January 1st I was horribly cold. Went to the gym with hubby on the 2nd (I wipe down machines before and after my use with antibiotic wipes that the gym has on hand for same purpose). I was feeling a little slugglish, but kind of threw it off. I did weights and a bit of the rowing machine. Saturday the 3rd I woke up with a horrid chest congestion and cough, which moved to the sinuses and basically kept me down for two weeks. I missed the first week of yoga due to the crud.
Then the 'ta da' feeling and I was feeling awesome last week. Woke up the 11th and I could breath and not cough every couple of minutes. I got out of the house, ran some errands and then Friday I hacked again and thought. oh no. I made an appointment with my doc for this past Monday, the 19th, and glad I did. I had to see her for that and something else we discovered Friday night. Doc fixed me up with an RX for a sinus infection! . . . and I go back on Monday for something unrelated to that. Tuesday, the second day of the RX I was feeling SOOOO much better. It was like awakening for the first time in weeks. It was like knowing recovery after a gluten attack. It was like sunshine, and daisies, and butterflies. (cue the trumpets and harps).
|Like a big sunny, happy, sunflower.|
Needless to say, I was wanting to get back to running, but decided I should still be taking it a little easy and easing into the program again. Yoga two days last week in class, two days this week in class and I thought "I think I'm ready". I was actually planning to run yesterday after yoga, but then we did the pigeon pose and I've been told not to run after doing those hip opening/flexing positions.
Today I got dudded up in my purple pancreatic cancer fighting clothes. Purple Athleta pants, purple (ahen) Lululemon tank and got on the treadmill during The Price Is Right. I walked during the show and ran during the commercials. Sounds simple. Sounds easy. WHOA. Hard stuff and I wasn't even running fast. Definitely going to take time to come back from the days off of the feet and hopefully it won't take too long.
|All red in the face after just a few running moments.|
|ARGH. What is THAT??!!!|
Showed it to the doctor (you know, they just *adore* when patients go in for one thing and ask them about a gazillion other things while we're there and their appointment goes from five minutes to thirty minutes!), and she said, "it's not fungus, come back next week and I'll remove it for you and send it out (to see what it is).
Here's the thing I just learned at the beginning of 2014 thanks to a Facebook page for my #1 illness, Colitis, that thanks to the medication I'm on, the infusion I get every eight weeks, that I am more likely to get weird skin things. Hmmm, in the eight years I'd been on Remicade, my GI never mentioned that to me. Sure, my PCP always says to stay out of the sun, stay out of tanning beds, not to sunburn, but hey, she's a PCP, she's *suppose* to say those things. I was shocked when I saw this tidbit of information on the CCFA FB page. I asked my GI's office about it and was given the 'eh, it's just something to be aware of'. I guess it's just something that is abstract in people's minds? not really important to tell a person? Kind of like the whole part they didn't tell me that I'd be on Remicade for life. I was on another immunosuppressant before that time and none of the three GIs I'd seen for that had ever mentioned anything about skin issues. I mean, I *know* I'm at increased risk for colon cancer, hence the colonoscopies every two years, but another thing I didn't even know about!From the CCFA page of 2014
"Today is #WorldCancerDay. [explanation of UC and Crohns]. . . Also, the rate of non-melanoma skin cancer and melanoma are increased compared to the general population among patients with IBD taking immunosuppressive medications such as azathiprine [Imuran]. 6-mercaptopurine [Purinethol], methotrexate, and anti-TNF agents [Remicade, Enbrel, Humira,Cimzia, and Simponi] . . . ."What? I've been on Imuran from 1994 to 2006 and Remicade since 2006.
I will be putting this out of my mind until I know what is what and if there's anything to worry about, but it's going to be hard.
I'm not sure how the biopsy will go or how my toe/foot will feel and I doubt I'll be able to wear my Injinji toe socks for a while.
. . . must remember to wear a slip on sandal on Monday. ..in Iowa. .. in January. Maybe I'll go buy those weird socks that have the four toes together and then a separate toe slot for the big toe. . .then I can wear those with my toe catching Born sandals? lol. That'll look swell.
Since pancreatic cancer is close to my heart, and the fourth leading cause of cancer deaths in the USA, I'll leave you with this. If you know anyone who is fighting pancreatic cancer, have them contact PALS at the below information. Patient And Liaison Services can help those who are fighting cancer by being there for them and talking about treatment options.
January is National Pancreatic Cancer Clinical Trials Awareness Month!
Contact firstname.lastname@example.org or at 877-272-6226 for information and free trial searches. You may also visit: http://bit.ly/1xhpOEO