Starting chemo August 2017 - would love some moral support!
Comments
-
Kritti, you should get it checked, it does look painful I am sorry and you feel better when they tell you it is nothing.
I will have my 4th Taxol and 2nd Herceptin injection on Monday and now I feel so tired that I just could go and sleep for hours even though I slept for ten hours at night I feel drained. I went to my appointment with psychological nurse at cancer rehabilitation center and cried a river there over this crap and my fears. She told me that I am worried over things that did not happened yet and may never happen, and how it is impairing my quality of life etc. I understand all that but it is so overwhelming, the hair are falling off, I did not dyed it for over a month and my grey hair is visible now, my face is full of pimples, I feel like I will never get to be my old self. I in some way regret that I did not considered ice capping more seriously, it will take the hair years to grow to the normal shoulder length and before I had hair to the middle of my back.
We bought a wig yesterday, a really expensive one, but only because insurance is covering 70% of the price. We paid the difference between the max amount and the price out of pocket, my husband thought that it was important because now it will be so obvious that I am sick. My youngest was fascinated with the wig, wanted to touch it and said that although one could see that it was not my hair it did not look that fake. It has my hair color and is long and wavy just like my hair used to be. My manager is coming to town next week and he wanted us to meet if I would feel good and I am going to wear it just to see how he will react.
We also went to the forest for a walk a couple of days ago, me and my mom, just walked there along the pathway, never got into the woods, the day after I found a tick that crawled under my tub sock I have over my piccline on my shoulder. The sock just came of and before I draw it back I was like: what is this and saw the tick, the place where it bite me is red, I just thought it will never end, now I got the tick bite and a possible infection threat. That it did not dye, now when my blood is full of Taxol.
Hugs to all of you, i am sorry for my rant, again.
Cherry
-
Oh Cherry - I wish I could make the worry go away - for all of us! If your not living it I don't think you can really understand that it is truly a trauma. Your fears are shared and understood by all of us. Some days are so hard. My mindset is to really take advantage of the good days. I handled the hair much harder than anticipated. My DH, I am so blessed to have him, is very good at focusing me on today. "Why are you dwelling on how long it'll take your hair to grow back!?" And he's right - geez, don't I have enough to worry sbout
At least let me reassure you about the tick. A tick has to be attached for around 36 hours for it is transmit disease, so you should be ok.
-
Hello my fellow gals,
Been a while. I had my 3rd infusions yesterday and they decided to skip the Perjeta (Pertuzumab) due to the D and they doubled my Carboplatin (Paraplatin®) because my kidney functions are much better than before. Thanks to the steroids I have small flushing on my face and wasn't that sleepy, so I'll try Benadryl tonight. I'm also taking Claritin (Loratadine) for hopefully preventing bone pain from the Neulasta shot that I get a day after Chemo. That I start the day of chemo and for a few more days, like until Sunday, once daily. One of the nurses recommended it, which surprised me since my onco Doc doesn't recommend much of anything in the way of OTCs that aren't on the "list". I also have a little case of bilateral Edema in my lower legs to feet but my Doc is reluctant to have me take diuretics; messes with other things like potassium, etc.
I still haven't made soup yet but I plan on doing it one of these days. I want to make a big batch of chicken noodle soup with dumplings, but don't know if the leftovers will freeze well for storage.
I hope that all of you are doing well with your treatments and having less SE. Hugs to you all
-
Cherry, I am so so tired too and like you have just lost it a few times and cried and cried. I blame some of the tears and anxiety on all the drugs in our body. Of course, we are worried too, and that is normal. I keep telling myself that if this chemo is making all my hair go away and die, it must be doing the same to the cancer. I hope so anyway! Hang in there. You can do this.
-
VL22, of what I red it takes 24-36 hours for borrelios to be transmitted but TBE that can cause brain inflammation can be transmitted very quickly, although it is not very common. My husband and the youngest daughter are vaccinated for TBE because we are often in the forest, but not me. I am usually very careful and check myself from top to toes when I get back from the woods, but this time we only walked along the pathway while I had a feather jacket because it is getting chilly here so how it crap got under my clothe I have no idea. This one was there for at least 16 hours.
My husband is exactly the same telling me that the chances are much bigger that everything will be fine, but uncertainty is awful. And the only tool I so far learnt to employ, when I feel like I am once again falling down the rabbit hole, is to say I am not going to die today, at least today I can live without this unbearable anxiety. I will continue with therapy because this lady soothes me a bit. I cannot even attribute it to the chemo SE, I have been like this since the diagnosis.
Strength to all of us, here is the only place where I post it as is without anyone asking each other behind my back: does she need to talk about it all the time. Well, it does occupy my mind even though I am having treatment, working part time and trying to keep things done at home. Life has changed and I do not know how long it will take my mind to adjust to it.
