24 Search Results for "phone"

• Dedicated to WorkComp1

  • From: chrisym
  • Description:

    For Workcom1:

     

    I have been trying to get a Radio (online mostly) Interview established so Ron's story can be exposed.  We appear to be waiting on the "reporter" and I think we need to come together as a community does to help one another.  Ron needs our help and each of us could do 1 small act towards the goal of helping Ron each week, think what we might be able to accomplish.  We all mostly are challenged ourselves and are limited by what we can do.  But how many of us here can make at least 1 phone call or 1 email.

    With that said I have contacted today RTIR.  So far the few stations I left a msg for have not returned my message.  RTIR came highly recommended by a PR company I found the PR company on the internet but they would not pursue Ron's story for fear of liability.  I am waiting on a call back from RTIR.  The link to their site is http://www.rtironline.com/blog/_WebPages/ContactUs.html. 

    Let's pray for Ron, and ask God what would he have us do....see if anything comes back to you and if so then act.  You want to call me you can do so at 512-496-6294.

    Blessings,

    Christine Messaros

  • Blog post
  • 2 days ago
  • Views: 771

• Muscle Therapy Device

  • From: heidiheidiho
  • Description:

    Does anyone know where I might find an EMG-Triggered Stimulation device?  The Care ETS unit, from CareRehab, is no longer available. 

    I need a device that combines a biofeedback (EMG) target threshold with muscle stimulation (FES or ETS) that kicks in to force the contraction of my arm beyond what I am able to perform actively.  I'm trying to work on muscle re-education in my lower arm and hand due to a trauma injury at the elbow. 

    Any information (product name, supplier name, phone #, e-mail address) would be appreciated. Please email me at heidiheidelberg@gmail.com.

  • Blog post
  • 1 month ago
  • Views: 23
  • Not yet rated

• the realization of being disab

  • From: gregg45365
  • Description:

    Most people take their bodies for granted.Everyday,they wake and rise from their beds and approch another day.A day of walking,bending,sometimes running,or kneeling.Never thinking about it,just doing it without thought.Lately,I've lost another one of those abilities.One that everyone does and never thinks about.For a time,I've always been able to ambulate with a cane,or crutch.This past few weeks it's become ever painful to to even that.It's so hard not to be so bummed about it.My wife and I were sitting our youngest grandson.He's 7 months old,and crawls pretty good.My wife was busy and our grandson was heading towards the desk where there are cords and wires for the phone and computer.I went to pick him up before he got into the wires and as I put my walker aside,I reached down for him and that fast he was out of reach,I again grabed my walker,took another step,went for him and he was out of reach again.I thought to myself...Man,a 7 month old baby is faster than I am.At that point I realized just how bad my condition was and that I'd never be able to have that special one on one relationship with my grandson like most are lucky to have.I can never be able to watch him without anyone else there ever.I can nolonger be unexceptable about my disability.The things we all take for granted everyday is no longer an option for me.I miss working,being able to do the things I used to love.Working on my own cars,walking along the river to a secluded spot to fish and take in nature.Taking my grandkids to the park and run after them,wressltling with them,or just walking with them.I am so bummed about my life as a disabled person.

  • Blog post
  • 3 months ago
  • Views: 64
  • Not yet rated

• GOVERNMENT PROPOSED HEALTHCARE

  • From: inside222
  • Description:

    So, why is it that Harry Reid and President Obama are pushing so hard and fast for this proposed Healthcare plan to pass without proper review by all parties?  Is it because because Harry Reid is not comfortable with his own State's Worker's Compensation System?  I would deduct YES.  Because I know of a case which I blogged about ( workcomp1 -  You can enter it in the search field with this title:This Man's Worker's comp Malpractice)

    ) that is still not being paid the proper attention to and has not garnered the attention of any media outlets as of yet, even with numerous phone calls, letters and emails, personal face to face meetings and letters from the editor of The Disability Digest...

    ...SCARY is the only word I can come up with, especially since the media is in such a fervor to find out about such menial news such as the Dr. that Michael Jackson used (which does not affect any residents of NV--other than he lived here and had a practice).  But this case certainly affects anybody that may get hurt on the job, YET the media CHOOSES NOT to pay attention to it in order to inform the general public of what could happen if they get hurt on the job as this gentleman did.

    So, once again, in this public forum, I will ask that the Media outlets in Nevada (more specifically Las Vegas) would please get in touch with this man so his case can be properly investigated and he gets the treatment appropriate for his disability which has not been appropriately & timely by the NV worker's compensation system thus far.  

    If this news does not sit well with any readers of this story, I would ask that you please (sooner than later) contact your Congress-people & Representatives, AS WELL as your local Media outlets, so that this will be brought to the forefront and help all the injured/disabled  workers experiencing a similar situation with this defunct Worker's Compensation system in Nevada.

