Concerned about the side effects of anastrozole

Unfortunately yes. I was diagnosed with plantar fasciitis 3 yrs. ago and still have it today. I did get some relief from taping for a period. I did all the exercises and even got the injections which lasted about 6 months. I took endocrine therapies for quite a few years, over 10. Interestingly this started as well as a few other annoying issues after I quit taking it. I always like to say, “I am still here to complain about it”.
Have any of you tried anything, that seemed to help? Has anyone tried any shoe inserts?

Oh sorry to hear that and hope it gets better now that you're taking a med break. I guess I will get a podiatrist appointment since my home remedies aren't cutting it. Thanks for sharing your experience.

I had similar but am not a runner. I’m an outside Walker or treadmill Walker but did it regularly 3-4 times a week. After 5 months on Anastrozole ( started July 2020, metastasis to my bones) I had the same
Thing, feel like plantars fasciitis on my left foot. It is finally better after 10 months but I still have some pain from time to time. Now it is starting on my right foot along the side (different position on the foot but same pain) Ugg! I were Crocs instead of slipper in the house and running shoes with a very cushioned insole and that makes a big difference. I also had some hair loss (I think one person who responded to your message spoke about hair loss) and now in the past three months it is starting to regrow and I have all these new baby hairs so that is encouraging. I think all of those side effects unfortunately are normal. As long as the medication’s are doing what they need to do, and I pray they are, the rest I will manage and I’m sure you were all the same. Stay strong ladies you are warriors!

YES !!!!!! Meeeeee!! I was on tamoxifen for 9 mos and one day I felt like I had small golf balls on balls of foot. I can’t wear heels any more or walk barefoot in my apt. Went to podiatrist and he diagnosed me with metatarsalgia , finally after too many side effects , dr took me off. We might try something new in January I am still in pain

Hi. Any runners out there on Anastrozole? Been running for years, decades, but stopped for a few months. Started training for a race and quickly developed very bad plantar fasciitis and other foot pain too, haven't gone to podiatrist yet but feels like could be bone related too. It's been about a month and still bothersome. Wondering if possible foot bones were weakened from Anastrozole but only been taking about 4 mo. Doesn't help that I gained about 10 lbs in last 2 years! Any one else have foot issues post med ? Thanks.

How are you doing today? Are you on any other AI or have an my reoccurrences? I pray not.

I was diagnosed with metastatic breast cancer in August of 2017. One sentinel node was involved and 2 axillary nodes. I had a right mastectomy and all axillary nodes were removed. Radiation was proton beam therapy over a three week course. Oncotype testing gave me a “1” rating which is extremely low therefore chemo was not necessary.
I started taking Arimidex or Anastrozole since December 2017 and side effects have been mild. My main complaint has been fatigue however I had 4 surgeries in 2 years which I felt factored in to the equation. I had frequent hot flashes which have subsided. I’ve had normal hair loss which it sounds may be a bit unusual. Fatigue is my main complaint but I’m willing to take Anastrozole if it will help me stay cancer free

My heart goes out to you. Best of luck finding relief on this journey.

Deloris this just sound awful, I am not familiar with (ACDF) but it sounds as if your pain might be related to that. I am going to post a link to a neuropathy group that will likely have some better information for you.
https://connect.mayoclinic.org/discussion/non-opioid-alternatives-for-chronic-peripheral-neuropathy/

on the 14 October I had (ACDF) to remove damanged disks. Now I have ALL of the above , full body nerupathy pain etc. as the above person .It started one morning with a cramp in the back of my left leg.I am only taking Gabapentina 300mgs at nights I am due to see the Neurosurgeon oth Monday 20th December I have had no releif since this started 2 weeks ago.Any advice will be welcome.It is the worse pain ever