Cherry
-
redeesides, I am also telling myself that that chemo must better be doing its job and we will have to endure, there is simply no any other choice. I am sorry you are crying too but in some way you may feel better that you are not doing it alone. I myself usually have tears near and these days it is just coming and coming for any reason.
I have been given a smaller booklet today in the clinic, called My book, it is for children whose parents have a serious illness. I was told to read it myself before I read it with my youngest. I red it and cried another river, the last chapter says: sometimes your parent may die, you did nothing to cause this illness and you will have adult people, friends and family, around you who will help you. I cried another Mississippi. I wonder if I should remove this last page, otherwise I do not feel like giving it to her.
-
Craps Cherry don't cry honey, you will be fine. Many prayers and please God don't let her down.
Gals I don't know what to say, so much sadness and cris and I know we will be fine as soon as we get through this journey. 🙏🙏🙏🙏
-
Marooshka -- thanks for sharing your experience about feeling hot and fever.
In term of icing, I tried using ice gel pack inserted into socks this Wed during the infusion. Not too complicated. There is a refrigerator in the infusion room that allows me to frige the replacement gel, which made everything easier. Not sure about the effect, but it doesn't hurt to try.
-
clearpath - Does the blood test result with WBC exceeds the limit and platelets below normal after neulasta hold you back from next round chemo?
And a question for the group: does anyone have muscle pain starting from the 3rd day and lasts about 3-4 days besides bone pain? I'm on Texotere and C
-
Walking - I saw muscle / bone pains in the weekly taxol group, they suggested taking Aleve or Advil I think.
Will start my taxol next Friday,
-
paullettek - thank you! I will try the pain reliever! And good luck toyour Taxel Journey!
-
Walkingintheclouds I did have muscle pain and some deep joint pain starting day 3. I was told to take Claritin and Aleve. I had tried ibuprofen with no luck and switched to Aleve after a couple days. I can't stretch enough to help with muscle pain either after the surgery so that made it worse. But I also took epsom salt baths which helped.
-
Cherry I wanted to send you a big hug. We here really understand the worry and fear that we have to try to keep at bay. We can do it pretty successfully most of the time but not all of the time. We need to have those good cries. I lay in bed in the wee hours (can't sleep) and sometimes my thoughts bring me to tears yet I am coping. You are as well. Just need to express the sad/scary stuff now and then.
My feet continue to tingle and burn with altered sensation up to above my ankle. I hope my Onc has a trick up his sleeve to help alleviate this. The other thing is my hair is slowly falling all over the house. Strange sad feeling.
Thank you Angie for checking in and giving us encouragement. It worked for me.
Prayers for everyone
-
Cherry,
If it were me I would not say the death part to my child. Geez why does a kid need to worry about that if it may not happen? No, you will have plenty of time for that if you get to that point. I think it is just TOO much to tell a kid that if you don't know it for sure. Screw that book.
-
cherry -- how's your tick bite? Hope it didn't cause infection. Also, I want to say the same as Rdeeside did: screw the book!
-
I agree about the book, leave the death part out! My 7yr old is such a good kid at understanding. he knows my hair is falling out and isn't scared, he's come with me to try on wigs, he knows that I am sick and lets me rest when i need to. so proud of him!
it sucks that we all have to be dealing with this and horrendous side effects! i wish there was a way chemo could just kill the cancer cells and not the healthy cells.
oh and i know im gonna get there with the crying, when my hair gets shaved off i know i will cry! im a crier in general.
Hugs to all, have a lovely weekend
-
Thank you girls for your support and all the kind words, I always keep telling myself imagine you would not have this forum but then I just say I would have found it sooner or later because I was turning the internet upside down for information. To handle it emotionally is the worst part, physically I am just following the stream, there is a schedule to follow and this is what I am doing. But to handle all these feelings is hard and I still do not fell for taking drugs because it would feel like a failure. The therapist did also say that people in this situation are going through trauma which leads to the sense that one cannot control the situation and brain is trying to resolve this.
I neither feel like giving this book to my youngest, I would rather see the therapist again to discuss it.
The tick bite is red and a bit swollen but of what I red it will takes weeks until one can tell whether there is any sign of Lyme disease. I found it on Wednesday evening and in the morning the same day I had an appointment with my oncologist. I am sure it was there already when she was examining my breasts it is just no one needed to take a look at what is happening with my piccline. They usually take care of it once a week during the infusion.
About the side effects, I noticed this week that my nails stopped growing. I keep those short now which means I cut them every week, but now I see there is nothing much to cut, they did not grow, almost not at all. Did any of you experienced that?
I wonder whether the doctors at my clinic are too conservative. I specifically asked about Epsom salt for joint pain and the oncologist just shook his head. How could it be that so many are saying that they experience relief and the doctors do not confirm it. Now I did not experience any joint pain yet but I have nine infusions to go.
