After completing radiation on my right breast in 2013 with very little side effects I assumed, wrongly,that my second time, now on my left breast would be a breeze.
I expected the burns and blisters and the tiredness, that was all just a part of having radiation. This time around though my side effects were much worse than the first time. I found myself feeling very tired immediately after having radiation, I found it hard to keep my eyes open sometimes whilst still driving home. I couldn't rest or sleep as much as my body wanted me to and it was months before I got some energy back.
What I wasn't expecting was damage to my esophagus. I now have reflux. I have had episodes where I get excruciating pain in my chest. I can't swallow without pain, not even fluid. My doctor calls it spasms in the esophagus, caused by the radiation. I've just had a gastroscopy, a camera down the throat, to see how much damage has been caused to my esophagus. I will get those results in a few weeks.
This is just another side effect of breast cancer. Does it ever end?
Welcome to My Breast Cancer Journey. I am 43 years old and I was diagnosed in February 2013. You can now also visit www.breastcancerandme.info
Showing posts with label breast cancer. Show all posts
Showing posts with label breast cancer. Show all posts
Thursday, 12 May 2016
Sunday, 3 April 2016
Oncotype Test
The Oncotype DX test is a genomic test that analyzes the activity of a group of genes that can affect how a cancer is likely to behave and respond to treatment. The Oncotype DX is used in two ways:
to help doctors figure out a woman’s risk of early-stage, estrogen-receptor-positive breast cancer coming back (recurrence), as well as how likely she is to benefit from chemotherapy after breast cancer surgery
to help doctors figure out a woman’s risk of DCIS (ductal carcinoma in situ) coming back (recurrence) and/or the risk of a new invasive cancer developing in the same breast, as well as how likely she is to benefit from radiation therapy after DCIS surgery
The results of the Oncotype DX test, combined with other features of the cancer, can help you make a more informed decision about whether or not to have chemotherapy to treat early-stage hormone-receptor-positive breast cancer or radiation therapy to treat DCIS.
Who is eligible for the Oncotype DX test?
You may be a candidate for the Oncotype DX test if:
you’ve recently been diagnosed with stage I or II invasive breast cancer
the cancer is estrogen-receptor-positive
there is no cancer in your lymph nodes (lymph node-negative breast cancer)
you and your doctor are making decisions about chemotherapy.
Most early-stage (stage I or II), estrogen-receptor-positive breast cancers that haven’t spread to the lymph nodes are considered to be at low risk for recurrence. After surgery, hormonal therapies such as an aromatase inhibitor or tamoxifen are prescribed to reduce the risk that the cancer will come back in the future. Whether or not chemotherapy is also necessary has been an area of uncertainty for patients and their doctors.
If you’ve been diagnosed with early-stage, estrogen-receptor-positive breast cancer, the Oncotype DX test can help you and your doctor make a more informed decision about whether or not you need chemotherapy. (Some research also suggests the test may help postmenopausal women with estrogen-receptor-positive breast cancer that has spread to the lymph nodes make chemotherapy decisions. Talk to your doctor if you are in this group.)
You also may be a candidate for the Oncotype DX test if:
you’ve recently been diagnosed with DCIS
you’re having lumpectomy to remove the DCIS
DCIS is the most common form of non-invasive breast cancer. DCIS usually is treated by surgically removing the cancer (lumpectomy in most cases). After surgery, hormonal therapy may be recommended if the DCIS is hormone-receptor-positive. Radiation therapy may be recommended for some women. Doctors aren’t always sure which women will benefit from radiation therapy.
If you’ve been diagnosed with DCIS, the Oncotype DX test can help you and your doctor make a more informed decision about whether or not you need radiation therapy.
