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	<title>Spinal Cord Resources Network &#187; congress</title>
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		<title>The ever increasing doughnut hole</title>
		<link>http://www.spinalcordresources.com/2009/12/the-ever-increasing-doughnut-hole/</link>
		<comments>http://www.spinalcordresources.com/2009/12/the-ever-increasing-doughnut-hole/#comments</comments>
		<pubDate>Tue, 29 Dec 2009 17:34:59 +0000</pubDate>
		<dc:creator>ghgeorge</dc:creator>
				<category><![CDATA[General]]></category>
		<category><![CDATA[Law Center]]></category>
		<category><![CDATA[Medical]]></category>
		<category><![CDATA[Roaring Mouse (advocacy)]]></category>
		<category><![CDATA[Technology]]></category>
		<category><![CDATA[congress]]></category>
		<category><![CDATA[disability]]></category>
		<category><![CDATA[drugs]]></category>
		<category><![CDATA[insurance]]></category>
		<category><![CDATA[Medicare]]></category>
		<category><![CDATA[prescriptions]]></category>
		<category><![CDATA[Social Security]]></category>

		<guid isPermaLink="false">http://www.spinalcordresources.com/?p=1075</guid>
		<description><![CDATA[
The doughnut hole, or the payment that Medicare patients make when their medications cost more than&#160; $2700 a year is going to get bigger. The new bill in Congress is supposed to close the payments over the next 10 years so that all pharmacy payments will be covered by Medicare. However, because of increases in [...]]]></description>
			<content:encoded><![CDATA[<p>
<input align="left" width="64" type="image" height="93" src="http://www.spinalcordresources.com/wp-content/uploads/image/Flag.jpg" />The doughnut hole, or the payment that Medicare patients make when their medications cost more than&nbsp; $2700 a year is going to get bigger. The new bill in Congress is supposed to close the payments over the next 10 years so that all pharmacy payments will be covered by Medicare. However, because of increases in pills and decreases in money coming in to pay for federal programs those on Medicare can expect to pay more for the next three years. After that the new legislation, if it becomes law will eventually catch up with those increases and will start to close the doughnut hole. <span id="more-1075"></span> That does nothing to help the people that take expensive drugs and have to come up with $2700 every year or just stop taking their pills. Many people that are on blood pressure medication or pain pills just stop taking their medication and for the rest of the year hope that their health does not decrease enough to be hospitalized until the beginning of the next year when Medicare picks up again. For those that can come up with the $2700, at $4300 Catastrophic Care kicks in and pays for 95% of all medications regardless of the amount. So those what are trying to live off of Social Security Disability payments have to somehow come up with over $2000 a year and give up on either a car or a place to live. This hole was put in place by the Republicans who said that the government could not pay for all drugs and this was a way to make sure that everyone would have access to the Medicare pharmacy program. However, it only creates a situation where people that need drugs cannot afford to keep taking them and are forced to stop taking them and put their health at risk. In the mean time the new Medicare bill requires pill manufacturers to give everyone a 50% discount to help individuals pay for their pills. No one knows how much that discount will help those that cannot afford their pills now, but the already existing programs to help those to pay for drugs only help a tiny fraction because the companies decide who their are going to help and by how much. (Source: <a href="http://www.washingtonpost.com/wp-dyn/content/article/2009/12/27/AR2009122701206.html?referrer=emailarticle">Washington Post</a>)</p>
<p>This political football has created a group of people that cannot pay for their drugs because of a crazy program that is based on Social Security that was never supposed to give people enough money to pay for their medical bills. So instead we have a drug industry that makes billions of dollars in profits on the backs of those that pay for research on the pills that we are charged $1000+ a month for. These companies due to keep generic drug makers from creating drugs that can be afforded by all. It is interesting that the costs of the same drug in the US is a fraction of that amount in Canada or even India. Each country pays a different amount but we are too stupid to make these same deals with the drug makers. To add insult to injury Medicare is not allowed by law to purchase drugs from other countries for less than what we are charged for them now. The US pays for all of the research but does not gain any of the benefits of that research. Instead the poor of the country are forced to pay outrageous amounts of money for drugs that they need to stay alive. We need to make some decisions as a country on how we deal with those that are disabled and elderly. Either we are going to pay for their medical care or not &#8211; not the bits and pieces we are now. By only allowing these people to take their drugs every 6 months, their health is deteriorating to the point that they are dying before they should because of the damage caused by not taking their medications. Lets close the doughnut hole and give people the medical care that they need to live useful lives.</p>
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		<title>Testify in congress for pain issues</title>
		<link>http://www.spinalcordresources.com/2009/12/testify-in-congress-for-pain-issues/</link>
		<comments>http://www.spinalcordresources.com/2009/12/testify-in-congress-for-pain-issues/#comments</comments>
		<pubDate>Fri, 11 Dec 2009 19:14:48 +0000</pubDate>
		<dc:creator>ghgeorge</dc:creator>
				<category><![CDATA[General]]></category>
		<category><![CDATA[Law Center]]></category>
		<category><![CDATA[Roaring Mouse (advocacy)]]></category>
		<category><![CDATA[chronic pain]]></category>
