Starting Chemo October 2012
Comments
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they tatoo the spot for radiation... kinda like a target... my mom had an X ... not sure if they do it like that to all tho
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The tattoos are tiny smaller than freckles, as if I had applied a dot to my skin from the tip of a marker. I have four that are to ensure I get lined up appropriately for the radiation. They have said that after chemo this will be a walk in the park, I was actually pretty excited yesterday to get mapped and ready to move on with treatment.
toots - try copying the hyperlink directly into your browser to open po-ke's facebook page: http://www.facebook.com/matchingdreams
Off to buy a compression sleeve today, apparently there are different colours?!
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Lou-Bar found it, liked it, appreciate it! Thank you. ..........can you get a purple one to remind of the purple bubbles???
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oooooo i like that idea toots
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Hi ladies, It's been a while since I checked in. Sorry...tomorrow I am four weeks PFC and I still am feeling totally exhausted. I've managed a few good walks but it kills my low back and legs. Even the arms ache and feel heavy. Everyday I force myself to get up and move around and I am so waiting for this to pass! Tomorrow I start radiation. Got my tattoos (three of them) and ready to get on with this phase. Glad to see so many of you finishing up too and still making this forum "home base". I check out other ones too, but you guys are "home". I will have to see about a sleeve as well ... are they recommended for flying as a precaution? Checked out the site Po-ke ... awesome idea! Hugs and happy thoughts all around!!! :-)
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Halfcan - good to hear from you! My lower legs (calves) seem to be giving me the most problems, they seem super tight and achy but still just so glad to be done chemo. Re. sleeve, yes they recommend for flying, there is custom and off the shelf, they told me to wear two off the shelf on top of each other and a glove when flying and my flight is only 2 hours. I was doing it as a precaution, yet it seems I do have mild swelling so will have to wear for other activities too. Good luck with rads tomorrow, what cream are you using? My hospital is recommending Glaxal, but I see the rads board ladies swear by aloe force. Apparently if I want to use something else I have to get the okay from RO in advance.
Toots / Celineflower - unfortunately, they didn't have purple sleeves, but you are on to a great marketing idea! My hubby wanted me to see if I could get the colours of the english soccer team he supports! But instead I have boring beige!
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LouBar - are you sure you don't have DVT in your legs? Have you mentioned your tight and achy calves to your MO? Hope you're feeling better!
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301724 - thanks for the information, oh my, I sure hope there is nothing else wrong with me, feel like enough is enough. I will be sure to mention now to MO. Was hoping it is because apart from the days post chemo and I didn't get out of bed, I have been walking about 6km daily. Last week we had tons of snow so I was hoping that from the chemo and a harder walk in the snow that this was the problem? But now will inquire further. Thanks
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Hi gals, LouBar - I am just using Keri lotion that I already had ...it was second on the list they gave me. First one was Glaxol Base. I'm in for 16 rads and have finished 2 today. Setup is quite the ordeal on day one but today was a breeze! I think this is going to be much easier than chemo for sure and I don't have to have that many rads either. But, they are zapping me in a huge area. Even from the backside and clean up one side of my neck. Crossing my fingers that my skin handles it well and I just get through it. Enough SE's leftover from chemo to deal with. :-) 301724 - What is DVT? Hugs and well wishes to all.
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It's deep vein thrombosis - AKA a blood clot in your leg. I only ask because I had one shortly after my surgery - and it felt just like tightness in my calf.
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Hello All,
I am super impressed with those of you able to keep up with the exercise. I have not, have to force myself to walk and usually 15 minutes before Im ready to fall out. I am tiiirrreeed , also suffer from the weak,tight legs. I am 3 weeks PFC today, herceptin only now but couldnt get my treatment, MO sent me to ER because bp was elevated and I had chest ,jaw and neck pain. Turns out I have a blood clot above my mediport. Shots in the belly and Coumadin now. Regarding the lymphedema sleeves, my therapist gave me a site to checkout, lymphedivas. I havent ordered from them but they do have some pretties. A little pricey for me.
