Healing Saint Peregrine of cancer healing

O Glorious Saint Peregrine, patron of those who suffer from cancer, I call upon you and seek your help. Please intercede for all those afflicted with cancer.

Obtain for them comfort during their sufferings, strength when they feel weary, hope when they feel discouraged, and joy when they are downhearted.

Help them know the Peace of Jesus and the certainty of His victory in their suffering, through Christ Our Lord, Amen.

Healing Prayer for Those with Respiratory Ailments

O Heavenly Father, God of Love, You gave us Your Son Jesus to be not only Physician of our souls but also Healer of our bodies and minds. Lord Jesus, I turn to You in this time of need. Please come to me now, and lay Your healing hands on Cindy Hudson. Let the warmth, peace and healing power of Your Spirit fill Cindy Hudson now with Your life and love.

Heal Cindy Hudson's respiratory ailment according to Your Divine Will, Lord Jesus, and enable her to serve You with a healthy body, soul, and spirit. May Your joy, O Lord, be her strength this day.

Amen.

Prayer to Saint Bernadine for those who suffer with respiratory ailments

Glorious Saint Bernadine, look down from Heaven and intercede for the many people who suffer from respiratory ailments in our world.

Help them to find patience in their sufferings and resignation to His Divine Will. Ask the Lord to grant them strength when they feel weary, hope when they feel discouraged and joy when they are downhearted.

O great Saint Bernadine, you who suffered from a respiratory defect was miraculously cured through intercession of the Blessed Mother, hear our prayers and obtain our petitions.

Amen.

Clinical Trial Drug is ASP-3026

Is an ALK ihibitor. It is similar to crizotinib (Xalxori), but it is a stronger form (more potent) than the crizotinib. The pharmaceutical company that is sponsoring it is Astellas Pharma.

All day at the START center and still there....

She is doing good today. She has been at the START center since a little before 8am. They did a phisical, drew blood, and an ekg before giving her the medicine around 10:30am. Since then they have drawn blood and ran tests on it about 9times so far. She has a few more before the day is over for her. She will be able to leave a little after 9pm. A very long day!!! She is doing well and has been able to nap a little bit. I hope it works!!!

She will go back tomorrow for one more blood draw in the morning and then after that she will return on friday.

Thank you and God bless!

-Vanessa

Merry Christmas!!

We hope everyone had a wonderful Christmas full of love, great memories, and good spirit!

Mom, John, Darinka, (Bathsheba-the dog and Katty[a.k.a Patches]-the cat) and I shared a wonderful Christmas Day together. We indulged in a delicious holiday meal of Honey Bake ham, green bean casserole, mashed potatoes, stuffing, and crepes! It was all very good and we were full for the day! Afterwards, we enjoyed opening presents from under the tree and enjoyed some laughs with each other.

The best Christmas present of all was received on friday from the START center when they informed us that mom has been accepted into the clinical trial and will amazingly start on tuesday the 27th!

We are so grateful and just thrilled with this good news!

Merry Christmas everyone!

Love and blessings,

-Vanessa Hudson Reyes and Family!

Understanding Anaplastic Lymphoma Kinase

Interesting article on Interpreting the Alk gene rearrangement:
http://www.mayomedicallaboratories.com/interpretive-guide/index.html?alpha=L&unit_code=60619

A youtube video explaining the FISH test for the Alk mutation in NSCLC.
http://www.youtube.com/watch?v=Bfsq5Vdr1OY&noredirect=1

ALKIn lung cancer, EML4-ALK is the most common 2p23 rearrangement associated with the ALK gene, which encodes anaplastic lymphoma kinase (ALK). EML4-ALK arises from fusion between the 5′ end of the EML4 gene and the 3′ end of the ALK gene. Patients with ALK rearrangements are younger than most patients with NSCLC.⁸ EML4-ALK rearrangements are more common in adenocarcinomas of never or light smokers whose tumors lack EGFR and KRAS mutations. Histology is typically characterized by mucin production and either a solid growth pattern containing signet-ring cells (more likely in Western patients) or acinar growth pattern (more likely in Asian patients).⁹

EML4-ALK and other 2p23 fusion products lead to the production of a constitutively activated kinase, which is likely to be sensitive to ALK inhibitors that have shown efficacy against ALK–rearranged lung tumors and cell lines. For example, in phase I testing, NSCLC harboring ALK rearrangements responded to PF-02341066 (crizotinib, Pfizer) treatment.¹⁰ Phase II and III clinical trials are underway. Patients who harbor ALK rearrangements do not benefit from treatment with the EGFR-specific TKIs and should be considered for ALK-targeted clinical trials.⁸

-More info on ALK
http://ghr.nlm.nih.gov/gene/ALK

Information on Alimta in regards to the ALK mutation.