		<category><![CDATA[conference]]></category>
		<category><![CDATA[congress]]></category>
		<category><![CDATA[CRPS]]></category>
		<category><![CDATA[government]]></category>
		<category><![CDATA[pain]]></category>

		<guid isPermaLink="false">http://www.spinalcordresources.com/?p=1034</guid>
		<description><![CDATA[Those having to deal with the federal government in the payment &#160;or remittance of equipment or services have an excellent idea of the red tape that is involved. For those of us with CRPS, it can be almost impossible to get the governmental people on the other end of the phone to understand. They have [...]]]></description>
			<content:encoded><![CDATA[<p><img align="left" width="75" height="70" alt="" src="http://www.spinalcordresources.com/wp-content/uploads/image/MicrophoneMouse.png" />Those having to deal with the federal government in the payment &nbsp;or remittance of equipment or services have an excellent idea of the red tape that is involved. For those of us with CRPS, it can be almost impossible to get the governmental people on the other end of the phone to understand. They have a list of what is needed and required, not what you need that ends up being paid for. So you don&#8217;t get what you need but rather what they think you need. <span id="more-1034"></span> To help get past these problems the CELA conference is looking for people that have CRPS and are willing to go in front of congress and tell them what you have gone through.</p>
<p>Have you or a loved one been denied Complex Rehab Equipment that would enable a healthier, happier and higher quality of life? Did you know your government is providing reimbursement based on which equipment they think is best for you? Their decisions are not based on what actually is best for your unique medical needs. So basically &#8211; you are getting rehab equipment &#8211; but what the government feels is appropriate for you. Not what is really best for you to live an independent healthy lifestyle. If this scenario sounds familiar and you would like to get involved and help change the way the government reimburses for Complex Rehab Equipment, go to</p>
<p>http://www.uptilt.com/ct.html?rtr=on&amp;s=6do,1afgq,2v1u,g8eb,cbdq,h55k,6y3w</p>
<p>and apply for a Consumer Scholarship to the CELA conference in April 2010. This is an expenses paid trip to Washington, DC where you can tell your story in person to members of Congress on Capitol Hill. Your involvement will help change the government&#8217;s perspective for you and others with disabilities. To apply for your CELA expense paid scholarship to Washington, DC go to</p>
<p>http://www.uptilt.com/ct.html?rtr=on&amp;s=6do,1afgq,2v1u,g8eb,cbdq,h55k,6y3w</p>
<p>To learn more about CELA 2010 go to</p>
<p>http://www.uptilt.com/ct.html?rtr=on&amp;s=6do,1afgq,2v1u,bh0q,f5pm,h55k,6y3w</p>
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		<item>
		<title>Massachusetts Governor cuts disability programs</title>
		<link>http://www.spinalcordresources.com/2009/11/massachusetts-governor-cuts-disability-programs/</link>
		<comments>http://www.spinalcordresources.com/2009/11/massachusetts-governor-cuts-disability-programs/#comments</comments>
		<pubDate>Mon, 23 Nov 2009 17:09:17 +0000</pubDate>
		<dc:creator>ghgeorge</dc:creator>
				<category><![CDATA[General]]></category>
		<category><![CDATA[Medical]]></category>
		<category><![CDATA[congress]]></category>
		<category><![CDATA[insurance]]></category>
		<category><![CDATA[Medicare]]></category>

		<guid isPermaLink="false">http://www.spinalcordresources.com/?p=993</guid>
		<description><![CDATA[With falling revenues hitting all states is was a matter of time before the programs that the disabled need were cut. Massachusetts lost revenue from families unable to pay for their property taxes or income taxes and has put the state in a tough situation. Many programs have been cut and state workers all over [...]]]></description>
			<content:encoded><![CDATA[<p><img align="left" width="64" height="85" alt="" src="http://www.spinalcordresources.com/wp-content/uploads/image/Point.png" />With falling revenues hitting all states is was a matter of time before the programs that the disabled need were cut. Massachusetts lost revenue from families unable to pay for their property taxes or income taxes and has put the state in a tough situation. Many programs have been cut and state workers all over the country have had their wages cut or had to deal with lay-offs in an effort to balance budgets. However, for the last two weeks of October disabled people and their caregivers held a vigil to let the Governor know that the disabled require state services to stay alive and healthy. <span id="more-993"></span> After the vigil the Governor said that he would keep the programs disabled people use funded but at the last minute he decided to cut many programs that are vital to the disabled community. The programs that have been cut include day rehabilitation, adult dental rehabilitation services, personal care attendant services, podiatry services and adult foster care. The disabled depend more on state and federal help than other groups because they typically live on Social Security Disability which typically pays for rent, food and a few other things. Anything after that is almost impossible to pay for and these state services make it possible for people to get foot care help or get their teeth cared for. Instead these people have to hope that family can find money to pay for these services, and many of these people are dealing with lay-offs and reduced pay as companies try to stay in business in our present economic environment. Because the disabled have no where else to turn to when these services disappear, they will be forced to live with foot problems or fillings that need repair. (Source: <a href="http://www.wickedlocal.com/reading/homepage/x1945259412/Cuts-stun-disability-advocates">Wicked Local Reading</a>)</p>
