Lupus and the War Within
An elder Cherokee Native American was teaching his grandchildren about life. He said to them, "A fight is going on inside me ... it is a terrible fight and it is between two wolves. One wolf represents fear, anger, envy, sorrow, regret, greed, arrogance, self-pity, guilt, resentment, inferiority, lies, false pride, superiority, and ego. The other stands for joy, peace, love, hope, friendship, empathy, generosity, truth, compassion, and faith. The same fight is going on inside you, and inside every other person, too. "They thought about it for a minute and then one child asked her grandfather, "Which wolf will win?" The old Cherokee simply replied, " The one you feed."
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Recent clinical studies into cancers have some researchers questioning the usual practice of attacking the disease. They believe now that current regimes based on drugs and radiation may only aggravate disease reaction and spur a more aggressive spread of cancer. These researchers hope that gentler, carefully thought-out individualized programs will calm cancer and give those coping with it a better chance of healing and survival. While battling my own inner wolf, I learned that fighting tooth and nail only provoked a more rabid response. Now, I strive for peaceful coexistence and though there are still difficult bouts and and occasional time-outs, Ol’ Wolfie and I tread more softly towards each other and I have lived with SLE for well over fifty years. If we think of lupus as our mortal enemy and feed it with our fear, we allow it to wage shock and awe on us. In this most intimate conflict, we must be armed with knowledge in order to win. When it comes to surviving the struggle within, the wise warrior learns to make love, not war.
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Throughout this work, we've investigated the multitude of environmental factors that can trigger and worsen lupus. I've written on the roles healthcare and medical support play in our well-being and the importance of knowing, understanding and enforcing our medical rights. I've reported on medications, supplements, nutrition, assorted chemicals and more and there's plenty more to come. Modern warfare, industry and "better living through chemistry" are rapidly changing our world and environmental science is finding out just how it all hits home.
We all carry some biological factors for various illnesses but they usually need specific stimuli to generate disease activity. After decades of debate, our ancestry is now one recognized component, thanks to our own persistence, improved medical record keeping and more specifically oriented research. Our ancestors' origins, their health and their diseases can have tremendous impact on our own health and many of us have relatives who also have autoimmune diseases.
Diseases like asthma, cancers including childhood leukemia and autoimmune diseases such as lupus, diabetes, fibromyalgia, multiple chemical sensitivity, scleroderma, reynauds, sjogren's and others are rapidly increasing over the last couple of decades alone. Cancer rates are expected to double within less time than that and many responsible researchers believe our chemicalized environment is the most toxic culprit. Researchers sometimes love to disagree but many factors have already been identified, with others under suspicion.
We need to know what lurks in our water, our air, our food, medications, cosmetics, household products, back yards, building materials, schools, hospitals, parks and playgrounds. Information that should splash across the front pages of every big newspaper and highlight every major broadcast is often buried in back pages or mentioned as an aside. There may always, unfortunately, be wars and rumors of wars but in this most intimate conflict, we must be armed with knowledge, in order to win.
The war on Iraq has unleashed its own army of chemical hazards in earth, water and air. Iraqi soil is contaminated by depleted uranium from spent weaponry used in both gulf wars yet gulf war illnesses are only now being officially acknowledged.Sometimes it seems like we're all living in Dodge City and everybody wants to be Wyatt Earp. My Cherokee grandfather knew Wyatt Earp and called him, "A back shootin' SOB" - not much of a role model. but despite my Grandpa’s colorful language, we can't necessarily blame his mother. Like us, he had the choice to blaze a war path or explore a path of peace.
In our lives with lupus, we often use warlike metaphors, with good reason. After all, we were drafted or conscripted by disease so we fight and survive battles, developing the gritty determination of seasoned warriors. In our efforts to combat our illness, metaphors dramatically accent our words, lace our thoughts together and influence our attitudes.
An assertive attitude can be a worthy and formidable weapon but if we view life as a battlefield, then we're always at war. If we think of lupus or any illness as our mortal enemy, it assumes far more power than it has naturally, because we allow it to wage shock and awe on us. When we're living in the stress of fight or flight mode, our adrenaline develops a hair trigger that's never fully holstered.
When we overload on built-up stress, we implode, blowing like bunker bombs, exploding from deep inside. We're bombarded with shrapnel from cluster bombs of hormones, cholesterol and systemic chemical assault. Our vital body fluids and essential nutrients are drained, leaving us prey to infection, virus and full blown flare. This is indeed biochemical warfare, with the warrior trapped inside enemy lines, caught in an endless internal firefight.
To win with lupus, we do need to be warriors when appropriate but we also need to be explorers, students, scholars and most of all, we need to be diplomats. We can't win this one by imposing sanctions or declaring war on ourselves - that will surely do us in. We'd better learn instead to observe, understand and nurture our true needs. When it comes to surviving the struggle within, the wise warrior learns to make love, not war.
Weapons are forged to attack, fight and destroy, while tools are crafted to reveal, create and refine. With supple hands and modeling tools, sculptors coax shapes from clay, freeing the art hidden within the lumpy dough. Weapons are effective in warfare but they're counter-effective overkill when negotiating a truce. If we want to shape and recreate our lives with as little collateral damage as possible, we'll accomplish far more with tools than with grenades.
We are the battleground, so we must learn to live in peace. Research and communication are powerful tools and we learn even more, by sharing what we learn with each other. We're connected by our health, our humanity and our hope. It is our shared experience, pooled research and stalwart support of each other that teach us how to survive this illness and can even teach us to thrive, despite war, within or without.
Easy Ways to Go Green
Green choices aren’t only good for Planet Earth; they're good for all of us, especially those living with limiting health conditions. By now there’s no doubt that chemicals in our environment affect everyone’s health and have a bigger impact on us if we are hypersensitized by allergies and illness. It amazes me how many folks think green thinking will break their brains and green living will break the bank. Not a chance.
For starters, just read
Easy Ways to Go Green from Good Housekeeping Magazine at IVillage.
Inheriting the tendency for making green choices has helped me live longer and healthier, while having a good time doing it. A little responsibility never killed anybody but a whole lot of us can die because of irresponsibility. How would you feel if someone trashed your creation? After all, if we believe this earth is a gift from the Giver of Life, shouldn’t we cherish the gift, to honor the Giver?
Pretty Green and So Good Looking
Despite Kermit the Frog's pitiful plaint, "It's Not Easy Being Green", it can not only be easy - see the going green bit above - but sweet-smelling and good-looking. Try the homemade beauty care tips in the
Kitchen Beautician another "You Go Green, Girl!" article from Good Housekeeping Magazine and iVillage. Good magazine, good website, good ideas - go for it and enjoy being a girl - or a guy. These are not gender specific tips. Anybody can appreciate soft skin, along with all the benefits that brings.
Read to Live - Be Lupus Literate
Low Health Literacy Puts Patients at Risk: The Joint Commission Sets Forth Solutions to National Problem. February 07, 2007
Knowledge is only power when we can understand the language it comes in. To survive well - or at all -with lupus or any other severe illness, we need to be sharp, smart and snapping it up.
If you don’t read well or at all, find someone who does and will read health information for you. Join an English as a Second Language class or find a literacy program in your community.
If someone you know can’t read to save his life, read him his rights and help him access them. This will make you a true hero and give him a chance to be a true survivor. He - and we - will love you for it!
Body and Mind: Melding to Meet Our Needs
Several LNL readers are Pastors’ wives and the stress of their mission can be difficult, especially while coping with family and serious illness. It can be isolating to stand on a pedestal, with little room for even one understanding person to stand beside you in solidarity.
Thankfully,
The National Coalition of Pastors’ Spouses.(NCPS) is a dedicated minority-inclusive support group, sending its 2500 members weekly emails and is very focused on responding positively to illness and healthcare needs.
