Tuesday, September 29, 2009

Cancer Reality - September 29th



Greetings Friends,

Didn't get much sleep last night, it was a restless night. I was up early today to go to the Radiology Center to have a sonogram done to locate the exact location of the Lymph node that will be removed tomorrow morning.

Here is the sonogram photo of the lymph node that is being removed:



The tech used a sharpie to mark the spot where the surgeon is to operate. I certainly hope the sharpie does not wear off and he operates on the wrong area.

                                              

Tomorrow morning I have to be at the Hospital at 6am for the post op blood work and then the surgery will be at 6:30. I am sure it will be a long day. I will update you tomorrow after I am awake...

Thanks for following, you can follow me on Twitter @CancerReality
or @danelson239


Face Book at www.facebook.com/buscando239

Thanks for all the support!

xoxo D

Monday, September 28, 2009

Cancer Reality - Sept 28, 2009



Hello My Friends,


Today was a difficult day. Monday’s are always full of conference calls for me and getting through the day being on the phone all-day and sitting in one place is often difficult. I try stay sane by checking my Tweets.

Tomorrow I go for a sonogram in the morning. They will be marking the exact location of the lymph node under my left arm, which will be removed on Wednesday during an out patient surgery.

The lymph node that will be removed will then be sent for a biopsy to determine the type of cancer. Hopefully it will be an easily treated cancer and will not require too much chemotherapy.

As I have been discussing, I am working on trying to get some musical artist to donate the use of a song to put together a benefit CD. The title of the CD will be ‘Cancer Reality Sucks’. The proceeds from the sale of the CD would benefit those who are unable to afford the high cost of Chemotherapy and other treatments for Cancer.

The idea came to me as I sat in the waiting room of my oncologist. There was a young woman in her early thirties and her husband sitting in the waiting room crying. I had a box of tissues sitting next to me, so I got up and handed the box to them and asked if they were okay.

I quickly learned that the tears were due to the fact that the young lady had lymphoma and had no insurance. The Cancer Treatment Center was requiring them to pay for the treatments in advance as most doctors do now to ensure they are paid. They had to make a decision, do they pay the mortgage payment and keep the place they live, or do they use that money to pay for the treatment, which would keep her alive. At that point, I needed the box of tissues.

I took my seat again and could not get them out of my mind. How do we allow someone to have to make a choice of a place to live versus life?

I got out of my seat and went into the financial office of the Cancer Treatment Center and had a brief conversation with the person in charge. After my conversation, the family was called back into the office where they learned that they would be able to receive the treatments without payment.

At this point, I realized that I needed to do something. A very wise man once said, “ You must be the change you want to see in the world.” that wise man was Gandhi.



The next day I made some calls to the Lymphoma Society where I quickly learned that the funds to assist Cancer patients had been already depleted for the year and there was no more help available.

Again, this is where I realized that I needed to heed the advise of Gandhi and LEAD THE CHANGE I WANT TO SEE IN THE WORLD. So despite my own battle with Cancer, I am going to put forth the effort to possibly make someone else's journey a little better.

I now ask that you share this message with everyone you know. I will continue to pursue the music industry in getting some songs donated to put together a benefit CD.

I am also working on a clothing line called “Cancer Reality”. More to come in future posts.

I hope to utilize this blog to share my journey through my second round of cancer as well as share information that I learn on treatment, prevention, and ways to help.

Please spread the word and help be part of the change I want to see in the world.

I am working on a logo for the site. I will post in a couple of days several logo’s and would love to get your opinion on which one is the best.

Until the next time… Be the Change – Work toward the Change – Pass forward the Change…

Xoxo Douglas

Sunday, September 27, 2009

Canadian Team Makes Cancer Diagnostic Breakthrough


According to an article, researchers say the University of Toronto have developed a microchip that could change how cancer and infectious diseases are diagnosed. This will allow doctors to conduct quicker and less invasive testing

The new technology, created by a team of experts, can determine the type and severity of cancer someone has by assessing molecular samples on a fingertip-sized chip, which is then fed into a device about the size of a personal organizer.

“We think this is very significant,” said Shana Kelley, the lead investigator for the research and co-author of a report released Sunday in the journal Nature Nanotechnology.

