

Tags: Cheese, Desserts, dips, food, football, guacamole, mexican food, nachos, party, pizza, recipes, salad, super bowl, Whoopie Pie


Tags: Cheese, Desserts, dips, food, football, guacamole, mexican food, nachos, party, pizza, recipes, salad, super bowl, Whoopie Pie
Hi! My name is Jamie and I’m the newest blogger at Boston Bakes
Currently, I manage grants at Dana-Farber Cancer Institute. I am passionate about food (especially sweets), fundraising for non-profits, and being active.
Expect to see a post from me every other Friday about my baking endeavors, food interests, and reports on the latest dessert trends.
Tags: Blog, Blogger, boston bakes for breast cancer, dana farber, Desserts, food, fundraising, Grants, non-profits, sweets
Today’s gadget is simple and subtle, but it might just find a permanent home atop your counter. A modernized version of an average wooden knife block, the Bistro Knife Block made by Bodum is stylish and very practical.
The outside casing of the Bistro is made of hard plastic and inside are thin plastic sticks packed tightly together, resembling the bristles of a broom.
The design allows you to place any size knife, anywhere, within the “block” itself. You can store your paring, chopping and chef’s knife all right next to each other.
It takes up only a small amount of space in the kitchen and it can hold a numerous amount of knives. My roommate got the Bistro Knife Block as a Christmas gift and its lived on our counter since.
Your knives will stay safe as well as clean and sharp, a much better option then storing them in a drawer. And you can remove the inside bristles from the shell to make sure you’re keeping it crumb-free. This gadget comes in several different colors including red, grey, lime green and orange, so it can suit any style!
Knives are an essential part to any cook’s kitchen, and an easy way to store them makes a huge difference in preparing your favorite meals. Available from bodum.com for $49.95 this helpful gadget is an awesome investment.
Tags: 2012, back bay, Bakes 4 Breast Cancer, baking, Blog, Blogger, blogging, blogs, Boston Bakes 2012, breastcancer, charity, charity boston, cooking gadgets, food blog, food bloggers, food community, fund raising, ideas for Mother, kitcehn tools, kitchen accessories, kitchen gadget, knives, knives skills, Living in today, Merry Christmas
The biggest change a diagnosis of breast cancer brings is the loss of feeling in control of your life, your body, your future.If our breast cancer is such that we can choose to have a lumpectomy; what method do we choose for radiation? External beam with its standard 36 treatments or Mammosite accomplished in two treatments a day for one week? What are the pros and cons of each? Am I a candidate for Mammosite? Does my hospital offer it? Does my insurance cover it? What kind of a physical outcome can I expect from each of these procedures?
In addition to the treatment decisions that breast cancer brings there are the financial, the employment, and the personal decisions to be made, especially if there are young children to be considered.
Once breast cancer surgery is over and treatment begun, we are challenged to cope with pain and feeling ill from treatments in ways that most of us have never encountered before. Fatigue is our constant companion. Many of us lose our hair and have to learn to wear a wig so it doesn’t look like we are wearing a wig.
We cope with the middle of the night “What Ifs” when it seems that everyone is asleep but us; when our minds run tapes on a continuous feed loop covering the same content over and over until we get too exhausted to think and fall asleep.
Somehow we do it all; we get through and treatment is over. Now we need to find ways to live our lives having experienced the physical and emotional changes that breast cancer brought to our lives.
For those of us who had estrogen fed tumors, there’s the continued challenge of coping with years of the physical changes brought about by hormonal therapy: weight gain, hot flashes, mood swings, bone pain, sleep disturbances and, for some, hair thinning.
Most of us make the adjustment to the new us. Given the coping mechanisms we had to develop in order to get through active breast cancer treatment it is not surprising that we do. Many of us get on with our lives with a new sense of purpose. We reinvent ourselves focusing on strengths and talents we have always had but may not have focused on developing. We are different; not bad different, just different. We cherish time and guard how we spend it. We still work at looking our best, but we spend more time on doing things that make us feel our best.
