Today, 8th March, is International Women's Day.
There are 1,000's of events happening around the world to mark the economic, social and political achievements of women.
As last year, we at WCSUK are taking part by asking people to take a simple pledge - to help raise awareness of womb cancer!
https://www.facebook.com/events/587352184627351/#!/events/587352184627351/
Please join us in raising awareness and help us cut the number of women being diagnosed with this cancer.
We know that it's not just a cancer that affects post menopausal women so all women need to be aware of the signs and symptoms and be aware of the factors that make it more likely that they might be at risk of getting it.
You can check out our page on the International Women's Day website too http://www1.internationalwomensday.com/wcsuk
So please share the links with all your female friends. We have to spread the word and raise awareness if we are to cut the number of women being diagnosed.
Kaz
Womb Cancer Support UK provide advice and support for women with womb cancer. We also work hard to raise awareness of womb cancer. We are on Twitter and have a Facebook page. https://www.facebook.com/WombCancerSupportUK
Friday, 8 March 2013
Monday, 4 March 2013
Your help required please!
We were contacted last week by Dr Jane Dennehey, the co-founder of the Gender Hub a research organisation interested in social issues with a focus on health and work.
She has asked if WCSUK would take part in a survey which is about understanding how women, their partners, families and friends cope and live with womb cancer on a day-to-day basis.
We have placed details of the survey on the Facebook page https://www.facebook.com/WombCancerSupportUK
and so far 27 of the women from the group have done the survey, so thank you very much to them.
The survey can be accessed via this link http://www.surveymonkey.com/s/2ZLQ2RM so if you are interested in taking part then please do so. There is the option of doing a follow up survey, either by phone or email, but there is no pressure on you to do so.
The initial survey is completely confidential.
She has asked if WCSUK would take part in a survey which is about understanding how women, their partners, families and friends cope and live with womb cancer on a day-to-day basis.
We have placed details of the survey on the Facebook page https://www.facebook.com/WombCancerSupportUK
and so far 27 of the women from the group have done the survey, so thank you very much to them.
The survey can be accessed via this link http://www.surveymonkey.com/s/2ZLQ2RM so if you are interested in taking part then please do so. There is the option of doing a follow up survey, either by phone or email, but there is no pressure on you to do so.
The initial survey is completely confidential.
Saturday, 23 February 2013
Advocacy Award
You may remember last year that WCSUK became a partner in the One Team One Goal worldwide coalition building campaign to unite gyneacological oncology practice and advocacy groups.
We are very pleased to announce today that we have recently has been honored with One Team One Goal Advocacy Champion (Europe) Award.
Debra and I are extremely honoured to receive this award.
We are very pleased to announce today that we have recently has been honored with One Team One Goal Advocacy Champion (Europe) Award.
Debra and I are extremely honoured to receive this award.
Wednesday, 20 February 2013
Support - when its needed, on your terms!
When I started Womb Cancer Support UK back in April 2011, I did so because I didn't want other women going through womb cancer to feel as alone and scared as I had been 16 months previously when I was diagnosed.
I was diagnosed on 23rd Dec 2009 and had my hysterectomy on 25th Jan 2010. I got my pathology results 3 weeks later and was then told that there were cancer cells still present and I would need chemotherapy and radiotherapy.
Thats when it hit me. Originally my Consultant had said he was 99.9% sure they could remove all the cancer through the hysterectomy - it was only when the pathology results came back and showed that there were cancer cells present in the stomach wash they did, did I realise that 99.9% wasn't good enough!
Cancer aside, the hysterectomy was the best thing I ever did. It put an end to over 30 years of extremely heavy, irregular and painful periods - sometimes lasting several weeks at a time.
So the thought of never having to worry about that again was great.
But being told that I was going to be pumped full of toxic chemicals, and have my hair fall out; and then have to go through 5 weeks of being irradiated every day scared the life out of me!!!
I didn't know anyone who had cancer; there was no history of it in my family. I had no one to talk to about it.
I live on an island off the west coast of Scotland and when I got my diagnosis, I was the only one on the island with womb cancer. I joined the local cancer support group but it was full of women with breast cancer and at 46, I was the youngest there by a good 15 years.
I felt scared, isolated and alone.
I was lucky enough to get (and still have) regular visits from a wonderful Macmillan nurse who has helped my immensely throughout the past 3 years.
When my treatment eventually ended in July 2010, a week before my 47th birthday, I felt cast adrift. My security blanket of regular visits to hospital and all the tests had gone.
Again, I felt alone. I expected my health to improve slightly after the end of the treatment. I had suffered with severe diarrhoea for the whole 5 weeks of radiotherapy aswell as cystitis but this lasted for several weeks after and indeed I now have long term bowel problems as a result of the treatment.