“At the moment, we don’t look for as many molecular markers as we actually could when doing clinical diagnosis of things like cancer because it’s too expensive to do the analysis There are some screening tests that are available, but there could be many more if the right kind of device is available.”

She said being able to determine the severity and type of cancer is critical is developing treatment programs for patients.

The new technology can get patients on track for the necessary procedures quicker, Kelley added.

“Prostate cancer, in particular, can be very aggressive or very slow growing and it’s quite important to be able to distinguish those types,” said Kelley, a professor in the department of pharmaceutical sciences at the University of Toronto.

“With this chip, we’re able to take samples from prostate cancer patients and see which markers they have and then correlate the outputs with the severity of the disease.”

Results from the chip, which used a test field of about 10 samples for Sunday’s report, can be seen within an hour, Kelley said. More conventional means of diagnosis, such as a biopsy, can take days to determine results.

The technology has so far been used only to test existing biopsy samples, but Kelley said she hopes it will eventually allow for cancer testing that is easier on patients.

“To do non-invasive testing, you need a very sensitive device that will pick up on the very low levels of cancer cells you see circulating in urine and blood and sites outside the tumour, where you can find some of the same molecules,” she said.

“We attained sensitivities we think will allow us to use our devices for non-invasive testing,” she said. “We have not yet done the work with clinical samples, but that’s the next step and the sensitivities we have make that possible in principle.”

While its main focus to date is cancer diagnosis, Kelley said the microchip can also be used to diagnose and assess infectious diseases, such as HIV and H1N1.

“You can detect different types of bacteria and viruses if you know which molecules to look for,” said Kelley.

“Any type of cancer where there’s an established molecular profile, we can modify our platform so we can gear it towards whatever disease is of interest.”

The current project, led by Kelley and engineering professor Ted Sargent, has been ongoing for about three years, said Kelley, who has personally invested about 10 years into the research.

“It’s very exciting to be able to make a device like this and have it perform as well as it does with patient samples,” she said. “It gives us confidence we’ll be able to take it to the next level and get it into the clinics.”

Kelley said a five-year time frame would be a “conservative estimate” to get the device on the market.

This is amazing. Five years seems like such a long time to get it on the market, I hope that the researchers will work diligently to get it to market faster. This could save lives....

Saturday, September 26, 2009

U.K. to Announce Quicker Cancer Testing


British Prime Minister Gordon Brown will unveil a plan to get patients suspected of having cancer to a specialist within seven days, sources said.


The sources told The Mirror that the plan will be announced Tuesday at the Labor Party conference in Brighton and will call for all National Health Services patients to receive diagnostic tests within a week of seeing their primary care doctor.

"If the NHS doesn't give you your tests within one week you will have the right to go to an alternative NHS or private provider," a source told the newspaper.

The Daily Telegraph said Saturday said the announcement is aimed at decreasing cancer deaths in Britain, but there are also political considerations. Sources said the plan would not go into effect until 2015 and could leave Labor vulnerable to charges the plan was aimed only at bolstering the party among voters.

This would be something amazing for us in the United States. In 2007 when they first diagnosed my cancer, it took three months for them to test the Lymphnode before determining a course of treatment. The Lyphnode they removed from my neck traveled from Florida, to Texas, to Boston Mass, and then back to Florida for a three month time frame before my treatment started.

Who says we don't need health care reform?

Friday, September 25, 2009

August 20th, 2009


So, I am finally in a room at the hospital, and thought that I was going to sleep. I am unsure what the logic is on the nurse coming into the room every 30 minutes, turning on the overhead light and asking me if I am sleeping. What did she think I was doing, baking a cake, making a grocery list, completing the NY Times puzzle? Of course, I WAS, sleeping untill she flipped the light on and scared the be-geezus out of me.

After she left the room, angry I am sure from my scoulding, I took two xanix which I snuck in to the hospital in my backpack and finally went to sleep.

At 4am a nurse flips on the light and says "Lab's". I was dazed a bit and slowly opened up my eyes. I am not sure where she got her training, but she was not able to hit a vein to save her life. She took a few vials of blood and then I was back to sleep. I think the nurse on the floor that night was scared, because she never did return to see if I was sleeping.

