sorry, not sure why the emotional content comment came on !!
Hi Clarence,
I am so sorry to read that you are having such a bad time. However, your are not alone and if you post on the Bone Mets thread there are lots of ladies with all kinds of mets that will be there to offer support, kindness and lots of knowledge.
Its a hard hard journey we are on and whilst I have it under control most of the time sometimes it just hits me and I feel overwhelmed by it all as I am sure everyone coping with this day to day does.
Try to find a nice thing to focus on doing each day, start off small and gradually build up to maybe a trip away or a night out. Most importantly though keep posting on here so that you don't think you are in this on your own.
(( )) hugs Maria
Niki, Wondering how you are feeling? Have you found any grieving support groups or breast cancer support. I remember when I was diagnosed with my primary breast cancer I felt OK and didn't feel I need support. Then when it came back in my lungs I felt entirely different. Friends and family don't get it!! They don't understand how lonely you can feel. It is not easy living this life! Part of my losing weight, beginning exercises and making a change every week was to help me concentrate on other things and keep my act together. My latest change is trying to find some little inexpensive things to do. I like nature and enjoy getting outside.Do you have any hobbies or activities you enjoy? Please tell us more about you! Hugs! Hang in there! FF
Hi Nicki, I just decided to take a look at this coffee lounge thread. Like Carolyn I post on the secondaries section. Your post about your mum and dementia brought you to my attention. I helped with my Aunt who had dementia. I also work at our local senior center and am in charge of a dementia program. Our senior center is a day program where seniors come to enjoy our programs or hang with their friends. Then we have the dementia program for early stage dementia we also take people in the program that need some extra help to enjoy the senior center. My job is to monitor their safety and guide them to have fun, since So many lose the ability to iniate socialization. It has always amazed me how people do not have any patience for dementia victims. Most of the other seniors have no patience for them. Complain how they repeat themselves, don't remember things, etc. They think their faking. My friends mother had dementia and her daughter in law thought she was faking it. She didn't understand that sometimes they are totally gone and other times they will have a lucid moment. This woman took peoples cameras. Lol no she wasn't stealing them, no she didn't have a thing for them, and no she didn't know she took them! They found 10 cameras in her bedroom. In drawers, closets and under her bed. Her daughter in law said look at all these cameras she stole. She said When they took her places and people woukd be looking for their cameras they would ask if she had it. Of course she would answer no. Her DIM said she is a liar and a thief and his them all. Well she didn't steal them she thought when she went places that it was her sons camera. She wasn't lying when she Saud she didn't have it, she truly forgot by that point that she had it. When she got home she was just stuffing it somewhere bc she didn't know where it came from and what to do with it. Even some professionals don't understand this and the limitations the people have. My cousin was a nurse and her husband a family Dr. They decided to take aunt out of the nursing home and take her home for 2 weeks. They bought her a goldfish and tank and tried to teach her how to care for it. They claimed she understood. They bought her anew TV and disposed of her old one. Well after 2 weeks they took her back to the nursing home with the new TV and gold fish. Well She killed the fish the first day bc she dumped in all the food, put the whole bottle of chlorine removing drops in the tank, and dipped out the water to water plants. Threw a glass in a nurses face bc she said I don't live here why are you keeping me prisoner. After being gone for 2 weeks she didn't remember the place. She though t someone stole her little TV and didn't know where the big TV came from or how to work it. She ended up in the psyche ward at the hospital til they got her squared away. So if professionals, family and other seniors can't understand what dementia people are going thru you can imagine others can't. Your friends might just not of understood.
Next and I will try to make this shorter. I've spent almost the last year trying to lose weight, get stronger and just have more control over myself. I decided that each week I would make one change in me and do it every day for a week and then try to continue it. If I didn't do it correctly I had to repeat it the next week without adding something else. I was also feeling lonely and felt I wasn't getting out and about enough. I knew I had to take the responsibility for changes to help my health and my happiness. This wasn't easy, but one step at a time made it nit So overwhelming. I did little things like this week you will cut portions, next no soda before noon, call up an old friend, make a date with an old friend, get out of the chair every hour, drink more water, start exercising doing 10 repetitions, after 2 months add more til you reach 25, leave a surprise on a gas pump at a convenience store (a note to have a good day and $2 to buy a coffee or other beverage), etc. I have lost 55lbs., I am able to walk for longer periods, I am happier and notice people are calling me to go out, I am able to do 40 sit-ups every night and couldn't do even one when I started, last night I decided to do 50! I haven't done that since high school! I'm 62! High school was 55 years ago! I thought the idea of changing one thing a week might help you out one foot in front of the other!
