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Six new BT Blog Buddies Added!

  • Saturday, 04 February 2012 20:00
  • Last Updated ( Saturday, 04 February 2012 20:02 )

We've added six new Blog Buddies to our list! Checkout their blog details below. Please pop by and show our new blog buddies your support as I know they would really appreciate it...

Name: Heather Roberts

Type of Brain Tumour: anaplastic astrocytoma

Grade of Brain Tumour: 3

A little about you: Heather (now 32) was diagnosed with brain Cancer Grade 3: Anaplastic Astrocytoma in April 2008; and on April 24, 2008, she had her first of two surgeries to retract her Tumor; her second surgery was June 12, 2008. Even though both surgeries were considered successful, the entire tumor could not be retracted. She completed 6 weeks of radiation with low dose Temador and then completed 11 months of high dose Temador.  After 11 months, her body said, “No more!” Her left side shows some deficit, but she is able to work and lead a mostly normal life.  She now travels to the University of California at San Francisco Medical Center (UCSF) to see Dr. Susan Chang every four months for her check-ups. She will be closely monitored for any changes for the rest of her life.  The past three years have brought many challenges: Heather lost a grandfather (2009) and a grandmother (2010).  Her 3-1/2 year relationship with her fiancée ended as her grandmother’s health was declining, and she was forced to call off her wedding in 2010.  Then later that year, she was diagnosed with Graves disease, which is now under control.  However, through all of this, Heather remains upbeat, positive, and thankful for so much. 

Blog name: Heather’s Journey

Blog link: leapforacure.org

Picture: Heather is in the middle.  Her two sisters, Michele (L) and Amy (R) stand with her.


Name: John Vang

Type of Brain Tumour: Oligoastrocytoma

Grade of Brain Tumour: Grade II

A little about you: Hello, I am a 34 year old male living in California. A CT scan in February of 2011 revealed a 3 cm-wide "dark spot" in my right Medial temporal parietal lobe. An MRI confirmed it most likely to be a tumor. Had a Needle biopsy which was inconclusive and ended up having a Craniotomy in August which diagnosed the tumor to be a grade II oligoastrocytoma. The craniotomy removed about 80% of the tumor with the remaining 20% too closely wrapped around an artery to risk removing. Opted for radiation therapy (December 2011 to January 2012) to treat this remaining 20%. 

Going through this experience, I've found connecting with others (either through direct communication or reading blogs) to be reassuring and comforting and I started my blog in hopes that someone who is also unfortunately sharing the same experience might find some level of reassurance and comfort in it as well.   

Blog name: My Life With a Brain Tumor

Blog link: http://havnot.blogspot.com/



Your Name: Kevin "Wash" Pratt-King

Type of Brain Tumour: Glioblastoma Multiforme 

Grade of Brain Tumour: IV

A little about you: 25 when diagnosed in late 2009, in school to be an architect. Lives in Arizona with his wife/caregiver Tashi. Now 27 and "retired" to spend his days writing sci-fi short stories and creating "steampunk" art. A huge couple of geeks and "Browncoats" - people who love Joss Whedon/ Firefly series.  They live with their two cats and various fish.

Blog name: Learning To Hope

Blog link:  http://washandtashi.blogspot.com/


Name: Jennifer K. Giliberto

Type of Brain Tumour: An Infultrating Grade II Astrocytoma was removed from my right Temporal Lobe

Bio: Wife to Paul and mother to three children and three rescue dogs. I’m also an advocate, volunteer and Domestic Goddess (I jest) of everything in-between in a place I fondly refer to as “crazyland”.

Oh, yeah… there’s this: I’ve got a brain tumor. Well, let’s be honest…shit happens and it could be worse.

Blog name: Grey Matter Life

Blog link: www.greymatterlife.com


Name: Jen Crowley Searle

Type of Brain Tumour: Oligodendroglioma

Grade of Brain Tumour: Grade II

Bio:

My name is Jen, and this is the journey of living the gift of life with my husband Mike and our 3 sons, while I also battle brain cancer.  Some days are good, some days are not so good, but all days are a blessing.  I promise to be open – sometimes painfully (sorry).  But this journey is all about trying to document this for my children, for being cheap therapy for me, and for hopefully helping a few others who might be going through something difficult in their own lives.  So come on in, pull up a chair and put your feet up.