     

    Thanks for Reading & PLEASE Rate this Blog,

     

    Inside222

  • Blog post
  • 3 months ago
  • Views: 743

• Bankrupkcty

  • From: lacey
  • Description:
    1. Here are some of the things we will be talking about: Chapter 7 may eliminate all your credit debts. Chapter 7 works best for those who: Have lots of unsecured debt, Here are some debts u can let go. All Credit Cards, Medical Bills, Ulilty bills, Personal loans and, pay day loans. Do u have alot of money: In order to qualify for chapter 7, you must meet certain income requirements. A local Bankuptcy Attorney can help u with your finances. U can go on line under Legal Aide, this lawyers go by your income. They do probono and go by your income. www. Legal Aide Helpers. The difference between Chapter 7 and Chapter 13: Chapter 7 Bankruptcy is often appropiate for people who have: fairly little property except basic necessities like furniture an clothing, little to no money left after paying basic monthly expenses each month. Chapter 13 Bankruptcy is often the answer for people with: alot of equity in a home or another piece of RealEstate or property; and or: a regular income and the ability to pay living expenses, but have fallen behind in all your bills, Just think no more phone calls........Sincerly Lacey
  • Blog post
  • 4 months ago
  • Views: 96

• Resource for Obtaining SSDI -

  • From: chrisym
  • Description:

    All:

    I know for a fact, that although I am disabled there are many with stories much more tragic than mine.

    In know way is this intended as gloating, but to be of help!

    I went through Allsup, no attorney, and received my SSDI within months of applying and received my SSDI retroactive payment within 6 months of losing my job to disability.

    After reading all these terrible stories on DD, I ask why was I approved with no problem?  I believe it is due to Allsup.  Please go t

  • 6 months ago
  • Views: 378
  • Forum: Fibromaylgi...

• Disability Approval

  • From: rhondaperreten
  • Description:

    Hello Sue and everyone here!

    I too am new to "the group".

    The most important thing in responding to your questions are the state you live in. Every state is different. I live in Texas, and at the age of 40 asked 3 attorneys to represent me in my effort to receive disability benefits. Every single one of them refused, saying I would not qualify. Well, not giving up and thinking, if I do nothing it's a 100% guarantee I will not get them. If I apply, it's 50/50. Even my friends said not to waste

  • 6 months ago
  • Views: 349
  • Forum: Fibromaylgi...

• kiki07430

  • Views: 39
  • Since: 7 months ago

• SSA new hiring initiative

  • From: diana53
  • Description:

    Welcome to my World! ( or should I say our World now)

    I believe in using every resource I can to fix my unstable financial situation and have it work around my disabilitiy issues.

    They say that what the mind can conjour up, the rest of you should be able to acheive it--ok --well something like that.

    Any way, I have my website up worldofdisability.com--and I put it together myself with the help of GoDaddy--at this point I could become a spokesperson for GoDaddy.  But I told them I had other goals ( ya right)

    So, my first project is to get those of you who might be intersted in going to work --to help you.

    I am pointing in some information about what SSA is doing--

    I have a lot of work to do yet with the website but you can follow updaste on Twitter.com--there is a direct link from my homepage to my Twitter Page.

    I found out the other day that Florida beaches hace all terrain wheel chairs that you can use on their beaches  and so does California.

     

    I totally believe that fun is the root of all happiness, so go have some fun!

     

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    The Social Security Administration recently received funding to hire a significant number of employees throughout the country. This hiring initiative offers a unique opportunity for individuals with disabilities who have are ticket to work ticket holders and veterans who may want to get a job with SSA. These jobs will be at various skill levels including a number of entry-level positions. .

    SSA is recruiting employees to work in field offices and teleservice centers where they will assist the public by phone and in person with a wide variety of program related activities such as filing claims, applying for new or replacement Social Security cards and other types of inquiries.  SSA also is recruiting employees to work in Program Service Centers where they will process claims and to work in hearings offices in legal and paralegal positions.

    All across the United States; for example, some are in the 1,300 local SSA field offices or SSA hearings offices, some in the 37 teleservice centers nationwide, some in SSA’s 6 program service centers and some at SSA headquarters in the Baltimore area.

    If you are interested in working or no some one, do not hesitate calling us and we can walk you through the process. SSA has simplified the process for you. We do not charge for this service.

    Just go to our website  worldofdisability.com and go to the contact page –put in your information and we will contact you about out next meeting.

    Or you can email me at questions@worldofdisability.com

    This is a really great opportunity for you!

    World of Disability, LLC

    Let me know what else I can help you with--I have a cool contact page over on the website and I am slowwwlllyy

    getting better at this email thing--so put in your info if you want and i will send you updates.

    Take care

    Diana
    

     

     

     

     

     

     

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    SSA new hiring initiative.