Many, many thanks to you brave ladies who have been posting your experiences, good and bad, and encouraging all of us. Great big hugs to you and those like me who visit but for whatever reason, aren't too comfortable posting yet. -
Hello Ladies, I hope everyone is doing well. HAPPY VALENTIN'S DAY TO YOU. i had treatment yesterday (Taxol & Herception). It went okay. Although it only makes me sleep. I spoke to this lady after treatment and she was saying instead of prolonger her treatment weekly she gotten it all in one day. As in if I was receiving mine 1x weekly for 12 weeks she got all 12 in one day for about 3 hours long. Has anyone heard of this? I was thinking about asking my doctor about it next week…just curious…
Caitgrace ~ thank you for that.
Laubar ~ I hope you are feeling better. I prayed your appointment went well at the lymphodema clinic. So glad to read things are getting better after the appointment. Good luck to you when you start your radiaton seesions.
Po-ke ~ Good you had your last treatment; congrats to you. Sweaty its okay to vent. We are here. I to hate to read of breast cancer ladies past away and wish its more survior stories that out weigh the bad stories but I am sure they are more positive ones out there. When I feel down that is all I think about is all this treatment I am doing going to keep me alive long or am I going to go in a few years. I think why me. My husband keeps telling me baby you got to think more postive because you have me and your son to live for. That seems to get me on track sometimes but it can be difficult. You try to keep the faith that your going to beat this cancer as much as you can. Wow your facebook page is a super good idea. I wish I can help but me and hubby live in a small one-bed room apt. I live in Bermuda and this island would difinit be an escape gate. Times like this I wish I owned my own place. I will pass the information on my facebook page as well. Good Luck I am sure this will take off.
Alco-70 ~ Is Taxol the same as Taxotere? I am on 12 rounds of Taxol & Hercepton weekly. My fingernails are all dark and I to have white lines on all of them. My doctor said it was from the Taxol and to keep them short and as dry as possible. I was a bit concern because I can’t handle my fingernails falling off like my toenails. Most of my toenails are dark colored and have lifted up but none have dropped off yet but very close. What you mean by “chemo induced menopause”. I get hot flashes then I am cold. This happens about an hour or so apart but worst at night. I am 37 years old I hope this is not menopause for me this early in age. . .
CelineFlower ~ I hope your feeling better now.
Marlene18 ~ I have five more treatments to go. Congrats on the birth of your child. I too have some stubs growing back on my head too…its not growing back dark brown but looks like its either white or gray…not so happy about that but its something. I just notice this week that my eye lashes were dimishing! I was shocked. I feel our concern about having chemo with a new born but try to look on the bright side like you said…you have your partner plus other people around who is there to help you during your treatment. I am positive things will work out for you in the long run. Good luck.
PatinMN ~ I am going through 12 rounds of Taxol and Hercepton weekly. I have 5 more left to do. I find that I sleep during and for the rest of the day. The day after treatment I am fine.
Jalessi92 ~ I am sorry you felt exhusted and emotional; I hope you feel better now. Its okay to complain my mom always say to me. Yes we must be thankful to see another day but we are only humans. So shout if you must we are here for each other. Hugs
Toots ~ Congrats on your last treatment!! Good for you.
HVV ~ Congrats on your last treatment too and thanks for the heads up.
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Hi ladies, sorry not been around, been wearing myself out, but getting back to normality. Went swimming for an hour yesterday morning, followed by an hour of aquaaerobics, felt so good afterwards but then went shopping, had lunch and slept for the rest of the afternoon. Had a quiet day today painting ready for the auction for funding for cancer research later this year. Planning on a repeat of yesterday tomorrow, swimming then aquaaerobics but have a reiki session booked for 14:00, the first but sounds like fun and has been rcommended by a few friends who have had cancer and they offer the service at the local CLAN centre, so available to anyone who has or has had cancer.............looking forward to it............
So hope that everyone is feeling good and that there are not too many SEs and lots of silver linings...........take care all lots of hugs from the NE of Scotland xxx
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So I'm back in the big chair this week
I've been dreading this week since Chloe was born but I guess it's time to suck it up and just get on with things. Actually, I had my first herceptin yesterday and it wasn't bad at all - no reaction, no side effects. Today is toxic taxol day though so I'm presently getting the steroid & Benadryl through my IV. Chloe is a nice distraction for everyone on the sixth floor here though
My mom is in town doing her share of the baby-holding so that helps a lot. I am really hoping I don't feel too bad, though my MO warns me that evening of day 2 is when I should get a taste of the discomfort beginning.