On Tuesday, June 12th 2007 I was diagnosed with a brain tumor, named Bob. The following month, I had brain surgery and pathology revealed brain cancer (oligodendroglioma, grade II). I have been doing well with MRIs every 3, 4 and then 5 months, until recently. I have a recurrence now (named Bozo), and we are going through the whirlwind of trying to research and figure out our next steps to defeat Bozo.
Blog name: Go Away Brain Cancer


Name: Lucy Cunnington

Type of Brain Tumour:

Grade of Brain Tumour:

Bio:

As of yesterday, 18th November 2011, I was told I have a brain tumour for the second time. THe first time was back in 2006, when I was halfway through my PGCE course. I came to a conclusion that higher education and I do not go well together. In 2001, I was in the final year of my English degree when I was hit by a car in a hit and run asccidet which nearly cost me my life, and left me permently disabled. I had to take a year out of my degree cours, was in hospital for 4 months, and spent about 10 months learning how to walk again and wondering why the UK wasn't more wheelchair friendly! So then I was faced with postponing my PGCE too!

Statistically if you've had a brain tumour (BT) you are more likely to have a reocurrance eventually, than never at all, so I always knew it was likely. Then literally two days after I got back from Taiwan, I had my first Seizure in five years, recognising the symptoms I phoned the hospital and following scans had my suspisions confirmed.

I have decided to write this as I found last time a lot of friends couldn't handle it and didn't know what to say, so hopefully this will bridge the gap. I don't feel ill at the moment and my lovely doctor has given me some snti-seizure drugs to make life more comfortable. I will Be updating this regularly. I am also asking people to make donations to BT buddies- a great charity that supports, sufferers, survivors and their friends and families. please go to my just giving page: Lucy Cunnington is fundraising for BT Buddies

Blog name: Statistic of One

Blog link: http://statisticof1.blogspot.com/

You can also click here to view a full list of our BT Blog Buddies...

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Over a million cancer carers miss out on vital support

  • Friday, 27 January 2012 08:28
  • Last Updated ( Friday, 27 January 2012 08:36 )

Over a million people who look after a loved-one with Cancer are potentially missing out on vital support and benefits, according to new research by Macmillan Cancer Support.


An Ipsos MORI report - which reveals for the first time ever the number and profile of the 1.1m people currently caring for someone with cancer in the UK[1] - found that almost none (just 5%) have received a local authority Carers’ Assessment which enables them to access practical, emotional and financial support with their caring role.[2]


Worryingly, half (49%) surveyed receive no support whatsoever – either formally or informally - to help them look after their family member or friend with cancer. As well as emotional support, cancer carers administer medicine; cook and clean; and provide personal care. 


This lack of support may explain why nearly half (46%) suffer with mental health problems such as stress, anxiety and depression, and one in eight (13%) say it’s causing physical health issues such as sleep and digestive problems. One in seven (15%) carers reported financial issues such as spending more on things like travel to hospital or giving up work.


One Carer who has struggled with her caring role is Rebecca Guyott, 19, Essex.[3] She says:


“I’d only just turned 18 when my mum was diagnosed with bowel cancer in 2010. It was left to me and my sisters to look after her and as a carer I found it a big strain.  At work I often had to leave the office because of the emotional stress.  I’d get home and do all the cleaning, washing and cooking as mum could hardly stand, let alone do anything for herself.  After just a week of this I slept so badly because of the worry and then could barely wake up the next morning to go into work and start all over again.


“Mum’s improved now and I’m hoping to return to college, but I still feel under pressure. I didn’t even know we could have been entitled to a Carer’s Assessment or benefits, it was never mentioned.”


The More than a million report identifies a number of key barriers to carers of people with cancer accessing vital support:


~ Less than half (43%) surveyed identify with the term ‘carer’ – men even less so (just 35% compared with 48% of women) – which means they are less likely to seek help.


~ Carers often don’t put their own needs first or think about what help they might need.[4]


~ Low awareness of the support available – from statutory services or other sources.[5]


Ciarán Devane, Chief Executive of Macmillan Cancer Support, says:


“Our research shows how unsupported cancer carers really are in the UK. Carers want to look after their family or friend with cancer – but it is often at the expense of their own mental or physical health.


“Cancer is no longer necessarily a death sentence and this means there is a growing need for people to care for their family member or friend with cancer. Often this is long-term care. But carers need support to cope with the significant demands of their role.


“The statutory sector must increase awareness and uptake of Carers’ Assessments. Both health and social care professionals need to be signposting cancer carers for assessments.”


If you’re caring for someone with cancer and need information or support, call 0808 808 00 00 or visit www.macmillan.org.uk/carers.


