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  • Pulmonary Fibrosis and Interferon

    I hadn’t heard about this article until just now so thought I’d share it. My doctor did not recommend that I try this treatment as he felt that the variety of IPF I had wouldn’t be helped by it, but I know of a lot of people who were really happy with the results they had on it. So I am kind of surprised at this report. At least there seems to be hope that it will help people with mild to moderate symptoms.

    Interferon a No-Go for Pulmonary Fibrosis

    WEDNESDAY, Jan. 7 (HealthDayNews) — A once hopeful treatment for pulmonary fibrosis, a fatal disease of the lungs, appears to have little or no effect on progression of the disease or on quality of life, a new study has found.

    There remains some optimism, however, that the treatment, interferon gamma-1b, might benefit patients with mild to moderate symptoms of the disease. The authors of the study, which appears in the Jan. 8 issue of the New England Journal of Medicine, are launching a new trial to test this hypothesis.

    The median survival time for patients diagnosed with pulmonary fibrosis is only two to three years. The disease results in a scarring of the lungs that eventually prevents the lungs from fulfilling their primary mission of delivering oxygen to the body. The only effective treatment is lung transplantation, although many people are treated with anti-inflammatory and immunosuppressive drugs, both of which have side effects… [www.medicinenet.com]

    As for me, I’m just waiting for a lung to come up for me on the transplant list and wondering why this article just popped into my aggregator now if the article is from January.

  • Fairy Tales – Redone

    Sequential Tart has a nice article with pointers to various retellings of fairy tales. I was happy to see it included one of my favorites, which is Sheri S. Tepper’s Beauty. And now I’ve got a few more books to add to my book list.

  • Yay! More Looney Tunes!

    Looney Tunes: Golden Collection: Volume 2
    I was just looking at Amazon.com and noticed they had a little ad up for the Looney Tunes Golden Collection: Volume 2. I loved the first collection, it was a great start to them releasing many old old cartoons that I hadn’t seen in their entirely in ages. This one looks to continue the trend with a lot of early material. And even better, it comes out on my birthday next month (November 2nd)! I’ve added it to my wish list, anyone wanna pick it up for me?

  • How to Cheer Oneself Up After a Boring and Dull Weekend

    I’ve been in an absolutely crappy mood all weekend. I dunno if it’s the phase of the moon or that time of the year or what. In an act of desperation I sent someone some songs anonymously, and got an absolutely wonderful response to the second one. I am now smiling. The End.

    ps. please don’t kill me.

  • More Developments in the Study of Pulmonary Fibrosis

    This one actually didn’t seem too surprising to me, but it is cool that they were able to find the connection.

    New Light Shed on Deadly Lung Disease

    TUESDAY, Aug. 3 (HealthDayNews) — New research holds out hope for people suffering from pulmonary fibrosis, a deadly lung disease, by discovering that cells that travel to the organ to repair damage end up doing more harm than good.

    The study found these biological repairmen, which experts had thought originally resided in the lungs, were actually adult stem cells that migrated there from the patient’s bone marrow — and this migration can be halted.

    “It’s certainly very exciting research, but the information is obviously very preliminary,” said Dr. Alfred Munzer, a lung specialist from Maryland and past president of the American Lung Association. “We have to see what meaning it holds.”

    Pulmonary fibrosis is a chronic and often fatal disorder that is characterized by extra scar tissue in the lungs. The disease, which affects some 80,000 individuals in the United States, has traditionally been treated with steroids and other immunosuppressive therapies, but with little effect. About 70 percent of people die within five years of diagnosis. “At the moment, there is no effective treatment for pulmonary disease, and it is not that uncommon a disease,” Munzer said. [medicinenet.com]

    What I think about this is that it gives me hope for people who get IPF in the future. I’m already well on my way to getting a new lung, but that honestly isn’t my first choice. And it isn’t something available to all people. In many ways I’m very lucky in that I haven’t gotten worse in well over a year (*knocks on wood*).

  • More Pulmonary Fibrosis News

    Here’s an interesting article from a few days ago:

    Adult Stem Cells Migrate to Lung, Contribute to Pulmonary Fibrosis

    09 Aug 2004

    UCLA researchers for the first time identified and then stopped a type of adult stem cell from migrating to the lung and contributing to pulmonary fibrosis in an animal model. Pulmonary fibrosis (i.e, idiopathic pulmonary fibrosis) in humans is a devastating terminal disorder that causes an overabundance of scar tissue to form in the lung.