<p>Hopefully the state will ask the federal government for help on these programs before large groups of people are effected by the cuts. These may not seem a big deal but if these people don&#8217;t take care of simple problems with their feet and teeth, those problems will become worse and will cost more to get fixed. This means going to the emergency room and putting strain on other state budget areas that would not normally have to handle these issues. Perhaps the state can look at all of the areas of the budget and spread the cuts over a larger area so that people are not hit as hard. If Boston were to cut the hours that state agencies were open by a few hours a week that could make a lot of money available to prop up services like the ones needed by the disabled community until either the economy improves or federal money becomes available. While families should be there for the disabled, they cannot always have money available because they have their own bills and children that need to be helped. Medical bills tend to be expensive and many people now do not have the extra money that they used to that could be used to pay for bills that popped up with out notice. Hopefully the work that has been done in the senate will make it easier for everyone to get health insurance and to get medical help. Otherwise hospital emergency rooms are going to be filled to capacity with people that don&#8217;t have emergencies, but do not have anywhere else to go to get help.,</p>
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		<item>
		<title>Medicare recipients already dropped</title>
		<link>http://www.spinalcordresources.com/2009/11/medicare-recipients-already-dropped/</link>
		<comments>http://www.spinalcordresources.com/2009/11/medicare-recipients-already-dropped/#comments</comments>
		<pubDate>Tue, 17 Nov 2009 15:28:55 +0000</pubDate>
		<dc:creator>ghgeorge</dc:creator>
				<category><![CDATA[General]]></category>
		<category><![CDATA[Law Center]]></category>
		<category><![CDATA[Roaring Mouse (advocacy)]]></category>
		<category><![CDATA[congress]]></category>
		<category><![CDATA[disability]]></category>
		<category><![CDATA[Doctor]]></category>
		<category><![CDATA[drugs]]></category>
		<category><![CDATA[insurance]]></category>
		<category><![CDATA[legislation]]></category>
		<category><![CDATA[Medicare]]></category>

		<guid isPermaLink="false">http://www.spinalcordresources.com/?p=987</guid>
		<description><![CDATA[For those that have not followed all the reports on the new medical bill making it&#8217;s way through the Senate, Medicare recipients are losing doctors, hospitals, and general care right now. My doctors have to be careful which medications that the prescribe because many times the company paid by Medicare will not OK the drug. [...]]]></description>
			<content:encoded><![CDATA[<p><img align="left" width="80" height="96" src="http://www.spinalcordresources.com/wp-content/uploads/image/SoapBoxMouse-small.png" alt="" />For those that have not followed all the reports on the new medical bill making it&#8217;s way through the Senate, Medicare recipients are losing doctors, hospitals, and general care right now. My doctors have to be careful which medications that the prescribe because many times the company paid by Medicare will not OK the drug. This is markedly different from standard insurance policies where you go in, talk to the doctor, and get your prescription all without&nbsp; having to beat up the insurance company or fill out all kinds of crazy reports explaining why you need the drug. This of course assumes that you can even get a doctor to see you. Many of us on Medicare are finding out that doctors will simply not see you anymore. <span id="more-987"></span> It is too expensive to see Medicare patients because the government keeps dropping the amount a doctor is paid to see a patient. So now it is to the point that no one wants to talk to you unless it is in the emergency room. Even there the last thing the hospital wants to do is to admit you. They will do the minimal amount of work necessary to make sure they are not sued for lack of medical care, and then kick you out the door. Many times blood work is pulled but you are still shown the door even if the results will be several days in coming. So you could have something that should be handled in the hospital, but you are tossed out before anyone figures that out. And if something is found what are the chances that the hospital will actually call you back to come in and be admitted? Winning the lottery is looking better all the time. We are all experiencing the healthcare breakdown, but we supposedly are not there. Guess what will happen after the new bill is passed? Not only will general practitioners refuse to see you, but specialists will also show you the door. Insurance companies have forced doctors to change from being healers to small business owners that have to carefully watch the bottom line. They have to be able to pay for nurses, malpractice insurance, equipment and an office. How does that happen if the doctor cannot make money off each patient.</p>
<p>Doctors cannot work like the government &#8211; run for years in deficit and then print up new&nbsp; money to pay for the previous losses. They need to be able to pay for bills and salaries as they come in and if they do not get enough money from patients coming in then they have to close down. That is in essence what is happening to the Medicare recipients and local doctors. They cannot afford to take care of us at the rate the federal government pays out so they flat out refuse to see us. So much for the medical coverage handed out by the government. I paid huge sums of money to the tax structure of this country before I was injured. As a software consultant I paid all that was owed so others could be helped and that I would be if something terrible happened. Well that time was three years ago when a hit and run driver ran me down and left me for dead in the street. As a tertraplegic stuck with complex regional pain syndrome I find it all but impossible to hold down a job because I am hospitalised as least once a month for pain or things tied to the pain. The last week of the month is back to back visits to all my doctors so we can figure out how to deal with problems with my spine and infections that are in the bone. So I live off of SSDI and hope and pray that Medicare allows my doctors and hospitals to continue to see me. My pharmaceutical issues would blow most people away and to show how fun things have been I hit the doughnut hole in June, and blew past it in August and am now having Critical Care government payments covering my drugs at 95%. That is until next year when I somehow have to find $2500 to get though the doughnut hole again. I&#8217;m hoping my pain doctor can get me on cheaper drugs soon, and that is assuming he will still see me after the new medical bill becomes law.</p>