Ever since I got my diagnosis I spent ages scouring the internet looking for information about womb cancer. Anything - treatment options, side effects, causes; symptoms.
I looked for support groups - there weren't any specifically for womb cancer patients. I used the forums on the Macmillan website and joined a US based support group on Facebook but it still felt like there was something lacking.
And thats where WCSUK came in. After a chat with a fellow womb cancer patient that I had met through FB I decided to start my own womb cancer support group!
The rest, as they say, is history!!
https://www.facebook.com/WombCancerSupportUK
I was diagnosed on 23rd Dec 2009 and had my hysterectomy on 25th Jan 2010. I got my pathology results 3 weeks later and was then told that there were cancer cells still present and I would need chemotherapy and radiotherapy.
Thats when it hit me. Originally my Consultant had said he was 99.9% sure they could remove all the cancer through the hysterectomy - it was only when the pathology results came back and showed that there were cancer cells present in the stomach wash they did, did I realise that 99.9% wasn't good enough!
Cancer aside, the hysterectomy was the best thing I ever did. It put an end to over 30 years of extremely heavy, irregular and painful periods - sometimes lasting several weeks at a time.
So the thought of never having to worry about that again was great.
But being told that I was going to be pumped full of toxic chemicals, and have my hair fall out; and then have to go through 5 weeks of being irradiated every day scared the life out of me!!!
I didn't know anyone who had cancer; there was no history of it in my family. I had no one to talk to about it.
I live on an island off the west coast of Scotland and when I got my diagnosis, I was the only one on the island with womb cancer. I joined the local cancer support group but it was full of women with breast cancer and at 46, I was the youngest there by a good 15 years.
I felt scared, isolated and alone.
I was lucky enough to get (and still have) regular visits from a wonderful Macmillan nurse who has helped my immensely throughout the past 3 years.
When my treatment eventually ended in July 2010, a week before my 47th birthday, I felt cast adrift. My security blanket of regular visits to hospital and all the tests had gone.
Again, I felt alone. I expected my health to improve slightly after the end of the treatment. I had suffered with severe diarrhoea for the whole 5 weeks of radiotherapy aswell as cystitis but this lasted for several weeks after and indeed I now have long term bowel problems as a result of the treatment.
Ever since I got my diagnosis I spent ages scouring the internet looking for information about womb cancer. Anything - treatment options, side effects, causes; symptoms.
I looked for support groups - there weren't any specifically for womb cancer patients. I used the forums on the Macmillan website and joined a US based support group on Facebook but it still felt like there was something lacking.
And thats where WCSUK came in. After a chat with a fellow womb cancer patient that I had met through FB I decided to start my own womb cancer support group!
The rest, as they say, is history!!
https://www.facebook.com/WombCancerSupportUK
Monday, 28 January 2013
Cancer and depression
We all feel a little down from time to time, especially when we are going through something like cancer. But when does it cross the line from being a bit down to being depressed; and what can you do about it?
Depression can affect your ability to cope with simple, everyday things such as sleeping, hygiene, eating, social activities and work.
If you are depressed, it’s impossible to simply "get over it". Well meaning family members or friends will often use this phrase and it's often difficult for people around you to understand how you feel.. Unless someone has been depressed themselves, it is almost impossible for them to understand what it feels like.
Depression is said to be the least noticed symptom in people with cancer. Yet it can be one of the hardest to cope with. GP's and cancer specalists are getting better at recognising and treating depression in people with cancer. But there is still a lot more significant research to be done.
According to CRUK, almost 60% of people with cancer will get depressed. It may happen soon after you are diagnosed, but it is also quite normal to become depressed after finishing treatment.
Depression can be triggered by a number of things. The impact of being diagnosed with cancer is enough to trigger a depressive illness in some people. Changes in hormone levels may contribute to depression in some people so the fact that most of us will have gone into surgical menopause after a total hysterectomy is also a factor.
Also once treatment has ended and you are no longer being seen frequently by your medical team you can sometimes feel lonely and isolated. You no longer have the security of having people looking after you and this can sometimes trigger depression.
It is important to remember that depression is not a sign of failure or an inability to cope. Never feel guilty about feeling depressed or not feeling positive all the time. It can usually be treated successfully and the first step to feeling better is finding appropriate help.
Speak to your GP, who may prescribe an antidepressant to help you. They can take some time before you feel any benefit but you should start to feel some improvement after a couple of weeks. There are different types of antidepressants, and your doctors may need to try more than one to find the type that suits you best.
If you’re very depressed, your GP may refer you to a psychiatrist or clinical psychologist.