Journal of Thoracic Oncology:

April 2011 - Volume 6 - Issue 4 - pp 774-780

doi: 10.1097/JTO.0b013e31820cf053

Original Articles

Anaplastic Lymphoma Kinase Gene Rearrangements in Non-small Cell Lung Cancer are Associated with Prolonged Progression-Free Survival on Pemetrexed

Camidge, D. Ross MD, PhD*; Kono, Scott A. DO*; Lu, Xian PhD†; Okuyama, Sonia MD*; Barón, Anna E. PhD†; Oton, Ana B. MD*; Davies, Angela M. MD*; Varella-Garcia, Marileila PhD*‡; Franklin, Wilbur MD‡; Doebele, Robert C. MD, PhD*

Abstract

Hypothesis: To explore whether the progression-free survival (PFS) with pemetrexed differs between anaplastic lymphoma kinase (ALK)-positive and other major molecular subtypes of non-small cell lung cancer.

Methods: In an ALK-enriched population, patients with metastatic non-small cell lung cancer were screened by ALK fluorescence in situ hybridization and for epidermal growth factor receptor (EGFR) and KRAS mutations. Triple-tested, pemetrexed-treated patients (monotherapy or combination therapy) were identified and PFS with pemetrexed captured retrospectively.

Results: Eighty-nine eligible cases were identified (19 ALK fluorescence in situ hybridization positive, 12 EGFR mutant, 21 KRAS mutant, and 37 triple negatives). Eighty-three cases (93%) were adenocarcinomas, two were adenosquamous, one squamous, and three had large cell histology. None of the ALK-positive patients had received crizotinib before pemetrexed. Pemetrexed was first-line therapy in 48% (72% as platinum-based combinations). Median PFS (95% confidence interval) data were EGFR mutant (5.5 months; 1–9), KRAS mutant (7 months; 1.5–10), ALK positive (9 months; 3–12), and triple negative (4 months; 3–5). In a multivariate analysis adjusting for line of therapy, mono- versus platinum and nonplatinum combination therapy, age, sex, histology, and smoking status, the only variable associated with prolonged PFS on pemetrexed was ALK+ (hazard ratio = 0.36 [95% confidence interval: 0.17–0.73], p = 0.0051).

Conclusions: In this exploratory analysis, ALK-positive patients have a significantly longer PFS on pemetrexed compared with triple-negative patients, whereas EGFR or KRAS mutant patients do not. This information should be considered when sizing randomized studies in ALK-positive patients that involve pemetrexed. Pemetrexed should also be prioritized as a cytotoxic to explore further in patients with known ALK-positive disease.

© 2011International Association for the Study of Lung Cancer

Yes!! Mom is in at the START Center for Cancer Care!!

We have an appointment monday morning at 11:30. We will be there a few hours. The website is www.stoh.com. It stands for South Texas Advanced Reseach Therapeutics center for cancer care. This is really cool and exciting! The START center is doing some really innovative research and treatment towards cancer. I can't wait to see the doctor and hear what they say. Mom is going to meet with the Director at the START center and the lead oncologist there. This is good and will give us more information about what genetic mutation is driving her cancer and how to fight it.

START CENTER FOR CANCER CARE OFFERS ROUTINE, COMPREHENSIVE GENOMIC PROFILING OF PATIENTS’ TUMORS. START is the first center in South Texas to make this sophisticated testing routinely available to patients and other oncologists. Testing will direct physicians in the selection of targeted therapies of both conventional and investigational drugs.

The START Center for Cancer Care has begun offering cancer patients routine comprehensive genomic profiling of their tumors using a unique combination of technologies -- array CGH and oncogene mutation anylisis. START is the only center in South Texas to make this molecular diagnostic testing of tumor tissue routinely available to patients, and the first to make both technologies available to any oncology patient as a clinical test. Patients do not need to be in treatment at START to have their tumors tested.