    This is great for those of you who want to use your ticket to work and maybe try working again ( Up to you)

     

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  • Blog post
  • 7 months ago
  • Views: 172
  • Not yet rated

• Emergency Medicade

  • From: quinncornwall
  • Description:

    Dear Lynette..Hi ,My name is john.To get "emergency medicade" you have to go to your local Social Services Office and ask for a medicade application.If you don't know where it is..look in your phone book uner your county of residense and then Social Services, if you still can't find it look up under food stamps.They will be able to give you the number and address.I was told to apply for everything..Medicade,Financial aid and food stamps.Even if your denied the other stuff,at least you applied and maybe y

  • 8 months ago
  • Views: 122
  • Forum: Fibromaylgi...

• Contract Between Verizon and L

  • From: missionbeach
  • Description:

     

    For Those who need additional income or want to start your own business, please read.  This business is changing what was left of my life after FM struck!
    
    If you had the opportunity to get paid every month not only on your wireless bill but on thousands of other peopleswireless bills, would that interest you??

    9 months ago

  • Views: 103
  • Forum: Employers P...

• Update on My Progress-Great Ne

  • From: missionbeach
  • Description:

    It's been awhile since I posted.  It's been a rough and rocky road for me.  No whining though because I am sure there are many who have it worse.  I know that Brian at least, may have been wondering where I've been so I thought I'd post an update...

    Well, I thought that once I got my SSDI, things would be ok.  What I learned was although it was practically impossible to live on NOTHING, living on $856 a month isn't much better.  Yeah, I know.

    So, I started seriously searching for a way to make some money.  My website, although "monetized" as much as I can possibly "monetize" it, hasn't made any money.  If anything, with the cost of hosting, advertising, etc.  it has cost me money.  December offered me one thing and that was a little extra cash from the "Letter From Santa" website.  I took advantage of that and having found what I hoped would be "the ONE perfect opportunity", I took the big plunge and signed up.

    Since joining the business in mid December, I have helped 4 others start their own business and I have received bonus commissions enough to cover my expenses, so I am not quite in the "green" yet but when my residual starts coming in at the end of this month, I will be in profit, FINALLY!

    I have enjoyed so much success so far with this company that I added it to my website as THE BUSINESS that I recommended for people like me who needed to make income from home.  Of course, the site doesn't receive that much traffic, so it's no big advertiser for me but the info is there for anyone who needs it.  Since my main goal with the website has always been to help people with Fibromyalgia, I hope that it helps just one person who needs a way to make residual income.

    The business, for any who may be interested, is Lightyear Wireless.  This Fortune 500 Co. signed a contract with Verizon back in July, 2008 to offer wholesale Verizon Wireless Service, thus creating one of the most lucrative opportunities for home based businsess owners in the US.  I have an online wireless webstore where people can order wireless service online from their home, without the high pressure salespitch and noone is denied due to poor credit.  It's an amazing website and I only pay $49.99 a month for it.  (I will pay for it with the 5% increase that SSA gave us this year, so it's not money that was already in my budget)

    I worked real hard to promote it and was promoted from "Manager" to "Senior Manager" in less than a month!  That's a good thing because it raised my residual percentages that I receive on my customer's cell bills and my managers' webstores.  It's a long walk to my next promotion but I am working really hard on getting new customers.  It's really been a positive experience so far and I finally have some hope of actually owning a successful business, despite my disability.

    So, I am seeing, just maybe some light at the end of the tunnel.  I use safelists to promote it and spend a buck or two here and there for a solo ad.  So far, it converts well and practically sells itself, being that EVERYONE either has or wants a cell phone, they give you one for free and you can't go wrong with the #1 Wireless Provider in the Nation, Verizon.

    I hope that everyone is doing well.  With FM, there are usually more bad days than good but when some of the stress is off of me, I feel a little better.

    Take care, everyone and if you do need a way to start your own business, a real business and not a system, scam or gifting thing, I can recommend Lightyear Wireless so far.  Should that change, I'll be sure and post here about any negative things that I encounter.  I'll include a couple of links so you can check it out.  Oh, and I also was able to finally afford a cell phone again, because their rates are wholesale and pretty reasonable.  That helps because who in this world can live without a cell phone, right?  LOL! 

    Here's my online wireless store:

    http://bestcelldeal.mywirelessrep.com

    And here's a page where you can check out the business opportunity, plans, phones, and get more info, all in one spot. 

    http://bestcelldeal.mywirelessincome.com

    I hope this info helps anyone that needs it.  I know I was about to go insane with insecurity and worry prior to starting this business.   Ya'll don't forget about the Ultimate Fibromyalgia Resource Center for those who have FM.  The Forum adds about a member or two a week and you can also request prayer if you need it.  Sometimes it helps just to vent to someone who knows how you feel.