Whether we recognize it or not, body and mind are wedded in teamwork till death they do part and both are greatly influenced by whatever affects the other. A cooperative mind-body relationship can help us be healthier and have more to share that may help others as well.
Introducing CarePlace
I’ve found a terrific website or, rather, it found me. Jenny, from CarePlace, sent me an invitation to check it out and share my impressions, opinions and ideas. She, Ben and the rest of the CarePlace team want to create a privacy protective, member only comfort zone for those dealing with their own challenges and those who care for them and want to help. I qualify on both issues, having lived my life on both sides. Lupus NewsLog has a similar intent and approach because the more we learn and the more we share, the more positive possibilities we will discover and everybody can benefit.
As the Internet grows older and wiser, our communities are adapting and expanding to meet our deeper needs. CarePlace is a resourceful site with a multi-dimensional mode, almost like an information mall made for morale-boosting and strongly encouraging individual involvement. We all have both needs and gifts and CarePlace is a gathering ground where both can be enriched.
Many years ago Margaret Mead wrote, “Never doubt that a small group of committed individuals can change the world; indeed, it is the only thing that ever has”. Those of us who are true believers always reach out together to create change.
Ben, Jenny and CarePlace have made such a powerful impression on me that I’ve joined, taking part in discussions and starting an onsite journal. As I wrote recently in
Who is this Strange Dame?I’m used to writing about lupus, not about me but I do believe it’s time for this ol’ wolf wrangler to learn some new tricks.
Luciano de Creszeno wrote, “We are, each of us, one-winged angels and we can only fly by embracing one another”. This has been my email signature quote and my personal motto for a very long time - it is the belief that gave wings to our Butterfly newsletter and still breathes life into these Lupus NewsLog pages.
A principal of Buddhism is, “Life is suffering”, but for a purpose. If we live, suffer and strive to grow beyond our pain, we gain so much that can elevate our own lives and help to uplift others. Come check out
CarePlacewith me - you’re likely to find something there, to give and receive, that will refresh your spirit.
Next Lupus Live Chat March 21st!
Don't forget to tune in for the next
Lupus Live Chat at the Lupus Foundation of America on Wednesday, March 21 at 3:00 p.m. Eastern Time, USA. This live online chat will offer recent research info on Kidney Involvement in Lupus. Renal or kidney problems are common in lupus and are among the leading causes of death. Please take your health seriously - even if this isn't an issue in your health, we never know what the future holds and the more we learn, the better we can plan for a healthier, happier, longer life.
Who is this Strange Dame?
Since my work is about lupus and not about me, that question has only been answered in relation to my life with lupus, in
"Living Beyond Acceptance" in our Lupus NewsLog Thrivers’ pages. Even getting that done took months of pleading, pressure and massive infusions of chocolate before it was published and still it was ordered back to the typewriter for more answers to more questions. I’ve had major surgery that was lots more fun.
Finally, in answer to the misplaced prayers of misguided friends, family, readers and my favorite publisher, I’ll be writing in a personal weblog - uh-oh, be careful what you pray for! Rose Harris, one of my favorite friends, kinfolk, writers and my co-columnist at the famed but now defunct Everyday Warriors has asked me to co-write her weblog, Strange Dame. Rose’s health makes it too hard for her to do alone anymore. I can’t refuse her anything and I’ve gotta admit the name is apt so I’ve already started.
Lupus NewsLog will continue, with my research and writing and Chris’s creation of more yummy, healthy recipes. This is such marvelous work; I meet the most heroic people, who don’t even know they’re exceptional - they’re just doing what they believe in, working in the way that fulfills them. Like Patricia Ionea, the creator of Lupus Romania who‘s also constructing the official Lupus Foundation of Romania. You’ll realize what an historical achievement and breakthrough this is once you read
"Welcoming Lupus Romania”and Patricia’s story,
"Learn To Live Again" (Invata Sa Traiesti Din Nou)in our Thrivers’ section.
It's no wonder why I love this work and I think my work at Strange Dame will swing in sync with my work at Lupus NewsLog, going full-circle and tying it all together with a zippy little bow. But whatever will I write about? Shall I discuss my tri-lingual cats, my Subaru-sized fish, my fascinating family and friends, my previously private sex life and unusual marriage proposals, my place in world events, my world travels and inter-planetary interactions or just stick to the truth? Which of these might be the truth and which might be delusions? What if all are both? Sufferin’ Succotash!
Whatever comes up at
Strange Dame it’ll be more sassy than somber because that matches Rose and me just fine. From our email conversations over the years and my lupie bio, some of you seem to have a pretty good idea of what I’m made of and what fuels my drive. Now, the word-portrait will be more dimensional. If you stop by and come up with comments or suggestions, drop me a line or two. Just don’t cuss me out or I’ll sic my cats on you and they‘ll lick, tickle and talk you to death in three languages.
Lupus Foundation of America - On Our Side
The next Live Lupus Chats at the
Lupus Foundation of America (LFA) will be "Kidney Involement in Lupus" on Wed. March 21st and "Diet and Nutrition for People with Lupus" on Wed. April 11th.
There is also an ongoing interactive poll at LFA that helps you contribute to greater understanding of lupus by answering the questions of the week. Both chats and poll are linked on the LFA's home page so check in often to learn more about lupus and to help others' to do the same.
The LFA has so much to offer us. A non-profit organization, it uses contributions to support clinical research, help provide education and support for lupies like us, to raise public and governmental awareness and to work for legislation that will help define and strengthen our patient rights while speeding effective research.
Get to know the LFA - they're volunteers, working hard on our side and they can use our support as much as we need theirs.
LFA Responds to Dr. Phil's Comments about Lupus
March 6, 2007
The Lupus Foundation of America is concerned about and wants to correct misinformation given by "Dr. Phil" on his USA television show on March 5th. This is an important article so I hope you'll read it. Please remember, even well-known 'experts' aren't always expert in all their opinions. I remember this TV personality in his first Oprah appearances telling women they were "fat" and it was their "own fault". I saw some of those women break down and cry in humiliation - so far, humiliation and public shaming have not proven to be weight-loss solutions and it doesn't take a PhD to figure that out. Even then, clinical obesity research proved there are many factors affecting people's weight, most of them having little or nothing to do with "fault". Dr. Phil is a television personality not a medically specific lupus or obesity doctor and sometimes speaks outside his area of education and expertise. For factual obesity or lupus information - or any medical condition - please seek out the real experts and act in your own best interests.
Alliance for Lupus Research Videos
Drop in to the
Alliance for Lupus Research (ALR) to view the Faces of Lupus and the Walk to Cure Lupus videos. The links only allow you to download and watch the videos from your desktop.
Welcoming Lupus Romania
Dear friends and readers,
As difficult and challenging as our lives with lupus can be, our experiences can also be educational, encouraging and mind/spirit expanding, when we stretch ourselves to exceed our limitations and surpass our expectations. One of the very best inspirations for personal growth in lupies like Chris, me and all of us is getting to know other lupies. I get so zinged by the sincerity, hope and determination in those I meet that it elevates me above my own pain and I leap to meet them in mid-air, reaching out beyond what life seems to be, to what life can become.
I’m so happy to introduce you to our new sister site here at Lupus NewsLog, the ground-breaking and incomparable
Lupus Romania.
The long history of Romania has been romantically colorful and politically complicated and, perhaps because of it, Romanians are very strong, passionate and resilient people. With the new year, Romania has joined the European Union, a move which can be politically and socially energizing for all member countries. This could be a great opportunity for scientific and medical research and our new friends Patricia and Stefan are right at the pivot point, surging forward to serve all those Romanians who are living with lupus.