The next three days were more torture with more blood drawn and lack of a nurse when one was needed. Hospital care is far below standard and I do not look forward to having another stay anytime soon.

Sunday the 20th, I was released from the hospital and able to return home to my own bed, my piles of emails, and all social network sites behind and in need of updating... does the ever ending road come to an end? Guess only time will tell...

xoxo D

Thursday, September 24, 2009

August 18,2009

It's been a few days since I have been able to make an entry. On Thursday morning, Sept 17th, I woke up with a fever and a rash covering my body. I debated for a few hours as to whether or not I should go to the emergency room or just wait and see. Well when the temperature hit 102.9, I made the decision that the hospital was probably the best bet. So I packed a few things and off to the emergency room I went, parents in toe.


I arrived at the emergency room and the woman at the entrance was a bit rude, as if I should have been surprised. She tossed a mask at me and told me to put on the mask. My mother started to explain the situation for me because I was feeling ill and needed to sit down.

I waited about an hour before they called me into the back so that they could examine me. I was there for a high fever and an unexplained rash, I'm not sure that I was speaking English because it took a good 6 hours for them to finally take a look at the rash. The nurse who put in the IV butchered me while trying to put the IV in. I am not sure if she was brand-new or just an idiot, but I could have done a better job. I have a 3/4" main vein in my right arm that would be a drug users dream vein. How she kept missing it is beyond me.

They ran some blood work, took a chest x-ray (not sure what that had to do with the fever or the rash, but hey, who was I to argue, our health care system at work) and then did an abdominal scan. Boy do I love the taste of the contrast that they have you drink.

Finally at 11:30pm the nurse came in and said that they did not have any answers to what was causing the fever or the rash, so they were going to admit me into the hospital.

At 1:45am, I was finally moved from the ER to a private room. At this point, I was exhausted, poked, prodded, and touched by more hands than I really desired. Sleep was all I was looking for....

to be continued....


Wednesday, September 16, 2009

Sept 16, 2009

I was finally able to get a few hours sleep last night with the help of a friend, xanix. My mind seems to wander on to what "if" and can't seem to stop getting that out of my mind. I have been having images of what it would be like not to wake up. Would anyone really notice I was gone? Would they miss me? What would I be remembered for? Strange how we as humans think in that capacity.

I have a long day today. Must get myself motivated and moving.

Hopefully, I'll have energy at the end of the day to tell you more...

xoxo D

Tuesday, September 15, 2009

Reality Check - Cancer SUCKS!

Today starts a new day for me; I am going to share my Reality of Cancer with you. As I undergo this journey a second time, I will share the experience and hope that it will help someone else who is also traveling this painful and unforgettable journey.


In Oct of 2007, I was diagnosed with non-Hodgkin’s lymphoma. It could not be a normal lymphoma; I had to have a rare B Cell Lymphoma. For three months the lymphnode, which was removed from my left neck, was flown from Florida, to Texas, to Boston, and then back to Florida. Determining a course of treatment was difficult.

Finally in Feb of 2008, my oncologist said they had found a chemical combination that was shrinking the cancer and could possibly put the cancer into remission. I happily agreed to the treatment and for eight months I went through what I would consider to be hell on earth.

By October of 2008, the cancer had begun remission and by Christmas of 2008 I was celebrating the fact that I was in remission. I was still not able to function an entire day, but I was celebrating that I did not have to have the treatments.

In August 2009, I went for a follow up PET Scan to ensure that I was still in remission and there were no signs of the Cancer returning.

On Sept 10th at 2:33pm, I received the news, "IT'S BACK!" I will not forget those words or the time of day. You cannot begin to imagine what was going through my mind at that time.

I have a biopsy scheduled for the 22nd of Sept to determine what type of Cancer I have... will it be the same? Will it be another strand? Will this be treatable? How will I make it through?

I will keep you posted as I travel this journey. Today, I will mourn the loss of a great actor and entertainer who loosed his battle to Cancer. Patrick Swayze was a remarkable entertainer. Visit my other blog, www.TheRamblingsofDouglas.blogspot.com to read more...and you can follow me on twitter at @CancerReality


Until next time,

Cancer Reality SUCKS!
xoxo D