Sorry, I have rambled so much! Btw I definitely live to far to go out for coffee! I live across the pond in the USA. I live in Pennsylvania about an hour west of Philadelphia! Good luck be good to you! FF
Hello again lovely Nicki - just to say I am thinking of you and hoping you are having an ok day. As you see lots of ladies here feel for you and want to send you our love. Also many of us have been through the bald with one breast stage or similar. Fortunately my hair is now growing back but before cancer I had long blonde hair and now I have short curly brown/grey hair which isn't quite the same look! I know how hard the hair loss is, but trust me it will come back soon and hopefully then you will start to feel better about yourself. Also I am currently sporting one natural E cup breast and one reconstructed C cup breast (no nipple yet) - hope they can be made to match better eventually but will take a further 12-18 months to get the finished set. Lots of us are happy to share our experience of reconstruction if that interests you - I would strongly recommend it if you can bear more surgery in due course. If you feel able to say what area you live in, there may be ladies near you who could pop by or being treated at the same hospital who could meet you for a coffee when you are there. Do take care. Susan xx
Hello again
So pleased that you have had such positive feed back from this lovely forum.
I am off for a short break today where wifi is intermittent , but I will try and see how you get on with that scan.
Those lymph nodes are a right nuisance. I don't remember any problems mentioned before they whipped them out. The talk after on lymphoedema was more frightening than the mastectomy!
Take care
Big hug
Joan
Hi Nicki 🤗You are amazing. You deserve more than a medal after looking after your dear mum and getting through the mastectomy and treatment given. You are aloud to grieve your mum for as long as you want because although they say it gets easier it is never ever forgotten so those days when you feel c--- its aloud and it's okay xxxxxxxxxxxxxxx
you have been through an awful testing time in your life but guess what ? You have got through your operation and you are making the choice to ask for a little help. I think you are super brave. I am only beginning my journey with chemo first, one session down and five to go 👍.
I wish I knew where you lived as I would say come stay at mine for a little break because you deserve zillions of friends and let me tell you there are lots of folk out there that will give you friendship and once you start meeting people there will be no looking back for you.
This site is the most lovely place to be when your feeling down, happy , frustrated etc etc.
Im so pleased your going to be referred for councilling because then you can speak in confidence and let all your feelings out , it will help you so much.
Last week I got a clot and I have spent lots of time in and out of hospital where the doctors and nurses were just amazing . When I was there I met two lovely ladies and I even swapped phone numbers as she was going through the same treatment as me. I was so happy to have the company.
Take care xxxx
Nicki
Hey hello mate :). Well I was shattered this morning it was a tough game, 3 hours long,but we did it. Trhough to the semi finals now so fingers crossed.
Is it possible that you have a seroma, they can be very uncomfortable, I had one under my arm from the lymph node surgery, which were all clear following surgery, mine did go down after several weeks, when I checked it with my bcn she confirmed that was what it was and said if I can tolerate it and not have it drained that would be a good thing to do. Mine felt like I had a golf ball under my arm.
Good to hear that you are having a nap, At least you are resting and your body will be working at healing itself. You are not selfish at all my dear
Helena xxx
Nicki
Hey mate, sorry I have only just got home from a bowls competition so first chance I have had to check in with you. You are sounding more positive which is really good. Lots of very useful ideas you are having and the mcmillan centre seems to be spot on for you.
As the others have said try not to be too hard on yourself, you really are only in the early weeks of recovery from your chemo and surgery, everything is starting to settle down which hurts like no business but you will get there. How about if you are feeling guilty about resting that you plan some time in your day where you say to yourself, this is my relax time, perhaps start off with a 15 minute slot and then build from there so that you can get used to resting without feeling guilty, resting is a big part of our recovery process. I often find even now, and I did not have as much treatment as you, that I will get to a point in the day where my shoulders go heavy and the next minute I am asleep for about 10/15 minutes, wake up and I am able to carry on for the rest of the evening, but I know and have got used to doing this so I have learned to accept this as part of my recovery process.
I am going to sign off for the evening my dear as I am shattered. I want to share with you that we won tonight so we are through to the semi finals of the competition for the first time as a team, so proud of the other ladies as they played amazingly.
Will be in touch tomorrow.
Night night Helena xxx
Hello Nicky
Glad that my humble posting helped a bit. If you go to the main menu you will find a thread called going through treatment ...there is several chemo threads there to help you with side effects of the treatment u r going through at the moment ...day at a time ...baby steps .
Once u settle in with the forum and get to know the other ladies ..you might just find a buddy to meet up with you but sadly it won't be me as I don't live anywhere near you in bethnal green !!!!