Patricia and Stefan have not only created the research based website, Lupus Romania but are in the process of establishing the Lupus Foundation in Romania. They are remarkable people with impressive drive and determination and it is my great pleasure to introduce them to you. Although their site is naturally published in their native language, I’m sure you’ll get a profound sense of their dedication, effort and high ideals, just as Chris and I have.
As our new sister site, Lupus Romania will be publishing our articles, translated by Patricia, sharing our research and our links. Lupus NewsLog will be publishing updates on news from Lupus Romania. This is one of the beauties of digging up clinical research, clarifying it from medical-speak into everyday terminology and carrying it forward for the benefit of us all; we all share the weight, responsibility and benefit as we pass it along.
Chris and I feel so honored and delighted that our work will help men, women and children in Romania to understand and cope with their own lupus. Yet, it isn’t only Patricia, Stefan and lupies in Romania who benefit from this new relationship - we are all enriched and enlightened by sharing and we all grow from such bonds. We really are all members of the same human family and what graces the life of one, enhances the life of another. In the words of Luciano de Cresenzo (and my signature quote for many years), "We are, each of us, angels with one wing and we can only fly by embracing one another." Together, we may even soar beyond the reach of the wolf.
Please visit our Lupus NewsLog Thrivers page and read "Learn To Live Again" (Invata Sa Traiesti Din Nou), Patricia’s story in her own words. In her graceful self-expression, you will touch and be charmed by the soul of Lupus Romania.
Jillian Leslie - Immortal Warrior
Those of you who’ve been with us since at least 2001 have read articles about and by our dear friend and mentor Jillian Leslie. Jillian’s website, Everyday Warriors, was one of the most informative, professional and heartwarming medical sites most of us will ever encounter. Truly one of a kind, Jillian confronted her own devastating illness by offering support and solutions to others. With her long background as a respected author and editor, Jillian sought out and published writers she believed in, giving them an audience of well over 250,000 regular readers. Friends of Lupus NewsLog including Rose Harris, Royce Sharp and me, were regular columnists or frequent contributors to Everyday Warriors. At Lupus NewsLog Thrivers, we honor and carry on that intimacy of true life, hard won and shared with hearts wide open.
When our Butterfly NewsBytes home site froze due to too many (4500+) members joining too soon, Jillian published our newsletter issues at Everyday Warriors. My short stories of life as a country mouse and a bay city kitty won her praise. The books she cradled for me like their own godmother are making progress, one on lupie life, with the recent discovery of once lost member contributions and another book with a darkly mysterious but true to life premise. She constantly urged me to write weblogs too, not just Lupus NewsLog but more personally and far more opinionated. She respected my backstage personality but never stopped shining a spotlight in my direction. That site she wanted so much for me to create will be online soon, largely due to her faithful encouragement.
Jillian and I were so close and so reflective of each other’s personalities that we exchanged countless emails and she sent me frequent effervescent voicemails which I treasure now as a vital inheritance. Those of us with incurable disease often live with internal time bombs, silently ticking, reminding us to savor every moment and every experience, teaching us to turn tragedy inside out, to offer others the acceptance we all deserve and shape our lives with creative expression.
With Jillian’s sharp intelligence, fluent artistry and surpassing compassion, she didn’t just help lift us up the ladder of life, she built it for us rung by rung in Everyday Warriors. Eventually her own pain and struggle became to much for her, making the heavy duty of a first-class, hugely popular website too exhausting to continue. Although she carried the copyright, owned the domain and never sought to earn a cent from it, an imposter has taken the name and is using it to make a buck off one of the finest, purest non-profits the world-wide web will ever weave.
Because Everyday Warrior’s name is being ill-used in this way, I’m removing every link to this famous site. Please ignore them in their last days at LNL. I won’t shill for any shyster and I won’t help anyone to cheapen Jillian’s considerable contributions. Jillian brought energy, humor and enthusiasm to everything she did and she will always be vibrantly alive in the memories of those she’s shared so much with and done so much for. Ti amo, dear sister, you are truly an Immortal Warrior!
Our Debt to a Great Scientist
Inflammatory pain in lupus and like diseases can drain our inner resources and speed the progression of our illness. Just imagine what life must have been like for folks like us before the development of cortisone. Without cortisone, a host of medications would be missing from our lives. Before cortisone, many of us lived much more painful and shorter lives, with more severe disability from deforming and debilitating disease effects.
Some of us must also cope with vision defects, such as glaucoma. In this, a drug named physostigmine has made the difference between darkness and light, smeary blur and sharp sight, for so many.
With all our struggles, coping with excruciating pain, with swollen, twisted joints and losing our sight at the same time can be devastating. Our job security, safety and survival all at risk and nothing to do but do our very best just to keep going. No medication works equally well for everyone but without these drugs, there’d be no chance of an equalizer at all, no protection for any of us.
Think of the beggars depicted in antique stories and pictures, hands and feet wrapped in rags to cushion against the cold and pain, cast out from employment because of their infirmities. People just like us struggled to eat, maintain any kind of shelter and simply survive, in the days before the medications that have changed and even saved so many lives since then.
We owe a huge debt to research scientist Percy L. Julian, who pursued a career in human service against incredible odds, labored long frustrating hours in research labs and developed these powerful medications for our benefit.
February 6th, 2007, Mr. Julian will be honored as one of the most important scientists of the 20th century. PBS television’s “Nova” science series will run “Forgotten Genius,” a documentary on the life of this high achiever and dedicated humanitarian. His accomplishments and concern for others without prejudice or reservation may be even more remarkable considering his great-grandmother bore deep scars from beatings inflicted during her days as human property, before America’s Civil War.
In America, February is Black History Month, when we formally honor the accomplishments and contributions of citizens whose ancestors came up from Africa. If we can remember Percy L. Julian when we ease our pain or see our loved ones faces, and then visualize his potential in those around us, we might be making a considerable contribution of our own.
NOVA “Forgotten Genius”Tuesday, February 6, 2007, 8:00-10:00 p.m. ET
Illuminating Links
Because of increasing scientific research on lupus, significant advances are being made. This proves the point made here, in "Lupus Awareness Month", just down this page. If we want to contribute to lupus research, we can accomplish more through direct donations. Not everyone who claims to support our cause is actually supporting our true interests. Some people are just in it for the money - we're in it for life.
"Thanks to a newly identified gatekeeper gene, lupus is now a preventable disease for mice. Humans could be next." The RU Scientist at Rockefeller University.
Lupus illuminated By Lynn Love.
"In the treatment of severe lupus nephritis, mycophenolate mofetil has emerged as an alternative to cyclophosphamide, offering a major advance in the therapy of lupus nephritis." JAMA Vol. 293 No. 24, June 22/29, 2005
Pharmacological Therapy of Lupus Nephritis Derek M. Fine, MD - JAMA. 2005;293:3053-3060.
Not all research is good for us or for our children. Without an ethical rudder and a moral compass, good intentions can be devoured by sharks in the water.
EPA rule loopholes allow pesticide testing on kids By Andrew Schneider, Baltimore Sun September 15, 2005 and reprinted by the San Francisco Chronicle.
There are some very interesting articles listed at the pages linked below. Please take a good look - you may find something that relates to your circumstances or those of someone you love.
Most Viewed Health News on Yahoo! News The top health news articles from Yahoo! News These next two links were contributed by an LNL reader who wrote "The first is on the disability process for lupus patients. The second is a good alternative med page for lupus.". I'd like to give due credit for the aid but didn't get a name. I'm very glad for the contribution and appreciate the consideration. As I've written before, this work and this site are of, for and by lupies, for the benefit of us all.
APPLYING FOR BENEFITS WITH LUPUS from Disability Secrets.com
Alternative Medicine and Lupus, Part 1 Vitamin Stuff .com. There's a link there, at the end of the article, that leads to its Part 2.