Genomic profiling represents a new tool in treating cancer and clinicians and researchers alike believe that it will enable them to better direct patients to targeted therapies of both conventional and investigational drugs. It is considered a major step in the delivery of personalized medicine. The new service will be coordinated through the new division, GenomeConsult at The START Center, and will be operated under the supervision of Shelly Gunn M.D., Ph.D. , a board certified clinical pathologist. The information her team provides will give oncologists important otherwise unavailable data concerning the specific mutations and unique pattern of changes detectable in each patient's tumor.

Info on cancer hospitals.

In general, MD Anderson in Houston is considered #1, Sloan-Kettering in NYC #2, etc. based on a US News & World Report listing of cancer centers. The Mayo Clinic in MN might an especially good one around you, or Cleveland Clinic in OH.

See http://health.usnews.com/best-hospitals/rankings/cancer
They are probably great for 2nd opinions, though some might feel a bit like a factory mill.

But it's not fair to rely on any one list of cancer centers. It really depends what kind of treatment is needed and whether the criteria any given list used is relevant to your needs. For example, for research-in-progress on mutation-targeted treatments, MGH in Boston (Alice Shaw) and maybe U of Colorado (Ross Camige) may be research leaders, although their discoveries eventually make it through the publication process a few months later and then all oncologists could know about them.

Cancer Treatment Center of America seem to be hit or miss. Some patients love them. They certainly to cater to their patients well and have good "image marketing" (e.g., "we give you options"). But I've heard a couple of adenocarcinoma patients who CTCA gave up on this year (i.e., 'can't anything more for you') without even doing any mutation testing. Yet some other patients have gotten mutation testing via their doctor at CTCA. There's also the issue of whether your insurance will recognize them or not (often not).
Here's another list, though not using a particular criteria:
https://www.inspire.com/groups/lung-cancer-survivors/discussion/node-sampli ng#cmnt_2691706

Best hopes

-This information was given through www.inspire.com from a Lung Cancer survivor who spends a lot of time researching and helping others find answers to their questions about cancer.

EMBO Mol Med. 2010 May;2(5):146-58.

Rapid targeted mutational analysis of human tumours: a clinical platform to guide personalized cancer medicine.

Dias-Santagata D, Akhavanfard S, David SS, Vernovsky K, Kuhlmann G, Boisvert SL, Stubbs H, McDermott U, Settleman J, Kwak EL, Clark JW, Isakoff SJ, Sequist LV, Engelman JA, Lynch TJ, Haber DA, Louis DN, Ellisen LW, Borger DR, Iafrate AJ.

Source

Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA. ddiassantagata@partners.org

Abstract

Targeted cancer therapy requires the rapid and accurate identification of genetic abnormalities predictive of therapeutic response. We sought to develop a high-throughput genotyping platform that would allow prospective patient selection to the best available therapies, and that could readily and inexpensively be adopted by most clinical laboratories. We developed a highly sensitive multiplexed clinical assay that performs very well with nucleic acid derived from formalin fixation and paraffin embedding (FFPE) tissue, and tests for 120 previously described mutations in 13 cancer genes. Genetic profiling of 250 primary tumours was consistent with the documented oncogene mutational spectrum and identified rare events in some cancer types. The assay is currently being used for clinical testing of tumour samples and contributing to cancer patient management. This work therefore establishes a platform for real-time targeted genotyping that can be widely adopted. We expect that efforts like this one will play an increasingly important role in cancer management.

Comment in

• EMBO Mol Med. 2010 May;2(5):143-5.

PMID:

20432502

[PubMed - indexed for MEDLINE]

We need a complete molecular test of mom's cancer!!! I hope we can get one soon!

<a href="http://www.rationaltherapeutics.com/cancer-testing/test-candidates.aspx#.TujhVw4ovf0.blogger">Cancer Treatment  Rational Therapeutics  Cancer Testing  Test Candidates</a>

 www.rationaltherapeutics.com

Today was interesting.. discouraging and encouraging.

So today was rough. We met with the doctor again to see about mom getting into a clinical trial at CTRC for lung cancer and to discuss treatment options. It was discouraging in that CTRC is limited in what they can offer and the clinical trial that the doc wanted her in is totally full. The good news is that he did encourage mom to seek out other clinical trials at other facilities. If anyone is curious how it works, the FDA approves different clinical trials for different institutions. So we may find a clinical trial somewhere else that we can get her in to. We are going to meet our doc again next week to see if there is anything we have found to get her in. He did say that because that one clinical trial he wanted her in was full, he did not think we should wait too too long before starting treatment again.