I don't post here very often but hang around the secondary bc threads mostly but I will dip in here to keep up with your posts etc.
Anyway ...try to stay close to your daughter and granddaughter ...you will find her a tower of strength and you will be surprised just how much it will help.
Xxx
Hi Nicky,
So glad you're feeling a bit better & you have some plans about courses, great idea!
Please don't be so hard on yourself, it's just your caring & sensitive nature. Goodness, it's not long since your treatment, so it does take a while to recover for anyboby, let alone the stresses you've had as well.
As well as some of the other threads, there is a lovely group of ladies chatting on 'Progesterone, other hormones & fluffy cakes' in the hormone treatment board in 'going through treatment.' Carolyn, Helena & myself hang out there, so will keep an eye out for you if you want to join in. Do look at the other threads as well.
ann x
Nicky
I am now much happier. Treatment now just hormone therapy until I'm 81!
l am nearly 30 years older than you, but we still experience the same problems .
I have been lucky. Lots to look forward to and determined not to keep looking back
You have made the best move contacting Macmillan. They were my lifeline when my sister was dying , and they can help you.
Good Luck
Strange when I hadn't been on the forum for ages. Glad I picked up on your post last night.
I could sense a thread of hope. Long may that continue
Joan
Nicki
I am just glad that I have been able to be of some help albeit that it is only a little bit. I can only imagine how hard it was to write it, but you are brave and you know you are in a safe comfortable place here surrounded by people who get you and understand which has enabled you to reach out. That goes a long way to your asking for the help that you know you need to get.
Many years ago I was in a situation where I did not know where to turn, I knew I needed to do something about the relationship I was in bit I really did not know what to do, in the end I rang Samaritans and spoke to this lovely gentleman who spent a long time, perhaps an hour or more just listening to me, I found it a real help just to talk to someone who could be objective as he did not know me. I made the right decision and i have never looked back.
When I was diagnosed with bc, there was a point where I felt rather overwhelmed by it, my wonderful boss arranged for me to have some counselling which I found sooo good and really helped me. Perhaps you could speak with your breast cancer nurse, I know mine mentioned that there was a counselling service available at the breast clinic if I needed it.
You will heal from all this and you will learn to let go, the fact that you have recognised this and what you want to do is such a huge step to make and well done you for doing it.
I am going to have to sign off now as I need to be up at 6.30pm tomorrow, but I will check in again tomorrow night to see how you are.
Helena xxxx
Hi Nicky,
So sorry to hear how you're feeling, it is tough enough going through cancer treatment anyway, let alone what you went through with your mum & family as well. Sadly, family & friends sometimes are not helpful, but that's not your fault, rather it's more about them. It certainly sounds like it's just all rather caught up with you a bit, but you are not alone.
Glad to see you have been in touch with Macmillan, there may also be volunteer support available if you feel that might be helpful, your treatment team may also be able to advise on this.
Also, there is the helpline above to talk things through if you need to.
Do come & chat here whenever you want to & take care.
sending hugs
ann x
Let's try to help.
l know how hard it is to get on with breast cancer and I have a family. My mother and sister died within 11months of each other. My mother died from old age and my sister struggled with cancer for four yrears. I also was the main carer for my mother in law and she died 3 weeks before my sister. I had travelled many miles over some years trying to care for them, so it seemed like a cruel reward when breast cancer was diagnosed.. No mum or sister - missed them more than ever.
lt was my friends who got me through it all , family are too traumatised, Mum isn't supposed to be ill and husbands can't cope.
So where can you find support, particularly female.
Is there a WI or something similar you could join. They are friendly with meetings and clubs to join. I hadn't been a member long but they were so supportive.. Any breast cancer or Macmillan groups near you?
You say you are bald with one breast, well you are not alone there , but you are only 7 weeks post op so don't expect too much.
It may be that you could try and make contact with some former friends. Explain how you felt, see if bridges could be built . If just one of them contacted you back it's a start. Perhaps you will have more insight into their rejection of you.
I probably have been no use, but I wish you well . You must still be under the care of a medical team or GP. Time to be honest with them, they might be able to help as well.
This forum is a friendly place .I am sure someone else will come up with ideas , better than mine.
Nicki
I have just read your post and wanted to just let you know that we are all here for you on this forum. I really do not know what else to say that will be of help, but I wonder if it might help you to call the helpline number where you will be able to speak to someone who might be able to give you help and support.
You have come through so much and done so well with everything that you have been through and no one can ever take that away from you.
Just sending you a lovely hug and hope that you can find the help and support you need. Dont stop coming on here and talking to us, that is what this forum is all about.
Helena xxx