    The UFRC addy is http://www.missionbeachsouth.com

    The forum addy is http://fibromyalgia.forumotion.com

    God bless ya'll,

    Tammy Elaine

  • Blog post
  • 9 months ago
  • Views: 398
  • Not yet rated

• My fellow quad's it's time to

  • From: EricCerra
  • Description:

    Hello my name is Eric Cerra. And I just joined the disability Digest. I would like to share something with you if you're interested go to my website www.24hourtour.net/EricCerra

     

    Check this site out I just signed up for by all means I am not pushing this on the one but this is a way we can make money a good friend of mine Danny got me involved in this in order to make the money you want to be a buyer broker/or website owner. All the stores are on their are all reputable. And if you want to sign up great will make some money "it is not a scam". I just feel in my position I am not able to get out all the time and I shop online quite a bit. So why not get paid for shopping online. If you have any questions e-mail me ericcerra1965@live.com  and I'll give you my phone number.

  • Blog post
  • 9 months ago
  • Views: 148
  • Not yet rated

• Free Cell Phone With free mont

  • From: tootall71
  • Description:

    I stumbled across this web site while surfing the internet and thought it might be helpful. It's called "Safelink Wireless". I received a free cell phone along with 68 minutes every month for free. If you haven't heard you might want to check it out.It's not available nationwide yet, but it is available in Florida, Tenn., Mass.,and Virginia as of right now. 

    How to Qualify

    The process to qualify for Lifeline Service depends on the State you live in. In general, you may qualify if...

    1. You already participate in other State or Federal assistance program such as Federal Public Housing Assistance, Food Stamps and Medicaid.

       OR

    2. Your total household income is at or below 135% of the poverty guidelines set by your State and/or the Federal Government.

       AND

    3. No one in your household currently receives Lifeline Service through another phone carrier.
    4. You have a valid United States Postal Address. In order for us to ship you your free phone you must live at a residence that can receive mail from the US Post Office. Sorry, but P.O. Boxes cannot be accepted.

    In addition to meeting the guidelines above you will also be required to provide proof of your participation in an assistance program, or proof of your income level.

  • Blog post
  • 10 months ago
  • Views: 232
  • Not yet rated

• Grants

  • From: ministerhanks
  • Description:

    My name is Monty and it's good to be here today. It's my understanding there are some folks out there that would like to find a individual grant, Well there are many grants that you can apply for, but as always you have to know where to look.

    If you go to the (Foundation Center) or just go to your google search or other and enter foundation center.

    Once the search page pops up it should be right there. If not go to any library website and they will have the address. Look for the Grants for Individuals on line. It will cost you $ 9.95 per month or you can contact me at wfh2356@aol.com send me your name, email, phone, address, or just the state that you live in and, email, and the type of grant you desire. I can add a attachment to my email and send you some info.

    I know how hard it is to find grants for individuals. The only other way is to pay a grant writer at a nonprofit 501(c)(3). Most foundations give only to them. However, there are a few that will work with individuals.

    Do not give any foundation your SS Number, Bank Account, or Date of birth unless you know who you are dealing with. I had to pay by credit card to get access to the list of foundations in the Foundations Center Website.

    There are a few other places that I have good luck finding grants for individuals. One is on MSN Live Search, in fact it is better than google I found. This time type in Individual Foundation Grants or Individual Disability Foundation Grants and Yes it does make a difference how you word it...