LNL's Articles With Attitude
Hello Dear Readers,
As I promised in my last post, we now have much more to read. Our log has rolled over to show us a whole new side, Lupus NewsLog's
Articles With Attitude. Here, you'll find updated and newly written articles on pain, nutrition, medical research and advances, our healthcare rights and more. When we exercise our bodies, our minds and our rights, life can really start to tone up.
Exercise your reading rights - there are more articles with attitude coming up and you're always welcome here among the pages of LNL. Remember, updated articles are as important as those fresh off the keyboard because research into autoimmune diseases is continually re-studied and new details or even radical reassessments are often made.
Our friend Kris has written up her lupie life story
Running With The Wolf as a worthwhile addition to our Lupus NewsLog Thrivers pages. Like many of us, including Sheila, another contributing Thriver, Kris is a nurse, dedicated to her patients and her work. It's now common knowledge that the risk factors for systemic lupus run higher among nurses like Kris, teachers as I once was and probably among hairdressers, too. The awareness is there but we're still seeking the reasons. Until we find them, shape them into tools and use them to change our lives, let's live like Kris, vibrant with love and laughter.
Reconstruction Blues-Pain Relief on Tap
Dear Readers,
Some of our links have fallen and they can't get up so I'm busy working on them right now. Ol' Wolfie may be gnawing on our Lupus NewsLog life-line but he's always biting off more than he can chew and our heart to heart connection's in far better shape than he'll ever be.
I'm also tapping out a couple of requested articles about pain relief for our new
Lupus NewsLog's Articles with Attitude pages. I could suggest y'all each buy a scattergun, fill the barrels with rock salt and let your wolves have it hard but since I am Buddhistically non-violent and, besides, these rangy wolves actually reside within us, this wouldn't be a good idea at all. There'll be much safer ideas in the articles. After you read data on some of the pain related research, you might be tempted to blast at a couple of specified others/agencies but, nope, we are loving - and legal, not lethal - lupies.
This is Sunday evening and I hope to have them all done, up and at ya by Tuesday or Wednesday night. They'll be going up one at a time so some will be up sooner, some perhaps later but all just as fast as I can make it. I aim to please - but not with a scattergun. To those whom much is given, much is required and we've for sure got our fair share of something so let's try to work it out, not throw it down.
Thank you for your patience and understanding.
Shar
Latest Links
Our good friend Julie, author of
Julie’s Journey at Lupus NewsLog Thrivers and publisher of The Lupie Bin has a new URL. The
Lupie Bin is one of the very best, most comprehensive and appealing lupus information websites around. You can learn a lot here and enjoy doing it.
Lupus Drug Fails Goals About LymphoStat-B for SLE, from Human Genome Sciences. New York Times, By REUTERS. (New York Times may require free registration to read full articles)
Human Genome Sciences offers a press release about the phase 2 clinical trial results of their SLE drug, LymphoStat-B. “While the trial failed its primary goals, it reduced the symptoms of the disease at 52 weeks in a subgroup of patients representing 75 percent of the study's patient population, the company said.”
Trying to Shut Off the Body's Friendly Fire By Andrew Pollack, New York Times.
Lupus News at Medical News Today “The latest lupus news and lupus articles published daily from Medical News Today. All articles are ordered by date.” There are several very interesting research based articles here.
“…and hold the onions” “What follows is a journal of a live donor liver transplant written by two people, Chris and Shari.”
Painkillers cut risk of mouth cancer Soy not so smart for lowering breast cancer riskDubious Antibiotic Cancer LinkWomen told to show breasts 'TLC' Low-income women in US underuse breast screening“The Basics” “3 legal papers you shouldn't live without” By Liz Pulliam Weston
Lupus Awareness Month
Over the years, I've know people to say, "There is nothing worse than lupus" and maybe we all feel that in our worst moments. There are times when symptoms are so invasive and pain is so severe we are almost shattered in mind and body and smashing our heads against the wall would seem like pain relief, at least while we'd be unconscious.
In some ways, when it tries to burn us down to the ground, lupus does feel like the worst thing that could happen to anybody. If we truly think it's the worst catastrophy ever, maybe we're not reading the daily news. Nowdays, there's a lot of competition for most horrible event ever. Lupus can be our catalyst for change and wisdom, but only if we know that, far worse than having lupus is thinking our lupus is the be-all and end-all of our whole lives, because then it surely will be.
October is Lupus Awareness Month, although, for those of us who have it or have a loved one who has it, it's every month of the year. Still, every October we are reminded that there is no cure for lupus, that there has not been a new and truly effective medication for lupus in decades, that many of us live with obvious symptoms but no definitive diagnosis and that somewhere, every day of the year, someone dies because they have lupus.
We may feel helpless sometimes against the force of this powerful disease but there are things we can do to assert ourselves, contribute to research and educate others. Lupus used to be one of the most unknown illnesses in the world but the mystery guest is signing in and we are speaking up. We can’t expect instant abracadabra results – ever tried to pull a wolf out of a hat? – but we can do a lot to rattle Ol’ Wolfie’s cage and loosen his grip on our lives.
We can document our symptoms on paper and give copies to our doctors to aid in diagnosis and treatment. We can share the URLs of good lupus websites and weblogs with family and friends. We can write letters to the editors of our local newspapers, to let them and their readers know the significance of this month and share non-profit phone numbers, URLs and addresses. These actions won’t cost us more than a couple of sheets of copy paper or envelopes and postage stamps.
We can buy pins, books, wristbands ($1. each + shp.), Lupus Now magazine subscriptions and more through the
Lupus Foundation of America (LFA) and support lupus community efforts and research.
St. Thomas’ Lupus Trust (STLT) in the UK offers wristbands in two sizes and charges are contributed to that charity. Click Now will contribute 50% of all revenues earned from your Ask Jeeves, Google, LookSmart and Yahoo searches if you set up your homepage at St. Thomas’ Lupus Trust. To do that, visit the STLT
Click Now page and encourage family and friends to make the switch, too.
If we’re well enough to get out and about, we can volunteer and help our local lupus organizations to disseminate information, help hold meetings and sit on boards.
Lupus Canada has a great need for volunteers right now.
Throughout the world, lupus organizations are made up of ordinary individuals who have lupus, love someone who does or just want to help others. They're all struggling to share information and compassion with those who need it badly. If we can afford it, we might donate funds each month or even once a year. We can ask those who might give us gifts to make donations instead for this crucial cause. There are many lupus research links on this page and other sites – please use them well.
Beware of those who offer lupus wristbands and other items at marked up prices - that money doesn't support lupus research, it supports their lifestyles. There’s no need to pay big bucks for lupus t-shirts with negative slogans made for profit. Why fill somebody’s personal pockets with your hard earned cash and take an emotional downturn, too?
You can make your own shirts and maybe a few for holiday gifts for less than $15. each plus shipping or maybe even with no shipping fees. If they’re upbeat, you’ll feel better each time you slip one on and you won’t just be informative, you’ll be positive and you’ll be remembered.
Check out do it yourself (DIY) sites like
Zazzle.com. Drop in on
CustomInk.com ,
CafePress and other DIY sites. Type “make your own t-shirt” into your search bar and explore. Don’t forget, when you search you can be automatically contributing to lupus research.
Just don’t anybody try to sell me any lupus items that prey on our fears and at a jacked-up price or I’ll sic my rabid wolf on ‘em. We should be promoting our community, not pilfering from it. To paraphrase an old Beatles song, I am you, you are me and we are all together – we are the faces of the wolf.
Support Breast Cancer Prevention All Year
By the way, October is also Breast Cancer Awareness Month. That cause and those whose lives have been affected could use our support, too. One of my dearest friends unintentionally donated her bosom to the cause of breast cancer research. My sister-in-law, in love and in spirit, died on Easter Sunday from cancer that began in her breast 15 years ago. Please help all you can in any way you can. You can even give a
free click everyday all year to donate the cost of mammograms and help save lives – maybe even your own someday or perhaps the life of someone you love. Life isn’t really about what takes us down – it’s about what we can do to lift each other up. And that, my friends, is plenty.