    IMPACT: The new study may offer novel therapies to treat idiopathic pulmonary fibrosis– currently there are no effective treatments and the mortality rate is approximately 70 percent within five years of diagnosis. Over 80,000 individuals in the United States suffer from the disease. [medicalnewstoday.com]

  • The Need For Patient Education

    One thing that amazes me is how much information is available on medical conditions and how few people ever find it. Hopefully things like this can help with that.

    Coalition for Pulmonary Fibrosis Announces Publication of New Educational Tools for Patients

    Preliminary Results From Latest Research Initiative Demonstrate Need for Lung
    Transplant and Pulmonary Rehabilitation Education for IPF Patients and
    Caregivers

    SAN JOSE, Calif., Sept. 17 /PRNewswire/ — The Coalition for Pulmonary
    Fibrosis
    (CPF) announced today the publication of two new educational
    brochures: ‘Lung Transplantation: What Every Patient with Idiopathic
    Pulmonary Fibrosis Should Know’ and ‘Oxygen Management and Pulmonary
    Rehabilitation for the IPF Patient’.

    The two brochures were created for patients, family members and physicians
    alike based on preliminary results of the CPF’s Basic Research Questionnaire,
    an education initiative launched last year to better understand the impact of
    idiopathic pulmonary fibrosis (IPF) on patients and families, and to help the
    foundation grasp the educational needs that arise for those fighting the
    disease.

    To date, the CPF has received more than 1,400 responses to this
    ground-breaking survey, and based on educational gaps identified by patients,
    discovered the need for improved education and awareness on two very important
    topics for IPF patients; lung transplantation and pulmonary rehabilitation.

    Interim results of the CPF’s research questionnaire found that among
    current patients, 30 percent responded that their physician has not discussed,
    or even mentioned the topic of lung transplantation, a potential treatment
    option for IPF patients under 65. Of those patients under the age of 60,
    fewer than half (47 percent) said they have been advised to seek a lung
    transplant. Additional data from a Duke University study also indicates that
    more than 50 percent of those with IPF who are on transplant lists will pass
    away before a donor lung becomes available. [via Feedster Search: Pulmonary Fibrosis]

    This also makes me very thankful that I found the doctors I did as I went through my diagnosis. I was quickly forwarded to a pulmonary specialist and he was able to give me a preliminary diagnosis almost immediately. Once it was confirmed that I did actually have Pulmonary Fibrosis we sat down and talked about what it all means, what treatments were available, how things tended to progress, what it meant long term, the whole thing. I still find it kind of stunning that other people have not had this same experience.

  • Possible New Treatments for Pulmonary Fibrosis

    I’ve started hunting for news items to do with Pulmonary Fibrosis in my news reader, so will be making note of interesting developments that I find.

    Treatment for pulmonary fibrosis may be achieved by blocking cell death in the lung

    A research team at Yale has found that blocking a kind of cell death called apoptosis in fibrotic diseases of the lung, also blocks the fibrosis, opening new ways of looking at treatment for lung diseases such as pulmonary fibrosis. [via Feedster Search: Pulmonary Fibrosis]

  • More Proof That Hartford Sucks

    I was looking through the list of places where Ghost in the Shell:Innocence was playing in the next month and Hartford, CT was nowhere to be seen. Heck, there wasn’t even anywhere in CT it is showing. I guess I’ll have to see it in the Boston area (where it is showing at two different places). Anyone up for going to see it next Wednesday afternoon?

  • Partisan Project

    I tend to stay away from discussing politics on this site, but my friend John just IM’d me a link to a pretty nifty site called PartisanProject..

    What We Did. We invited 15 designers and artists to each create one, two-color poster (18.5″x24″) urging a vote against the current administration. The posters were printed, stacked together, folded in half and in half again – like a newspaper. These poster packs are being distributed much like a free newsweekly – dropped in bookstores, coffeehouses, restaurants, grocery stores, libraries, etc. throughout the city of Pittsburgh and the surrounding areas of southwestern Pennsylvania. people can choose a poster (or posters) they like and hang it outside their home or somewhere in their neighborhood. The posters can also be downloaded at this website. We are also wheat-pasting the posters in various locations through the city. And in September, we will host a gallery event where each poster will be displayed en masse along with speakers, voter registration booths and live music. [Partisan Project. INFO]

    Neat idea. Given that I’m not a fan of the current administration, I thought this sounded pretty cool. I also think they’re a bit short-sighted and should also be pushing this for other areas beyond Pittsburgh. And someone needs to tell them that you really shouldn’t have all the text in your site be images. It makes it impossible to quote things easily.