    Well I have to run now, so if you need some help, just dial me up,,,

    Monty  wfh2356@aol.com

  • Blog post
  • 1 year ago
  • Views: 391
  • Not yet rated

• Baa Also gets a hug

  • From: BlackSheep
  • Description:
    Some favorite photos of what I stand to lose before the year is out. At one time, we took in abused and neglected farm animals. Dogs of course showed up as well. All our animals are castoffs and everyone - those who have passed on and those who are still with us - have been angels passing through our lives. At the very time we were going to apply for non-profit status, my husband suffered a massive heart attack in 2005 that left him disabled and a barely tolerable quality of life. Self-employed for most his life, he only gets SSI. I had growing health concerns of my own, but my doctor was able to carry me on knowing I was now the sole provider. The dream of a refuge for the neglected died the night of the heart attack. Our home - now is in default. Because in 2007 I was terminated. Reason: "no longer able competently perform my job." I have been a programmer for over 15 years. I knew my health was a growing concern: having CFS and fibro long before my husband's heart attack. But in 2006 those around me (including my employer) noticed other changes. Only my husband sought help, for I was in my first (and only) manic phase and I sensed no problems. My employer did, but never mentioned anything, yet that and more are in my files - never to see the light of day for fear of the fact the broke every employment law on the books (ones I never knew of and they never revealed to me). The changes involved those Cognitive and behavioral. Only until 2007 was it clear to me my ability to be productive was drawing to a close. And since that time, all has grown worse, with the added Dx of early onset Alzhiemer's/Dementia. That was a shock but it fits. In fact, on one scale of 1 to 8, I am now at 5. Last week I finally pulled the best of all: I got lost on my own property. True it was dusk, but I was so disoriented only the light of the house led me home. Added to all that, I am also a long-time sufferer of depression of over 30 years. Once a super-achiever (which brought on anorexia at 18), I still managed to graduate summa cum laude. But the shooting star soon burned out. I qualify for SSDI and in June I went (with no insurance) to my doctor to ask his advice as to whether I had a claim. He all but shouted "You have BEEN disabled!" He also advised me to apply for all categories applicable. In my case they are many, but the problem is that there is NO diagnostic evidence - only empirical and the word of my doctor. Because of caregiving duties, I missed more days at work than I cared to. The doctors ordered the usual MRI, EEG, EMG, et. al, but I canceled all for fear of losing a job I lost anyway. Joke is on me. I am now approaching 6 months since the initial filing. The stats are against me I know, and because of our financial situation, denial is not an option. Uninsured, I have no medications to control the fibro pain, the depression, the narcolepsy, the ADHD, and the rapid decrease in mental ability. In despair last March, I hate to admit I attempted suicide (not the first, but this one would have worked). I found the vessels in both wrists. No emotion, it was almost like some experiment. Only when I lost enough blood that I grew dizzy, cold and blue did the fear of living in Hell pull me back - THAT time. My fear is that when that denial letter comes it means that all is lost. The home, the animals that are left, no place to go and an end stage cardiac patient homeless. With that knowledge - and knowing so many are denied (even my husband was at first and he only has less than 1/2 of a functioning heart, with an EF of 20, and a prognosis of 3 to 5 years). I fear what I started in March this time I will finish because surely God cannot expect someone to endure this much loss and this much pain. DSS is useless. I was denied Medicaid - a sure sign of things to come. I applied immediately after I filed my SSDI claim. The mortgage company, notified before we were behind, did nothing for 60 days and then sent a letter for payment that was not possible. I paid one payment, but it was late and I was informed that the 'deal is off'. Foreclosure is their solution for troubled homeowners (Bank of America). Even HOPE NOW cannot offer any solutions other than CCCS. There is nothing to budget - no credit cards, no income (my IRA being exhausted months ago), I even ordered the house phone cut off. I canceled my life insurance. All is cut to the bare bones to no avail. Help from family is not an option - leave it at that. I have nowhere to turn and found this website (or rather the lessons on how to win a SSDI claim). I found it too late, I fear. I did everything right and tidy, but being uninsured means there is no updated or continued treatment to add weight to the claim. So much is at the discrection of those who know nothing. Pressured under an impossible workload, they rubberstamp most claims 'denied' just to get them out of their department and onto the next stage. I have seen three of their doctors: one psychologist (whose memory tests I failed), one medical doctor who spent 10 minutes and never said a word, and one psychiatrist whose accent was so strong, I spent the entire time saying "Can you repeat that?" She grew exasperated after 20 minutes, never even got to the crux of any of my 'section 12' issues and terminated the session. No more appointments are scheduled and from experience I know that I can now expect my denial in the next couple weeks. God help me. God help all of us in this boat. I see the pictures of what was, what could be, but reality sets in and I have lost all hope.
  • 1 year ago
  • Views: 95
  • Not yet rated

