Marching Healthy 2012
Comments
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I walked 2 miles with one of my friends I met at the park.. First time I made it that far in 4 months!... One day down anyway... Tomorrow maybe a slow Dance Revolution..
I'm getting ready to leave for a week. Going to go see my kids and grandkids.. Long drive and I'm going without DH... I am bringing my computer with me so I can still work while I'm there..
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Great job GMA! 2 miles is sooo good. Over the course of my treatment i've recently seen 3 MOs. The head honcho says walk an hour a day to stay strong. The one I saw today (for a future ooph) said it is not necessary, prudent, to walk when you're feeling really bad as that can do more damage than good. What a relief as the day I was in a fetal position there was no way...or today was a full day driving to chemo/shopping/home (5am to 7pm).
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Its been quiet in here.. thought I would bump it up ... Walking has not been happening - stormy weather but did get on the beginning dance revolution until it wouldn't work anymore.
I don't know what to do any more.
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Does everyone know about this FREE 12 week LIVESTRONG program at your local YMCA?
http://www.livestrong.org/What-We-Do/Our-Actions/Programs-Partnerships/LIVESTRONG-at-the-YMCA
http://www.livestrong.org/What-We-Do/Our-Actions/Programs-Partnerships/LIVESTRONG-at-the-YMCA
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Hi healthy Marchers!
I haven't posted in a while. It has been 5 weeks and 5 days since my final TCx4 treatment. This is day TWO of the daily Tamoxifen pill.
I kept putting it off. Partly to detox some from the TC before adding the tamox. Had it in my head to join 'Hot yoga" -- AKA "Bikram yoga". I've been alternating between Bikram and Vinyasa flow.
After a few classes, I discovered these were power yoga classes. POWER yoga! Turned out to be a great mistake since I would never have signed up for power yoga if I knew what I was doing... !! I am the worst one in the classes... but I'm also the only bald chick... so it's like I'm wearing a sign that says "Hey... after what I've been through, I'm just happy to be here". And it's the truth... actually.
The classes bug my TE a little bit. Anyone else here taking yoga or doing other exercise that stresses the pectoral with TEs? Has your surgeon limited any of your activities?
I left a message with my surgeon to make sure it was ok -- the nurse told me he said no problem to yoga...I asked her if he understood its power yoga and stressing/challenging the pectoral quite a bit...she wasn't sure, so she supposedly asked him and got back to me with a "yes thats fine".
Way too many posts to read and catch up -- but hope everyone is getting through and/or recovering from treatments quickly. Hope your hair is growing fast! The hair thread is just too long to get through it all... wish there was a smaller thread with ONLY hair regrowth tips. If there is... please share!
Shera
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Hi all
I feel a little bad, haven't been on this forum for weeks now.
Have had 5x doses of Paclitaxel now. 7 more infusions left to go.
Overall, I'm feeling better on this one than on Doxorubicin and Cyclophosphamide.
I haven't done a lot of exercise, although today I got up and did 30 minutes flat walking on my elliptical machine. Felt good to do it, and I plan to do that every day... at least while the aches and pains aren't too bad.
I hope everyone's doing well.
Angela
PS. I must admit that a big reason I haven't been here much lately is because I don't like this new forum format.
It just doesn't look good or flow well for me.
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Hello Ladies. I just finished last chemo tx (6 TCH) this past Thursday and I feel soooo lethargic. I felt better after #4 & #5. I have had no desire to work out. Hopefully, I get over this hump in the next day or so. My weight is at an ALL TIME HIGH. It doesn't look bad...yet. I HAVE to get back to my workout plan though.
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I'm with you - I know I should work out, but other than walking, really haven't broken a sweat or anything. One more chemo left then radiation, so hoping I will get my mojo back soon and get back to my workout program!
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I've managed two mornings of walking, at around 6 am, because it is do very stinking hot here right now... Even managed a few blocks of a jog.
This is all inspired by my RO informing me that some of the radiation, a small slice, will probably reach the heart, and that you want to make sure all other heart health risk factors are reduced. I mean, really, don't we have enough to think about...I have alot of heart disease in my family. Excellent. So I can get my body moving, that's what I can do...