<p>There are many things to be fixed in our medical system, but the way we are doing it now will guarantee the death of thousands. If we cannot see our doctors and hospitals and get the drugs we need at a rate we can afford, then we might as well throw in the towel and stop pretending that Medicare pays for things. Lets start thinking about how doctors pay for their bills and how they can stay in business and allow Medicare the pay at those rates or we will soon see a time where Medicare is a terrible thing to have to deal with. Here is to our Senate and House members to talk to everyone involved and forget about the insurance companies and lawyers who are killing out medical system. With the bill going through congress we are all running out of time.</p>
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		<title>HIPAA costing lives in longrun</title>
		<link>http://www.spinalcordresources.com/2009/10/hipaa-costing-lives-in-longrun/</link>
		<comments>http://www.spinalcordresources.com/2009/10/hipaa-costing-lives-in-longrun/#comments</comments>
		<pubDate>Mon, 05 Oct 2009 14:44:43 +0000</pubDate>
		<dc:creator>ghgeorge</dc:creator>
				<category><![CDATA[General]]></category>
		<category><![CDATA[Law Center]]></category>
		<category><![CDATA[Roaring Mouse (advocacy)]]></category>
		<category><![CDATA[congress]]></category>
		<category><![CDATA[legislation]]></category>
		<category><![CDATA[Medicare]]></category>
		<category><![CDATA[prescriptions]]></category>

		<guid isPermaLink="false">http://www.spinalcordresources.com/?p=893</guid>
		<description><![CDATA[All of us are worried about our personal data getting out to the Internet so that identity thieves can steal our bank accounts. Plus, health insurance companies have used personal data to drop patients or deny services based on items found in old health forms. To make sure that these types of things cannot occur [...]]]></description>
			<content:encoded><![CDATA[<p><img width="64" height="85" align="left" alt="" src="http://www.spinalcordresources.com/wp-content/uploads/image/Scale.jpg" />All of us are worried about our personal data getting out to the Internet so that identity thieves can steal our bank accounts. Plus, health insurance companies have used personal data to drop patients or deny services based on items found in old health forms. To make sure that these types of things cannot occur the government created HIPAA. <span id="more-893"></span> HIPAA is a group of laws that determine who has access to your personal data and for how long. This is why doctor&#8217;s offices constantly ask for your signature to access forms and data from hospitals and other health centers. Overall the laws have been successful in keeping data breaches down and making sure that your data is only accessible to those that need it. However, as more data is being collected, some doctors are asking for data mining capabilities that they can&nbsp; link up records from multiple locations to determine trends and issues in your medical care. Since doctors only have access to a sliver of your whole medical record they may not see trends in pills that you are taking that may cause problems later on with your liver or kidneys. By connecting data together into large data sets, they can be &quot;mined&quot; for data that shows the early signs of ailments or drugs that are causing problems based on earlier blood tests. This means that we would have to open up our medical records to more doctors and new companies that we do not&nbsp; have any experience with.</p>
<p>Considering the omnibus health care bill that is slowly making it&#8217;s way through congress, all, of us needs to tell our congressmen what we need in health care. Protection of personal data is extremely important as more and more companies depend on the Internet to send your data to hospitals and payroll companies. This gives more people access to your data, but without it you could not get the care you need. Call and tell your congressman and senators what you think about security and health care. Are you happy with Medicare or Social Security as it is? Doubtful. Everyone we talk to have major problems with all governmental agencies and that translates into drugs that insurance companies won&#8217;t pay for or services that your doctor needs that will not be ok&#8217;d. We have said this before but unless out voices are heard you can expect medical coverage to get worse and tyhe disabled to be forgotten about in all aspects of medical care. If you don&#8217;t want to be at the bottom of the barrel in the medical system now is the time to open your mouth. Congress wants to hear from you because you are a voter (you vote don&#8217;t you??) and as such have power. Once the bill is passed into law we are done. There is little we can do to change things for a long time. Don&#8217;t let this time pass by without getting involved.</p>
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		<title>Medicare overpays again</title>
		<link>http://www.spinalcordresources.com/2009/09/medicare-overpays-again/</link>
		<comments>http://www.spinalcordresources.com/2009/09/medicare-overpays-again/#comments</comments>
		<pubDate>Sat, 26 Sep 2009 14:59:26 +0000</pubDate>
		<dc:creator>ghgeorge</dc:creator>
				<category><![CDATA[General]]></category>
