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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
Thanks Finita and Pollyanne58 for your lovely comments. My Son (who is now 40) has A.D.H.D. and his Doctor used to tell me that I was a very strong Woman because he said most Women would turn to drink or drugs in the same situation but that I just kept on going. Until then, I never thought I was because I am very quiet and felt insignificant. I can be determined and stand up for what is right and have been told that I am strong a couple of times before. I just look for the light at the end of the tunnel., never thinking of giving up. I guess it's a good thing. Thanks for my prayers. I am disassociated from my Siblings for religious reasons, but I am very fortunate to have a lot of good Friends and the support of all you lovely Ladies as well. I do miss my Siblings and love them so much but I can never go back to something that I lost faith in growing up. So, thank you all for being there and listening to all my troubles. I really appreciate your support and am here with a listening ear if you need to vent at any time. Love, Ruth xx
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Hi Ruth,
I just want to say that you are a true inspiration to us all...here you are with your back ache , no energy and still socializing with your friends under such incredible circumstances . You are a pillar of strength and very appreciative of your good fortune for having such good friends and family , it is no wonder that God is looking over you ...you are beautiful ! . I will also be asking a favour of our Australian Saint Mary Mackillop ( Mary of the Cross) to pray for you and all of us BC sisters. Myself like your cousing always feel an inner peace after praying .
All my love
Finita xxxxxxxxxxxxxx
Sign in to react to this post - Pollyanne58MemberRuth sometimes what we are dished up doesn't seem fair but they say we are never given more than we can deal with so that means that you are a very strong woman. My thoughts are with you and all the other lovely Ladies on this site. XxSign in to react to this post
- Pollyanne58MemberRuth sometimes what we are dished up doesn't seem fair but they say we are never given more than we can deal with so that means that you are a very strong woman. My thoughts are with you and all the other lovely Ladies on this site. XxSign in to react to this post
Hi Finita,
Thanks for the encouragement. I know that God has been with me along the way. My Cousin has been praying for me and feels very peaceful when he does. I am finding it hard with my back ache and no energy but at least I am still able to socialise with my Friends. If I was housebound it would be harder to cope with. I am so fortunate to have good Friends and Family and the Friends on this site. It has just been a bit overwhelming with everything going on but I know that God will me the strength to carry me through like he always has. Love, Ruthxxx
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I want to thank you all beautiful ladies for making a difference in my life by making me feel that "I do matter " I am already feeling so much better ...thanks a million again .
love you all
Finita XXXXXXXXXXXXXXXX
Sign in to react to this post - finitaMember
Thank you so much Pollyanne and yes, I will be doing as Kathleen suggested and will be talking it over with my oncologist . I am very happy for you spending beautiful and precious time outdoors in your motorhome ...as for the flies...don't forget the 'Aerogard !!! lol .
my love to you
Finita xxxxxx
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Hi Kathleen, I hope that you are doing well . I am taking your advise and will be talking to my oncologist about it on the 30th of june when I will be having my other test done. Will stay in touch and thank you so much,
all my love
Finitaxxxxxx
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My darling girl, what can I say, except that you are really pretty much full on with so mcuh and the double whammy really tops it . I really do wish you all the very best with your left kidney .and with your breasts surgery . As for having a colonoscopy done yearly, that is not so bad ...I had it done too and found to have diveticullum disease . Continue to feel positive among all the negatives and be strong . I wish you all the very best and may God give you all the necessary strength to see you throught it all .
my love to you
Finita xxxxxxx
Sign in to react to this post Finita, I can not believe that they wouldn't do your gene test. I know the Government is tightening up on Health. I was sent there by the Hospital as I had just lost my Mum and other Family members. I was tested for Lynch Syndrome as I lost my Father and my Brother has Bowel cancer. I recieved the results on Wednesday and found out that I have this mutated gene as well as Braca 2. A double whammy. I was very upset to get the results because I thought I was fine. Now I have to have colonoscopies every 12 Months. On top of that I only have one Kidney functioning and there is a large cyst with hydronephrosis on my left Kidney. As well as seeing the Urologist and having tests, I am awaiting propalaptic surgery on my breasts. Thankfully, I have had my ovaries and uterus removed so that solves that problem. It has been very draining and I will be glad when it's all over but at least I am still here.
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