Source: breastcancer.org
to help doctors figure out a woman’s risk of early-stage, estrogen-receptor-positive breast cancer coming back (recurrence), as well as how likely she is to benefit from chemotherapy after breast cancer surgery
to help doctors figure out a woman’s risk of DCIS (ductal carcinoma in situ) coming back (recurrence) and/or the risk of a new invasive cancer developing in the same breast, as well as how likely she is to benefit from radiation therapy after DCIS surgery
The results of the Oncotype DX test, combined with other features of the cancer, can help you make a more informed decision about whether or not to have chemotherapy to treat early-stage hormone-receptor-positive breast cancer or radiation therapy to treat DCIS.
Who is eligible for the Oncotype DX test?
You may be a candidate for the Oncotype DX test if:
you’ve recently been diagnosed with stage I or II invasive breast cancer
the cancer is estrogen-receptor-positive
there is no cancer in your lymph nodes (lymph node-negative breast cancer)
you and your doctor are making decisions about chemotherapy.
Most early-stage (stage I or II), estrogen-receptor-positive breast cancers that haven’t spread to the lymph nodes are considered to be at low risk for recurrence. After surgery, hormonal therapies such as an aromatase inhibitor or tamoxifen are prescribed to reduce the risk that the cancer will come back in the future. Whether or not chemotherapy is also necessary has been an area of uncertainty for patients and their doctors.
If you’ve been diagnosed with early-stage, estrogen-receptor-positive breast cancer, the Oncotype DX test can help you and your doctor make a more informed decision about whether or not you need chemotherapy. (Some research also suggests the test may help postmenopausal women with estrogen-receptor-positive breast cancer that has spread to the lymph nodes make chemotherapy decisions. Talk to your doctor if you are in this group.)
You also may be a candidate for the Oncotype DX test if:
you’ve recently been diagnosed with DCIS
you’re having lumpectomy to remove the DCIS
DCIS is the most common form of non-invasive breast cancer. DCIS usually is treated by surgically removing the cancer (lumpectomy in most cases). After surgery, hormonal therapy may be recommended if the DCIS is hormone-receptor-positive. Radiation therapy may be recommended for some women. Doctors aren’t always sure which women will benefit from radiation therapy.
If you’ve been diagnosed with DCIS, the Oncotype DX test can help you and your doctor make a more informed decision about whether or not you need radiation therapy.
Source: breastcancer.org
Monday, 28 March 2016
My Book Currently in the top 10
My book is available as an e=book or paperback on Amazon.com Fighting The Storm - My Breast Cancer Journey
http://www.amazon.com/Fighting-Storm-Breast-Cancer-Journey-ebook/dp/B017UTFFRQ/ref=sr_1_1?s=digital-text&ie=UTF8&qid=1453013528&sr=1-1&keywords=fighting+the+storm
http://www.amazon.com/Fighting-Storm-Breast-Cancer-Journey-ebook/dp/B017UTFFRQ/ref=sr_1_1?s=digital-text&ie=UTF8&qid=1453013528&sr=1-1&keywords=fighting+the+storm
Saturday, 26 March 2016
Monday, 1 February 2016
Monday, 11 January 2016
Sugar
This Common Dietary Ingredient May Increase Breast Cancer and Lung Metastasis Risk
According to a recent study, 30% of mice in a controlled group developed breast cancer after six months compared to 50%-58% of mice that were given this ingredient commonly found in your kitchen.
This dietary ingredient could be a trigger for breast cancer and lung metastasis
One commonly hypothesized "trigger" of cancer metastasis that researchers have been focused on for years is an item found in basically every American household: sugar. Sugar is a source of energy for healthy cells in our bodies, but researchers have long postulated that it could also be the energy source that kicks cancer cells into overdrive. However, proving this hypothesis has been a challenge -- until now.
Thursday, 10 December 2015
Fighting The Storm
Also now available in paperback
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Headscarf or Wig?