		<category><![CDATA[Law Center]]></category>
		<category><![CDATA[Roaring Mouse (advocacy)]]></category>
		<category><![CDATA[congress]]></category>
		<category><![CDATA[disability]]></category>
		<category><![CDATA[drugs]]></category>
		<category><![CDATA[Equipment]]></category>
		<category><![CDATA[insurance]]></category>
		<category><![CDATA[legislation]]></category>
		<category><![CDATA[Medicare]]></category>

		<guid isPermaLink="false">http://www.spinalcordresources.com/?p=865</guid>
		<description><![CDATA[A US Inspector General has reported that Medicare overpays almost $1000 on every wheelchair that they rent rather than purchase. The idea behind the Medicare program is that the disabled will have someone to go back to if there is a problem with their chair and that the repairs will be included with their monthly [...]]]></description>
			<content:encoded><![CDATA[<p><img width="64" height="93" align="left" alt="" src="http://www.spinalcordresources.com/wp-content/uploads/image/Flag.jpg" />A US Inspector General has reported that Medicare overpays almost $1000 on every wheelchair that they rent rather than purchase. The idea behind the Medicare program is that the disabled will have someone to go back to if there is a problem with their chair and that the repairs will be included with their monthly payment. However the costs do not pan out and it is not economical to rent the wheelchairs. Medicare ended up paying suppliers $2970 for services that suppliers paid $1048. These overpayments cost Medicare $686 million for the first half of the year. There is no system in place that allows Medicare to pick the lowest supplier of powered wheelchairs so they end up paying much more than they should. This is on top of the rental costs of the wheelchairs that are almost four times what it would cost to purchase the equipment directly. There are no bills in congress to deal with this issue which is costing tax payers much more then they have to. (Source: <a href="http://www.upi.com/Top_News/2009/09/02/Medicare-overpaying-to-lease-wheelchairs/UPI-65881251900301/">UPI</a>)</p>
<p><span id="more-865"></span></p>
<p>Americans are used to dramatically overpaying for equipment and services for some time. The all time classic was the military spending over $1000 for a hammer that anyone could purchase at the corner hardware store. It is sad that government contracts allow this type of insanity to continue, but many parts of congress do not have rules to purchase from the lowest bidder or to even try and negotiate with the supplier. It is bad enough when the military buys things that they can get cheaper, but Medicare is costing a fortune as it is so any savings would be helpful. If we are to get a handle on Medicare and Medicaid costs, then we need to start here. There is no reason to overpay on items merely because the government is used to doing business with a particular company. There is no way that we can keep overpaying on medical care and expect our tax structure to keep up with the increases.</p>
<p>All of us have a stake in making medicare care in this country affordable and safe. Doctors need to be able to order procedures and drugs without having to worry about what will be paid and what will not be. No one&#8217;s health ca be tied to a price tag and no one should have to worry that someone else will decide whether they will be healed or nor. As is stands now under Medicare Part D, insurance companies can decide what drugs to cover and which they don&#8217;t. If you pick a company that covers what you are taking now but get sick, you may not be able to get the drugs you need. This is especially true of expensive drugs that do not have a generic to purchase. Powerful pain drugs like Actiq are not covered so if you have chronic pain there may be no drugs you can take that are covered. So you get to suffer because of bureaucratic red tape. This needs to stop. There is no reason why a drug a doctor prescribes is not made available and covered by insurance. Unless this is fixed we will have a group of have and have nots. WHile that is bad enough in schools, it ks inexcusable for medical care.</p>
<p>Everyone deserves the best that we can properly afford. Please contact your congressman and senators to let them know what you think about this. The new bill going through congress will never be the best it can be unless we all participate and let everyone know what we need. Democracies are not spectator sports. If we don&#8217;t participate, don&#8217;t complain about what happens with the new Medicare changes.</p>
<p style="margin-bottom: 0in;">&nbsp;</p>
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		<title>Disabled heckled at meeting</title>
		<link>http://www.spinalcordresources.com/2009/09/disabled-heckled-at-meeting/</link>
		<comments>http://www.spinalcordresources.com/2009/09/disabled-heckled-at-meeting/#comments</comments>
		<pubDate>Thu, 17 Sep 2009 13:51:27 +0000</pubDate>
		<dc:creator>ghgeorge</dc:creator>
				<category><![CDATA[General]]></category>
		<category><![CDATA[Law Center]]></category>
		<category><![CDATA[bigotry]]></category>
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		<category><![CDATA[disabled]]></category>
		<category><![CDATA[fair housing]]></category>
		<category><![CDATA[Heckling]]></category>
		<category><![CDATA[legislation]]></category>
		<category><![CDATA[Medicare]]></category>

		<guid isPermaLink="false">http://www.spinalcordresources.com/?p=827</guid>
		<description><![CDATA[At a town hall meeting in New Jersey a disabled woman who spends half her day in a wheelchair was heckled. She started to explain that she has Rheumatoid Arthritis and Sjogren&#8217;s Syndrome, both which destroy healthy nerves. Then she explained what she thought should be in the health care bill for the disabled when [...]]]></description>
