You've blogged your way to Bowman's Thoughts and Things. Before you leave I hope that you will leave having been informed and introduced to some pretty good products. Because I have Lyme Disease I do hope that you learn something about Lyme and the need for more research. If you know someone with Lyme disease-show kindness and understanding. Believe me, it will be very much appreciated. The very best of health to you all!
Friday, November 27, 2009
Monday, November 23, 2009
Under Our Skin .. a possible Oscar!
Hello everyone,
I saw this on for and wanted to pass it along to you about the movie, "Under Our Skin" that I hope most of you have heard of and taken the opportunity to watch. It has made the short list of 15 for the Oscar nomination. I sincerely hope this film wins the Oscar. It will do wonders for the increase of knowledge around the country for Lyme disease.
Be well,
Richard
The Academy of Motion Picture Arts and Sciences today announced that UNDER OUR SKIN was selected as one of the 15 finalists competing for “Best Documentary Feature” in the 82nd Academy Awards®.
Unfolding like a real-life thriller, UNDER OUR SKIN exposes the hidden epidemic of Lyme disease and reveals how our corrupt medical system is failing to address one of the most serious illnesses of our time. Open Eye Pictures is thrilled that the Academy has honored the courageous Lyme patients and physicians whose stories are told in this film. And we hope that this nomination will help spread awareness about this devastating disease and serve as a catalyst for fixing our country’s broken health care system.
The Documentary Branch Screening Academy Committee viewed all eighty-nine qualifying documentaries during the preliminary round of voting. Academy members will now select five nominees from among the 15 titles on the shortlist, and Academy Awards nominations will be announced on Tuesday, February 2, 2010.
This was taken from the "Underourskin.com home page.
I saw this on for and wanted to pass it along to you about the movie, "Under Our Skin" that I hope most of you have heard of and taken the opportunity to watch. It has made the short list of 15 for the Oscar nomination. I sincerely hope this film wins the Oscar. It will do wonders for the increase of knowledge around the country for Lyme disease.
Be well,
Richard
The Academy of Motion Picture Arts and Sciences today announced that UNDER OUR SKIN was selected as one of the 15 finalists competing for “Best Documentary Feature” in the 82nd Academy Awards®.
Unfolding like a real-life thriller, UNDER OUR SKIN exposes the hidden epidemic of Lyme disease and reveals how our corrupt medical system is failing to address one of the most serious illnesses of our time. Open Eye Pictures is thrilled that the Academy has honored the courageous Lyme patients and physicians whose stories are told in this film. And we hope that this nomination will help spread awareness about this devastating disease and serve as a catalyst for fixing our country’s broken health care system.
The Documentary Branch Screening Academy Committee viewed all eighty-nine qualifying documentaries during the preliminary round of voting. Academy members will now select five nominees from among the 15 titles on the shortlist, and Academy Awards nominations will be announced on Tuesday, February 2, 2010.
This was taken from the "Underourskin.com home page.
Wednesday, November 18, 2009
A personal note to all who suffer from Lyme disease!
Hi everyone,
It has been a long time since I have made personal note to the Blog. I have been experiencing a flareup of My Lyme disease problems and it makes me realize even, even more, why we have to defeat this disease. It has been over 8 years since I was stricken with this awful disease. Since then I have gone through working at my business from putting in over 60 hours a week on the average to now having to stay at home. It is an adjustment not easily made. My attempts on this Blog and on the Internet to develop new businesses for me to do from home has been more than frustrating because of the small amounts of time I can work on them. Tasks which I used to do in a few hours, now take me several days of months to accomplish. As a result, a person ends up spending more money than they are taking in. As many of you know having Lyme disease is expensive and debt can be accumulated quickly. So the new business attempts, although starting to trickle in some income, are not doing what they need to do. Brain fog, insomnia, headache, extreme arthritic type pain, overwhelming fatigue, and many other symptoms don't make it easy to accomplish what you have planned in any given day. I am finding how important it is to focus on only one thing at a time, work when I can and then listen to what my body is telling me to do. Those who are experiencing these types of frustrations know and understand the urgency of finding doctors and specialists who ar qualified to treat Lyme disease. I don't know how many times I have heard doctors tell me that they know nothing about Lyme disease and how to treat it. It is if those of us who have this disease are supposed to go home and suffer the debilitating conditions it places on our lives. Why aren't doctors required to stay trained on diseases affecting their patients? This question remains as one of the many unanswered questions of the day. If we have Cancer, we can find specialists to help us. It is that way with most of the other diseases. But Lyme disease patients find little to choose from. Ironically, the ones who are trying to help us are embroiled in the CDC's failure to properly recognize treatments that are working for Lyme disease. Many are afraid of losing their license to practice medicine if they treat Lyme disease with working treatments. In the meantime, thousands of Lyme disease patients are stuck in the middle and continue to see their lives ruined. All in all, some days it becomes quite frustrating. Thank goodness most of us are fighters and we arise the next day ready to continue the battle. For those of you out there going through similar problems, I know how you feel and how much you want to get better. I will continue to try and continue my meager efforts to keep us informed about this brutal disease. I apologize that I have not posted more information in the past couple of years. I hope to do better in the future. If any of you have any concerns or you would like to comment, I urge you to do so. Your struggles are our struggles and hearing them from you makes us all feel better. The main purpose of this blog remains Lyme disease. Yes, I do post some products and services that I have found interesting over the past few years. I list the products only in the attempt to make a little money to pay my medical bills. You are under no obligation to purchase anything from me to visit this blog or to find Lyme disease information. The cure and successful treatment of Lyme disease is why this blog exists. As the holidays are approaching, may I wish you all a wonderful Thanksgiving, a Merry Christmas and a healthy and happy New Year!