When you are about to start chemo and you know you will lose your hair one of the big decisions you will have to make is whether to wear a headscarf or wig,some people also decide not to wear anything. What will you choose? A headscarf or wig? Whatever you decide you have to choose the option that you feel most comfortable with. I couldn't bring myself to buy a wig, for me it was an easier option to choose to wear headscarves, beanies and hats. They were comfortable, pretty, and fun. I wore an under scarf/headwrap of cotton fabric and wore slouch beanies over the top when I went out. Some days I wore a headscarf but I was most comfortable with my beanies. When I was in the privacy of my home I wore only the cotton under scarf/ head wrap. My beanies were pink, black, white and beige.They became a kind of security blanket. I have kept them as a reminder. I wore the slouch beanies because they are larger than the average beanie and fit better on my head so people couldn't see my baldness.
Tamoxifen and Zoladex
I was on tamoxifen and zoladex for two and a half years. My belief was that both of those together would stop any recurrence, especially a recurrence of the same er+ pr+ breast cancer. After all, tamoxifen is used to block or kill any cells and zoladex puts my ovaries to sleep, so I will be producing little to no estrogen. For two and a half years I was in menopause, hot flashes, the works. I was safe, at least from getting breast cancer again, maybe I would get a secondary cancer but it wouldn't return in my breasts, right? WRONG.
Apparently, there is only a 4% chance of a recurrence or being diagnosed with breast cancer in the other breast when on this treatment . I am in that 4%.
My point, if you are on this treatment, keep checking your breasts, don't think that this treatment will stop your chances of getting breast cancer again. It does lower your chances, yes, but it doesn't stop the cancer from coming back. Be and stay vigilant.
Tamoxifen and Zoladex (chemical name: goserelin) are hormonal therapy medicines used to lower the risk of breast cancer coming back (recurrence) in premenopausal women diagnosed with early-stage, hormone-receptor-positive breast cancer. A study found that tamoxifen and Zoladex work about the same to lower the risk of breast cancer coming back.
Estrogen can make hormone-receptor-positive breast cancers grow. Hormonal therapy medicines treat hormone-receptor-positive breast cancers in two ways:
by blocking the action of estrogen in the body
by lowering the amount of estrogen in the body
Apparently, there is only a 4% chance of a recurrence or being diagnosed with breast cancer in the other breast when on this treatment . I am in that 4%.
My point, if you are on this treatment, keep checking your breasts, don't think that this treatment will stop your chances of getting breast cancer again. It does lower your chances, yes, but it doesn't stop the cancer from coming back. Be and stay vigilant.
Tamoxifen and Zoladex (chemical name: goserelin) are hormonal therapy medicines used to lower the risk of breast cancer coming back (recurrence) in premenopausal women diagnosed with early-stage, hormone-receptor-positive breast cancer. A study found that tamoxifen and Zoladex work about the same to lower the risk of breast cancer coming back.
Estrogen can make hormone-receptor-positive breast cancers grow. Hormonal therapy medicines treat hormone-receptor-positive breast cancers in two ways:
by blocking the action of estrogen in the body
by lowering the amount of estrogen in the body
Monday, 30 November 2015
Radiation Treatment
Radiation can reduce breast cancer recurrence by up to 70% — but it can also have unfortunate side effects. This is because it damages healthy cells while it’s zapping cancerous cells. It’s common to be nervous or scared of what may happen to your skin during this type of therapy, so we’re here to break it down.
The side effects tend to gradually appear a couple weeks after the treatment has started, and can last for up to six months after it has ended. The severity of the symptoms can vary from person to person, especially when you factor in how many weeks the therapy is required. In some cases, the onset of side effects won’t occur until months or even years after treatment, but this is fairly rare.
What Are The Side Effects Of Radiation Therapy?
The most common effects include damage to skin (like sensitivity, skin weepiness, burning, dryness, blisters, peeling, and itchiness) and fatigue that won’t improve with rest. Less common effects include heart problems, lung problems, low white blood cell count, and lymphoedema. In extremely rare cases, radiation can lead to a secondary cancer, like sarcoma (cancer of the connective tissues).
Your breasts may change slightly in size (due to fluid build-up or scar tissue), the skin may appear thicker, your pores may be more noticeable, and your skin may even become darker in the treated area. In addition, your changed body image will definitely take some getting used to, and then there are other emotional side effects like fear and anxiety that come from not knowing the outcome of your treatment.