For the full research report, please click on the link below:  http://www.macmillan.org.uk/Documents/Cancerinfo/Ifsomeoneelsehascancer/More_than_a_million.pdf


Notes to Editors:


[1] Research methodology:


People currently supporting someone with cancer were defined as carers for the purposes of this research if they provided more than five hours of care a week (‘care’ was determined by asking them if they did any of a range of activities for someone because they had cancer) or provided 1-4 hours of care a week but said it had an impact on their lives. It does not include those who provide care as their paid job or voluntary work.   Please see the full report (on the link below) for a more detailed explanation of how carers were identified as part of this research.


Research carried out via Ipsos MORI’s face-to-face omnibus survey of the general public. Fieldwork conducted between 20 May and 25 August 2011. 18,449 members of the UK public aged 15+ were screened to identify current carers of someone with cancer. In total 386 fitted eligibility criteria and were interviewed in more depth. Results have been weighted to be representative of the UK adult population.


From the sample of the public interviewed, 2.1% of the UK population aged 15+ were identified as currently caring for someone with cancer (using the ‘carer’ definition outlined earlier). Converted to a population estimate (using ONS 2010 Mid Year Population estimates) this equates to 1,080,000 adults aged 15+. As a sample of people were interviewed rather than the whole population, this estimate could lie within a range calculated to be 960,000 – 1,200,000. [2] 5% of carers surveyed say they have had a local authority Carers’ Assessment. Using the estimated total population of current carers (of 1,080,000) as a basis - this equates to just over one million carers (about 1,040,000) who do not report having ever had a Carers’ Assessment. Carers are legally entitled to an assessment of their needs by their local authority if they provide a substantial amount of care to someone on a regular basis. The purpose of the assessment is to ascertain what help they need with caring, and what services and support social services can provide.


[3] Rebecca is a member of Macmillan’s own panel of cancer carers who have agreed to comment and be quoted on their experiences of looking after someone with cancer. She was not a participant in the Ipsos MORI research.


[4] Ipsos MORI conducted a series of qualitative depth interviews with carers who took part in the survey and who agreed to be contacted for further research. These interviews suggest that carers don’t think to ask for help for themselves, partly because they aren’t aware of any services that are available, but also because they feel they should deal with things themselves. In addition to this, carers often feel that the best support for them is additional support for the person with cancer, because making things easier for that person would in turn make things easier for them.


[5] 44% of carers have never heard of Carers’ Assessments. Not being aware of the support available is one of the most common reasons given by carers for not receiving support that would be helpful to them (mentioned by 27%).

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Young Britons have 200 Facebook friends but can only turn to two friends for support

  • Tuesday, 24 January 2012 10:13

Young Britons have an average of 237 facebook friends but nearly two out of three people (61%) say they could only turn to two friends at most for support in a crisis, according to a new poll by Macmillan Cancer Support for Cancer Talk Week (23-29 January 2012).

A poll of 1,000 people, age 18-35, reveals that one in eight (13%) surveyed couldn’t even turn to one single friend for support when faced with a serious problem. Men were more likely (16%) than women (12%) to have no-one to turn to. This is despite the ‘boom’ of social networking sites such as facebook and twitter in recent years.

The poll also shows that social networking sites have also sometimes had a negative impact on friendships, as one in six (18%) of those who use these sites say they see or talk to their friends less often.

Jeannie Wilkinson, a Macmillan-funded Relate counsellor, says:

“It is surprising and concerning that people confide in such a small number of friends and family – and more so that others may not confide in anyone. It is important that, when going through something tough, like a cancer diagnosis and treatment, you can speak openly about what you’re going through to ensure you get the right support you need. We meet a lot of patients and people caring for someone with cancer who feel like they need to be ‘strong’ and bottle up their emotions. This causes great strain on relationships.

‘If anyone does want to talk to someone impartial or wants advice on how to talk to their friends and family, the Macmillan team can always help.”

Cancer Talk Week (23-29 January) is encouraging people to talk about cancer. Macmillan Cancer Support can help you with those difficult conversations, call free on 0808 808 00 00 or visit www.macmillan.org.uk.

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IBTA E-News January 2012

  • Tuesday, 17 January 2012 00:11

Dear All,

Patient resource: There is a very useful podcast explaining a CT scan to patients that was released on 2 January by ASCO. It is available here and lasts for 5 mins 40 secs. While intending to cover all cancers it answers most questions asked by a patient referred for a CT scan of the brain.

Paediatric Brain Tumour research: In a recent report US Phrma identified 53 medicines in clinical trial development or FDA review for paediatric Cancer of which 12 were specifically associated with brain tumours, while several others were being investigated for solid tumours in general. 