Once again, thank you all and hope the next week infusions will go smoothly for everybody.
Hugs, Cherry
-
Hi Walkingintheclouds - The oncologist is happy with high WBC. The platelet count is just under normal and they said that is expected with chemo. So in response to your question,no problem with being approved for treatment.
-
Leatherette and PauletteK thanks for the tip re dry mouth - will order Nuun.
-
I've been reading the postings in this group for a couple of weeks and decided to join the discussion. I started my first of 12 weekly chemo on August 22, and will have my fourth infusion of Taxol/Herceptin on Tuesday. All previous treatments have been uneventful but yesterday I started to have some mild digestive issues...nothing too bad. I'm also cold capping and experienced my first freezer burn which I'm nursing with aloe vera, coconut and vitamin E oil. I've enjoyed all of the suggestions and tips from all of you and look forward to joining in. In the meantime, I pray that you all have a great weekend and upcoming week!
-
Welcome Ivy sorry you are here with us but nice to know some of use don't have much SE.
-
Ivygirl121, welcome, sorry you had to join us. I will have my fourth Taxol and second Herceptin on Monday, I had my first on August 21. I do regret that I did not do ice-capping, is it working? My hair is coming off, probably lost half of it by now and I got a wig. Cherry
-
Cherry, I would also caution you on using that book with your children. Children don't really understand the nature of serious illnesses. Take diabetes for instances. Can it kill you, absolutely, but at the same time it does not mean it will kill you. Now if your kidneys started to fail and the doctors are telling you their is nothing they can do to help this from happening, time to get the book out. Breast cancer can most definitely kill people, but not all people who have breast cancer will die from it. Each case is different with different circumstances. Your prognosis is a good one. I personally would not be using that book at this time.
As far as the Lyme disease, it is a good thing you know you had a tick on you. If you start to develop symptoms and get tested and medication in a timely fashion your prognosis will be good. It is those that never knew a tick bit them and come down with symptoms, and it takes doctors many months or years to figure out what is going on before a diagnosis and/or medication is given. Many may have a worst prognosis. Just be vigilant.
-
Shellsatthebeach, our daughter is 11 and by the time we explained to her that I have bc she already started to figure it out on their own. We waited to meet the therapist and according to her you have to explain to your child what is going on and not keep it a secret, because the research show it can lead to depression in the future. So we have explained everything and she was scared of course but she is taking it well after the circumstances. But this time we were given this book and it was just to much for me to read and I decided not to give it to her until I talk to the therapist next week. This is our child and I know that the decision will only be made of us so at this point I do not see me giving it to her. I told it because I was so upset about the whole bc situation. I will monitor for the symptoms for this tick bite too, thank you. Cherry
-
Cherry,
It looks like I am one day behind you with treatments. I'll have my fourth on Tuesday. In spite of the small freezer burn on my scalp (which is slowly healing) I don't regret the cold capping process. I don't think I've lost any hair so far. Although it's a hassle to get the dry ice, pack the cooler and keeping track of everything, it helps the time pass very quickly. I will say that I wish the process was more affordable and accessible for all who want to use it. I often wonder if insurance would pay if BC was primarily a male condition. I'm just saying....
-
Ivygirl121, In my clinic they offer ice mittens and socks but no capping, I am not in US, I am in Europe, we have public health insurance and some things are just covered and some are not. I asked my oncologist and he said that they do not think that ice-capping was necessary. They did not think the mittens were needed either but I insisted. I do not know whether it were better if it was a male cancer, before my diagnosis I did not know many with cancer and was just like average people thinking that cancer happens to others, Cherry
-
Has anyone else had a little cold while on chemo? I have a slightly runny nose and an annoying cough. Feel ok otherwise and no fever. Wonder what I can take for the cough.
-
redeesides, now I do not know what medication you can take because we do not have similar meds, you can ask your doctor, but whenever I had lingering cough from the flu I used to grate a bit of ginger, pour boiling water on it and squeeze half of lemon, you can also add a spoon of honey, then just sip it hot. I hope this brew does not contain anything we are not allowed to eat while on chemo.
-
redeesides, I can't tell if I had some cold symptoms or it is just irritation from the smoke from all the fires. We are right in the path of so many of the fires and the hazy air has been a real irritant. For persistent cough my naturopath had shared a study on cough that used a mixture of coffee and honey that I have used in the Winter. You can mix about half a cup of honey with 1/2 oz instant coffee (I've used that instant espresso powder which I have for baking) then dissolve a tablespoon or so in some hot water and drink it a couple times a day.
-
rdeeside- could it be post nasal drips? Since we lost most of the nasal hair my nose runs more often then before. But my nasal drips are clear I know it is not a cold. Post nasal drips will make you cough.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team