+++ Laurissa, Kari, Marsha, how are you three pink sisters doing now on chemo? Please post an upda
Hugs, Angie
Comments
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Thinking and praying for you
Thinking and praying for you three too!
Hugs, Jan0 -
Shouting out and hoping tosurvivorbc09 said:Thinking and praying for you
Thinking and praying for you three too!
Hugs, Jan
Shouting out and hoping to hear back soon.
Big hugs, Megan0 -
Wanting to add BJ Mom's to this list ... of SistersMegan M said:Shouting out and hoping to
Shouting out and hoping to hear back soon.
Big hugs, Megan
battling another round with this dreaded beast. Also, Myturnnow as well.
Strength, Courage and Hope for all of these breast Sisters in PINK.
Vicki Sam0 -
I also wish that the pinksVickiSam said:Wanting to add BJ Mom's to this list ... of Sisters
battling another round with this dreaded beast. Also, Myturnnow as well.
Strength, Courage and Hope for all of these breast Sisters in PINK.
Vicki Sam
I also wish that the pinks sisters that are fighting the beast again would post some news for us.0 -
not much to reportDebbyM said:I also wish that the pinks
I also wish that the pinks sisters that are fighting the beast again would post some news for us.
I really don't have much to report. Last Friday I had my third round of Abraxane and Herceptin. First, I saw my onc because he wanted to see how the side effects were from this combination. At this point (and in comparison to Xeloda and Tykerb), this is a breeze (knock on wood!). I feel good but do get a little tired each Sunday. Unless something unforeseen happens, I'll continue this combo for 2 - 3 more months and then have another scan...so for now, it's stay the course and wait and see.
Looks like I might lose my hair again because I have sore spots on my scalp. Through all the different chemos I've had, I only lost it in the very beginning while on Taxol and Herceptin. None of the others caused this even though they were "likely" to. It's not that I want to lose it, but I'm well aware that there are many things so much more important. I must say after 73 weeks of chemo, that would have been a very long time to be without hair!
Thanks for checking on all of us again. I hope the others are all feeling as well as I am right now. Please join me with continued hopes and prayers that our current treatment plans are effective in fighting the tumors.
OFF TOPIC - I hope this finds everyone safe from the weather events that continue to batter our country!
My best to all, Marsha0 -
I am knocking on wood forMarsha Mulvey said:not much to report
I really don't have much to report. Last Friday I had my third round of Abraxane and Herceptin. First, I saw my onc because he wanted to see how the side effects were from this combination. At this point (and in comparison to Xeloda and Tykerb), this is a breeze (knock on wood!). I feel good but do get a little tired each Sunday. Unless something unforeseen happens, I'll continue this combo for 2 - 3 more months and then have another scan...so for now, it's stay the course and wait and see.
Looks like I might lose my hair again because I have sore spots on my scalp. Through all the different chemos I've had, I only lost it in the very beginning while on Taxol and Herceptin. None of the others caused this even though they were "likely" to. It's not that I want to lose it, but I'm well aware that there are many things so much more important. I must say after 73 weeks of chemo, that would have been a very long time to be without hair!
Thanks for checking on all of us again. I hope the others are all feeling as well as I am right now. Please join me with continued hopes and prayers that our current treatment plans are effective in fighting the tumors.
OFF TOPIC - I hope this finds everyone safe from the weather events that continue to batter our country!
My best to all, Marsha
I am knocking on wood for you too Marsha! So glad to know that you are feeling pretty good. I always think of you and always say a prayer for you. Keep posting so we know how you're doing.
Hugs, Megan0 -
As usual Marsha, you alwaysMarsha Mulvey said:not much to report
I really don't have much to report. Last Friday I had my third round of Abraxane and Herceptin. First, I saw my onc because he wanted to see how the side effects were from this combination. At this point (and in comparison to Xeloda and Tykerb), this is a breeze (knock on wood!). I feel good but do get a little tired each Sunday. Unless something unforeseen happens, I'll continue this combo for 2 - 3 more months and then have another scan...so for now, it's stay the course and wait and see.