Reaching Through the Wreckage
Hurricane Katrina has caused perhaps the greatest sudden loss of life worldwide since the recent tsunami. It's so hard to believe that such horrible things could happen again - Katrina is the worst disaster on American soil since September 11, 2001 and the largest displacement of Americans since the
Dust Bowl migrations in the 1930’s. We are all struggling to cope with the shock and anguish, trying to make sense of this trauma. And we are not alone in our shock and grief, in America, in Indonesia, anywhere in the wake of the ocean's wrath.
In the USA, Florida, Alabama, Louisiana and the Mississippi Gulf Coast have been battered and shattered by nature running wild. Along the coastline, thousands of homes have been flattened by the winds or swallowed up by the sea. Entire towns are reduced to rubble and sewage. Some of these towns may be reclaimed and rebuilt but many will sink into the marshlands and the memories of those who’ve lost so very much. Katrina and the tsunami are kin as close as we all are, in the horror and the agony of their ravage and waste.
Now, hurricane Ophelia seems to be biding its time offshore, as if debating whether to strike or settle down. (Update: Ophelia is now heading for the Carolinas, aiming at North Carolina’s south coast and South Carolina’s north coast. Residents are evacuating.)
New Orleans, Louisiana is celebrated world-wide as the birthplace of the blues and jazz music. It is renowned for its cuisine, architecture, friendly folks and culture. This unique city has always attracted visitors from around the world. Now, it's almost wiped off the map and all the lives lost will probably never be accurately counted. With Katrina, the tsunami and as with the twin towers in New York, the victims of these tragedies are international.
One of the kindest, most courageous people I've ever known is Sharon Sanders, a warm and wise
Lupus NewsLog Thrivers contributor and LWLupus co-moderator. As I’ve written in
A Tribute to True Soulmates her husband George died recently, at home with her, in Louisiana. We’re very grateful that Sharon is not among those lost or in the wreckage.
Our friend Kris Kutz is also a contributor to
Lupus NewsLog Thrivers and one of the brightest lights in Alabama. We are fortunate that she and other friends who may have been in harm's way are safe. Linda, our long and loyal ally, publisher of
The Lupus Chronicle lives in Florida and I hope to hear from her soon.
Sheila Wilder one of the architects of LNL, lives in Texas and I pray she is safe and well. Our friend and fellow LWLupus member Shine Rivai, her husband Yoel and their baby boy Mika (born on the fourth of July) live in Indonesia. I am little Mika’s true though honorary aunt and it worries my heart that I haven't heard from them since the tsunami.
Our challenge in any catastrophe is not to assign blame – that’s always easy and ain't it a shame – but to accept responsibility for what must be done and do our part. In the 20th century, Mahatma (“Great Soul”) Mohandas Gandhi said, “The difference between what we do and what we are capable of doing would suffice to solve many of the world’s problems.” In this 21st century, mothers, fathers and their children still die not just during but in the aftermath of hurricanes, floods, famines, fires, tornados, earthquakes and wars. On this planet of plenty, millions of children slowly starve to death every year, day by day. Can we even imagine what that must feel like - how it is to be abandoned by the world?
For all our techology, life still comes down to individuals reaching out to help others, one person recognizing and connecting to the precious life of another. By ourselves alone, we cannot save the entire world but those of us who care enough to try can comfort, change and even save lives.
In the opinion of philosopher/writer Luciano de Crescenzo, "We are, each of us, angels with one wing and we can only fly by embracing one another." According to all major religions, God, and the highest nature of humanity, is love. Our ability to recognize, feel and return such love can unify us and help us all to heal.
Life Saving Links
New Orleans, Louisiana A fascinating history. (Wikipedia)
Faith in the Eye of the Storm"
The Deluge Survivors and religious leaders comment on Katrina.
Katrina: Not God's Wrath--or His Will By Dr. Tony Campolo Oordained minister and author of 28 books, including 'Following Jesus Without Embarrassing God.'
Deep Waters: A Spiritual Response to Hurricane Katrina Wisdom and comfort from Billy Graham to Lama Surya Das.
Hope and Faith After the Storm A daily blog chronicling inspiring and brave stories of survival, hope, and faith in the wake of Hurricane Katrina.
Katrina Thanks Blog "A Public Forum to Express Thanks to Individuals, Organizations and Countries that Have Assisted with Katrina Relief Efforts"
Click for Free to Create Donations:
Click to End Hunger "For each click, Dannon will contribute $1. to America's Second Harvest (up to a total of $75,000). Every $1 donated helps America’s Second Harvest provide 15 meals to children in need."
The Hunger Site Corporate sponsers act on your clicks to feed children in the aftermath of the tsunami and hurricane Katrina.
The Animal Rescue Site Dedicated to rescuing and sheltering animals in need.
Send money, goods and/or volunteer your services:
Mercy Corps “92 cents of every dollar” is applied to good works.
The Humane Society of the United States' (HSUS) Disaster Relief Fund “Helping animals and their caregivers” after Katrina.
USA Freedom Corps represented by former presidents George H. W. Bush and Bill Clinton solicts cash, goods and services to help disaster victims.
Manilow Fund for Health and Hope “… You donate $1.00… Barry will match your $1.00… and the Manilow Fund will match another $1.00…. so your one dollar becomes $3.00.”
ASPCA – American Society for the Prevention of Cruelty to Animals “to help the animal victims of Hurricane Katrina.”
Best Friends Animal Society “A better world through kindness to animals.”
Check Out Charities:
Network for Good “an e-philanthropy site where individuals can donate, volunteer and get involved with the issues they care about."
Charity Navigator and
Guidestar rate charities for effectiveness.
In Tribute to True Soulmates
For our Lupus NewsLog Thrivers, my beloved friend
Sharon wrote so touchingly of her faith, her lupus, her loyal husband George and his own struggles for survival. Sharon’s SLE has been extremely fierce and George has had severe heart related problems with repeated surgeries. Through all the pain and anxiety they’ve endured, their faith in God and in each other, purified by fire, has grown stronger, deeper and richer in wisdom. Their marriage has been a true meeting of minds and blending of spirits, with compassion flowing like a stream between them and pouring like a waterfall onto their family and friends.
On July 7th, 2005, after twenty-two years together, George flew free of his pain, because his body, made so fragile by his suffering, could no longer shelter his buoyant spirit. As they have always done for each other, Sharon quietly, gently, tended his needs, this time, through his last good-bye. My heart breaks for them both but I know they are only parted by time and not by spirit.
Sharon and George are two of the most exceptional people I’ve ever known and my life, like all the lives they’ve touched, is enriched and strengthened by their kindness. Nowdays, we often speak of ‘soulmates’ but Sharon and George have exemplified their marriage vows with a rare devotion to each other. Some people become teachers or mentors by profession, some through character and conscience. I am grateful to Sharon and George, for all I’ve learned by loving them and I am thankful to be their true friend.
The ABCs of IBS
Irritable bowel syndrome (IBS) is often either the topic of bad jokes (groaners in more ways than one) or too embarrassing to discuss at all. If we have SLE, we're likely to have IBS too so we need straightfoward information to ease our toxic tummies and debilitating digestive systems.
Sophie Lee publishes a very informative website,
IBS Tales, writes a very personal
IBS weblog and has written an interesting ebook, IBS and Me: Living with Irritable Bowel Syndrome, which costs only $9.99.