In the mean time I will be researching and calling all kinds of places to see what I can find. The doc said he would be happy to look over any trials I find and he will share his opinion if he thinks its right for her. It is important to mom that she gets his input. She likes him and is comfortable with him and that is important to all of us.

In todays meeting, I had suggested all kinds of chemo treatments that I have researched and discussed with other NSCL cancer patients, but he insisted that the best option for her at this point is still Tarceva. Tarceva is more of a maintenance chemo drug by itself. It does have some really good results in cancer patients especially those who are EGFR positive. Unfortunately mom is EGFR negative so it would probably not be quite as beneficial for her as it has shown for those who are EGFR positive. One thing everyone has to remember in all this is that each cancer affects each individual person differently and in knowing that each person reacts differently with each treatment. So just because some drug works one way for most and not others doesn't necessarily mean it won't do the same for those its not expected to work as well for. There have been many cases where Tarceva has done wonders for patients who were EGFR negative. Everyone is different. Needless to say our doctor is absolutely amazed at how well mom looks, feels, and is doing. She is staying strong.

It is difficult because there is no easy solution. We all just have cherish each moment with each other, forgive and accept each other, support and love one another, and know that God is with us.

Vanessa

Made some headway today.

Mom, is currently not on any treatment, but I went to the START Cancer Care center and spoke with a wonderful woman who shared the faith and hope that I have in healing my mom. She really cared that all treatment options would be discussed and that every resource be utilized. She was so sweet and I thank God for bringing her forth in our lives.

Mom has signed the release papers so that they can get her complete file and we are one step closer to getting another evaluation and second opinion. 

I would like to point out that we have nothing personal against CTRC or the doctor, but I truly believe it would be irresponsible of us not to seek out a second/third opinion. Our doctor has stated that he is not completely familiar with all treatments for NSCL cancer and it is important that we are presented with all available opportunities. Also, CTRC does not offer all types of treatment. There are several new types such as Proton Therapy (available at MD Anderson) and there is also Photodynamic Therapy (available at the Cancer Treatment Centers of America) and I am not sure if CTRC offers the extensive genetic and molecular typing that the START center does. So, I don't want anyone to think that the Doctors or CTRC is not appreciated, because my family is grateful for what they have done. I just really want to be sure that my mom is getting every opportunity presented to her that is possible. This is an extremely frightening journey and it has been very difficult.

My mom has always been a role model and she has taught me to Never give up and don't take no for an answer. She taught to me to stay strong and to continue whatever journey we are on no matter what obstacles or challenges we face. We will fight this battle together and with all your help.

Thank you and God bless.

-Vanessa

Tomorrow I will ask if they did a complete genetic profile on mom.

Tumors In Majority Of Patients With Advanced Lung Cancer Found To Have Genetic Mutations That Can Be Treated With Targeted Therapies

CHICAGO, IL, June 4, 2011

Mark Kris

Screening tumor samples for cancer-causing genetic mutations can help physicians tailor treatment to specifically target those mutations in patients with advanced lung cancer.
A new study detected one of ten such mutations in 54 percent of the 516 lung cancer patients tested at diagnosis. The results enabled doctors to select the most appropriate drug designed to block the identified mutation and choose other treatment options for those patients whose tumors did not have a mutation.
The results of the multicenter study are being presented today by the study’s lead author, Mark Kris, MD, Chief of the Thoracic Oncology Service at Memorial-Sloan Kettering, at the 2011 annual meeting of the American Society of Clinical Oncology.

“The key to treating men and women with lung cancer lies in understanding the genetic makeup of each person’s tumor,” said Dr. Kris. “Pinpointing specific mutations known to play a role in one-third of lung cancers can help maximize the chance of treatment success with personalized medicine.”

Memorial Sloan-Kettering is one of 14 institutions participating in this ongoing study, which has collaboratively tested a total of 1,000 patients who have been newly diagnosed with stage IV lung cancer that has returned after initial treatment with surgery, chemotherapy, and/or radiation. All 14 hospitals are members of the National Cancer Institute’s Lung Cancer Mutation Consortium (LCMC), an initiative created to identify the frequencies and characteristics of genetic mutations found specifically in lung cancer and research treatments that target them.