This week I also have appointments for scans I couldn't have last year while pregnant - MUGA yesterday (EF 61% - yay!) and bone scan Friday. Hoping was very uninteresting results...
Thanks everyone for continuing to check in - you can prepare me for what to expect with rads, which I guess won't be starting until at least May for me.
Oof, getting woozy from Benadryl. Time to curl up and zone out! -
WB Chloemommy .. the chair isnt as bad when your not alone
So today i will tell my OD, That I feel his time is to limited to properly meet my needs as a patient and that , in this war to kill my cancer, i must feel trust and a connection with each member of the team, and from various incidents , i do not feel a connection, nor the trust i need to fight this battle with you.
Sigh... i dont do well at confrontation...
And this is on of the times my sister Cathy will not be with me ... shes my "pit bull" with the medical world...
We come from medical family.. kinda..
Dad was a hospital admin... mom a psy nurse , and involved with unions for nurses ...
So dinner table convo's were fun... lol
And my sister has worked in admin positions in hospitals as well.. so she knows how to work the system
So i will do my best to channel her and try to remain calm... lol
There are some positives about today's treatment... after its done, there will only be 2 left... and i get to show off pictures of my new grandson! -
Celine Flower:
Thinking of you and wish you the best today. As an RN, I always tell my patients that they really are their own best advocate for medical treatment. As a patient, YOU decide who your team members are, YOU decide what treatments or procedures you are willing to undertake, YOU decide what medications you will and won't take.
I sometimes see patients who are upset...that they're not being listened to or their questions are not being answered, and then that is my call to be their advocate. RNs are patient advocates...we know the doctors, we know the medications and the procedures, we want what's best for you.
Several years ago, I had to drop my primary care doctor from my medical team. I was having pain under my right ribs and occasional nausea which went on for almost 8 months. She sent me for an ultrasound which showed no gallstones, so she blew off my complaints and never took the next step. I also was feeling aching in my left armpit which she blew off for 6 months as muscle pain from my job as a nurse. She finally ordered an ultrasound.
My new primary care doctor ordered a HIDA scan which clearly showed that my gallbladder wasn't working (an 8 % ejection fraction). I had gallbladder surgery in 2010 and haven't had any more problems. The armpit ultrasound showed one of my lymph nodes was 2.4 cm...fairly large for nodes in that area and I was urgently sent to a surgeon for evaluation. I had two nodes removed which were determined to be reactive hyperplasia...fortunately not cancer.
If you are not comfortable with your medical team, it is your right to leave their care and find a new doctor, Don't feel bad about doing that! I now have an OBGYN that I've been going to for 15 years, a primary care doc who listens and aggressively treated my pneumonia in November, a general surgeon with wonderful bedside manner who performed my gallbladder removal, mastectomy, and port placement, and an oncologist who is up to date on the latest cancer research, genuinely cares, and is aggressively treating me for IDC.
I would be there with you if I could!! Thinking of you today!!!
Jen
Jalessi92 -
Hi Ladies, had another Taxol and Hercepton treatment yesterday. It went somewhat okay as the nurse told me after treatment my white blood cells were too low and they might hold out my Taxol next week and only give the Hercepton. In Bermuda they do the blood work the day before your treatment and they may not get the results in time when your treatment is due. I was very upset by this. I told the nurse I am sure my white blood cell will be fine next week. I really hate to miss any of my treatments being so close to finishing up. I told them I am losing more feelings on the tips of my finger and my toes and part of my feet. I hope it dosen’t get to bad…here is what they look like…I wish I can do something about it….
Toots ~ so glad your getting yourself back to some form of normality. I need to start doing some things too. All I do is lay in bed all day and only Saturdays I go out and spend time with my family/cousins. I need to start acting like I have a life again.
Marlene18 ~ sorry the big chair has you again. Its nice to hear your mother is in town helping you out and that having your baby Chloe with you during treatment is a positive distraction. I hope the rest of your test continue to be positive results your looking for. Good luck.
CelineFlower ~ I agree with Jalessi92 with having a team that you feel that will work with you in what your looking for. In the end its all your choice in what medical treatment you choose and you should feel comfortable with who is looking out for you in that area too. I know you will find the best medical team. I hope all went well today even though you didn’t have your sister aka pit-bull there to help you. I am sure you did well.