We are no longer naive about our health. Sometimes the sense of vigilance that comes from living with a schedule of routine follow up visits to surgeons, medical and radiation oncologists and the usual blood work and other tests leaves us yearning for the “Un Days”; the days when no one is examining us or asking the same questions asked so many times before . We hold our breath until we hear those words, “Your Fine.”
We learn to manage our fears because if we don’t there will be no quality of life, just a constant state of apprehension and that is not living. One day we realize that the things that used t upset us to the point of ruining our day or robbing us of a night’s sleep before our breast cancer don’t pack the same punch anymore. We’ve learned who is there for us and who isn’t. We know what matters to us and will always matter to us.
We coped and continue to cope with the changes that breast cancer brought into our lives with the support of other survivors, friends and family and for many, a faith in a power greater than ourselves. We are confident in our ability to care for ourselves proven by all we survived.
Do we regain that sense of being in control of our lives after breast cancer? I can only answer for myself. I have come to accept that I control how I care for myself both physically and emotionally. Beyond that I can only control how I react and cope with what happens to me, when it happens to me. That will have to be enough. Breast cancer has taught me that.
For more information about navigating breast cancer please visit my website…www,noboobsaboutit.com
Tags: breast cancer surgery, breasts, constant companion, continuous feed, coping mechanisms, diagnosis of breast cancer, diagnostic tests, external beam, lumpectomy, mammosite, mastectomy, personal decisions, presence of mind, pros and cons, radiation, reconstruction, treatment decisions
Last week pasta was the main topic of conversation. But naked pasta isn’t my thing…I need the sauce! My favorite is stewed tomatoes with spaghetti, preferably linguini, farfalle or rotelle.
When I lived in the North End, pasta was king. In the summertime, the Italian family who owned my building made massive amounts of tomato sauce which they would jar and use throughout the rest of the year. They set up shop in the courtyard a few floors below my window and the sweet smell of simmering tomatoes filled the apartment. It was magical.
Although you’re probably not planning on making quite as much sauce, you can still have the delectable homemade flavors, just in a smaller portion. The Roma Tomato Milling Machine is perfect for counter-top use. 
There’s no need to peel the tomatoes or remove the seeds. Just rinse your fresh, ripe tomatoes and plop them into your mill. Once you start turning the handle the skin and seeds are separated from the puree, leaving you with the perfect sauce blend.
Next, just put the guts into a pan, add some spices, extra virgin olive oil and whatever else you think will give it a good kick, and let your sauce simmer to perfection.
The Roma Tomato Milling Machine made by Weston is available online from tomatomilling.com for $49.00. And, to make this gadget even better, this awesome milling machine can produce jams and jellies from fresh fruit!
This gadget is a gardener’s delight.
Tags: Boston Bake, Boston Bake for Breast Cancer, Boston Bakes 2012, cooking, cooking gadgets, north end restaurants, pasta sauce, yum
As you hopefully I know I recently returned from an amazing trip to Dubai. The city itself was great, very modern and a cool place to visit but the one of the main parts of what made my trip so spectacular was the food. I want to share with you some of the wonderful things I ate while there but I don’t want this to just be a brag-post. Rather I hope this will be an inspirational post on food that you too can enjoy. Middle-Eastern food in general is something I love and it’s a great way to mix up your cooking routine at home. I know everyone loves pasta, but not seven nights a week. I hope that reading about food from another country will not only make you want to try it out yourself but even explore foods from other countries as well.
Now you have to keep in mind that I am a vegetarian, and so is my best friend whom I traveled with. When her family found out they would be hosting two vegetarians they went into panic mode. I think her cousin was actually convinced that we would starve to death and tried to compensate the lack of meat by severely over feeding us. One of the things that she always had on hand, that we basically ate every single day for breakfast was Labneh and Za’atar. We ate them very simply, spread over a flat pita – and they were absolutely delicious. Labneh is a very thick yogurt spread, almost like Greek yogurt but a little less yogurt tasting, if that makes sense, a little creamier too I would say but still tart. Labneh can be served with most middle-eastern dishes, as its flavor lends nicely to a variety of foods. Like I said though, our favorite way to eat it was with Za’atar, which is a spice blend that is used on essentially everything in the Middle East to just add a punch of flavor.
