...it means one more year on this beautiful planet earth . Many happy returns and may you live to be 100 !!
lots of birthday hugs and wishes
finita xxxxxxxxxxxxxxxxxxxxxxxxxxxxxx
Sign in to react to this post - finitaMember
Hi bella,
I am sorry to hear about your results, and as I don't know much about it , what I do know is that the ovaries as well as the breast are usually removed, but you will need to do more research and don't leave any stone unturned. As for my Brac test, they made it very clear that the fact that my sister died at the age of 47, was unfortunate and that there is no explanation, because my mother did survive. Also the fact that on my mother and my father side, all family members lived to old age and no cancer involved that is known ! I have four more sisters, and they said that if anyone of them were to be diagnosed with breast cancer, then and only then will they take my family into consderation. So, I will just leave it at that and pray for the best...in the meantime I just try to go on and forget . Also I still get a few side effect from the arimidex, I have gained 5 kilos but it is stable , and pains and aches but winter is not helping , so I use lots of heat packs . I have recetly been put on Lovan , anti-depressant and anti -irritability...because my moods swings were getting bad...two weeks on, and so far I feel like I just want to sleep for ever but already I am feeling more relaxed, and that is good. Good luck with your research and all the best ...keep in touch .
Love and hugs
Finita xxxxxxxxxxxxxx
Sign in to react to this post - finitaMember
Hi ruth,
I am so very happy for you but do take care and don't over do things ...what a blessing !!
lots of hugs
Finita xxxxxxxxxxxxxxxxxxxxxx
Sign in to react to this post Hello again Bella, I also forgot to mention that I turn the big 60 next Month.
Sign in to react to this post- Bella314Member
thank you
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