Jalessi92 ~ Thank you for your story and advice. At times I felt like CelineFlower too and your comment as a RN really hit the spot for me to take note too.
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Hi 35 smiling.....I hope it's not too late but you can try icing your fingers and toes during the taxol. It will help prevent neuropathy and nail damage. Best to you!
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neuropathy?? never heard of that. the nurse always said to keep hands and feet as dry as i could. but will try it next wednesday when i go back for my next treatment. thanks
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35 smiling - be sure to wear thin knit gloves and socks - put ice in a plastic bag. That way your skin will stay dry and get chilled but not too cold. Good luck!
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Hello everyone! Sorry I have been out for awhile, I was in St. Lucia last week for the wedding of some of my college friends. I hope everyone is doing well! I had my first Herceptin-only infusion yesterday which was exciting and I also started tamoxifen two days ago. I have been very tired and going to bed super early even with naps! Did everyone hear about the new drug approved yesterday? If not google it, interest stuff! They are basically linking chemo to Herceptin so that healthy cells are spared! What a great idea. Love to all!!! xoxo
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Hi Ladies; been a while for me checking in, just back from visiting my family out of province. It was great to get spoiled and looked after by the family, realize how lonely this journey has been and how much I missed my family. I have two young neices that I love to bits and was worried how they would react to how I look...needless to say they were fine with my baldish head and couldn't get enough feeling it
I wore two sleeves and a hand guantlet on my flight and that seemed to work well and tonight I have another appt. with a different lymphodema specialist. The funny thing was I measured both my mom and sister's arms and they also have one arm bigger than the other and didn't have lymph nodes removed! perhaps my slightly larger arm is just a genetic anomoly?
I have had a bit of a pain (very slight) on my shoulder blade when it is touched, expect to see it bruised but it looks fine. I switched over my purse (had an over body one) that may be was rubbing? I also went back to the gym and have been doing some weights recommended by physio for my "swollen arm" so may be the shoulder blade is the stretched skin from the lymph node dissection? Yes, trying to convince myself that there is nothing seriously wrong with the bone (original bone scan clear) so surely after all this chemo I'm in the clear for a while? But, certainly I have had the sad realization that any soreness moving forward will be so worrying:(
Start rads tomorrow, can't wait, let's get this show on the road and get it over with. I'm also going back to work two days a week for the duration of rads, also really excited.
Okay - enough about me...sorry for my blabbering.
Toots -how great for you to be getting back into your normal life. As much as I am exercising, my legs still feel like they are lead weights, being in the water sounds like a good idea!
Marlene - how lucky for everyone to have the lovely distraction of your daughter, you must be brightening the spirits of everyone in the room. I can imagine seeing you with your new baby would give everyone so much hope and pleasure.
Celineflower -I hope everything went well with your appt. and you were able to channel your sister to advocate for yourself, so sorry that you have this to worry about on top of everything else. Looking forward to hearing a positive update from you. Lots of good advice from Jalessi92.
35_smiling: so sorry about your nails. As per 301724 I also iced and so far so good. In addition before each treatment I cut my nails really short and applied a clear nail hardener that I kept on between treatments, good luck.
po_ke: hope you had a great trip, what a nice get away! Also, how wonderful to have such positive news about the efficacy of your treatment!
New information regarding benefits of omega 3's inhibiting breast cancer: http://www.uoguelph.ca/news/2013/02/omega3s_inhibit.html seems flaxseed delivers lots of omega 3's this is now on my grocery list
Love to all xxoo
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Hi everyone and I hope we all had a wonderful day today as I say this because today I turned 38 years old and I am so thankful God allowed me to see and spend another year with my family and friends. I pray I see much more. My husband is taking me out to dinner tonight and I am looking forward to it. Tomorrow is another treatment day already. I try not to look at it as a drag but finding it difficult which is odd. I am just glad my treatment isn’t on my birthday.
301724 ~ Thanks again I will try it out tomorrow.
Po-Ke ~ It sounds like you had a wonderful time in St. Lucia! Good luck on your treatments.