Many people will not experience severe symptoms, so don’t fret: just be prepared. Since radiation therapy can seem overwhelming and scary, we’ve included a list of items that will help you get through your weeks of treatment.
Tips To Stay As Comfortable As Possible:
Wear loose clothing
Try not to wear a bra if areas are raw, try a sports bra.
The treated area will be more susceptible to sunburn than the rest of your skin, so be sure to use sunscreen.
Use warm water in the shower
When you wash the area, use only water and mild soap, eg dove.
Balance activity with plenty of rest.
Sweat can irritate the affected area.
Stay hydrated, water is crucial.
source-the breast cancer site
The side effects tend to gradually appear a couple weeks after the treatment has started, and can last for up to six months after it has ended. The severity of the symptoms can vary from person to person, especially when you factor in how many weeks the therapy is required. In some cases, the onset of side effects won’t occur until months or even years after treatment, but this is fairly rare.
What Are The Side Effects Of Radiation Therapy?
The most common effects include damage to skin (like sensitivity, skin weepiness, burning, dryness, blisters, peeling, and itchiness) and fatigue that won’t improve with rest. Less common effects include heart problems, lung problems, low white blood cell count, and lymphoedema. In extremely rare cases, radiation can lead to a secondary cancer, like sarcoma (cancer of the connective tissues).
Your breasts may change slightly in size (due to fluid build-up or scar tissue), the skin may appear thicker, your pores may be more noticeable, and your skin may even become darker in the treated area. In addition, your changed body image will definitely take some getting used to, and then there are other emotional side effects like fear and anxiety that come from not knowing the outcome of your treatment.
Many people will not experience severe symptoms, so don’t fret: just be prepared. Since radiation therapy can seem overwhelming and scary, we’ve included a list of items that will help you get through your weeks of treatment.
Tips To Stay As Comfortable As Possible:
Wear loose clothing
Try not to wear a bra if areas are raw, try a sports bra.
The treated area will be more susceptible to sunburn than the rest of your skin, so be sure to use sunscreen.
Use warm water in the shower
When you wash the area, use only water and mild soap, eg dove.
Balance activity with plenty of rest.
Sweat can irritate the affected area.
Stay hydrated, water is crucial.
source-the breast cancer site
Tuesday, 24 November 2015
Tattoos
Many women opt for getting their first tattoo post breast cancer treatment. I have one on my arm and am hoping to get another for Christmas this year. I remember my surgeon commenting on my tattoo when he first saw it. He said does having breast cancer mean you must get a tattoo? Well, no it doesn't, how ridiculous, but for many it is a significant sign of what we have been through. Why not, I say. Here are some of my favourite tattoos...













FIGHTING THE STORM - MY BREAST CANCER JOURNEY
Monday, 16 November 2015
Radiation
First radiation treatment today. I had forgotten how tired I would feel afterwards. The treatment itself was fine, it took about ten minutes,but the tiredness has hit me almost immediately this time. I met with the rads nurses who gave me a list of possible side effects. This time around I will see a nurse every week to check on my burns. Today I was given some sorbolene cream to use everyday. The joys of breast cancer treatment.
Life Without Ovaries
So, for the past two and a half years I have been in what they call 'medically induced menopause'. I have been on tamoxifen and have had zoladex injections every 4 weeks. The zoladex puts my ovaries to sleep. The whole reason for this treatment was to lower or stop the production of estrogen in my body. As my breast cancer was estrogen positive. Having my ovaries removed was not an option I was given. That was until my recent recurrence - also estrogen positive breast cancer. I had my ovaries removed two weeks ago. Tomorrow I will see my gyno for any results. The surgery wasn't as easy as what I had expected. I had a few complications and oh so much pain. Apparently, I had a lot adhesions due to a previous cesarean and they had to be removed so the surgeon could get to my ovaries.
