Monday, 2 May 2016

60 Things to Do to Raise Celiac Disease Awareness | BeyondCeliac.org

60 Things to Do to Raise Celiac Disease Awareness | BeyondCeliac.org
Make the most of Celiac Awareness Month 2016! How many ways can you spread awareness?

I found this article 60 Things to Do to Raise Celiac Disease Awareness | BeyondCeliac.org

60 Things to Do to Raise Celiac Disease Awareness | BeyondCeliac.org

And added TWO of my own !!!

AND 61 - Share my book with a local cafe or restaurant so that they prepare gluten free correctly http://ebook-cafes-restaurants.what-is-gluten-free.org/



AND 62 -  Share my gluten free book for the home with family and friends http://www.cooking.what-is-gluten-free.org/


Sunday, 24 April 2016

Tick Bites Have Made Red Meat A Nightmare For Thousands

I found this article By CLARISSA BYE in The Daily Telegraph - I thought it may be of interest.

Ticks cause health problems other than Lyme Disease - I wonder if any of you Lyme sufferers have experienced an allergy to red meat which could not be previously explained? 

Cooper Westaway with his mum Rebecca at their Warriewood home. Cooper, 16, was bitten by a tick at
school late last year.

TICK bites have caused more than 1000 Australians to develop a life-threatening allergy to red meat, with numbers of people affected rising dramatically over the past decade.

Immunologist Sheryl van Nunen sees between one to two victims every week at her Chatswood practice.

The allergy can cause an anaphylactic reaction up to eight hours after a person eats red meat, and the allergy can develop months after a bite.

Cooper Westaway with his mum Rebecca and dog Harvey: “I end up eating chicken all the time and I’m so sick of it.” Picture: Troy Snook
The Australian paralysis tick, which cause the mammalian allergy, is most common on the north shore and the northern beaches in Sydney, but are also found all along the east coast. “The numbers have increased markedly since 2003,” Dr van Nunen said.
“The important advice is to kill the tick where it is by freezing it with a spray from the pharmacy. Don’t squeeze it with tweezers.”

Sixteen-year-old Cooper Westaway (pictured) loves meat pizzas but can’t eat them any more. The Year 10 student from Warriewood now carries an epipen with him wherever he goes — all because a tick bit him at school last November.

“The tick gave me a meat ¬allergy, which is really annoying as I end up eating chicken all the time and I’m so sick of it,” Cooper says.
He is one of a growing number of Sydney-siders — and residents up and down Australia’s east coast — who have become victims of the unusual meat allergy caused by common bush ticks. A tick had attached itself to his head when he ran through bushes at his school, Mater Maria College.

Later in class he scratched it out and the bite site became really itchy. Being new to school, he didn’t want to speak up, and the reaction passed.

But a fortnight later, after a dinner of chilli con carne, he woke up in the night “going insane with itches” and with a swelling throat. The next day the GP sent him to see Dr van Nunen and blood tests confirmed the allergy diagnosis.

Cooper’s mother Rebecca Westaway said the state health department should be sending letters to schools to alert them to the dangers of ticks


Find out more about Lyme http://www.amazon.com/dp/B015PG1M1O


Australian Senate Inquiry Into Lyme-Like Disease

I have just become aware that the Australian Senate is conducting a review into Lyme-like disease in Australia. I am so pleased that the government is now taking this very seriously. Unfortunately, The submissions closed at the end of March so it is too late to give your point of view - but this is what the terms of reference are.
On 12 November 2015, the Senate referred the following matter to the Senate Community Affairs References Committee for inquiry and report:
The growing evidence of an emerging tick-borne disease that causes a Lyme‑like illness for many Australian patients.
The terms of reference are:
  1.  the prevalence and geographic distribution of Lyme-like illness in Australia;
  2.    methods to reduce the stigma associated with Lyme-like illness for patients, doctors and researchers;
  3. the process for diagnosis of patients with a Lyme-like illness, with a specific focus on the laboratory testing procedures and associated quality assurance processes, including recognition of accredited international laboratory testing;
  4. evidence of investments in contemporary research into Australian pathogens specifically acquired through the bite of a tick and including other potential vectors;
  5.  potential investment into research to discover unique local causative agents causing a growing number of Australians debilitating illness;
  6. the signs and symptoms Australians with Lyme-like illness are enduring, and the treatment they receive from medical professionals; and
  7. any other related matters.  
Submissions should be received by 31 March 2016. The reporting date is 20 June 2016.