Have a good day, all. -
Wow - this is weird..this thread was so slow and all of a sudden people have moved from March Chemo to Marching Healthy! This is good news, I guess. I was doing pretty well with walking during chemo, 4-5x a week for a hour a day, but my walking partner took a hiatus preceding and during my last dd Taxol. Teaches me I can't be so codependent on someone to get my exercise! I think I paid for that as my fatigue factor shot way up after I slowed down on the walking (mind you, this is not a balls to the wall sweatfest, but slow and steady walking on flat ground for an hour). The Taxol really did a number on me during tx#4...fatigue, but worse, the nueropathy of my hands and feet. I continue to walk, but it is uncomfortable and I'd rather go 45 minutes than 1 hour 20 minutes, which I had started to do. I did manage to lose 5 lbs during chemo....despite being told that people gain weight during chemo. Exercise does help fight the fatigue, so keep it up Marchers......!!!
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KCB: That's interesting that your RO has indicated that radiation will hit your heart. I've met with two different RO's and they both have ASSURED me that my heart will not be touched by radiation. They did say that a sliver of my lung would be hit but that it would have absolutely no effect on lung capacity. They were very adamant about that. You might want to meet with another RO, maybe he's using older technology.
On the fitness front, I did do a leg routine today and walked on the treadmill for 20 minutes. I sweated so much you would have thought I was outside in the 90 deg weather. It didn't bother me though. I wanted to sweat out as much chemo crap as I could.
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Tc9876: thanks for that feedback. I will definitely ask around.
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Its nice to see familiar names from the March chemo thread over here. I know many of you are in mid-treatment or almost done. My last tx was May 2... making me 8 weeks and 3 days out. I didn't exercise much during treatment... other than walking. Lucky to have a dog that needed walking because she forced me to go outside much more than I would have. More power to those of you exercising during treatments.
I am exercising now though -- joined up and taking Bikrim yoga -- known also as hot yoga. All I can say is wow. It is intense. The heat and moves are meant to detoxify body, and I am litereally dripping with sweat during class -- which is great, thats why I'm taking them. I don't try to keep up with anyone else in class... and adapt moves as needed... so no star yogi here, thats for sure. Just so happy to be able to take them at all.
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Shera - woohoo to be done with treatment! I keep wanting to try hot yoga - great idea after finishing treatment to sweat all those toxins out! Thanks for the idea!
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Hi All! At the cottage swimming, kayaking, walking trails.. Exercising is so much easier when it's all outside on your doorstep... If only life were like that!
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New to this thread. Started chemo in July, started doing long walks in 2002 when I decided to do a half-marathon. I've done 11 half-marathons since then. Only had to skip a year when I had open heart surgeries to repair 3 leaky valves.
Well, the first week after each of the 2 chemos I've had so far, I have NO energy. After that, I can do 3-4 mile walks, but not very speedy. How discouraging! But I worked my way back from heart thing, it took 9 months of hard work...I'll work my way back from this.
Send some encouraging stories my way please.
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NatL: yours is the most amazing encouraging story YET! thank you!
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I'm on a roll. I have exercised everyday the last 3 weeks. I even did P90X (modified,of course) with my daughter. I have since emailed Tony Horton (Mr P90X) and suggested he create a new P90X program and call it " The Survivors Boot Camp". Maybe he will listen?? I'll let y'all know. He may need us for video?? Haha
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wow p90x is tough even modified! Good for you msbelle!
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msbelle - You are doing so well. Something for the rest of us to look forward to and to motivate us.
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msbelle - what is p90X?
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Tamoxifen is kicking my butt!!! Well, it's not that bad but it's making me all achey. I'm still working out but I often feel as if someone beat me. My M.O. said that it was residuals from the chemo but I think otherwise. If I sit too long, my body stiffens up something terrible. But from the exercise viewpoint, I am working hard to stick with my 3-4 day/week workout schedule.
Msbelle, I've heard great things about the P90X workout program. That is awesome that you are hanging in there with it!
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P90x is an exercise program you order and do at home. It's claim is muscle confusion, work different muscles daily. It is tough but you modify the exercises to what you can handle. I am just starting so I am only doing it 2-3 days a week. I have woken some muscles that have been sleeping for quite awhile. Very sore but determined to get in shape and do some 5k walk/runs without dying.
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