Imagine that - a usful ebook, for a reasonable price. She isn't trying to stick us up for our gas tank funds or chow down on our lunch money. Basically, it'a a trade up from a large latte. It's just a simple negotiation - she gets $9.95 = you get a pretty good read. Sophie invites you to visit her sites, to share your IBS experiences and those of others. She’s put together a triple-hitter there that packs a mighty wallop and, with all she has to offer, you're bound to learn something new and useful.
Dr. Weil's Lifestyle Tips for Lupus and Other AI Diseases
Here at LNL, rolling down our log, you'll find research based information (with links to clinical study data) on lupus nutrition and healthy habits. Dr. Andrew Weil's Daily Tip for August 10, 2004
Help for Autoimmune Disorders further verifies that documentation and is a good reminder.
To sleep, perchance…
We lupies crave sleep about as much as we do chocolate, mostly because we can indulge in it even less. Often, our sleep cycles are spinning wheels on deflated tires and we’re tossed out of dreamland every time we hit a speed bump or pothole. Many of us might as well try sleeping on rotisseries, since we wake up and roll over several times every night, just to rearrange our aches and pains.
If not for naps - when we can get 'em - we might not sleep much at all but, stubborn as the wolf who rides our backs, we often come to accept our need for naps slowly and reluctantly. Thanks to
Life With Lupus, the weblog of Loretta, another sleep-deprived lupie, we’ll learn we’re not the only needful nappers. Just follow her sleepwalk to
Famous Sleepers at MySleepCenter – open all night.
In Rhythm with Health Beat
Carla Johnson of Health Beat does a fine job of tracking health care news items. Check out
New antidepressant approved; stockholders rejoice and
Heart health: Supplements little help. Read
Arthritis pain news: creams lose effectiveness. The full story link opens a BMJ (British Medical Journal) file.
Scroll down the
Health Beat main page to read “A top-shelf idea”, about nasal irrigation for easing sinus problems and improving general health. Learn about “Tampons with something extra” devised to prevent toxic shock syndrome and, in “One study, many headlines”, about the reported link between antidepressant use and suicide.
While you’re there, read “Compare your local hospitals with new web-based tool” – this is a must-read item, for your own protection. This is an excellent weblog to bookmark and visit often.
Soft Skin and Laser Vision
We lupies are notorious for our sensitive skin and our junk drawers overflow with failed hopes packaged as dreams come true. Can one cleanser actually cope with hair, face and body and not cause a skin rash somewhere around the curves? According to LNL Code Warrior Sheila, it can, at least for one whole monh so far – a rarity in our world. Sheila loves
Philosophy's Willpower Shower Gel and provides a shopper’s link, too. If you decide to try it, just remember, it’s skeeter season and mosquitos love lavish scents as much as they love biting tender lupie skin.
While you're at Sheila's place, cast a glance at
Shooting Laser Beams From My Eyes - especially if you're considering lasik, aka optical laser surgery. Read around, while you're there - told ya this is one smart, witty blogger and she proves me right.
Smart Summer Reading
If the summer heat has got you beat, get off your feet and READ for your health! There are terrific newsletters and weblogs you'll be glad you found. They'll educate you and even make you laugh.
Purple Medical Blog is still one of the very best and most interesting medical weblogs I’ve ever found. Drop by for a quick read and you’re likely to find yourself getting very involved and widely educated with the wide range of stories and unusual links at PMB. Smart, quirky and cool at any temperature, this is a great blog.
American Medical News, aka AMNews and amednews.com, is the free newsletter of the American Medical Association. Geared towards physicians, it’s a smart read for anyone interested in health and medical news. You can sign-up for their free
email alerts to stay in step with your doctors.
New Scientist offers weird, wacky and worthwhile science and medical news.
The Last Word (Questions & answers on everyday scientific phenomena) is my fav bit. Folks ate ice cream in ancient Pompeii? How else you gonna beat that volcanic heat? Questions with answers of interest to most lupies include
Why do we have headaches? What are they?! Best of all, reading these bits is absolutely free and they go on forever. This isn't just weird science, it's smart and relevant, too.
The Literature Network has classic literature, poems, and quotes you can read online. They have over 300 full length books and over 1000 short stories and poems by over 90 authors and over 8500 quotes. They've got Shakespeare, Dante, Thoreau, O. Henry, Louisa May Alcott, Hans Christian Andersen, Lewis Carroll, Mark Twain, Sun Tzu, Jules Verne and Bram Stoker, along with that old favorite, Anonymous. Best of all, you don't have to whisper in this library and there are no fines for overdue books.
Season Of The Switch
I deeply appreciate the input of our readers, the support of our hardworking compatriots and our impressive technical assistance. Still, I’m your lupie scribe so the bulk of the newslog’s and ezine’s medical research, writing and site maintenance is my responsibility.
This year, along with setting up and refining our LNL pages, I’ve also been restructuring my offline life. I’ve been moving to a new town, in a new state of mind, while coping with a ferocious lupus flare and a cantankerous computer. Lately. I’ve been as frazzled as a cat with a litter of nine two-headed kittens.
Jillian, our ally at(the once famed but now defunct Everyday Warriors - please read
Jillian Leslie - Immortal Warrior) and publisher of our Butterfly NewsBytes (BNB) ezine is seriously ill right now and may also be moving soon. Must be the season of the switch, since our fellow Thriver Julie, webmaster of
The Lupie Bin, recently relocated. Her move riled her wolf, too. Right now, BNB is a mighty rocky row to hoe, with Jillian and me caught between my wolf and her hard place.
To ease the load on Jillian’s generous shoulders and balance the burden on mine, we’re suspending publication of new Butterfly NewsBytes issues for now. You can follow our BNB links, to read this year’s past issues and you’ll find related bits here at Lupus NewsLog. Thank you muchly for your patience and your support.
Rion - In Flight
Lupus Support and Survival is the worthy website of Brenda Rion Sewell and
Rion's Reflections Life Thoughts and Healing Words, is her gift of love. Visiting her pages is like finding an oasis in the desert. This thoughtful and compassionate lupie is no longer with us but her family maintains her site so that we may share in the beauty of her spirit. Rejecting tragedy, she found triumph in her struggle - may we all be so blessed.
LNL Updated
Dear reader-friends,
These weblog pages haven’t looked too active just lately but deep down in the pits of the Lupus NewsLog coalmine, this canary’s been working her tail feathers off. There’ve been twitchy site glitches to tweak (for one, posts don't always show up when published) and new Blogger.com tech changes to implement. Thankfully, I’m not the only bird working this wire.
With the technical talents of Jared, LNL’s web-wiz, our weblog’s pages are now more user-friendly. Chris has been cookin’ up a storm to blow the wolf away, with luscious lupie recipes on our
WolfBytes page. We also have new true life stories to share on our
Thrivers page.
Each Thrivers’ story is hyperlinked in that page’s left side menu box, to open into its very own page. I’ve also made each link in our main Lupus NewsLog and
Library pages open into a new window, for your ease and convenience.
This summer, there will be more fine-tuning, with new research information and weblog pages added. Our LNL Library is growing too, with more great links to share. If you’d like to suggest a link, please email me the URL. Remember, your questions, suggestions and bright ideas are always appreciated and help keep this log rolling.
Lupus Meetup Day 3rd Tuesday of Every Month
As I wrote in an earlier post, on the 3rd Tuesday of every month, there is a
Lupus Meetup Day worldwide. At 7PM, on these Tuesday evenings, lupies and those who care about them gather in small towns and cities, meeeting each other to share information, lend support and make friends.
These meetings are set up online through Lupus Meetup but they're grassroots level, with individuals in local communities choosing where to meet and how to get together. Folks with any form of lupus and/or any related condition are welcome, as are their friends, family and those who want to learn more about these illnesses.
Lupus makes us ill but it need not make us foolish or lonely. People arrange to meet in coffee shops and other public places and personal information such as addresses and phone numbers can be kept private. This gives participants a chance to check each other out and control just how deeply involved they wish to become.
