Karenhi

YAY!! You made it through 8 treatments! Everyone IS different, and I have read stuff on this site where people had NO skin burns (or very minor ones) I try to prepare for the worst and hope for the best.
My next chemo is TUES. Hair is coming out in clumps. I think of you all the time when I am "pulling"....lol. I just want it all out now.
I am not working. I am retired.
I hope you are having a good weekend off. It is getting a little chilly here in New England. A few of the trees are starting to change color. I hope the colors are spectacular this year.

You are too funny! I saw this picture in my head of the client "on the couch" and the therapist with the notepad in one hand and a handful of hair in the other. lol Client" I don't know Doc...I 'm at my wits end....I feel like pulling my hair out!" lol
I shaved it first time around but thought I could just let it fall out but I am tired of having hairs all over the place. So I am compulsively pulling......lol.
My hair will come in white as I have been dying it for years. But I have really straight hair and last time it grew back curly, for a little while anyway. I am glad yours is finally starting to grow a little. You can always take care of the color later.

Karenhi, just wondering how you are doing with the radiation. I hope you are still doing well with it.

Karen, hope you are doing well. I was dx'd Feb 2012, did lumpectomy, 16 rounds of chemo and 33 rads (finished in Nov). I just wanted to reach out in case you wanted to know about a BC support group. We meet the 4th Tuesday from 5 - 6:30pm at the Allina Clinic on France Ave in Edina. I live in EP. feel free to contact me if you wish kheuchert at yahoo dot com.

How funny.....I was thinking the exact same thing about the number 33!

I know what you mean about compulsively pulling...lol. Its day 14. I did have chemo 11 yrs ago and I did lose my hair so its nothing new. Seems like you lose it so quick but takes forever to grow back. I have straight hair but when it grew back it was curly...for a little while anyway. I do not have mouth sores or reflux yet. I get a little winded on my walks and a little tired but so far, so good (knock on wood)
When you get radiation do they do a big area? Do they do different areas?

Sounds like radiation is a breeze, hope it stays that way for you. Try to concentrate on how many you have done not on how many you have to go.
I have recovered sufficiently though my hair is really starting to fall out today. Kinda want to get it over with. I think I have it all hairsprayed to my head today,lol I go for round 2 on Mon.
Thanks for the update. Makes me feel better knowing its doable. Keep in touch if you can........:)

Hi Harenhi, I was just wondering how the radiation went. I hope it is going easily for you. Thoughts and prayers are with you.....:)

Wow! A chiropractor messed up your back? Geesh! I'm sorry to hear that. The whole concept IS a little scary but it did help me. I don't know if I will be going back after all this cancer treatment. I will have to think about it. I tried it in the first place because it was one of the few things i HADN'T tried yet.
I think it is so cool that you will be participating in clinical trials. It will benefit you as well as so many others down the road.
I hope radiation goes well for you. I am following in your footsteps so to speak.Keep me posted if you can...........:)

Chronic pain IS a @#$%!!! It wears you out. I have tried many things for the Fibro pain. Acupunture, Yoga, Cranial-Sacral massage and on and on. Most recently I have been getting Chiropractic adjustments and that helped enough that I could start going for short walks. The more mobile I am the better I feel. This whole surgery and chemo thing put a dent in that routine but I am determined to get back to it. I don't really take a lot of pain meds as they do a number on your digestive system. Also I want them to really work on the really bad days when I HAVE to take something..
How many times do you have to go to radiation? Did they tell you Arimidex might cause pain flare-ups?
I hope all goes smoothly for you. Keep me posted.....:)

i had bone/nerve pain from Neulasta for about 2 days. I have Fibromyalgia too so that pain got amped up too. I did have a port put in with the first mastectomy. I got 4 rounds of Adriamycin, Cytoxan and 5FU. Then no radiattion. Then 5 yrs on Tamoxifen So this tine 6 rounds of Taxotere and Cytoxan, probably radiation and then Femara or Arimidex. Are you getting neuropathy symptoms already? Are they giving you chemo and radiation at the same time?

Karenhi....wanted to let you know its been roughly a week since 1st chemo and my belly pain is much improved...no pain meds today. Hope you are feeling better as well.

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