We didn’t eat a lot of big entrée type meals, we mostly had little bits and pieces, which is definitely how I prefer to eat – that way you get a little taste of everything. Some of my favorite small bites I will detail below
Stuffed Grape leaves are little bite sized appetizers that are quite delicious. They can be stuffed with a variety of things, from meats to vegetables, but we mostly had them stuffed with rice, olive oil and lemon juice to play off the bitterness of the leaves themselves and give a full flavor to the rice.
Babaganoush is almost as common as hummus in Middle Eastern cuisine. It is an eggplant spread that is often plated with pomegranate seeds. It is served along side hummus, pita and olives as an appetizer type dish.
Fattoush was the salad we had with most meals and by far one of my favorite dishes that we ate. It is essentially a salad with lettuce, tomatoes, cucumbers etc. in it but they are cut up into larger chunks. What makes this salad so good though is the “croutons” they use, which are little flat squares of fried pita bread, the perfect crunch to the salad. They also traditionally use sumac in the dressing to give the salad a sour tinge that makes it unforgettable.
And of course, no dining experience would be complete without dessert. Although at heart I am a chocolate girl I did enjoy a lot of the pastries that they served (mostly because they had cheese in them, another love affair of mine). My favorite one that we had is called Kenfe, which is a circular bread hollowed out and filled with sweet cheese and topped with sesame seeds and is absolutely delicious.
These are just some of the highlights of my food adventure in Dubai and I hope that this will inspire you to have a food adventure of your own. You don’t need to travel somewhere far to try new things, all you need is a kitchen!
Tags: babaganoush, Cheese, Dessert, dubai, eggplant, fattoush, grape leaves, international cuisine, knefe, labneh, Middle Eastern, new foods, pastry, pita, salad, spice blend, spices, sweet cheese, travel, vacation, yogurt, za'atar
Part of dealing with a new cancer diagnosis involves deciding how to let those around you know what’s happening. While you’ll probably want your loved ones to know about your diagnosis and treatment, deciding whether to tell your employer can be a more challenging process.
Here are some tips if you’re weighing the decision to share your cancer diagnosis at work.
Start with a clear picture of your treatment. Before you go to your employer, talk with your doctor about what to expect. Ask whether you’ll need time off to recover from chemotherapy or surgery. It’s also a good idea to ask how other people typically feel during and after your types of treatment. Let your doctors and nurses know what your job involves and ask what type of work schedule they might recommend. This also makes them aware of another important aspect of your life that is being affected by your cancer care.
Make a list of work-related changes you think you might need while you’re in treatment. For example, if you’re worried you’ll feel tired or ill after chemotherapy, note that you may need to change your work schedule or take certain days off.
If you’re worried about approaching your boss with such requests, keep in mind that federal laws protect cancer patients from discrimination. For example, employers are legally required to help you do your job during or after cancer treatment by providing reasonable accommodations, such as an adjusted work schedule or time off for doctor’s appointments.
You may also want to talk to your human resources department about work accommodations you may need during treatment.
As you make your plans, be sure to enlist the help of others. Think about how friends or family may help. And take time to talk with a professional, such as a social worker, who can help you address the challenges of managing work and cancer care.
Decide who to tell. While you aren’t required to tell your employer or coworkers about your diagnosis, you may get questions if you miss a lot of work or your productivity lags.
Rather than not telling anyone, you might want to tell just a few people, such as your boss or coworkers you trust. Or you might decide to tell everyone, depending on your work environment. The most important factor in this decision is your comfort, so do what you feel is best for you.
Use this as an opportunity to educate. Whether you’re talking to your boss or your coworkers, think of your conversation as a chance to help others understand what you’ll be going through. People often have a lot of misconceptions about cancer. They may assume it’s going to be terrible and you’ll never be able to work during treatment, but that’s not necessarily the case.