Check out "Lupies Meeting Face to Face" on this weblog for more information on Lupus Meetup. Lupus Meetup is linked to the left of this column in "Lupus Links" and under "Lupus Community Health/Medical and Support Sites" at our Lupus NewsLog Library.
If you've participated in a Lupus Meetup Day, I'd love to hear from you. It could be very informative for us all if you'll share your insights on just how these get-togethers take place and how well they work out.
Lupies Meeting Face to Face
Lupus can be an isolating disease and many of us have never met another lupie in person. No matter how much information we can find, it can be lonely, when we’re the only wolf-bait we know, one on one. Talking with others who share similar challenges and experiences can be educational and empowering.
Meetup.com has posted information on a lupus community event called International Lupus Meetup Day. On Tuesday, March 16 at 7:00PM, people with lupus and others affected by this disease will meet in their communities worldwide. So far, 202 people in 53 countries from America to Vietnam have signed up to host local meetings and get to know each other.
There’s no information onsite telling who started this global lupus get-together and no indication that any lupus affiliated organization is directly involved. It seems to be a grassroots, ground-level movement. If you’re interested in meeting with other lupies who live in or near your area, you can check out
Lupus Meetup at meetup.com.
If you’d like to meet with fellow lupies on a regular basis, the Lupus Foundation of America has volunteer chapters in communities in the USA and around the globe. LFA has been around for a very long time, connecting us to each other to share information and lend support. Check out LFA’s
Chapter Locator and
International Groups at the home site and find out about the benefits of joining in.
Lupus Nephritis and CellCept Study
According to statistics, nephritis or kidney disease occurs in about 50 to 75% of those diagnosed with lupus and patients often ultimately require permanent dialysis or kidney transplants. If you have lupus nephritis and you’re unsure which treatment is best for you, a recent study may give you more hope and confidence. However, before you accept anything as a possible “miracle drug’, research the clinical study background, the parent drug company and learn what wasn’t included in the press release.
The most common treatment for lupus nephritis has been the intravenous chemotherapy medication, Cytoxan (cyclophosphamide). The problem with this drug is that the cure can be as bad as the disease. Chemotherapy is a poisonous assault on the system, which, if one is fortunate, will kill the disease without taking down the patient. Side effects of Cytoxan can include hair loss, shingles, unusual infections, increased risk of malignant tumors, bladder bleeding, leukemia, temporary or permanent sterility and fetal damage.
CellCept is becoming popular because of reports of reduced side effects In CellCept use, bloating, nausea and diarrhea are the most commonly reported side effects but are said to be usually temporary. A recent study declares that CellCept (mycophenalate motifil, as a pill, taken by mouth) can reduce antibody levels in the kidneys, minimize disease effects, decrease kidney damage and perhaps even stop disease progression. This could mean dialysis and kidney transplants will become unnecessary, with CellCept.
This study was done by Rheumatologist Ellen Ginzler, M.D., M.P.H., of State University of New York Downstate Medical Center. According to Dr. Ginzler, 140 people enrolled in this study received either CellCept or Cytoxan With CellCept, 16 people went into remission, as opposed to only 4 on Cytoxan.
In this study, reported by
Ivanhoe Newswire and picked up by
HealthCentral.com, CellCept also had more positive than negative results among African-American patients, who usually have more severe lupus, a higher rate of side effects and are often less responsive to the usual Cytoxan treatment. As many as 2/3 of the patients overall were able to tolerate CellCept’s high dosage of 3,000 milligrams. CellCept is generally a 6 month treatment, which is said to cost “a few thousand dollars” but most insurance companies are expected to offer coverage.
This study was funded by the National Institutes of Health (NIH) and
Roche Pharmaceuticals the makers of CellCept. Roche has prepared a PDF document, which describes CellCept oral tablets and intravenous medication. Intravenous CellCept was not used in this study. In this
PDF, under “Warning”, Roche lists “increased susceptibility to infection and the possible development of lymphoma may result from immunosuppression”, which was not cited in the Ivanhoe study report.
CellCept was developed to prevent the rejection of transplanted organs and treatment of lupus nephritis is a new use of this medication. Roche’s warning recommends only doctors “experienced in immunosuppressive therapy and management of renal, heart or hepatic transplant patients should use CellCept. Patients receiving the drug should be managed in facilities equipped and staffed with adequate laboratory and supportive medical resources. The physician responsible for maintenance therapy should have complete information requisite for the follow-up of the patient”.
NIH has posted an
Important Warning on CellCept, which should be read in full, along with the other information on that page. These warnings make clear that anyone considering using this drug should first learn everything they can about it, take all precautions very seriously and deal only with doctors and medical staff who are experienced as described by Roche and who will communicate openly, fully and clearly.
If you’re considering this treatment, be sure to discuss these official warnings with your doctor. Remember, even the most glowing clinical report can be subject to change, once the drug is in wider use.
Aspirin and Ibuprofen Don’t Mix
An aspirin away may not keep the doctor away, if you take ibuprofen or other NSAIDS, too. A study done by Brigham and Women's Hospital in Boston shows
Ibuprofen may blunt aspirin so we’ll have to choose whether to take baby aspirin as a protection against heart attack and stroke or certain NSAIDS for pain relief.
Aspirin Study in Pancreatic Cancer
Does aspirin increase the risk of pancreatic cancer? (The study concludes, yes, but the official assessment is that the risk is probably not enough to outweigh the benefits of aspirin against cancer overall.
"The results showed that compared with never taking aspirin twice weekly on a regular basis, taking two tablets a week for more than 20 years increased the risk of pancreatic cancer by 58% (there were 34 cases). Further analysis showed that long-term use (at least four years) of 14 tablets a week or more was associated with an 86% increase in the risk of pancreatic cancer (20 cases in total). When regular use of aspirin was defined as taking five tablets a week or more, there was an association between longer duration of use and risk of cancer, such that when the duration of regular use exceeded 10 years the risk of pancreatic cancer was increased by 75% (37 cases).
" - "Furthermore, the total number of cases of pancreatic cancer identified from almost 90,000 women over a period of 18 years was only 161.")
National electronic Library for Health Centre for Reviews and Dissemination, University of York, England.
But Aspirin May Help Fight Some Cancers
Studies conducted in the UK and the US show aspirin, for those not allergic, may be a powerful weapon against cancer. The Uk has also now begun a 10 year trial, to end in 2014. British study results are reported
here at Cancer Research, UK.
Aspirin and ulcer drug tested as cancer fighters (the ulcer medication is Nexium) CNN News/Reuters
NCI-Funded Clinical Trials Show
Aspirin Reduces Recurrence of Polyps
Dr. Andrew Weil on Herbal Remedies
Dr. Weil answers the question,
Can Herbs Combat Inflammation?
He offers suggestions for our health in
Lupus: A Natural Approach?
Black-Currant Oil, a plus for us lupies, from Dr. Weil’s Herbal Medicine Chest.
Ginger is well-known for its anti-inflammatory benefits. Learn the best way to eat it in
Rooting for Ginger? at DrWeil.com
Dr. Weil recommends
horse-chestnut seed extract over grape seed extract, for alleviating varicose veins and improving vascular elasticity.
In answering
Pain Relief From Grape Seed Extract? he writes on grape seed extract and Pycnogenol, which is processed from maritime pine extract and makes specific recommendations for proven alternatives for pain relief.
A Chest Full of Heart Health Links from DR.Weil.com
Search Dr. Andrew Weil’s archive of
heart healthy articles with tips on exercise, herbs, heart attack prevention and more.
Dr. Weil offers dietary recommendations and lots of luscious recipes below for
countering inflammation. See the right-side list, too.
More
anti-inflammatory recipes from Dr. Weil.
The good doctor Weil explains,
Why No Milk?