• My 140lb Lab Dodger

  • From: BlackSheep
  • Description:
    Some favorite photos of what I stand to lose before the year is out. At one time, we took in abused and neglected farm animals. Dogs of course showed up as well. All our animals are castoffs and everyone - those who have passed on and those who are still with us - have been angels passing through our lives. At the very time we were going to apply for non-profit status, my husband suffered a massive heart attack in 2005 that left him disabled and a barely tolerable quality of life. Self-employed for most his life, he only gets SSI. I had growing health concerns of my own, but my doctor was able to carry me on knowing I was now the sole provider. The dream of a refuge for the neglected died the night of the heart attack. Our home - now is in default. Because in 2007 I was terminated. Reason: "no longer able competently perform my job." I have been a programmer for over 15 years. I knew my health was a growing concern: having CFS and fibro long before my husband's heart attack. But in 2006 those around me (including my employer) noticed other changes. Only my husband sought help, for I was in my first (and only) manic phase and I sensed no problems. My employer did, but never mentioned anything, yet that and more are in my files - never to see the light of day for fear of the fact the broke every employment law on the books (ones I never knew of and they never revealed to me). The changes involved those Cognitive and behavioral. Only until 2007 was it clear to me my ability to be productive was drawing to a close. And since that time, all has grown worse, with the added Dx of early onset Alzhiemer's/Dementia. That was a shock but it fits. In fact, on one scale of 1 to 8, I am now at 5. Last week I finally pulled the best of all: I got lost on my own property. True it was dusk, but I was so disoriented only the light of the house led me home. Added to all that, I am also a long-time sufferer of depression of over 30 years. Once a super-achiever (which brought on anorexia at 18), I still managed to graduate summa cum laude. But the shooting star soon burned out. I qualify for SSDI and in June I went (with no insurance) to my doctor to ask his advice as to whether I had a claim. He all but shouted "You have BEEN disabled!" He also advised me to apply for all categories applicable. In my case they are many, but the problem is that there is NO diagnostic evidence - only empirical and the word of my doctor. Because of caregiving duties, I missed more days at work than I cared to. The doctors ordered the usual MRI, EEG, EMG, et. al, but I canceled all for fear of losing a job I lost anyway. Joke is on me. I am now approaching 6 months since the initial filing. The stats are against me I know, and because of our financial situation, denial is not an option. Uninsured, I have no medications to control the fibro pain, the depression, the narcolepsy, the ADHD, and the rapid decrease in mental ability. In despair last March, I hate to admit I attempted suicide (not the first, but this one would have worked). I found the vessels in both wrists. No emotion, it was almost like some experiment. Only when I lost enough blood that I grew dizzy, cold and blue did the fear of living in Hell pull me back - THAT time. My fear is that when that denial letter comes it means that all is lost. The home, the animals that are left, no place to go and an end stage cardiac patient homeless. With that knowledge - and knowing so many are denied (even my husband was at first and he only has less than 1/2 of a functioning heart, with an EF of 20, and a prognosis of 3 to 5 years). I fear what I started in March this time I will finish because surely God cannot expect someone to endure this much loss and this much pain. DSS is useless. I was denied Medicaid - a sure sign of things to come. I applied immediately after I filed my SSDI claim. The mortgage company, notified before we were behind, did nothing for 60 days and then sent a letter for payment that was not possible. I paid one payment, but it was late and I was informed that the 'deal is off'. Foreclosure is their solution for troubled homeowners (Bank of America). Even HOPE NOW cannot offer any solutions other than CCCS. There is nothing to budget - no credit cards, no income (my IRA being exhausted months ago), I even ordered the house phone cut off. I canceled my life insurance. All is cut to the bare bones to no avail. Help from family is not an option - leave it at that. I have nowhere to turn and found this website (or rather the lessons on how to win a SSDI claim). I found it too late, I fear. I did everything right and tidy, but being uninsured means there is no updated or continued treatment to add weight to the claim. So much is at the discrection of those who know nothing. Pressured under an impossible workload, they rubberstamp most claims 'denied' just to get them out of their department and onto the next stage. I have seen three of their doctors: one psychologist (whose memory tests I failed), one medical doctor who spent 10 minutes and never said a word, and one psychiatrist whose accent was so strong, I spent the entire time saying "Can you repeat that?" She grew exasperated after 20 minutes, never even got to the crux of any of my 'section 12' issues and terminated the session. No more appointments are scheduled and from experience I know that I can now expect my denial in the next couple weeks. God help me. God help all of us in this boat. I see the pictures of what was, what could be, but reality sets in and I have lost all hope.
  • 1 year ago
  • Views: 306
  • Not yet rated

