Forum Discussion

DAR_Travelbug's avatar
13 years ago

Femara and Crestor

I joined this blog today as I am looking for answers about the joint pain, lethargy etc I have been feeling recently and I am starting to think its a side effect of Femara or Crestor.  Off to the doctor I go tomorrow to  discuss whether I need to change my medication.  I read a lot of posts about fish oil - are people finding relief taking this? 

I am nearly 5 years post Grade 3 IDC - three surgeries and large amount of lymph nodes removed, chemotherapy and radio therapy.

It feels good to be so close to my 5th year anniversary - its been one hell of a journey and not all bad in so many ways - I think you are forced to re-evaluate what's important and you can't help but grow from this experience.   I have mixed feelings about being cut loose by my doctors - a little scary as well as feeling good to have beat this.

17 Replies

  • Hi Dar Travelbug/Friends

    I was pleased to hear your comment about Femara. For months now I have been having terrible pain in my feet and ankles and days when I can hardly walk. The Doctor said Planter Faciitis. Strangely enough I have been reading up on this subject from women who have Bone Mets and they say surely we all can't have Planter  Faciitis.I would love to hear from anyone if they have experienced the same pain in their feet. I still take Femara, Xgeva and Vit. D.It just takes the life out of me as I hesitate even to play nine holes of golf or go shopping.I think I would be relieved to just have someone say it could well be the Femara. Thank -you morry

  • Thanks for coming back to me Jill - I might get onto the fish oil - it can't hurt and if it helps blood pressure that's got to be a good thing.  All the best to you, kind regards from Deb xx

  • Hi DAR Travelbug,  Joint pain and lethargy sure are side effects of Femara.  I have been taking Femara since February 2010 and still suffer these side effects.  I do take Fish Oil as well which I really started to lower my blood pressure but it has made a little difference to the pains, mainly in my legs and feet.  It is 4 years today since I was diagnosed and like you I will be feeling a little edgy when I reach my 5 year anniversary.  Best of luck in the future,    Jill  xx