Trigger Finger/Thumb exercises
I've found a Youtube presentation that explains how Trigger Finger/Thumb occurs & some rubbing & exercises that may help it. https://www.youtube.com/watch?v=V0FfMzemLnU The info from the 2min 20sec mark is more about locating the nodule at the base of the thumb/finger that is restricting the tendon from working smoothly - and how deep tissue massage may help to help break down the scar tissue. This is very similar to what my husband has done in the past when he gets a running injury - he will give deep massage to the muscle, to 'free it up'. I found that I have quite a BIG nodule at the base of my left thumb - it is much smaller on my right thumb. I started the rubbing of the nodule quite aggressively yesterday & I am surprised to say that it already feels 'freer' today! I still can't bend the thumb tho the pain is less (the magic oil may also be helping here too!) - so I am stretching it & forcing it to bend as well, to try & free it up more. Good luck - it is definitely worth a try!
Counterpart
I attended a Cancer and Wellbeing day run by Counterpart this week. We did Feldenkrais, some light aerobics and theraband work, Qi Gong and a fantastic deep meditation. There was a very good lunch and lots of time to chat and connect with the other participants. For Melbourne and Victorian folks (they're running a wellness day in Gippsland later this month), if you haven't heard of Counterpart check them out. They do all sorts of workshops and seminars. The events I've attended have always been very well run and they are free. Their new calender is coming out soon but there are also several events on in the rest of April. https://www.counterpart.org.au
Well meaning..but not helpful (for me)
I've recently been diagnosed. I let the initial shock subside and embraced that part of my brain & personality which is about process and planning rather than panic. So lots of information gathering, talking with close friends and contemplating available choices & options. At this point I am sure of my treatment decision. However one friend in particular has responded by insisting she will help 'cure' me through a range of naturopathic potions, powders & pills. Additionally, she suggested I have not looked after myself in terms of diet and exercise. I do have some appreciation for natural remedies, and as I have a lifelong disability I have always taken care of my nutrition and well being. Whilst I think her approach is well meaning, it's not helpful or respectful. I don't have any family, live on my own and so my close circle of friends are important. But I need to focus on my decisions and choices without gestures and comments that are intrusive or not supportive of my own path. Any advise is welcome, thank you.
The things people say
Someone posted this link on fb. Enjoyed it and sharing for you all. 3 weeks ago someone suggested i juice 8 times a day, especially carrot juice. Ive been given crystals, essential oils. I was warned by well meaning friend about chemo - err sorry I said, Id like to give myself a chance. Someone else said to me "if you ever need go talk....i have a friend who had breast cancer 10 years ago, actually she has died". Bit of a conversation stopper. What are some if your real liffe conversation killers? https://m.youtube.com/watch?v=mKovm8HINjI&noapp=1Early Days on Letrozole
So, I started taking Letrozole on the 1/6/18. My oncologist says I have to be on it for 10 years as several ongoing studies are indicating cancer preventing benefits beyond the seven year mark. It's a watching brief though, so I'm prepared that the advice might change in this time. Three days after starting it my ankles started to ache. A lot. It got worse and started to wake me up at night. Whether I exercised or not didn't make any difference. I took some osteo-panadol for when it was really painful but I didn't fancy living on that, so on the advice of many people here, and my oncologist, I started taking krill oil. Within a few days the pain was down to a manageable level. Hooray! Three weeks later though the ache ramped up. At exactly the same time my hot flushes, which had subsided to a bearable level after chemo, suddenly got a lot worse. Longer, stronger and now with extra bonus sweat! I persisted with the krill oil for another week but there was no change. So in my personal clinical trial, I came off the krill oil for a (painful) week, and then started magnesium. Again on the anecdotal evidence from the good folk here, many of whom say it helps. I also had a foot, ankle and lower leg massage at one of those mall massage joints on the same day as I started magnesium. It was utter bliss having my aching ankles worked on! Something changed, because again the ankle pain subsided to a bearable level. Now whether this was something to do with the massage, or the magnesium, a combination of both, or my body simply adjusting to the rapid withdrawal of oestrogen, I simply don't know. My oncologist says no evidence that magnesium works on anything other than cramps. However I'll keep taking it for a couole more weeks and then stop. I'll observe what happens and then, if the pain returns, I'll move on to the next thing in my 'clinical trial', which is curcumin. The onc says her patients have reported success with that. There'll be a magnesium spray test at some point as well! My ankles still ache but it's at a lower level at the moment. All our bodies are different, der, but I thought I'd share my experiments in managing Letrozole side effects. It might be useful to someone! K xox
