Wegener's granulomatosis is a rare blood vessel inflammation



DEAR DR. ROACH: In March 2009, a family member was having terrible flu-like symptoms accompanied by horrific headaches. The symptoms lingered on for what seemed like forever, getting worse, even with hallucinations and cold sweats. At first, the doctor he visited thought he had mesothelioma, but after numerous tests and much research, decided it wasn't cancer, and in July 2009 he was diagnosed with Wegener's granulomatosis. He ended up in the critical-care unit for four weeks and was given only two days to live, even being revived twice while there! He survived and is fairly healthy today. He is in remission and is now being weaned off prednisone, methotrexate and perhaps other drugs. Do you know what caused him to contract this awful autoimmune disease? He had been very healthy, and luckily was in good physical condition when it was diagnosed. Thank you. -- S.R.

ANSWER: Wegener's, also known as granulomatosis with polyangiitis, is an autoimmune disease of unknown cause that commonly presents with oral or nasal inflammation or ulcers, lung symptoms, abnormal X-rays and kidney problems. A biopsy of the affected tissue shows inflammation and granulomas (giant cells) around blood vessels. A blood test, ANCA, usually is positive. Unfortunately, we don't really understand why the body attacks the cells around blood vessels. Infection, genetic predisposition and drugs all have been postulated.

Early diagnosis can lead to effective treatment, often involving prednisone or other steroids, and medicines that partially suppress the immune system. More information is available at http://ift.tt/1oHBLpf. DEAR DR. ROACH:One daughter was put on estrogen, which has helped her cramping, but she still is getting migraines. The other daughter has been referred to three physicians who all told her there was nothing that could be done but go on estrogen. She is now 49 years old and concerned that if she goes on estrogen at this point, she will simply have the same migraine issues again when she goes off it and wonders if that is actually worth just delaying having to deal with the migraines. Is there any other solution besides estrogen for severe hormonal migraines? -- S.S. Both of my daughters are in their 40s and going through menopause (according to their doctors, so they are not guessing about this). Both daughters are having migraine headaches that are so severe that they are missing work (and both are practically workaholics who usually are able to tough it through physical problems). The migraines occur almost every time they have a period. Migraines are not daily during that time, but episodic (usually one per period). They do not have migraines except during menses.

ANSWER: Estrogen-associated migraine is common. However, it usually is the drop in estrogen that triggers the migraine. That's the reason many women get migraines around the time of their periods, as estrogen levels normally decline then.

For many women, migraines get worse years before menopause -- and by "menopause," I mean when periods stop altogether. As the periods become erratic, and sleep cycles are interrupted by hot flashes, migraines become worse, as they have in your daughters. However, once periods stop entirely, episodic migraines usually get dramatically better on their own.

During the erratic time before menses completely stop, estrogen pills, cream or an insertable ring can be used to maintain a more constant estrogen level, which usually improves the headaches. This can be slowly tapered off when the periods could be expected to be finished. Dr. Roach regrets that he is unable to answer individual letters, but will incorporate them in the column whenever possible. Readers may email questions to ToYourGoodHealth@med.cornell.edu or request an order form of available health newsletters at P.O. Box 536475, Orlando, FL 32853-6475. Health newsletters may be ordered from www.rbmamall.com.

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New fund will help families affected by mesothelioma



AS a new fund is announced which will see significantly higher payouts awarded to sufferers of mesothelioma and their families, minister of state for work and pensions, MIKE PENNING, addresses the residents of Barrow



THE shipbuilding industry of Barrow has brought with it jobs and opportunities for scores of local people, writes MIKE PENNING, minister of state for work and pensions.

Few would have ever thought earning your keep from doing a hard day's work could bring with it hidden dangers.

But exposure to asbestos has devastated families across the region. Despite being banned in 1999, people are still living with the toxic effects, with many battling unsuccessfully for years for reparation. Two hundred and forty one people in Barrow have tragically lost their lives over the past 30 years to the aggressive cancer mesothelioma.

It's particularly endemic in areas with heavy industry.

It's a crippling disease, which can take 40 and 50 years to present symptoms, but once diagnosed it leaves victims with just months to live.