I have been in menopause for the past two years. I also have medication to help relieve those symptoms. Efexor. Unfortunately, that stopped working for me a long time ago. I get all the not so wonderful symptoms of menopause. Instead of feeling like a 45 year old I now feel more like 75.
Since having my ovaries removed I had a brake from the sweats and hot flushes for the first week. I couldn't walk straight and I was in pain but at least I wasn't sweating. Roll on last Saturday and I woke early in the morning dripping wet like I had been sleep walking and had a shower. Most of the day was spent with my body overheating. Sweating was out of control and hit with no warning. Luckily for me I had no where to go. So, I hid inside my house, sweating and hot flushing all day. The flushes were so strong that I also had nausea. What a rotten day.
Just as I am thinking, this will be my life now. I doubt there is any other medication out there that I can take to help with my menopause, everything has stopped again.No hot flushes or sweats since Saturday. I have a feeling that at the moment I am on a roller-coaster ride, not able to get off. Hopefully, the ride will stop soon and let me get off and leave my menopause symptoms behind.
I have been in menopause for the past two years. I also have medication to help relieve those symptoms. Efexor. Unfortunately, that stopped working for me a long time ago. I get all the not so wonderful symptoms of menopause. Instead of feeling like a 45 year old I now feel more like 75.
Since having my ovaries removed I had a brake from the sweats and hot flushes for the first week. I couldn't walk straight and I was in pain but at least I wasn't sweating. Roll on last Saturday and I woke early in the morning dripping wet like I had been sleep walking and had a shower. Most of the day was spent with my body overheating. Sweating was out of control and hit with no warning. Luckily for me I had no where to go. So, I hid inside my house, sweating and hot flushing all day. The flushes were so strong that I also had nausea. What a rotten day.
Just as I am thinking, this will be my life now. I doubt there is any other medication out there that I can take to help with my menopause, everything has stopped again.No hot flushes or sweats since Saturday. I have a feeling that at the moment I am on a roller-coaster ride, not able to get off. Hopefully, the ride will stop soon and let me get off and leave my menopause symptoms behind.
Saturday, 3 October 2015
Breast Cancer Recurrence
It has been two and a half years since I was first diagnosed with er+ pr+ her2- breast cancer in my right breast. Most of my treatment was well over. I was still on hormonal treatment, including my monthly zolodex injections and tamoxifen tablets daily. I was stage 2b with my first diagnosis and the chances of recurrence were supposed to be slim. I was still on three monthly visits with my medical oncologist and surgeon. My life was beginning to feel almost normal again. I had just started to relax. I stopped fearing, everyday, that every ache in my body was cancer. After two and a half years I was finally feeling calm again.
My G.P(general practitioner) suggested that I have a mammogram and ultrasound as he didn't have any records on file since September last year. He figured I was due and should have the left breast checked as well because "sometimes cancer can return in the opposite breast". Now, I owe my doctor a second time as the mammogram picked up a cancerous lump in my left breast.Again, I thank my doctor for being so thorough as he has probably saved my life for a second time.
Two weeks ago I had a lumpectomy on my left breast and lymph node removal with all clear margins. This time I won't be having chemotherapy but I will have radiation therapy again, starting in a few weeks.
My G.P(general practitioner) suggested that I have a mammogram and ultrasound as he didn't have any records on file since September last year. He figured I was due and should have the left breast checked as well because "sometimes cancer can return in the opposite breast". Now, I owe my doctor a second time as the mammogram picked up a cancerous lump in my left breast.Again, I thank my doctor for being so thorough as he has probably saved my life for a second time.
Two weeks ago I had a lumpectomy on my left breast and lymph node removal with all clear margins. This time I won't be having chemotherapy but I will have radiation therapy again, starting in a few weeks.
Tuesday, 3 June 2014
Sunday, 1 June 2014
Eating Well During Chemo
Eat to beat the pain of chemo
BEATING cancer is never easy but understanding the right way to eat can help you recover and give you energy and strength to fight on. This isn't a matter of fad diets or cramming yourself with special foods but of good, sound nutrition.