			<content:encoded><![CDATA[<p><img width="64" height="93" align="left" src="http://www.spinalcordresources.com/wp-content/uploads/image/Flag.jpg" alt="" />At a town hall meeting in New Jersey a disabled woman who spends half her day in a wheelchair was heckled. She started to explain that she has Rheumatoid Arthritis and Sjogren&#8217;s Syndrome, both which destroy healthy nerves. Then she explained what she thought should be in the health care bill for the disabled when she was repeatedly heckled. <span id="more-827"></span> People were screaming that she should drop her cable television and air conditioning. She was repeatedly heckled as she explained that she cannot afford her prescription medication and her mortgage. Thee hecklers were yelling that she spent too much money on her home and that she should move into public housing. (Source: <a href="http://jfactivist.typepad.com/jfactivist/2009/09/health-care-town-hall-jeers-woman-with-disability.html">American Association of People with Disabilities</a>).</p>
<p>We have all heard of the hecklers in the town meetings over the last few weeks but it is unbelievable what happened to this woman in New Jersey. Regardless of where you are in the political spectrum, there is no excuse to verbally assault someone who has the floor during a meeting. Plus there is no reason to attack someone personally because you do not want to hear their view. In a democracy we expect different ideas on how things are to be done so we can pick the best one for our country&#8217;s needs. No one has exclusive rights to good ideas such that no one else can speak their mind. Those that believe that&nbsp; need to take an American government class so they can get a grasp on how this republic operates. Everyone has a right to speak their mind, regardless of how horrible it sounds to you.</p>
<p>How many of those that heckled this woman would be willing to drop their cable and Internet connection and live in public housing. If you do not have a chronic medical problem then you truly do not understand how things work for those that rely on Medicare and Medicaid. Many pills and procedures that are used everyday on those with private insurance find they cannot get help with Medicare. The dough nut hole requires people to come up with thousands of dollars of their own money before catastrophic care kicks in. Many live on social security and do&nbsp; not have thousands to throw around so stop taking their medication until the beginning of the new year. That can be a death sentence to those on heart or cancer medications. Issues like these need to be fixed so that we do not kill our citizens in the name of controlling costs. Those on social security are not people that should not have rights. We have all worked hard and paid into the system and now find ourselves severely injured because of an auto accident or have been forced to retire at 65 and now are trying to make ends meet. </p>
<p>If we don&#8217;t deal with this soon, we will truly have two type of people in America, those that have and those that have not. Money should not be the only measurement to determine if someone should live or have constitutional rights. Those that work and are in power have a responsibility to help those that cannot&nbsp; help themselves. If we don&#8217;t then we will not continue to be a world power as social issues will eat away at the basic structure of how our country works. Lets help everyone to be the best that they can be so we don&#8217;t have situations like we are creating now. Lets make sure we keep a country that gives everyone a chance to succeed so that everyone wants to emigrate here. If we don&#8217;t we will experience the brain drain that many countries experienced over the 20th century.</p>
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		<title>Olmstead Act turns 10</title>
		<link>http://www.spinalcordresources.com/2009/09/olstead-act-turns-10/</link>
		<comments>http://www.spinalcordresources.com/2009/09/olstead-act-turns-10/#comments</comments>
		<pubDate>Tue, 15 Sep 2009 14:04:26 +0000</pubDate>
		<dc:creator>ghgeorge</dc:creator>
				<category><![CDATA[General]]></category>
		<category><![CDATA[Law Center]]></category>
		<category><![CDATA[Roaring Mouse (advocacy)]]></category>
		<category><![CDATA[ADA]]></category>
		<category><![CDATA[bigotry]]></category>
		<category><![CDATA[congress]]></category>
		<category><![CDATA[disability]]></category>
		<category><![CDATA[fair housing]]></category>
		<category><![CDATA[job discrimination]]></category>
		<category><![CDATA[legislation]]></category>

		<guid isPermaLink="false">http://www.spinalcordresources.com/?p=800</guid>
		<description><![CDATA[Ten years ago the Olmstead Act was put into law. This act removed the last of the &#8220;ugly&#8221; laws that controlled where and how disabled people lived in the state of Georgia. A lawsuit then started where land owners and home owner associations tried to make their rules against the disabled the official law of [...]]]></description>
			<content:encoded><![CDATA[<p><img width="80" height="96" align="left" alt="" src="http://www.spinalcordresources.com/wp-content/uploads/image/SoapBoxMouse-small.png" />Ten years ago the Olmstead Act was put into law. This act removed the last of the &ldquo;ugly&rdquo; laws that controlled where and how disabled people lived in the state of Georgia. A lawsuit then started where land owners and home owner associations tried to make their rules against the disabled the official law of the land. They lost their case and now the disabled can live anywhere they want, thanks to the lawyers and judge tied to the case. <span id="more-800"></span> A symposium, &ldquo;Toward the Future: A constitutional right to community services&rdquo; is coming to Atlanta. This is a chance to talk to the judge presiding over the case, the last living plaintiff, and other experts in disability law. Everyone who is a care giver or the disabled themselves should come to this symposium. We need to keep up to date on what is happening in disability law so that we never have to fight &ldquo;ugly&rdquo; laws ever again. Information about the symposium can be found at this website. We will keep you up to date on this symposium as it comes up in the calendar so you can fit it into your schedule.   