Over 300 sufferers every year struggle to find a relevant party to sue for damages because their ex-employer has become insolvent or insurance records have gone missing.

It's a serious issue that's sadly been ignored by successive governments. Until now.

After hard negotiations with the insurance industry, I'm pleased to say that from this month anyone diagnosed with mesothelioma since July 2012 will be able to apply for compensation worth up to £123,000. The families of loved ones will also be able to apply posthumously.

This scheme represents a major breakthrough for the many victims of this terrible disease.

Politicians and the insurance industry have for years ignored the plight of the innocent victims of this awful disease. It will end years of injustice that has left many tragic victims and their families high and dry.

As we approach what experts believe will be the high-water mark of diagnosed cases in 2016, I can assure more than 3,500 families they will benefit over the next 10 years from this £380m package.

Until now sufferers have at best scraped a few thousand pounds from statutory schemes. By striking a deal with the insurance industry we have secured substantially higher packages of support that will help 800 people or their families in 2014 - and 300 every year after that.

They will also get £7,000 towards legal expenses.

Cancer is a terrible and horrid disease. But when it's contracted in the course of earning a living, it's all the more difficult to comprehend.

The hard work of the people of Barrow has helped Britain ride the waves and make our country what it is today. I would urge victims of mesothelioma to apply to this fund. While it will never replace a loved one, it will hopefully at least go some way towards getting the justice hard-working families deserve.

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New fund will help families affected by mesothelioma



AS a new fund is announced which will see significantly higher payouts awarded to sufferers of mesothelioma and their families, minister of state for work and pensions, MIKE PENNING, addresses the residents of Barrow



THE shipbuilding industry of Barrow has brought with it jobs and opportunities for scores of local people, writes MIKE PENNING, minister of state for work and pensions.

Few would have ever thought earning your keep from doing a hard day's work could bring with it hidden dangers.

But exposure to asbestos has devastated families across the region. Despite being banned in 1999, people are still living with the toxic effects, with many battling unsuccessfully for years for reparation. Two hundred and forty one people in Barrow have tragically lost their lives over the past 30 years to the aggressive cancer mesothelioma.

It's particularly endemic in areas with heavy industry.

It's a crippling disease, which can take 40 and 50 years to present symptoms, but once diagnosed it leaves victims with just months to live.

Over 300 sufferers every year struggle to find a relevant party to sue for damages because their ex-employer has become insolvent or insurance records have gone missing.

It's a serious issue that's sadly been ignored by successive governments. Until now.

After hard negotiations with the insurance industry, I'm pleased to say that from this month anyone diagnosed with mesothelioma since July 2012 will be able to apply for compensation worth up to £123,000. The families of loved ones will also be able to apply posthumously.

This scheme represents a major breakthrough for the many victims of this terrible disease.

Politicians and the insurance industry have for years ignored the plight of the innocent victims of this awful disease. It will end years of injustice that has left many tragic victims and their families high and dry.

As we approach what experts believe will be the high-water mark of diagnosed cases in 2016, I can assure more than 3,500 families they will benefit over the next 10 years from this £380m package.

Until now sufferers have at best scraped a few thousand pounds from statutory schemes. By striking a deal with the insurance industry we have secured substantially higher packages of support that will help 800 people or their families in 2014 - and 300 every year after that.

They will also get £7,000 towards legal expenses.

Cancer is a terrible and horrid disease. But when it's contracted in the course of earning a living, it's all the more difficult to comprehend.

The hard work of the people of Barrow has helped Britain ride the waves and make our country what it is today. I would urge victims of mesothelioma to apply to this fund. While it will never replace a loved one, it will hopefully at least go some way towards getting the justice hard-working families deserve.

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New fund will help families affected by mesothelioma



AS a new fund is announced which will see significantly higher payouts awarded to sufferers of mesothelioma and their families, minister of state for work and pensions, MIKE PENNING, addresses the residents of Barrow



THE shipbuilding industry of Barrow has brought with it jobs and opportunities for scores of local people, writes MIKE PENNING, minister of state for work and pensions.

Few would have ever thought earning your keep from doing a hard day's work could bring with it hidden dangers.