Understanding the right way to eat can help you recover from chemo
There is nothing worse than trying to eat when feeling sick or if you have been bringing up your food. There are many reasons for nausea and vomiting and any problems should be discussed with your doctor.
There is now a potent range of anti–nausea and anti–sickness medication but an effective dietary option is to take extra protein throughout the day.
Research has shown many people experience less nausea by sipping high–protein (whey) drinks with powdered ginger twice a day.
Nausea is worse on an empty stomach so if you can't manage meals try to keep nibbling small amounts of food or sipping drinks containing sugar. I often suggest keeping a couple of dry water biscuits on the bedside table to nibble before getting out of bed.
Food fixes: Avoid foods that are hot, greasy, fried, spicy, fatty or high in sugar.
Sip lemon–flavoured barley water or suck ice–lollies. Snack on cheese, rice pudding, nuts, olives, ginger biscuits, salt and vinegar crisps, toast and Marmite and drink salty broths or soups, ginger beer and cola.
TASTE CHANGES
Losing your sense of taste or experiencing metallic, salty or sour flavours in your mouth is one of the side effects of chemotherapy and radiotherapy that is most difficult to manage.
There are no medications available to help restore the taste buds. It is up to you to discover what tastes or flavours you can register. Work out what mixtures of flavours to incorporate into your foods.
If you have completely lost your sense of taste it is important to use lots of colours and different textures and temperatures to help keep food interesting and manageable. Keeping your mouth clean and fresh is a must. Use non–mint flavoured toothpaste.
Low zinc levels can cause taste problems so ask your doctor to have your zinc levels screened. Food fixes: You might prefer strong flavours, such as Asian sauces or Lebanese spices including harissa or preserved lemons.
If meat tastes bitter soak it in wine, soy sauce or fruit juice. Avoid foods with saccharine.
Ease the side effects of cancer treatment with these top tips
This is a common side effect of chemotherapy and radiotherapy. The cause is often related to pain–control medications along with the impact of certain drugs. Experiment with building up your fibre intake.
It is important to balance fibre between soluble and insoluble types. The best results come when they are consumed together, for example wholegrain cereal and fruit, wholegrain pitta bread and salad or jacket potato and steamed vegetables.
There are times when the problem cannot be rectified by diet and you will need laxative medications prescribed by your doctor or clinic. If your doctor has suggested you work on your diet to help manage constipation the following should be considered. Food fixes: Choose wholegrain cereals such as Bran Flakes or All–Bran and wholegrain bread, pasta and crackers and brown rice. Increase your intake gradually and only if you can tolerate it.
Eat five to seven servings of fruit and vegetables daily and sip fluids throughout the day. Add two teaspoons of flaxseeds to your diet each day, perhaps left in yogurt overnight or added to muesli.
If you have wind or bloating, limit food such as broccoli, onion, garlic, cabbage, pulses, apples, carbonated drinks and refined wheat products.
LOSS OF APPETITE
Struggling with a poor appetite is a difficult side effect for many having cancer treatment. If you want to build yourself up you have to eat more calories than your body is using. For many this means aiming at 2,500 to 3,000 calories a day.
Typically individuals with no appetite are taking in 800 to 1,400 calories daily. If you have little or no interest in eating it is important to organise a strict diet routine. Nibble or pick your way (every hour or two hours) through lots of regular mini–meals or snacks. Food fixes: Try to eat nourishing snacks such as eggs, smoked salmon, cheese, minced meat, nuts, peanut butter on toast, wholegrain crackers or a bowl of cereal with milk, milkshakes, scones or a piece of cake. Also use high–protein milk rather than regular milk.
Eat puddings and desserts after a break following the main course. If the smell of food affects the appetite, eat cold or tepid dishes.
Keep nutritious snacks including nuts, cereal bars, yogurts, cheese sticks or dried fruit to hand.
Eat in front of the TV or with the radio on. People often tend to eat more when they have a distraction.
Source:express.co.uk
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