This is an awesome opportunity to see and hear what happened in a landmark civil rights case in the United States. It is sad that ten years ago there were laws in place to make sure the disabled had to live in nursing homes and away from loved ones or the community. These laws, created by land owners, home associations and others tried to control where the disabled lived and how they lived their lives. The communities didn&#8217;t want to see people in wheelchairs, walkers, or other implements because they were &ldquo;ugly&rdquo; and detracted from neighborhoods and malls. These people felt that nursing homes were the ideal place to live out the remainder of your life if you were disabled. There was no need to leave the nursing home or to live anywhere else. The Olmstead Act changed the landscape of civil rights in the state of Georgia by allowing the disabled to live anywhere they wanted regardless of any local laws.   It is our job to watch over our civil rights so that they are not trampled by those that hate the disabled. African Americans are very aware of how important it is to stay on top of civil rights issues because they directly effect their day to day lives. As an example, insurance companies have been caught &ldquo;red lining&rdquo; neighborhoods that had minorities and dramatically increased their rates. The disability community as a whole has to fight these kinds of attacks on our civil rights. That means we all need to get involved and keep in touch with our elected officials as well as each other. Spinal Cord Resources Network has comment sections for each article exactly for the reason to get your ideas out to the media and each other. This is something all disabled people need to do. Elected officials that are able bodied don&#8217;t understand what we are up against until we call or write to let them know. Things like the ugly laws in Georgia will never change until those in the Olmstead group did something about it and demanded their rights. Everyone pitching in will make the difference that we are all looking for.</p>
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		<title>Senator Kennedy Dies</title>
		<link>http://www.spinalcordresources.com/2009/08/senator-kennedy-dies/</link>
		<comments>http://www.spinalcordresources.com/2009/08/senator-kennedy-dies/#comments</comments>
		<pubDate>Mon, 31 Aug 2009 19:17:18 +0000</pubDate>
		<dc:creator>ghgeorge</dc:creator>
				<category><![CDATA[General]]></category>
		<category><![CDATA[Law Center]]></category>
		<category><![CDATA[Roaring Mouse (advocacy)]]></category>
		<category><![CDATA[ADA]]></category>
		<category><![CDATA[bigotry]]></category>
		<category><![CDATA[congress]]></category>
		<category><![CDATA[disabilities]]></category>
		<category><![CDATA[disabled]]></category>
		<category><![CDATA[fair housing]]></category>
		<category><![CDATA[job discrimination]]></category>
		<category><![CDATA[legislation]]></category>

		<guid isPermaLink="false">http://www.spinalcordresources.com/?p=764</guid>
		<description><![CDATA[
One of the longest sitting senators in history has died. Mr. Kennedy was always a champion of the disabled and pushed legislation through for the disabled in education and was instrumental in getting the Americans with Disabilities Act (ADA) pushed through the senate. Many of us would not have a place to call home or [...]]]></description>
			<content:encoded><![CDATA[<p>
<input width="64" type="image" height="93" align="left" src="http://www.spinalcordresources.com/wp-content/uploads/image/Flag.jpg" />One of the longest sitting senators in history has died. Mr. Kennedy was always a champion of the disabled and pushed legislation through for the disabled in education and was instrumental in getting the Americans with Disabilities Act (ADA) pushed through the senate. Many of us would not have a place to call home or a had place to go to work without this law. Very few of us actually call or write congress as most people think that it is a waste of time and that there is too much behind the scenes negotiating. <span id="more-764"></span>Spinal Cord Resources does not believe that and the types of legislation that Ted Kennedy voted for and helped to get through compromise committees show that one person can make a tremendous impact on how America treats her disabled community. While the constitution guarantees rights for all it took additional laws to force schools to be physically accessible tot he disabled. .Most building would not be accessible by those in wheelchairs or walkers if the ADA was not the law of the land. There are still places in virtually all cities that the disabled cannot get into hot because it is hard or expensive, but because of those that hate the disabled. From the 1940&#8217;s through the 1970&#8217;s &quot;ugly&quot; laws made sure that the disabled lived in nursing homes a long way from those that didn&#8217;t want to see them. Malls and other building were made with steps so that the disabled could not get in. Many single family homes have steps that are not required in the plans so that the disabled could not buy them. Laws like the ADA changed all of that and now we have a court system that works with us to make life safe and worth living.</p>