But exposure to asbestos has devastated families across the region. Despite being banned in 1999, people are still living with the toxic effects, with many battling unsuccessfully for years for reparation. Two hundred and forty one people in Barrow have tragically lost their lives over the past 30 years to the aggressive cancer mesothelioma.

It's particularly endemic in areas with heavy industry.

It's a crippling disease, which can take 40 and 50 years to present symptoms, but once diagnosed it leaves victims with just months to live.

Over 300 sufferers every year struggle to find a relevant party to sue for damages because their ex-employer has become insolvent or insurance records have gone missing.

It's a serious issue that's sadly been ignored by successive governments. Until now.

After hard negotiations with the insurance industry, I'm pleased to say that from this month anyone diagnosed with mesothelioma since July 2012 will be able to apply for compensation worth up to £123,000. The families of loved ones will also be able to apply posthumously.

This scheme represents a major breakthrough for the many victims of this terrible disease.

Politicians and the insurance industry have for years ignored the plight of the innocent victims of this awful disease. It will end years of injustice that has left many tragic victims and their families high and dry.

As we approach what experts believe will be the high-water mark of diagnosed cases in 2016, I can assure more than 3,500 families they will benefit over the next 10 years from this £380m package.

Until now sufferers have at best scraped a few thousand pounds from statutory schemes. By striking a deal with the insurance industry we have secured substantially higher packages of support that will help 800 people or their families in 2014 - and 300 every year after that.

They will also get £7,000 towards legal expenses.

Cancer is a terrible and horrid disease. But when it's contracted in the course of earning a living, it's all the more difficult to comprehend.

The hard work of the people of Barrow has helped Britain ride the waves and make our country what it is today. I would urge victims of mesothelioma to apply to this fund. While it will never replace a loved one, it will hopefully at least go some way towards getting the justice hard-working families deserve.

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Advocate of the Month



MCA Warrior Stories

Inspiring Stories from Courageous Men and Women Dedicated to Increasing Mesothelioma Awareness

The Mesothelioma Cancer Alliance would like to thank Sara Gapasin for sharing her story about how asbestos exposure affected her family's life as the April Advocate of the Month. Asbestos-related cancer took the life of her grandfather, breast cancer claimed her grandmother, and Sara also lives with her own disease, Rheumatoid Arthritis. Being no stranger to health adversity, Sara still shares a message of hope. Read on to learn Sara's story and share it to help raise awareness of the dangers of asbestos.

It is a great honor to be featured as the Mesothelioma Cancer Alliance's Advocate of the Month! I feel inadequate at receiving this honor. This past year I was writing a blog about my experience with Rheumatoid Arthritis (before I had to stop due to RA) and I was approached by mesothelioma survivor Heather, who shared her incredible story of survival with me. Her story touched me personally as my maternal grandfather had passed away from lung cancer from exposure to asbestos when I was very young.

My grandfather worked in construction during the late 1930's and early 1940's to pay for college and, unfortunately, the materials used at that time contained asbestos. He developed an asbestos spot on his lung, which his doctors did not diligently observe and it eventually metastasized and led to his untimely death at the age of 65. Though I was young when he passed, the ripples of his early demise can still be felt every holiday and in the many everyday happenings that trigger memories of him for my grandmother and mother.

That is why when Heather approached me with her own story of how she developed mesothelioma from exposure to asbestos, I felt personally drawn to it and felt compelled to share it. Heather is just one of the many "female warriors" who have approached me since I started blogging. I have received messages and emails from so many amazing women battling different types of cancers and diseases, it has been truly touching. Cancer has not just been limited to my grandfather, my paternal grandmother passed away from breast cancer in 2008. Due to my family experience, along with my own increased risk to develop certain cancers like lymphoma as a person with Rheumatoid Arthritis, I have learned to enjoy every moment of life with my family and loved ones.

Though cancer has been fatal in my family, it is important to remember that a diagnosis is not a death sentence. You just have to look at all the amazing stories of survival out there, like Heather who was given 15 months to live in 2005. Her story like so many others, is truly inspirational and gives hope to the many people battling cancer and mesothelioma. That is why the Mesothelioma Cancer Alliance, and other organizations like it, are so very important as they spread hope for patients and work to increase awareness about the stories in addition to their advocacy work.

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