Pinpointing specific mutations known to play a role in one-third of lung cancers can help maximize the chance of treatment success with personalized medicine.

Mark Kris, MD, lead author and Chief of the Thoracic Oncology Service at Memorial Sloan-Kettering

The sophisticated technology needed for such extensive testing of cancer-causing, or “driver,” mutations is currently available at only a handful of centers in the world, including Memorial Sloan-Kettering, which began to screen all of its lung cancer patients for driver mutations in 2009.
Study researchers are screening lung tumors using multiplexed assays for mutations in KRAS, EGFR, HER2, BRAF, PIK3CA, AKT1, MEK1, and NRAS and are using flourescence in situ hybridization (FISH) for ALK rearrangements and MET amplifications. The most common mutations found so far have been KRAS (23 percent) and EGFR (17 percent).
Patients whose tumors are found to have the driver mutation EGFR-1, which was discovered by researchers at Memorial Sloan-Kettering and two Harvard institutions in 2004, are treated with the targeted drug erlotinib (Tarceva®), an FDA-approved drug that is currently the standard of care. Patients whose tumors exhibit one of the nine other mutations avoid being treated with erlotinib - which would not likely benefit them - and are offered participation in one of several LCMC-linked clinical trials investigating new medicines that target these specific genetic defects. For example, patients who have the EML-4ALK mutation may enroll in a clinical trial studying the experimental drug crizotinib, which is currently under FDA review for the treatment of lung cancers that have that mutation.
According to Dr. Kris, the next step is to expand this concept of customizing treatment based on a patient’s unique genetic tumor profile to all lung cancers and all stages of lung cancer.

“In fact, this process can work for any cancer and our assay panel already includes important mutations in colorectal cancer (KRAS) and melanoma (BRAF),” noted Dr. Kris. “As additional mutations are discovered by efforts like The Cancer Genome Atlas, these mutations can be quickly included in the routine molecular analyses. At the same time, our investigators will continue researching new therapies that target these genetic abnormalities, providing hope for the 220,000 people diagnosed with lung cancer each year.”

The study was funded by a grant from the American Recovery and Reinvestment Act (ARRA).
Members of the LCMC include Dana Farber Cancer Institute, Boston; Massachusetts General Hospital, Boston; The University of Texas MD Anderson Cancer Center, Houston; Partners Health Cancer Center, Boston; Vanderbilt-Ingram Cancer Center, Nashville; The Sydney Kimmel Comprehensive Cancer Center, Los Angeles; University of Texas Southwestern Medical Center, Dallas; H. Lee Moffit Cancer Center and Research Institute, Tampa; Medical University of South Carolina, Charleston; National Cancer Institute, Bethesda; Vanderbilt University, Nashville; University of Colorado Cancer Center Denver, Aurora; and University of Colorado Denver, Aurora.

IP6 and Inositol- Information from the American Cancer Society website

Inositol Hexaphosphate

Other common name(s): IP6, IP-6, InsP-6, inositol, phytic acid, phytate, myo-inositol hexaphosphate
Scientific/medical name(s): inositol-1,2,3,4,5,6-hexakisphosphate

Description

Inositol hexaphosphate (IP6) is a chemical found in beans, brown rice, corn, sesame seeds, wheat bran, and other high-fiber foods. It is converted into compounds in the body that are used by cells to relay outside messages to the cell nucleus. IP6 also aids the body in its use, or metabolism, of calcium and other minerals.
IP-6 is a very specific form of inositol, and there are several other forms of it found in the human body. It is different, for instance, from myo-inositol, which is another form being studied because of its possible role in illnesses such as depression and anxiety.

Overview

Animal and lab research has found that IP6 may be effective in lowering tumor incidence and slowing tumor growth. However, studies of IP6 have not yet been done in people. Clinical trials are needed to find out how it might work in preventing or treating cancer in humans.

How is it promoted for use?