• Our Home before all went south

  • From: BlackSheep
  • Description:
    Some favorite photos of what I stand to lose before the year is out. At one time, we took in abused and neglected farm animals. Dogs of course showed up as well. All our animals are castoffs and everyone - those who have passed on and those who are still with us - have been angels passing through our lives. At the very time we were going to apply for non-profit status, my husband suffered a massive heart attack in 2005 that left him disabled and a barely tolerable quality of life. Self-employed for most his life, he only gets SSI. I had growing health concerns of my own, but my doctor was able to carry me on knowing I was now the sole provider. The dream of a refuge for the neglected died the night of the heart attack. Our home - now is in default. Because in 2007 I was terminated. Reason: "no longer able competently perform my job." I have been a programmer for over 15 years. I knew my health was a growing concern: having CFS and fibro long before my husband's heart attack. But in 2006 those around me (including my employer) noticed other changes. Only my husband sought help, for I was in my first (and only) manic phase and I sensed no problems. My employer did, but never mentioned anything, yet that and more are in my files - never to see the light of day for fear of the fact the broke every employment law on the books (ones I never knew of and they never revealed to me). The changes involved those Cognitive and behavioral. Only until 2007 was it clear to me my ability to be productive was drawing to a close. And since that time, all has grown worse, with the added Dx of early onset Alzhiemer's/Dementia. That was a shock but it fits. In fact, on one scale of 1 to 8, I am now at 5. Last week I finally pulled the best of all: I got lost on my own property. True it was dusk, but I was so disoriented only the light of the house led me home. Added to all that, I am also a long-time sufferer of depression of over 30 years. Once a super-achiever (which brought on anorexia at 18), I still managed to graduate summa cum laude. But the shooting star soon burned out. I qualify for SSDI and in June I went (with no insurance) to my doctor to ask his advice as to whether I had a claim. He all but shouted "You have BEEN disabled!" He also advised me to apply for all categories applicable. In my case they are many, but the problem is that there is NO diagnostic evidence - only empirical and the word of my doctor. Because of caregiving duties, I missed more days at work than I cared to. The doctors ordered the usual MRI, EEG, EMG, et. al, but I canceled all for fear of losing a job I lost anyway. Joke is on me. I am now approaching 6 months since the initial filing. The stats are against me I know, and because of our financial situation, denial is not an option. Uninsured, I have no medications to control the fibro pain, the depression, the narcolepsy, the ADHD, and the rapid decrease in mental ability. In despair last March, I hate to admit I attempted suicide (not the first, but this one would have worked). I found the vessels in both wrists. No emotion, it was almost like some experiment. Only when I lost enough blood that I grew dizzy, cold and blue did the fear of living in Hell pull me back - THAT time. My fear is that when that denial letter comes it means that all is lost. The home, the animals that are left, no place to go and an end stage cardiac patient homeless. With that knowledge - and knowing so many are denied (even my husband was at first and he only has less than 1/2 of a functioning heart, with an EF of 20, and a prognosis of 3 to 5 years). I fear what I started in March this time I will finish because surely God cannot expect someone to endure this much loss and this much pain. DSS is useless. I was denied Medicaid - a sure sign of things to come. I applied immediately after I filed my SSDI claim. The mortgage company, notified before we were behind, did nothing for 60 days and then sent a letter for payment that was not possible. I paid one payment, but it was late and I was informed that the 'deal is off'. Foreclosure is their solution for troubled homeowners (Bank of America). Even HOPE NOW cannot offer any solutions other than CCCS. There is nothing to budget - no credit cards, no income (my IRA being exhausted months ago), I even ordered the house phone cut off. I canceled my life insurance. All is cut to the bare bones to no avail. Help from family is not an option - leave it at that. I have nowhere to turn and found this website (or rather the lessons on how to win a SSDI claim). I found it too late, I fear. I did everything right and tidy, but being uninsured means there is no updated or continued treatment to add weight to the claim. So much is at the discrection of those who know nothing. Pressured under an impossible workload, they rubberstamp most claims 'denied' just to get them out of their department and onto the next stage. I have seen three of their doctors: one psychologist (whose memory tests I failed), one medical doctor who spent 10 minutes and never said a word, and one psychiatrist whose accent was so strong, I spent the entire time saying "Can you repeat that?" She grew exasperated after 20 minutes, never even got to the crux of any of my 'section 12' issues and terminated the session. No more appointments are scheduled and from experience I know that I can now expect my denial in the next couple weeks. God help me. God help all of us in this boat. I see the pictures of what was, what could be, but reality sets in and I have lost all hope.
  • 1 year ago
  • Views: 149
  • Not yet rated

• BOOKING HOTEL FOR DISABLED TRA

  • From: gottitravel
  • Description:

    Booking Hotels-Helpful Hints for the disabled

    

    Few things can prove more disappointing or challenging for a disabled traveler than discovering that an allegedly accessible hotel room is anything but. Unfortunately, all too few lodgings have any real idea of what accessibility means, and while the United States is, no doubt, the leader in the access movement, the ADA (American with Disabilities Act) does still not guarantee that transportation and lodgings will adhere its requirements. Since businesses often claim that the law is vague, the interpretation of the ADA is constantly being interpreted in court.

    While such vague interpretations of access exist, a disabled traveler must act assertively to locate suitable lodgings. Here is a short list of helpful hints that will maximize your chances of booking a suitable room.

    1. Be wary of calling the 800 numbers for the hotel/motel chains. The phone reservationists who work these lines aren't often located anywhere near the hotel you're calling about, and they rarely have a clue about a room's accessibility. Call the hotel's direct number (which you can get from the 800 line) and ask to speak to the manager, who should be able to provide you with access info. Be specific about your requirements. How wide are the doors? Does the bathroom have a roll-in shower and grab bars? What about a handheld shower spray? No one knows your traveling needs better than you, so if you need a shower chair or TDD, it's up to you to ascertain if the hotel actually has them.

    Since hotels require a credit card to hold your room, be certain of your dates when making a reservation as cancellations can be costly. If you cancel, the hotel may keep all or part of the cost of your room. Every reservation should be confirmed in writing through a letter or FAX. If you're traveling overseas, send your message with the international wheelchair symbol on it to remind the hotel that a disabled person is heading their way.
    