Looks like I might lose my hair again because I have sore spots on my scalp. Through all the different chemos I've had, I only lost it in the very beginning while on Taxol and Herceptin. None of the others caused this even though they were "likely" to. It's not that I want to lose it, but I'm well aware that there are many things so much more important. I must say after 73 weeks of chemo, that would have been a very long time to be without hair!
Thanks for checking on all of us again. I hope the others are all feeling as well as I am right now. Please join me with continued hopes and prayers that our current treatment plans are effective in fighting the tumors.
OFF TOPIC - I hope this finds everyone safe from the weather events that continue to batter our country!
My best to all, Marsha
As usual Marsha, you always have kind words and thoughts for everyone else. You truly amaze me! I am so happy to see you posting, as, I also get worried about you.
I will continue to pray that your treatment plan will be effective and rid you of the beast.
You take care and remember how loved and admired you are by all of us.
♠♣ Love, Susie ♠♣0 -
Thanks Marsha for seeingsusie09 said:As usual Marsha, you always
As usual Marsha, you always have kind words and thoughts for everyone else. You truly amaze me! I am so happy to see you posting, as, I also get worried about you.
I will continue to pray that your treatment plan will be effective and rid you of the beast.
You take care and remember how loved and admired you are by all of us.
♠♣ Love, Susie ♠♣
Thanks Marsha for seeing this post and for posting. Sending lots of hugs, prayers and strength to you.
Hugs, Angie0 -
Hi Angie
I haven't been on til now. Chemo is really hard this time. Now I'm due for another one on Monday, just when I'm starting to feel a little better. I have to have 6 months to a year of it, 3 times a month. Its rough. I don't have an appetite this time around and have lost almost 30 lbs in 2 months. My husband and sister help me out alot. Husband is very depressed about the recurrance. Our anniversary is today and I know he's wondering if it will be the last. I worry about my girls, 19 and 21. Money issues are not good either. He's on sick leave getting only half pay for the next 4 months or more, and his job may be moving after that. I also wonder about the other girls and how they are doing. I hope things will get better soon. And a money tree would be fantastic. Thanks for thinking of me.0 -
Always looking for postslaurissa said:Hi Angie
I haven't been on til now. Chemo is really hard this time. Now I'm due for another one on Monday, just when I'm starting to feel a little better. I have to have 6 months to a year of it, 3 times a month. Its rough. I don't have an appetite this time around and have lost almost 30 lbs in 2 months. My husband and sister help me out alot. Husband is very depressed about the recurrance. Our anniversary is today and I know he's wondering if it will be the last. I worry about my girls, 19 and 21. Money issues are not good either. He's on sick leave getting only half pay for the next 4 months or more, and his job may be moving after that. I also wonder about the other girls and how they are doing. I hope things will get better soon. And a money tree would be fantastic. Thanks for thinking of me.
Always looking for posts from you Marsha and Laurissa. I so wish each of you had better news, but, I am going to keep praying and sending lots of positive thoughts.
I pray that Kari is doing well. I haven't seen her post in quite awhile.
Sue0 -
For MarshaMarsha Mulvey said:not much to report
I really don't have much to report. Last Friday I had my third round of Abraxane and Herceptin. First, I saw my onc because he wanted to see how the side effects were from this combination. At this point (and in comparison to Xeloda and Tykerb), this is a breeze (knock on wood!). I feel good but do get a little tired each Sunday. Unless something unforeseen happens, I'll continue this combo for 2 - 3 more months and then have another scan...so for now, it's stay the course and wait and see.
Looks like I might lose my hair again because I have sore spots on my scalp. Through all the different chemos I've had, I only lost it in the very beginning while on Taxol and Herceptin. None of the others caused this even though they were "likely" to. It's not that I want to lose it, but I'm well aware that there are many things so much more important. I must say after 73 weeks of chemo, that would have been a very long time to be without hair!
Thanks for checking on all of us again. I hope the others are all feeling as well as I am right now. Please join me with continued hopes and prayers that our current treatment plans are effective in fighting the tumors.
OFF TOPIC - I hope this finds everyone safe from the weather events that continue to batter our country!
My best to all, Marsha
If I could do one of those "happy dances" that women do on these forums, I would.
So very please that this new combo is being kinder to you. Hair lost in the scheme of things of what you been through is no doubt tolerable.