Macmillan have a very good section on their website about depression and remember that you can always contact them for help and advice. http://www.macmillan.org.uk/Cancerinformation/Livingwithandaftercancer/Emotionaleffects/Depression.aspx
Remember, you are not alone and you don't have to go through depression on your own. Never be afraid to ask for help.
Depression can affect your ability to cope with simple, everyday things such as sleeping, hygiene, eating, social activities and work.
If you are depressed, it’s impossible to simply "get over it". Well meaning family members or friends will often use this phrase and it's often difficult for people around you to understand how you feel.. Unless someone has been depressed themselves, it is almost impossible for them to understand what it feels like.
Depression is said to be the least noticed symptom in people with cancer. Yet it can be one of the hardest to cope with. GP's and cancer specalists are getting better at recognising and treating depression in people with cancer. But there is still a lot more significant research to be done.
According to CRUK, almost 60% of people with cancer will get depressed. It may happen soon after you are diagnosed, but it is also quite normal to become depressed after finishing treatment.
Depression can be triggered by a number of things. The impact of being diagnosed with cancer is enough to trigger a depressive illness in some people. Changes in hormone levels may contribute to depression in some people so the fact that most of us will have gone into surgical menopause after a total hysterectomy is also a factor.
Also once treatment has ended and you are no longer being seen frequently by your medical team you can sometimes feel lonely and isolated. You no longer have the security of having people looking after you and this can sometimes trigger depression.
It is important to remember that depression is not a sign of failure or an inability to cope. Never feel guilty about feeling depressed or not feeling positive all the time. It can usually be treated successfully and the first step to feeling better is finding appropriate help.
Speak to your GP, who may prescribe an antidepressant to help you. They can take some time before you feel any benefit but you should start to feel some improvement after a couple of weeks. There are different types of antidepressants, and your doctors may need to try more than one to find the type that suits you best.
If you’re very depressed, your GP may refer you to a psychiatrist or clinical psychologist.
Macmillan have a very good section on their website about depression and remember that you can always contact them for help and advice. http://www.macmillan.org.uk/Cancerinformation/Livingwithandaftercancer/Emotionaleffects/Depression.aspx
Remember, you are not alone and you don't have to go through depression on your own. Never be afraid to ask for help.
Friday, 18 January 2013
Win at all costs?
So Lance Armstrong has finally admitted to being a cheat. http://www.bbc.co.uk/sport/0/cycling/21066354
The thing is, the people that he's really cheated, as far as I am concerned, are the millions of cancer patients who read his books and believed in him.
He says that his battle with cancer gave him a "win at all costs" attitude. Well, most of us have that when we've been given a diagnosis of cancer. But we don't turn into lying, cheating cowards!
Because thats what I think he is, a coward.
He was scared of dying and couldn't admit it to himself. I read his books and what struck me was his attitude to having cancer. Most of us have this "I'm going to fight this and I'm going to win" attitude but it seemed to go far beyond that with Armstrong.
Looking at all the news reports today about his interview with Oprah Winfrey, its all about how he's ruined the sport; ruined the reputation of "sportsmanship"; bought cycling into disripute! Its all about money, success, ego.
I can't find much about how the millions of cancer patients feel about being let down by someone they believed in. Someone who gave them hope.
http://www.freep.com/usatoday/article/1842777&usatref=sportsmod?odyssey=mod%7Cnewswell%7Ctext%7CSports%7Cp
The Doctor who treated him says that "his legacy is going to be his legacy as a cancer survivor and what he's meant to the cancer community.''
Really? I'm not so sure! With all the calls for him to be tried in a court of law and sent to prison - its obvious that most people (maybe those who havn't had a cancer diagnosis!!) feel differently.
But I guess what it really boils down to is this. We live in a society that worships success. We want winners! Doing your very best and not coming first isn't good enough!
The people calling him a cheat are probably the very same ones who think its ok fot their teams top striker to take a dive in the penalty area to score the winning goal.
I guess as always we need to look at the bigger picture. Without his Tour de France wins there would bever have been the Livestrong Foundation. This has helped many hundreds, thousands of people with cancer. Despite the admission from Armstrong of having taken performance enhancing drugs during his racing career, the Foundation will continue to help cancer patients around the world - and in the end, thats all that really matters as far as I am concerned.
The thing is, the people that he's really cheated, as far as I am concerned, are the millions of cancer patients who read his books and believed in him.
He says that his battle with cancer gave him a "win at all costs" attitude. Well, most of us have that when we've been given a diagnosis of cancer. But we don't turn into lying, cheating cowards!
Because thats what I think he is, a coward.
He was scared of dying and couldn't admit it to himself. I read his books and what struck me was his attitude to having cancer. Most of us have this "I'm going to fight this and I'm going to win" attitude but it seemed to go far beyond that with Armstrong.