Proponents call IP6 a "natural cancer fighter" and claim it slows or reverses the growth of various forms of cancer, including breast, colon, and prostate cancers. It is thought to be an antioxidant, a compound that blocks the action of free radicals, activated oxygen molecules that can damage cells. It may help to prevent the abnormal signals that tell a cancer cell to keep growing from reaching the cell's nucleus. Some research shows IP6 slows abnormal cell division and may sometimes transform tumor cells into normal cells. Supporters also claim it effectively prevents kidney stones, high cholesterol, heart disease, and liver disease.
IP6 is one form of inositol. Inositol is a kind of sugar formed by 6 carbon atoms, 6 oxygen atoms, and 12 hydrogen atoms. This combination of atoms can also form glucose, but the atoms are arranged differently in these 2 sugars. There are actually several forms of inositol, each with subtle differences in the arrangement of atoms, with myo-inositol being the most common form. IP6 is formed by substituting phosphate groups (each with a phosphorous and three oxygens) for each of the 6 hydroxyl (an oxygen and hydrogen) groups of inositol. Thus, IP6 is related, yet chemically distinct, from myo-inositol, which is being studied for its possible role in illnesses such as depression and anxiety.

What does it involve?

Many high-fiber food sources contain IP6, and it is also available in pill form as a dietary supplement combining inositol and IP6. Scientists do not know enough about the chemical to recommend a standard supplement dose. It is not known whether taking a supplement provides the same effect as getting IP6 from food sources.

What is the history behind it?

The existence of IP6 has been known for several decades. Interest in its potential anti-cancer properties emerged in the mid-1980s when Abulkalam Shamsuddin, MD, PhD, a pathologist at the University of Maryland, began to conduct research studies on inositol in the lab. He published a book on the subject in 1998. He and other researchers continue to study the effects of IP6.

What is the evidence?

All of the evidence regarding the anticancer effects of IP6 has come from laboratory cell cultures and animal studies. Laboratory studies of cell cultures have shown that IP6 may help put cancer cells on a path toward normal cell death and may help keep them from spreading to other parts of the body. It may also affect the growth of blood vessels that supply the tumor and the immune system in general. These studies have shown IP6 may have activity against cancer of the pancreas, breast, prostate, colon, and other types of cancer. Results of some studies in cells have also suggested that IP6 may help certain chemotherapy or hormone therapy drugs work better.
Studies in animals have found that supplementing the animals' diets with IP6 may help prevent tumors from forming in the prostate, lung, colon, skin, and other areas. While animal and laboratory studies may show a certain compound holds promise as a helpful treatment, further studies are needed to find out if the results apply to humans. One preliminary human study suggested that IP6 may cause regression of precancerous lung changes in smokers. IP6 has not yet been studied in humans as a treatment for cancer.
Inositol hexaphosphate and similar chemicals have also been studied for treating polycystic ovary syndrome, panic disorders, autism, obsessive-compulsive disorders, Alzheimer disease, post-traumatic stress disorders, and depression. Researchers have reached no firm conclusions about its impact on these conditions.

Are there any possible problems or complications?

This product is sold as a dietary supplement in the United States. Unlike drugs (which must be tested before being allowed to be sold), the companies that make supplements are not required to prove to the Food and Drug Administration that their supplements are safe or effective, as long as they don't claim the supplements can prevent, treat, or cure any specific disease.
Some such products may not contain the amount of the herb or substance that is written on the label, and some may include other substances (contaminants). Actual amounts per dose may vary between brands or even between different batches of the same brand.
Most such supplements have not been tested to find out if they interact with medicines, foods, or other herbs and supplements. Even though some reports of interactions and harmful effects may be published, full studies of interactions and effects are not often available. Because of these limitations, any information on ill effects and interactions below should be considered incomplete.
When taken in moderate amounts, IP6 appears to be safe. However, no studies have been done to determine its safety. Some experts advise those who wish to increase their intake of IP6 to add beans, whole grains, and other foods rich in IP-6 to their diets before resorting to supplements.
Inositol hexaphosphate may reduce the body's ability to absorb some minerals such as zinc, calcium, and iron. This concern has been raised mainly in regard infants. IP-6 can also reduce the amounts absorbed from mineral supplements. No studies have tested the safety of IP6 in women who are pregnant or breast-feeding. Relying on this treatment alone and avoiding or delaying conventional medical care for cancer, may have serious health consequences.

Mom had a good weekend!