Committee Secretariat contact:

Committee Secretary
Senate Standing Committees on Community Affairs
PO Box 6100
Parliament House
Canberra ACT 2600

Phone: +61 2 6277 3515
Fax: +61 2 6277 5829
community.affairs.sen@aph.gov.au
For those of you who would like to know more about the controversies associate with Lyme disease - my book is available on  the  Amazon KDP programme 

DOWNLOAD IT NOW 






Wednesday, 6 January 2016

My Brother-In-Law Won His Battle With Lyme Disease - You Can Too!

Lyme Disease Case Study - Could this be you?


This is  the story of my brother-in-law John (not his real name) who suffered for so many years with Lyme disease and his amazing recovery once the real cause of his symptoms was discovered and appropriate treatment given. 



John moved to southern Humboldt County in Northern California in 1983. His wife (my sister) and two small children had bought a house on 20 acres that was two miles down a private gravel road. The land is hilly, mostly forested with grassy meadows and brush. They maintained their own power and water systems and use wood for heat. All this requires a lot of hiking around the property to maintain the long pipe from the spring and the gathering of wood for the winter. 

The insect pests around their home are mosquitoes, chiggers and ticks. Deer wander freely on the land. If you have to walk in the grass and bush you may get bitten.

John can’t remember when he first heard about Lyme disease, but it was some years after he had moved there. He learned that a bite from a Lyme infected tick would give you a bull’s-eye rash and mild flue like symptoms. Later the symptoms would develop into swollen and sore joints.

John never experienced these particular symptoms, even though in retrospect, he now suspects he did have Lyme disease as far back as the 1980’s or early 1990’s. Lyme disease is a subtle disease. He says that you can feel fine most of the time and when you don’t, well sometimes you don’t feel your best and that’s life. It happened that Lyme disease had just been discovered in this area about 10 years earlier. Lyme disease is now found in many areas of the US besides its hot spots in the Northeast.

John started having symptoms he could not ignore around 1997, and overall body soreness mainly centered in his upper body. It was painful to take a deep breath and the pain interfered with his sleep and left him with very low energy. The answer to the pain was Aleve (noproxen sodium) one tablet morning and evening. For the low energy he started taking Ritalin, a mild time release amphetamine, 10 mg morning and midday. The Aleve and Ritalin treated the painful symptoms and allowed him to perform in a high stress job.

Around 2004 his mind seemed clouded, he had trouble controlling his emotions and was quick to anger. When he explained this to his doctor, he was prescribed Wellbutrin and that controlled those symptoms.

His years of treating the symptoms and not the disease came to an abrupt end in 2009 when he was hospitalized for bleeding ulcers, the result of taking Aleve for all that time. Now that he was allergic to the most effective pain reliever he became desperate to discover the reason for his symptoms and the permanent cure for his sore body.

A neighbor suggested he see a new doctor at the local clinic. After many negative test results for a variety of other diseases, the doctor asked if he had ever been tested for Lyme disease. He had not because he did not have the classic symptoms of joint swelling and joint pain.

The doctor took a sample of blood and sent it to the laboratory to be tested for Lyme disease.  It was POSITIVE in the screen test and confirmed by the more specific Western Blot method. John had late stage Lyme disease which was diagnosed with a simple blood test and after all these years of suffering, proper treatment could be started to treat the cause of his symptoms.

Testing was also done to see if he had two of the common co-infections associated with Lyme disease: - Babesia, which was positive; and Ehrlichia which was negative.

His general blood count and the test CD-57+ to check his immune status were all normal.

John went on a two month regime of doxycycline antibiotics. Though taking antibiotics for that long was tough he was happy to finally find and treat his disease. Within a couple of months he started feeling less pain and went from taking twelve Tylenol a day to just two at night. His mind also became clearer; he was better able to focus, was less anxious and had better control of his temper.

He feels that the multi-year onset of the symptoms of Lyme disease were subtle. As he aged he was less able to cope with them. The recuperation was long as well. In the five years since the end of his treatment he still feels like his health both physical and mental is improving.

He has since discovered many people of his area were also treated for Lyme disease. He asks newcomers now if they have been tested for Lyme disease. He wishes someone had mentioned it to him years ago. Find out more about Lyme disease and the controversies surrounding it by clicking here.