Looking at all the news reports today about his interview with Oprah Winfrey, its all about how he's ruined the sport; ruined the reputation of "sportsmanship"; bought cycling into disripute! Its all about money, success, ego.
I can't find much about how the millions of cancer patients feel about being let down by someone they believed in. Someone who gave them hope.
http://www.freep.com/usatoday/article/1842777&usatref=sportsmod?odyssey=mod%7Cnewswell%7Ctext%7CSports%7Cp
The Doctor who treated him says that "his legacy is going to be his legacy as a cancer survivor and what he's meant to the cancer community.''
Really? I'm not so sure! With all the calls for him to be tried in a court of law and sent to prison - its obvious that most people (maybe those who havn't had a cancer diagnosis!!) feel differently.
But I guess what it really boils down to is this. We live in a society that worships success. We want winners! Doing your very best and not coming first isn't good enough!
The people calling him a cheat are probably the very same ones who think its ok fot their teams top striker to take a dive in the penalty area to score the winning goal.
I guess as always we need to look at the bigger picture. Without his Tour de France wins there would bever have been the Livestrong Foundation. This has helped many hundreds, thousands of people with cancer. Despite the admission from Armstrong of having taken performance enhancing drugs during his racing career, the Foundation will continue to help cancer patients around the world - and in the end, thats all that really matters as far as I am concerned.
Sunday, 13 January 2013
Raising Awareness
Womb Cancer Support UK was set up back in April 2011 on Facebook as an online support group for women going through womb cancer.
It soon became clear that many of the women who joined the group had never heard of womb cancer before their diagnosis, myself included.
So bit by bit, we began to add awareness raising to our efforts and this took many forms.
During September 2011, we held out 1st Womb Cancer Awareness month, following the lead of our US peach sisters, who regard September as Uterine Awareness month.
We had a "Turn Facebook Peach" event where we asked people to change their profile pic to something peach for the month. Some of us held tea/coffee mornings in our own local area. I had a short article published in my local paper.
After the success of that first awareness campaign, we began to look at ways of doing more to raise awareness of womb cancer throughout the year and not just during September.
We had some leaflets printed that list some of the signs and symptoms to look out for and some of the women kindly agreed to distribute them at their local Health Centres, GP surgeries and Hospitals.
One of the best ways of raising awareness is to "come out" as a womb cancer survivor and a lot of the women in the group have done that by either wearing one of the peach wristbands or even getting a peach ribbon tattoo!
Its surprising the number of people who will ask about a wristband, especially if it's in a colour they don't recognise. I myself have been asked on numerous occasions why I wear mine!
Its often as ice breaker to a conversation and then you are able to do a bit of awareness raising which helps every woman out there!!
If you'd like a wristband (£1.50 each including p+p) then contact us via the FB page https://www.facebook.com/WombCancerSupportUK or email us at wombcancersupportuk@hotmail.co.uk
Also, if you are able to take some of our leaflets to leave at your local Health Centre etc then again please contact us and we'll get some in the post to you.
Awareness raising, in whatever form it takes, is vital if we are to inform women of the signs and symptoms of womb cancer and help to stop the increase in the numbers of women being diagnosed.
Thank you. xx
It soon became clear that many of the women who joined the group had never heard of womb cancer before their diagnosis, myself included.
So bit by bit, we began to add awareness raising to our efforts and this took many forms.
During September 2011, we held out 1st Womb Cancer Awareness month, following the lead of our US peach sisters, who regard September as Uterine Awareness month.
We had a "Turn Facebook Peach" event where we asked people to change their profile pic to something peach for the month. Some of us held tea/coffee mornings in our own local area. I had a short article published in my local paper.
After the success of that first awareness campaign, we began to look at ways of doing more to raise awareness of womb cancer throughout the year and not just during September.
We had some leaflets printed that list some of the signs and symptoms to look out for and some of the women kindly agreed to distribute them at their local Health Centres, GP surgeries and Hospitals.
Its surprising the number of people who will ask about a wristband, especially if it's in a colour they don't recognise. I myself have been asked on numerous occasions why I wear mine!
Its often as ice breaker to a conversation and then you are able to do a bit of awareness raising which helps every woman out there!!
If you'd like a wristband (£1.50 each including p+p) then contact us via the FB page https://www.facebook.com/WombCancerSupportUK or email us at wombcancersupportuk@hotmail.co.uk
Also, if you are able to take some of our leaflets to leave at your local Health Centre etc then again please contact us and we'll get some in the post to you.
Awareness raising, in whatever form it takes, is vital if we are to inform women of the signs and symptoms of womb cancer and help to stop the increase in the numbers of women being diagnosed.
Thank you. xx
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