Even though tuesday was a very difficult day for us, mom has continued her focus on being positive and staying strong. She has been working and keeping life as normal as possible. She has agreed to drink Kombucha tea again which makes me really happy. Its an awesome tea that just really helps boost the immune system and full is of good enzymes and probiotics. Anyway, its just good for her and its healthy. She also has agreed to take the IP6 and Inositol supplements which are also awesome in boosting the immune system. Both of these things are something that in my research and in communicating with other Non small cell lung cancer stage 4 survivors say they take are going on years of survival and some are now No Evidence of Disease (NED). I don't if these will really help and there is no such thing as a miracle cure, but the way I look at it is that its not gonna hurt and in researching it, it really is just good for the immune system. The immune system is very important to monitor in fighting cancer. So, I'm just glad she's taking it anyway. I will post some info on these after.

Anyway, I spent the night on friday with mom and I made spaghetti for dinner. We watched NCIS and talked about seeing another doctor to get another opinion. I showed her some of the discussion forums that I have joined where other people around the world who are fighting this disease come together and talk about what they are going through and how we can all help each other. There are many  people that feel like we do when our doctors just aren't trying enough or don't know enough specifically to want to try. They see that you are stage 4 and don't really see a point in trying. Now that I've said that, other people on these forums come through saying that they were in that same position and decided to go get another opinion (even though their doctors were supposed to be the best in their area as well). Anyway, they got another opinion and are doing extremely well today. They found new doctors who didn't stick with standard protocol and did what they thought would be right for those individual people. I am just hoping that we find another doctor who will fight as hard as my mom is. She really is an inspiration!!

So friday night was good and on saturday we got up and went for a drive to the outlet mall. It was packed with christmas shoppers. Mom and I went to only a couple stores- Yankee candle, bath and bodyworks, and neiman marcus last call. We both got a candle, a hand soap, and sweater (and all at extremely great discount savings plus we had gift cards! Cool). We weren't there too long, maybe an hour and a half and then headed back home in the rain and almost ran out of gas too! After that, we went to mom's good friend and hair dresser Michael and he trimmed her bangs a little and gave her a big hug and kiss. It was nice and I think mom had a good day. We went back to the house had enchiladas for dinner and then mom needed to rest.

This morning, John (my older brother), Darinka (his wife), and I met at the house to get a christmas tree for mom. We picked out a really nice noble fir maybe 8-9feet and we all decorated it together. It was fun and it was really great being together. We had a good weekend.

This week is going to be interesting. Mom will continue to work and I will continue to research treatment options. We are going to discuss options with her doctor on tuesday. He is supposed to be giving us several options and inform us about several clinical trials. Regardless, I am going to be prepared and have lots of questions. I am also hoping to hear from MD Anderson and I will go to the START center and seek out an another evaluation. I just want to be thorough and be sure that all bases are covered.

Keep praying and continue your faith!! God bless.

-Vanessa

Option Tarceva

Possible Benefits of Tarceva

Related Links

• How to Take Tarceva

Maintenance treatment with Tarceva has been shown to extend overall survival time and increase the time until the cancer gets worse.
In a large study in people with advanced NSCLC who received Tarceva as maintenance treatment:

In a large study in people with advanced NSCLC who have not taken Tarceva before and whose cancer has grown or spread after at least 1 prior chemotherapy regimen:

Tarceva may offer convenience

You take the pill by mouth once a day on an empty stomach.
In addition to understanding the benefits of Tarceva, it is also important to know the side effects and safety information about Tarceva. This information appears below.
*Median is the midpoint of a range of numbers. This means that half the patients had a shorter overall survival time and half had a longer overall survival time.
Indications and Usage for Advanced Non-Small Cell Lung Cancer Patients Tarceva is prescribed for patients with advanced-stage Non-small Cell Lung Cancer (NSCLC) whose cancer has not spread or grown after initial treatment with certain types of chemotherapy. (Maintenance treatment)
Tarceva is prescribed for patients with advanced-stage Non-Small Cell Lung Cancer (NSCLC) whose cancer has spread or grown after receiving at least 1 chemotherapy regimen. (2^nd/3^rd-line treatment)
Tarceva is not meant to be used at the same time as certain types of chemotherapy for NSCLC.

Important Safety Information

Possible effects on the lungs

There have been reports of serious adverse events involving the lungs in a small number of patients taking Tarceva. These events have included death in some patients. The medical name for these types of events is interstitial (in-tur-STISH-ul) lung disease-like events (or ILD-like events).