Be well,
Richard
It has been a long time since I have made personal note to the Blog. I have been experiencing a flareup of My Lyme disease problems and it makes me realize even, even more, why we have to defeat this disease. It has been over 8 years since I was stricken with this awful disease. Since then I have gone through working at my business from putting in over 60 hours a week on the average to now having to stay at home. It is an adjustment not easily made. My attempts on this Blog and on the Internet to develop new businesses for me to do from home has been more than frustrating because of the small amounts of time I can work on them. Tasks which I used to do in a few hours, now take me several days of months to accomplish. As a result, a person ends up spending more money than they are taking in. As many of you know having Lyme disease is expensive and debt can be accumulated quickly. So the new business attempts, although starting to trickle in some income, are not doing what they need to do. Brain fog, insomnia, headache, extreme arthritic type pain, overwhelming fatigue, and many other symptoms don't make it easy to accomplish what you have planned in any given day. I am finding how important it is to focus on only one thing at a time, work when I can and then listen to what my body is telling me to do. Those who are experiencing these types of frustrations know and understand the urgency of finding doctors and specialists who ar qualified to treat Lyme disease. I don't know how many times I have heard doctors tell me that they know nothing about Lyme disease and how to treat it. It is if those of us who have this disease are supposed to go home and suffer the debilitating conditions it places on our lives. Why aren't doctors required to stay trained on diseases affecting their patients? This question remains as one of the many unanswered questions of the day. If we have Cancer, we can find specialists to help us. It is that way with most of the other diseases. But Lyme disease patients find little to choose from. Ironically, the ones who are trying to help us are embroiled in the CDC's failure to properly recognize treatments that are working for Lyme disease. Many are afraid of losing their license to practice medicine if they treat Lyme disease with working treatments. In the meantime, thousands of Lyme disease patients are stuck in the middle and continue to see their lives ruined. All in all, some days it becomes quite frustrating. Thank goodness most of us are fighters and we arise the next day ready to continue the battle. For those of you out there going through similar problems, I know how you feel and how much you want to get better. I will continue to try and continue my meager efforts to keep us informed about this brutal disease. I apologize that I have not posted more information in the past couple of years. I hope to do better in the future. If any of you have any concerns or you would like to comment, I urge you to do so. Your struggles are our struggles and hearing them from you makes us all feel better. The main purpose of this blog remains Lyme disease. Yes, I do post some products and services that I have found interesting over the past few years. I list the products only in the attempt to make a little money to pay my medical bills. You are under no obligation to purchase anything from me to visit this blog or to find Lyme disease information. The cure and successful treatment of Lyme disease is why this blog exists. As the holidays are approaching, may I wish you all a wonderful Thanksgiving, a Merry Christmas and a healthy and happy New Year!
Be well,
Richard
Tuesday, November 3, 2009
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About Me
- rbowman838
- Pueblo, Colorado, United States
- I am a Chronic Lyme disease patient. I was bitten by a tick in 2001 and have been very sick ever since. Subsequently, you could say I am a Lyme disease junkie.I thirst for any information about it,any treatments, research etc. It has been a life altering experience, which has kept me away from our business and at home most of the time. I use to own A-1 Barricade and Sign Inc. here in Pueblo, Co, but because of the Lyme disease, my sons are running the business for the most part with my wife. I have been married for 48 years to a wonderful woman who is also my best friend. We have five children, all grown. Four boys live here in Pueblo and my only daughter lives in Bonney Lake, Washington. We miss her a lot. I have 7 grandchildren, which are the greatest of all. They are all exceptionally beautiful! The last thing you need to know about me is that I am proud to be a member of The Church of Jesus Christ of Latter-Day Saints. Because of this I have the knowledge that life is eternal and that it does not end here, but it will go on after death because of the Atonement of Jesus Christ. This truth I bear witness of!