GAGWTA!!
Happy weekend to all, esp Laura and DH at the BC!!

Hope there are no ill effects from the fall!!
I feel like a wuss complaining, especially when others are in much worse situations, but I just want to "unload" and move on....
I feel as though I'm 91 not 51! Shortly before my RFTC trip, my left wrist bothered me, felt like a bruise on the inside edge of the wrist joint, but nothing visible. It got worse, such that the thumb hurt and with certain movements there were shooting pains radiating into the hand and up the arm. Went to my new PCP for the first time (my old one left and a new one took his place--this doc had been there before my time and left and then returned to replace mine, who I really liked

) He diagnosed it as deQuearvain's tendonitis, gave me some presc Naproxen, exercises, and told me to ice and wear a wrist/thumb brace esp at night. It improved with that over the following several weeks though I still have twinges with certain movements,nothing like before. But now the right one is a little sore....I'm being careful and exercising that trying to head it off. Now, for the last week or so I have had lowback pain esp towards the right side/right hip....again with no known trauma or overextertion

That's improving with self-care and no trip to the doc. I was e-mailing with my sister in Co, and the one here who had the phyllodes and pneumothorax.....they both recently were found to be severely Vitamin D deficient and told me to get checked for that, and it apparently can cause joint pain

So on top of my "usual" fatigue and the sore feet/ankles each day until I get "loose" I have been having a pity party. And getting depressed when I go the msg boards on Breastcancer.org and read of some women's side effects from the hormonal therapy

I want to chalk some of this up to normal aging, but thinking having almost 2 more years to go onthe HT clinical trial is getting me down sometimes. And I need to schedule my annual physical with the PCP soon, and hope that he doesn't think I'm nuts for wanting the bone density scan every year (instead of every 2 which is what they "usually recommend, even when I tell them an aromitase inhibitor,which is likely what I'm on in the trial, can accelerate bone loss) and will probably have to beg for the Vit D to be checked too......unless the onc chekcs that in the every 6 months labs, I guess I should call there first and find out. OK, if you're still with me....thanks for reading my whiiine, please pass the cheese and crackers

I feel better now!