Still Weil-ing, with tips and recipes for
hypertension.
DrWeil.com Question:
Searching for Safer Sprouts? Why alfalfa isn't good for us and what is better.
Heart Smart Health Links
In America, February is Heart Month and Black History Month so the
American Heart Association has information on protecting our hearts while eating well and dishing up savory soul food. Please check out
Lupus And a Wolf-Wise Diet for more healthy heart tips. This article is based on current research into lowering inflammation, which can not only minimize our lupus symptoms but help protect us against heart attacks and strokes.
Frankenfoods, Frank Answers and Fair Play
Eye-catching boxes line store shelves and many look like our old favorites but everything old is new again and nobody’s telling us what’s really in the food we eat. Genetically engineered foods are nearly everywhere and we never got a chance to vote on whether we even wanted them.
Here in America, biotech food products are almost impossible to avoid, whether we want them or not. They’re in flour, spices, herbs, processed foods and snacks. You won’t find them on the labels but they’re in baby foods and animal foods. They’re silently served on airlines, at restaurants, salad bars and in vending machines. We’re fed them in hospitals, school cafeterias and nursing homes. It’s a genetically engineered diet plan, from cradle to grave. Many experts say it’ll probably get us from one to the other a whole lot faster and a lot more expensively.
The frankenfood industry is not held accountable for what their products might do to us and generations of children. Meanwhile, the US government admits over 44,000,000 folks (a deceptively low count) can’t get medical insurance and, for many of us, medical services are unavailable or in jeopardy.
Insurance conglomerates and politicians complain about the rising demand for and cost of healthcare, deciding who to kick off the gurneys and lock out of the hospitals. Meanwhile, disease rates rise and freaky foods may be a factor. The frankenfood kings are in their counting houses, counting out their money while we’re getting shortchanged at the market. They’re not at all concerned but then, they don’t have to eat what they sell.
The industry, its political lobbyists and our politicians have mutual interests and the public health doesn’t seem to be their highest priority. We aren’t corporate executives, their well-funded mouthpieces or politicians with free lifetime first-class health care. We’re real live, really vulnerable human beings with the right to gain knowledge and make our own choices.
We need to know what we’re eating, in order to know what’s eating us. Independent consumer protection organizations like
Public Citizen,
Environmental Working Group and
The Center for Food Safety are on our side. These groups help fund or run clinical studies and they all have educational websites, with the food and supplement facts we need to know.
Biotech is big business, despite opposition in countries worldwide. Soybeans, maize, corn, tomatos, sweet potatos, bananas, wheat and more are being farmed from genetically altered seeds, along with cotton (which shows up in some new foods) and other crops. GE brings good things to life, for those who cash the checks but, somehow, these biotechies can’t afford to give us answers.
Rather than take up a collection to benefit the communicatively challenged – they really don’t need the money – we can educate ourselves to eat well and wisely. That’ll teach ‘em – their classroom is the marketplace and if we don’t buy, they fail. We won’t make positive changes in food quality and consumer protections until we learn to be selective and make our voices heard. Stomachs, get ready to rumble!
Biotech’s Frankenfoods
Bizarre Living Through Chemistry?
GM (Genetically Modified), GMO (genetically modified organisms) or GE foods (genetically engineered) are a boon to the biotech biz but a puzzlement and a problem to much of the world. It’s troubling to many that technology with such extreme potential to impact our health wouldn’t be put up for a vote or at least openly discussed and clearly identified before it landed on our plates.
The experts in the freaky food field insist genetically engineered foods are good for us but all we know for sure is that they’re good for the growing industry. These folks are busy in the labs, whipping up menus but they won’t share their formulas. Scientists in the real food industry tell us these “enhanced” foods are a recipe for disaster.
Since these frankenfoods are disguised as products we know and love, we might not notice the difference in the flatter flavors of our favorite foods or we might just learn to tolerate them. Our bodies, however, will feel the effects of diminished nutrition and unacknowledged, untracked side-effects.
We’re eating mystery meat, fabricated fruit, virtual vegetables and sneaky snacks, while garbed in cotton devised by designing minds. Even tobacco has been genetically modified. Try to identify these products in your local market – you can’t, without honest labeling.
As for that mystery meat, it may be a fungus among us.
Victims Urge “Whole Foods” Supermarkets Not To Sell Quorn Fake Meat Made From Fungus Causes Vomiting, Diarrhea, & Worse, According to CSPI
The genetically engineered food industry should tell us what to look for but won’t. If their products are so good for us, why are we being force-fed everything but the
facts?
The industry secrecy gives, “shop till you drop” a whole new meaning and wary American consumers are getting a bellyful.
Green groups sue USDA to stop bio-pharm planting with
BioDemocracy Spreading in California because folks would rather not plant their crops or choose their menus while blindfolded.
Before you go shopping, digest a little food for thought.
AGRICULTURE: Biotech Boom Linked to Development Dollars - Critics NEW YORK, Dec 3 (IPS) – “Even as an international debate rages over the safety and wisdom of planting genetically modified (GM) crops, they continue to spread like wildfire, particularly in developing countries”.
Even if you grow your own, check out the technology in the seeds you buy or you might yourself growing freaky foods in your own back yard. After all, we truly are what we eat and with lupus, that can be freaky enough already.
A Truly Rad Diet – Irradiated Foods
Lupus is greatly influenced by the food we eat and a clean diet of whole foods is best for us. The irradiation of our food, we’re told, increases food safety and promotes health. In truth, irradiation actually strips foods of most nutrients, leaving them essentially useless in a healthy diet. If only that were the worst of it but, this being the real world, it naturally, or unnaturally, isn’t. The irradiating process alters pesticides and chemicals already present in these foods, creating new combinations, with sometimes dire effects.
Escalated tumor rates, miscarriages and kidney damage are reported among animals fed irradiated foods. The range of irradiated foods includes fresh and frozen poultry, pork, lamb and beef, native and imported vegetables and fruits, wheat, eggs, spices, herbs, herb teas and sprouting seeds like alfalfa. Read the
facts on food irradiation at OrganicConsumers.org.
On November 25th, 2003, consumer watchdogs
Public Citizen and the
Center for Food Safety filed a
petition with the U.S. government, urging the Food and Drug Administration (FDA) to finally ban irradiated ground beef. This action was taken after lab tests detected carcinogenic chemicals and genetic damage in meat samples.
USDA Approves Irradiated Meat for Schools On May 29, 2003, the United States Department of Agriculture (USDA) ignored overwhelming opposition from students, parents and teachers across America. Involuntarily, schoolchildren have been put on the mystery meat diet. Our new government policy seems to be to Leave No Child Behind on the way to the hospital. Come back in 10 or 20 years to see how little Jessie and Joey are doing.
Andrew Kimbrell, director of the Center for Food Safety, says "Allowing our national school lunch program to distribute this irradiated meat would be to use 27 million children as unknowing guinea pigs to test the safety of these products." Read the
press release at Public Citizen.
It’s very difficult to know just what we’re buying and although we’re told irradiated foods are originally labeled, those notices don’t always make it to our local markets. Visit Organic Consumers to read
Background and Status of Labeling of Irradiated Foods and feel your stomach churn.
Uncle Sam wants to be Big Daddy, ordering our food for us and telling us to clean our plates. This fatherly attitude is going global, as the US pressures other countries to buy American seed and food products for their own citizens’ consumption. After years of discussion and dissent,
Leaked Documents Show Britain Ready To Allow Limited GM Crops and other countries are caving in.
Whether we have lupus, diabetes or other diseases to contend with or not, we're better off when we're eating whole, healthy foods, not reinvented versions of them. We were all taught not to play with our food and, with these new games, everybody could lose but the profiteers. Please learn how to protect yourselves by watching what you eat.
©Shar Phoenix, Lupus NewsLog.
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