<p>If the many laws that Mr. Kennedy championed never became laws, we would all be living in a much different America. The Senator proved that one person could make a major difference in congress and America. We at SCRN ask you our readers to call or write your congressmen to let them know how you feel about the issues of the day. Most probably believe that Washington D.C. is too impenetrable or that no one wants to hear from them. Nothing is further from the truth and Senator Kennedy proved it every day. We called our congressman about two weeks ago to get information about a town hall meeting and to discuss our medical system. The person on the phone was helpful and sent to a another person who listened to what we had to say and asked good questions back. This is not the way indifferent people work, these folks want to do the right thing and the only way they know how is to listen to you. It is hoped that this death gives you a few moments to think about what our government provides to us and what can be done better. Sure things are frustrating and everything may not go your way but that is not a reason to give up. The disabled have usually had to deal with way more than a bad day and we all need to do our part. Democracy is not a spectator sport and Senator Kennedy was there to make the important votes, even when he was very sick for the last year of his life. Lets all take the opportunity to do better than we have before, help those around us and let your officials that you pay know what is on your mind. That way we all win with a better country and you knowing that you helped to make a difference &#8211; just like Ted did for all those years in the senate.</p>
<p>&nbsp;</p>
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		<title>Medical insurance changes on the way</title>
		<link>http://www.spinalcordresources.com/2009/08/medical-insurance-changes-on-the-way/</link>
		<comments>http://www.spinalcordresources.com/2009/08/medical-insurance-changes-on-the-way/#comments</comments>
		<pubDate>Tue, 25 Aug 2009 14:45:23 +0000</pubDate>
		<dc:creator>ghgeorge</dc:creator>
				<category><![CDATA[Law Center]]></category>
		<category><![CDATA[Roaring Mouse (advocacy)]]></category>
		<category><![CDATA[congress]]></category>
		<category><![CDATA[insurance]]></category>
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		<category><![CDATA[Medicare]]></category>

		<guid isPermaLink="false">http://www.spinalcordresources.com/?p=749</guid>
		<description><![CDATA[The Department of Health and Human Services has developed a website to educate the public on the new medical insurance bill going through congress now. Pundits on the left and right have been discussing this  bill for the last two months but no one has taken the time to actually write down what to [...]]]></description>
			<content:encoded><![CDATA[<p style="margin-bottom: 0in;"><img width="64" height="85" align="left" alt="" src="http://www.spinalcordresources.com/wp-content/uploads/image/Scale.jpg" />The Department of Health and Human Services has developed a website to educate the public on the new medical insurance bill going through congress now. Pundits on the left and right have been discussing this  bill for the last two months but no one has taken the time to actually write down what to expect from the changes to our health insurance. Regardless of where you stand on the issue changes must be made because medical costs are rising faster than we are able to pay for them. While most Americans do not appear to want a government run health care system, we do pay significantly more per patient than Britain, Canada or Switzerland. <span id="more-749"></span> We expect that the latest and greatest drugs and procedures will be used when older, well established procedures work just as well. Those alternate procedures tend to cost a fraction of the latest and greatest, dramatically ballooning our medical costs without seeing the same increase in life expectancy or positive results from procedures. Doctors need to have specific rules to follow so we get the type of care we all expect at a price we can afford. This will is going to be changed as it makes it&#8217;s way through the house and senate and we need to add our requirements in as well. To start this, we all need to read what will change and what will be removed from healthcare. That means we all need to read this and then call your congressman and senators so they know what we want. (Source: <a href="http://jfactivist.typepad.com/jfactivist/2009/08/hhs-how-health-insurance-reform-will-help-people-with-disabilities.html">JFActivist</a>)</p>
<p style="margin-bottom: 0in;">We have seen or read about the town hall meetings on healthcare and the yelling matches they have turned into. While it is easy to see why everyone is upset at the possible changes that will be made to our medical system, working to get things fixed is a better place to put your energy. We all want medical care that is affordable, safe and effective. Some stores like Walmart have made deals with the drug companies to reduce the cost of their medications and we should have the government do the same. The drug companies need to make money so they can research new drugs, but the spiraling costs are going to make it impossible for an of us to afford them. The disabled are in the worst possible situation because most are on SSDI and cannot afford the more expensive drugs with the already existing plan. Add that to the doughnut  hole and we have a need to do dramatic changes so that everyone has access to the drugs and services they need.</p>
<p style="margin-bottom: 0in;">Not changing anything is guaranteeing that thousands of people will die because they cannot afford their medication after hitting the doughnut hole. The new plan has worked out a deal for the drug companies to charge 50% of the cost while in the doughnut hole. That is a good place to start, but more work needs to be done. When you need to spend two thousand of your own dollars before you can get out of the hole and into catastrophic care something needs to be done. Most in SSDI cannot afford thousands of dollars let alone hundreds. The doughnut hole needs to be removed so that those that run out of benefits under medicare automatically move into catastrophic care without a giant outlay of money. People on heart medication only take it six months out of the year because they run out of benefits and don&#8217;t have the money to pay for it themselves. That is something worthy of being fixed and should be agreeable to everyone. No one should have to die before changes are made so that those that need medical care can get it at a price they can afford. Having world class care that we all can afford is a worthy endeavor we can all work toward.</p>
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