While every situation is different and there’s no crystal ball, many people continue to work successfully through treatment. You could also use this as a chance to let others know where and when you might need help in your work during treatment.
Keep a record. Employers are usually very supportive of employees going through cancer treatment, but this isn’t true 100 percent of the time. It’s a good idea to keep track of discussions you have with your boss or human resources office. Hang on to copies of work reviews, emails or letters about your performance, or requests for accommodations. This documentation will be helpful if you need to take action to uphold your rights in the workplace.
If you’d like to learn more about your rights as an employee, you can contact the U.S. Equal Employment Opportunity Commission, which enforces Title I of the Americans with Disabilities Act. Depending on where you live, you may also have state laws that apply to your situation.
If you’re a Dana-Farber patient, you can speak with one of our licensed social workers to help you think through your situation, learn more about your rights, and what options to consider as you move forward. Everyone is different and the process of responding to a cancer diagnosis is very personal, so meeting with a social worker who is familiar with your cancer may be a good starting point.
Nancy Borstelmann, LICSW, MPH, is a licensed clinical social worker who serves as Dana-Farber’s director of patient and family support and education.
Courtesy of Dana-Farber Cancer Institute
Tags: discrimination, Equal Employment Opportunity Commission, federal laws, how to tell your boss you have cancer
Once I knew I was having a bilateral mastectomy, I realized I had some practical planning to do, beginning with my home. I did a walk-through of my two bedroom apartment to identify what changes I would need to make for my comfort, not only while recovering from surgery, but permanently.
I began with my kitchen. I enjoy baking and cook daily. My traditional oven with the front door opening and low broiler unit was not going to be practical once I had weight restrictions on my arms from the surgery. I bought a counter top oven that is a regular oven, convection oven and broiler. This unit eliminates the need to bend and lift. I still use the burner units of my stove, but the oven is now a much needed storage space for pots.
I purchased a jar opener, which eliminated the need to use my hands with hard to open containers. I made sure the appliances, dishes, cooking utensils and foodstuffs that I used regularly were counter top or on the lowest shelves above the counter tops and within easy reach.
My office needed to be rearranged, making frequently used supplies and equipment within easy reach, similar to the kitchen. My computer notebook that I used for demonstrations at meetings became another office computer and I purchased a small, lightweight computer notebook that I transport in a carrier with wheels.
The bedroom, bath and living room did not need any adaptations, but the closets needed rearranging to allow for easy access to most frequently used items.
After the apartment was made accessible for the new me, I turned my attention to what I anticipated my personal needs would be. Knowing that I would be spending two nights in the hospital following surgery, I decided to call the hospital registry and hire private duty caregivers to be with me. The first night, I had a registered nurse; the second night a certified caregiver (nursing attendant). It was the best money I have every spent! If you have a family member who can stay with you, that’s great. Not everyone does. It was comforting to know there was someone there with me. I was on an IV, and needed the bedpan every hour or so. Waiting for a floor nurse or attendant to be available would have been very uncomfortable.
Prior to surgery, I purchased two camisoles that I would wear for 12 days following surgery. The camisoles had pockets for the drains carrying fluid from the incision sites on my left and right sides.
The day of my surgery, I wore sweat pants and a zip front sweatshirt with a hood, which I also wore home. It was an easy outfit to get in and out of, especially over bandages and I didn’t have to lift my arms.
For the first two weeks after my surgery, the hospital arranged for a visiting nurse service to look in on me several times to check my bandages and the amount of fluid draining from my incisions. They were on call for emergencies and when one of the drains stopped functioning they sent a nurse. It really was a comfort to have this service available.
Most importantly, having the company and care of a loved one and the visits of friends and family, from time to time, really helped me to recuperate. Having my kitchen and office easy to use made all the difference.
Recently, I came across a site that provides insight into all the aspects of planning for having and recovering from a mastectomy covering the medical, physical and emotional as well as the practical tips for making the process easier. I will share this information in my next post.