I know, I know…it’s been a while. But no need to worry excessively – I’m doing okay. Just struggling a bit with motivating myself to write something.
Here’s a slightly overdue recap of recent events:
12/28/09 – I went in for an ultrasound on my right arm to see if the blood clot(s) had resolved. Thankfully, the answer was yes (no clot!). So, I got the “all clear” to have the port removed (although I still have to keep giving myself the Lovenox shot every day for a few more months as a preventative).
Later that day – Off to the cath lab for the port removal procedure. Two nurses told me it would be easy, with no sedation necessary, and nothing to worry about – so, I didn’t. Then, the doctor came in while they were prepping me and gave me a slightly more detailed version of what to expect: the procedure would take about 20 minutes, they’d give me local anesthesia to numb the area, and “most people do fine without sedation, but if you feel anything sharp, let me know…” (What!?) They tented my head again, as they had when I got the port installed, so I couldn’t see what they were doing, but I could feel tugging and pulling and hear the sound of clamps being used. At one point I swear it felt like the doctor put his foot on my shoulder and yanked the thing out of me. I’m sure that’s not what really happened, but it felt like it! They sewed me up and I went home. For a procedure that was supposed to be “nothing” I ended up on the couch for the next two days. I was really fatigued and it felt like someone had slugged me hard in that soft area between the shoulder and the collar bone. But I survived (once again), and the dreaded port is gone!
12/30/09 – I had my follow-up appointment with Dr. Brown at four weeks after the surgery. He looked at all the wounds and said they were healing properly and he was happy with my progress. He also commented that when he saw me walk down the hall to the exam room “it didn’t look like you just got off a horse.” I understood this to be a positive indication of how well I was doing. We discussed the things I’d been concerned about (the stoma bleeding, the wounds still seeping, the bulge on my belly just above the incision…). Everything I brought up was met with his nonchalant “that’s normal.” I’m to see him again at eight weeks after surgery.
1/8/10 – I was having a few problems with the colostomy bag, so I went to see Carla, the ostomy nurse, for a follow-up. She looked at everything and, like Dr. Brown, declared that all was well and normal for this stage of things (being less than six weeks after surgery). I talked to her about the features of the different bags I’d tried so far. There was one bag I liked everything about, except for the wafer (the part that adheres to your skin). I preferred the wafer on another bag, but it didn’t have other features I wanted. Carla looked through her enormous ostomy appliance catalog and found a bag that has the combination of things I wanted, including the “microskin” wafer I liked. I’m waiting for the new bags to arrive any day now so I can see if they’ll make dealing with this a little easier!
Other than that, I just seem to have days when I simply do not feel like doing anything. I think I’ve actually been just a little depressed – which, in Dr. Brown’s and Carla’s words, is “normal” under the circumstances. I’m still adjusting to a having a colostomy (a huge adjustment, I might add). My body is still recovering from the months of being poisoned, burned and cut open. Plus, the chemo and radiation brought on instant menopause, meaning my hormones are whacked on top of everything else. And, it’s been downright cold! So, a tiny bout of depression doesn’t seem out of line, does it?
The good news: It’s a New Year. I’m cancer-free. I’m well enough to get out and walk, drive, go to the grocery or the post office, and generally do many things I once took so much for granted. Only now, I usually remind myself how blessed I am to be able to do these simple chores of daily life. Okay, sometimes I’m sad. Sometimes I’m silly! But, mostly, I’m just grateful for life.
Next time: Ostomy 101 (I’m giving you fair warning about the topic in case you’re squeamish…)
Dear Karen,
I am sooo glad to see your posting. I knew you weren’t feeling so chipper, but I was checking, sometimes, several times a day. You will never know how much you inspire me. Everytime I worry about something, I look at what you have been. and are going through, and it helps me put things in to perspective.
I knew you were amazing when I worked with you at Kindred, but I didn’t know JUST HOW MUCH!!!
I mean it!! And the fact that you share your experiences so honestly constantly influences my life. I just had the best pot of Chun Mee ever. With 4 inches of snow on the ground, I am “working” the tea thing.
I send you strength and love.
Karenda
Karen
It’s sooo good to hear your “voice.” Miss you, love you, and am sending you lots and lots of hugs. You will feel stronger with each new day, REALLY. And if you have a day that you don’t: well, heh, snuggle in a warm blanket and rest that svelt body of yours, and those warm, beautiful eyes.
Big Love comin’ your way, Amazing Lady! So happy to hear you’re getting your health and strength back!! Happy ’10!!
Sooo very glad to hear from you. How selfish of me to think that you have nothing better to do than to make me feel better!! Glad to see your ostomy nurse found the right combo of wafer and bag for you. Hope they have arrived on your doorstep by now.
so now i have a prject for you…go and explore the HGTV dream home. i do believe it is in your town. I have tried to win the one in Key West, Port Saint lucie (yes my home town) and now Santa Fe. so far I am not doing too good. If I win this one i can come visit a lot. I thought that this might cheer you up. By the way, if i had just gone through all that you have i would be depressed as hell so you have the right. i think that you are doing amazingly great dear Karen.
i send my love and can’t wait for your next post.
Love,
Candy