The name, indication  and status of the brain tumour medicines or therapies are:  ARC-100 (medulloblastoma) Phase I/II; cintredekin besodotox  ( Glioma) Phase I; GliAtak ( Malignant brain tumors), Phase I; Nexavar (glioma), Phase II; nimotuzumab (recurrent glioma), Phase II; PTC299 (CNS cancer) Phase 1; SL-701 (glioma) Phase I/II; Tarceva (recurrent/refractory ependymoma) Phase II; TheraCIM (recurrent DIPG) Phase II; vismodegib (medulloblastoma) Phase II;  Xeloda (gliomas) Phase I; Xerecept (brain Edema associated with brain tumors) Phase I/II.

Those therapies listed above appear to be company-initiated studies, as opposed to investigator-initiated studies. For example, the CERN Foundation also has an on-going paediatric study  (CERN08-01) of bevacizumab and Lapatinib for recurrent or refractory ependymoma.

MRS and IDH1: Scientists have used magnetic resonance spectroscopy (MRS) to identify the IDH1 mutation in both tumour samples and patients with glioma brain tumours by searching for the molecule 2-hydroxyglutarate (2HG). It has been suggested that this may "dispense with the need for invasive surgery". Hopefully, the results of this technique will be used to develop targeted therapies, rather than just tracking a patient's progress. 

At the present  time surgery is used not only to identify the type and grade of tumour but as a debulking process prior to use of the concomitant therapy.  Patients are likely to be puzzled should a Doctor say: "We don't need to operate, from the MRS we know you have a glioma with the IDH1 mutation".  In a recently released US Patterns of Care (POC) study for 2006 approximately 65% of patients with a GBM received a partial or total resection. There might be a relevance for the MRS technique in the case of Inoperable tumours.

Drug shortages: The USA has continued to experience shortages of drugs, particularly sterile injectable drugs, including those relevant to cancer treatments.  It is not known if this has had a flow-on effect in other countries. Drugs currently on the FDA's  shortage list, which shows individual supplier shortages and alternative sources, and which may be relevant to brain tumour treatments, include: Cisplatin injection 1 mg/mL solution,  Dexamethasone Injection, Methotrexate Injection-Preservative Free, Midazolam Injection,  Ondansetron Injection 2 mg/mL, Vincristine Sulfate Injection.

Commemoration and conference days: 7 February has been designated as International Childhood Cancer  Awareness Day. Now that CNS tumours have overtaken all leukaemias as the greatest childhood cancer killer in many countries it represents an opportunity to raise awareness about the need for greater support and research for paediatric brain tumours.

Rare Disease Day will be marked in Europe on 29 February - chosen because that date is a "rare date".  In the USA on 29 February the National Institutes of Health will also hold a Rare Disease Day. On the following day (1 March) the FDA will host a Rare Disease Patient Advocacy Day. By definition all paediatric cancers are "rare diseases".  In Brussels on 10 February the European Society for Medical Oncology (ESMO) and Rare Cancers Europe (RCE)  will jointly sponsor a conference on clinical trial methodology for rare cancers.

Trabedersen: On 11 January  Antisense Pharma  announced  that  they have decided to terminate  the ongoing Phase III trial (the Sapphire trial) for recurrent or refractory anaplastic astrocytoma (AA) or secondary glioblastoma (GBM ) due to slow patient recruitment. The company will pursue 1st line treatment of GBM with standard of care.  We will advise when any information about the next  trial in high grade glioma is available.

The company stated: " Recruitment delays are a result of changes in the histopathological grading of patients, introduced by the WHO, which considerably reduced the number of patients diagnosed with AA, already a rare, orphan disease. In addition, advances in the standard of care for 1st line patients have rendered many treated patients unsuitable for inclusion, as they no longer receive Radiotherapy. Attempts by the management to identify and implement an effective solution, such as amendments to the study design, have not yielded significant improvements in the recruitment rate."

Recent developments and promising therapies: Two researchers from Barcelona have discovered that the molecule CPEB4 turns on hundreds of genes that play critical roles in the progression  of pancreatic cancer and brain tumours. Inhibiting the process might be a useful form of targeted therapy.

Dutch company to-BBB has received a grant of €600,000 from a Dutch government agency to support a brain drug delivery partnership with a (as yet unnamed) top-5 pharma company using its G-Technology which enhances the delivery of specific drugs to the brain. In June 2011 the Company announced approval for a Phase I/II clinical trial testing its product  2B3-101 for brain Metastases from breast cancer.