Possible effects on the kidneys and liver

Liver and/or kidney problems (including deaths) have been reported in some patients taking Tarceva. Let your healthcare provider (HCP) know if you have a history of liver or kidney disease.

Possible effects on the stomach and intestines

Some patients taking Tarceva have developed a hole in the lining of their stomach or intestines (including deaths). It may happen more in patients who are taking certain other medicines or who have had certain stomach or intestinal diseases.

Possible effects on the skin

Some patients taking Tarceva have developed serious skin conditions. Some patients have died from these conditions.

Possible effects on the eye

Some patients taking Tarceva have developed eye irritation and damage to the cornea. The cornea is the clear part of the eyeball that covers the colored part of the eye and the pupil. Other eye problems such as abnormal eyelash growth, dry eyes, or changes in eyesight have also been reported. Patients should tell their HCP about eye problems that get worse, including eye pain.

When to call your HCP

Call your HCP right away if you have these signs or symptoms:

• New or worsening skin rash
• Serious or ongoing diarrhea, nausea, loss of appetite, or vomiting
• New or worsening shortness of breath or cough
• Eye irritation

Before you start taking Tarceva

Some patients taking Tarceva have experienced difficulty with blood clotting, and bleeding events, including gastrointestinal and non-gastrointestinal bleeding. Patients taking blood thinners (Coumadin^®, warfarin or other coumarin-derivatives) should be monitored regularly.

Taking other medicines and herbal supplements with Tarceva

Certain medicines and herbal supplements can affect how Tarceva works in the body. It is important that you tell your HCP about all of the medicines and herbal supplements you are taking. DO NOT start taking any new medicines or herbal supplements before talking with your HCP. Tarceva may also affect other medications you are taking.
In addition, grapefruit and grapefruit juice have an effect on how Tarceva works. DO NOT eat grapefruit or drink grapefruit juice while on treatment with Tarceva, except under the care of your HCP.
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Common side effects of Tarceva

The most common side effects in patients who took Tarceva were generally mild to moderate rash and diarrhea. You may also have other changes in your skin.
The rash from Tarceva therapy may appear on your upper body or face. Typically rash occurs within 8 days of starting treatment, but it may occur any time during treatment with Tarceva.
The rash is not an allergic reaction. It may look like acne or dry skin. It is not acne. Talk to your HCP if a rash occurs.
Typically, diarrhea may develop within 12 days of starting Tarceva.
Hair and nail changes have been seen with Tarceva.

Not so good

Unfortunately, mom's scan results from the crizotinib showed that the medicine did not work at all. It had zero effect on the cancer and the tumors have grown 2-3 times the size. We are all so upset from this news because we all believed that this miracle drug would work. We have another appointment on tuesday to discuss new treatment options and clinical trials. Whatever we decide is going to be labeled as third line treatment. The clinical trials we have so far been told of are stage 1 clinical trials which means that they are completely new and have not been tried yet. If she decides to do a clinical trial the next one doesn't start for 5 weeks. This means she cannot be on any other treatment during that waiting "washout" period. Even then, I don't know if she will get in the trial because she is on a waiting list and then when the time comes they run tests to see if she is even eligible.

The other choice is to just start taking either Tarceva or Taxol. I will post info about both.

Mom, is extremely positive and so incredibly strong. We must all continue to pray because God can heal her. I believe it is his will and that this is another bump in the road.

Psalm 41:3
The LORD sustains them on their sickbed and restores them from their bed of illness.

Let us pray:
 
Dear Lord of Mercy and Father of Comfort,

You are the One I turn to for help in moments of weakness and times of need. I ask you to be with your servant, Cindy Hudson, in this illness. Psalm 107:20 says that you send out your Word and heal. So then, please send your healing Word to your servant, Cindy Hudson. In the name of Jesus, drive out all infirmity and sickness from her body.
Dear Lord, I ask you to turn this weakness into strength, suffering into compassion, sorrow into joy, and pain into comfort for others. May your servant trust in your goodness and hope in your faithfulness, even in the middle of this suffering. Let her be filled with patience and joy in your presence as she waits for your healing touch.
Please restore your servant, Cindy Hudson, to full health, dear Father. Remove all fear and doubt from her heart by the power of your Holy Spirit, and may you, Lord, be glorified through her life.
As you heal and renew your servant, Lord, may she bless and praise you.
All of this I pray in the name of Jesus Christ.
Amen.