Best wishes in this continuing to be endurable and helping,
Doris0 -
Hello Angie and all my other
Hello Angie and all my other fellow "Kindred Spirits". Checking in and giving my update as well. It's been a tough week...Tue. my counts were VERY low, with my platelets coming in at 2, yep only 2, WBC was 1.0, HGB was 8, along with everything else running dangerously low. So Wednesday I received a platelet transfusion, Thursday I received 2 units of blood (was hoping it would be super-hero blood so I could fly out of there). Yesterday my HGB was up, my WBC was up and platelets made it up to 43, still very low but way better than 2. Today I'm doing ok, feeling better for sure, like I got my oil changed, lol. Hope this finds everyone else doing well and as always, you're all in my prayers every day.
Miles of Love,
Kari0 -
Kari, Laurissa and Marshapinkkari09 said:Hello Angie and all my other
Hello Angie and all my other fellow "Kindred Spirits". Checking in and giving my update as well. It's been a tough week...Tue. my counts were VERY low, with my platelets coming in at 2, yep only 2, WBC was 1.0, HGB was 8, along with everything else running dangerously low. So Wednesday I received a platelet transfusion, Thursday I received 2 units of blood (was hoping it would be super-hero blood so I could fly out of there). Yesterday my HGB was up, my WBC was up and platelets made it up to 43, still very low but way better than 2. Today I'm doing ok, feeling better for sure, like I got my oil changed, lol. Hope this finds everyone else doing well and as always, you're all in my prayers every day.
Miles of Love,
Kari
Thank you for your updates. I am glad to see you posting, however very sorry for rough rides, low blood counts, transfusions, all Chemo side effects.
My son as many college students always gives blood, hopefully you will get energy and young , "can do everything" spirit from transfused blood.
Please know you are always thinking and praying for your effective treatment and easy side effects.
Hugs0 -
Marsha, Kari and Laurissa--as well as all the others strugglingNew Flower said:Kari, Laurissa and Marsha
Thank you for your updates. I am glad to see you posting, however very sorry for rough rides, low blood counts, transfusions, all Chemo side effects.
My son as many college students always gives blood, hopefully you will get energy and young , "can do everything" spirit from transfused blood.
Please know you are always thinking and praying for your effective treatment and easy side effects.
Hugs
through treatment, just wanted to add that my thoughts and prayers are with you all every day. Wish I could do more for each and every one of you. Praying that all your treatments are quick, tolerable and getting the perfect results you need to keep moving forward.
Hugs and hugs,
Renee0 -
I am so glad that you each
I am so glad that you each checked in. I am praying for each of you and sending lots of (((hugs))) and healing energy.0 -
ThanksCypressCynthia said:I am so glad that you each
I am so glad that you each checked in. I am praying for each of you and sending lots of (((hugs))) and healing energy.
Thanks for the update ladies. You are all in my prayers and thoughts daily.
Stay strong!!
Hugs,
Debi0 -
Great to see your postingCypressCynthia said:I am so glad that you each
I am so glad that you each checked in. I am praying for each of you and sending lots of (((hugs))) and healing energy.
Great to see your posting too Kari although I wish you also had better news. Each of you are always in my thoughts and prayers.
Sue0 -
Marsha, Laurissa and Kari
so glad to see your posts but sorry you are all having a rough time of things. Laurissa - happy anniversary - let's hope you'll celebrate many years to come. I wish all of you calm, strength and courage as you continue to fight this battle. I will keep you in my thoughts and prayers.
{{hugs}} Char0 -
Think of you guys too...
Thanks for posting Angie.
I think of you ladies too, quite often. I want you to recover and be well. Thanks for the update. My prayers will continue.0 -
I thank you too for updatingmissrenee said:Marsha, Kari and Laurissa--as well as all the others struggling
through treatment, just wanted to add that my thoughts and prayers are with you all every day. Wish I could do more for each and every one of you. Praying that all your treatments are quick, tolerable and getting the perfect results you need to keep moving forward.
Hugs and hugs,
Renee
I thank you too for updating us. I think you all know that you have all of the pink sisters praying for you.
Please do check in when you can and feel like it, as, we do worry.0
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