Northwest Biotherapeutics: On 9 January the company announced plans to have at least 30 sites open and enrolling by the first quarter of 2012 for its DCVax immune therapy for GBM and will pursue programs in Europe.

On 4 January Celldex Therapeutics announced "...  that patient screening has initiated in a Phase 2 trial of rindopepimut in combination with avastin in patients with recurrent epidermal growth factor variant III (EGFRvIII)-positive glioblastoma, called the “ReACT Study.” This new study will run in parallel with Celldex’s Phase 3 trial (ACT IV) evaluating rindopepimut in patients with newly diagnosed EGFRvIII-expressing glioblastoma (GB)."

On 5 January the German-based company Apogenix announced the raising of further funds to advance the Phase II clinical trial of its drug APG101 to treat GBM. Final results of the trial are expected in the first quarter of this year. One of the investors is the German Cancer Research Centre.

Brain tumours and weather forecasting: The complete novelty of a scientific paper which seeks  to apply principles of weather forecasting to the spread of an individual's GBM was bound to attract attention in the popular media. The open-access paper can be downloaded here. In a subsequent interview the principal author Eric Kostelich from the University of Arizona revealed that he was prompted to focus on brain tumours because he had a family member with a brain tumour. 

The authors believe that  "... this preliminary study demonstrates the potential feasibility of ensemble forecasting and data assimilation methods for short-term prediction of the growth and spread of malignant brain tumors." They warn that "considerable work remains before our approach can be seriously considered in clinical settings." In the interview referred to earlier Kostelich suggests that the research (essentially based on MRIs and the behaviour of GBMs in other patients) might enable pre-emptive action to forestall development of a GBM in a certain direction, or a forecast that continuation of a Chemotherapy might be unproductive.

In all such research the evaluative criteria should be "will this be of benefit to the patient", rather than simply helping the clinician to confirm the accuracy of a rather dire Prognosis.

Danish brain tumour statistics: The 2010 report of the Danish Cancer Registry notes an increased incidence of CNS tumours in men. In the rather uncertain language of a Google translation it is stated: "There was a significant increase of tumors in the brain and Central Nervous System in men. The increase is 16 percent. in incidence rate, the responses to (which corresponds to?) an increase in the number from 638 to 748 (between 2009 and 2010?). There is no similar increase among women. The reason for the increase in men is uncertain. Over the past 10-year period (we have) seen a steady increase, which to some extent (is) a reflection of increased diagnosis as a result of a general focus on the detection of cancer with highly increased imaging activity."

IBTA Co-Director Kathy Oliver will attend the Drug Information Association  conference in Copenhagen in March and in April it is hoped that IBTA officials can meet with representatives of the Scandinavian brain tumour support and advocacy groups to discuss areas of common interest.

magazine.  The suggestions about content made by 279 respondents to the IBTA's 2011 satisfaction survey have been carefully analysed and incorporated where possible in the magazine planning. Two recommended subjects we would like to cover and for which we are seeking authors are: (1) the relevance of stereotactic radio surgery for meningiomas, and (2) the use of boswellia in Germany for brain oedema as an example of a useful complementary treatment.  Please contact This e-mail address is being protected from spambots. You need JavaScript enabled to view it if you know of possible contributors on these subjects.  Limited copies of the 2011

Thank you for your continuing support. We wish all our readers a successful New Year.
 
This e-mail address is being protected from spambots. You need JavaScript enabled to view it (Chair and Co-Director)                                     
International Brain Tumour Alliance IBTA 
www.theibta.org

This e-mail address is being protected from spambots. You need JavaScript enabled to view it (Co-Director)
PO Box 244, Tadworth, Surrey
KT20 5WQ, United Kingdom
Tel:+ (44) + (0) + 1737 813872
Fax: + (44) + (0) +1737 812712
Mob: + (44) + (0) + 777 571 2569
 
The International Brain Tumour Alliance is a not-for-profit, limited liability company registered in England and Wales, registered number 6031485.  Registered office: Roxburghe House, 273-287 Regent Street, London W1B 2AD, United Kingdom.  All correspondence should be sent to the Co-Directors address above, not to the registered office.

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David G. updates his Story of Hope

  • Monday, 09 January 2012 23:39


Diagnosed with a Glioblastoma Multiforme in 2005, David, was one of our very first BT Buddies and we are very pleased to be able to share with you the last update in his story.

It gets off to a great start with Tom saying "76 months post op and still going strong!"

To find out more about David and to read his latest update in full CLICK HERE.

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