LouBar ~ Glad you had a wonderful time being spoiled with your family. Don’t worry your not blabbering at all ha ha I hope the radiation goes well tomorrow. I have some nail hardner so I will put them on before I go for treatment. Thanks.
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Happy birthday, 35 smiling!
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301724 ~ Thank you so much!
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Hello ladies. I'm overdue to check in ... where do the days go? LouBar - rads will feel like a piece of cake compared to chemo! I've done 10 and have 6 to go. My skin is a bit pink but doesn't bother me so far. For some reason though my shoulder/socket hurts. Dr. thinks maybe physio after rads may help. 35_smiling - HaPpY bIrThDaY tO yOu!!! Po-ke, Congrats on finishing chemo! You are one, tough young gal! :-). Marlene - how's mama and baby doing? Haven't heard for awhile. Toots - glad life is getting normal feeling again!?! Celineflower - thinking of you too. 301724 - glad to see you still here! Hope we all have a good day today! Hugs.
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35-smiling - Hope you have a wonderful birthday, and heres to many many more of them x
Marlene - hugs to you and little one x
Loubar - legs particularly muscles in calves like lead weights but the exercise in water is great - but I will have to stop once I start radiotherapy because oncologist says there is a big chance that the chlorinated water will burn...........
Poke - sounds like you had a good trip
Had a friend sent me something the other day which I thought was lovely - she sent 'wishing Hope for the fighters, Peace for the survivors and Prayers for the taken' hope you don't mind me sharing with you all x
Take care all, lots of hugs and silver linings x
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My treatment went okay yesterday. Well…I cried for about 15 minutes and had idea or clue why…it was strange. This is the second time I start to cry and have no reason for it. I mean it’s not that I am going to my treatments alone; my husband and cousin (who also is a survivor of Breast Cancer) are there with me every week! Has this happen to anyone? I am not going crazy am I
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Well I did try iced my feet and hands during treatment (the nurse looked at me strange so I explained to her what I read on this site) but I woke up today and good lord my toes feels more numb then before and my finger nails are hurting now. My finger tips still feel numb like before and haven’t gotten any worst like my feet. I also noticed last night my hot flash was coming on hotter too. Talk about no sleep for me and my poor husband. All well…. I will try it again next week and see what happens.
halfcan ~ Thank you so much for the birthday shout out
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Toots ~ Thank you so much for the birthday shout out! Also, thank you for sharing to us what our friend sent you. That was so beautiful and inspiring to read
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I have been thinking about this for some time now trying to have a baby. We have been married for four years and we have had seven miscarriages and successful one birth (when I was 17yrs old). I would love to have given my husband a child of his own because he has no kids. I feel like I am cheating him out of having children. We still don’t know if the cancer caused them or not because I had five of them between 2010-2011 and two in 2012 then I was diagnosed in August of 2012 of the stage IV HER2 Neu+ breast cancer which spread to my spine. I’ve read on this site that some women had all their chemo and radiation treatments then stopped tried to conceive and given birth then return to receive their final treatment for the next five years. I know it’s a risk but there isn’t much data out there stating otherwise. I feel lost…my husband said he would do whatever I decide but really doesn’t mind not having children if it’s going to cause my life. I am not too sure if they would allow us to adopt knowing I have cancer either. Has anyone of you heard of any successful stories from women who has their cancer similar to mine?
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35 smiling, taxol is well known for causing numbness and tingling in hands and feet. I don't believe icing will help with that - it's more for nail problems. What was suggested to me for the numbness/tingling was this: Vitamin B6 - 100 mg per day, and glutamine powder - 30 grams per day, split into 2 or 3 doses. You can get the glutamine powder at GNC (if you have GNC where you are) or I'm sure you could order it over the Internet. For the GNC kind, 30 grams is about 2 heaping tablespoons. I mixed 1 heaping tablespoon in 8 oz of iced tea and drank that twice a day. You can mix it in whatever you want. I had 12 weekly taxol and used the glutamine on the day of treatment and 3 following days. You could use it every day if your tingling and numbness continues. These 2 things seemed to help me. My chemo nurse told me I should continue the glutamine for a few weeks after finishing taxol. I didn't because I didn't think I needed it, but then about 2 weeks PFC I developed a numb big toe. It's going away - mostly gone now at about 12 weeks PFC. I did start up the B6 again. Good luck to you.
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