    Want to lodge a complaint against a hotel or other facility governed under the ADA? Call the Department of Transportation at (800) 514-0301 (voice) or (800)514-0383 (TDD).

    The U.S. and many European nations demonstrate the most concern for access issues. The high-speed trains of Europe (specifically Britain, France) even provide accessible bathrooms aboard.

    Disability Digest Resource Page - http://www.thedisabilitydigest.com/Members.htm

  • Blog post
  • 1 year ago
  • Views: 288
  • Not yet rated

• How to Care for Yourself

  • From: geekygranny
  • Description:

    From The Arthritis Foundation

    (I think many of these would apply for everyone with a disability! - GG)

    Think there’s nothing you can do about arthritis? Great news! You can act right now. Some of the ideas here are simple, one-time actions. Others are first steps toward longer-term goals. All can directly or indirectly improve your health, outlook or pain level, and can generally make life with arthritis a little easier.

    • Pay attention to symptoms, see your doctor and get an accurate diagnosis

    If you have pain, stiffness or swelling in or around a joint for more than two weeks, it's time to see your doctor. These symptoms can develop suddenly or slowly. Only a doctor can tell if it's arthritis. But "you have arthritis" is not a diagnosis. Ask for a specific diagnosis of the type of arthritis you have. There are more than 100 types, each of which has different treatments. Getting the right treatment requires getting the right diagnosis.

    • Start early

    The earlier an accurate diagnosis is made and treatment started, the better. Early treatment can often mean less joint damage and less pain. Your doctor may recommend a combination of treatments that may include medication, weight management, exercise, use of heat or cold, and methods to protect your joints from further damage. See your doctor for an early diagnosis and immediate treatment plan!

    • Protect your joints

    Avoid excess stress on your joints. Use larger or stronger joints to carry things. Assistive devices can make tasks at home and work easier. Staying close to your recommended weight also helps relieve damaging pressure on hips and knees.

    • Get moving

    Exercise helps lessen pain, increases range of movement, reduces fatigue and helps you feel better overall. Your doctor, a physical therapist, or other specially trained health professionals can show you range-of-motion exercises and strengthening exercises that are good for arthritis. The Arthritis Foundation also offers water exercise and other classes. Contact your local office for details.

    • Tune in

    Listening to your favorite music can lighten your mood and may even help you to forget your pain – at least for a little while. Make a tape of your favorite upbeat tunes and listen to it when you need a lift.

    • Pick, pour or peel

    If you are looking for a tasty healthy treat, reach for an orange – or a tall glass of orange juice. Why? Recent research has shown the importance of vitamin C and other antioxidants in reducing the risk of osteoarthritis and its progression. Another bonus: oranges and other citrus fruits are good sources of folic acid, which can help alleviate the side effects of the arthritis drug methotrexate and reduce the risk of cardiovascular disease in women who have lupus.

    • Check out your options

    In the past two years, the FDA has approved several drugs for rheumatoid arthritis, osteoarthritis and other arthritis-related diseases. If your current medication isn’t working as well as you’d like – or if it’s causing unacceptable side effects – ask your doctor about these new treatment options. Check out the online drug guide and supplement guide.

    • Let yourself go

    On vacation, that is. Make yours a good one by remembering to bring extra medication, a spare prescription, insurance card, comfortable shoes, your doctor’s phone number and, of course, your camera.

    • Face facts.

    Learn something new about arthritis. Building an understanding of your disease is an important step in managing it. Start by ordering some of our free brochures.

    • Play in the dirt

    Buy the seeds for three of your favorite veggies or flowers and plant a garden. Digging in the dirt can be therapeutic for sore hands and can yield beautiful and fragrant – or delicious and nutritious – results.

    • Have a good laugh

    Read a book of jokes, rent a funny movie or watch your favorite sit-com or stand-up comedian. Laughing – even when you feel like crying from agony – can relax muscles, relieve pain and even boost your immune system.

    • Play it safe in the sun

    Protect yourself when you go out into the sun — wear sunglasses, a hat and sun screen. Some forms of arthritis, as well as certain medications, can leave you more vulnerable to the sun’s harmful rays.

    • Do Tell

    Take an opportunity to tell someone — co-worker, friend, and family member — about arthritis. Start with an interesting fact: Did you know that arthritis affects 46 million people? Then go from there. They’ll understand you – and the way arthritis affects your life – a little better. Or share your feelings with others who have arthritis on the Arthritis Foundation's message boards.

    • Resolve to reduce

    Lose weight. You won’t just look better, you’ll feel better, too. Why? Every extra pound you carry around translates to added stress to your knees and hips. Excess weight can mean more pain, no matter which form of arthritis you have. It can also contribute to and aggravate osteoarthritis, while increasing your risk of gout. Learn more in the Exercise Center.

    • Bone up

    Stock up on your favorite source of calcium. A diet rich in this important mineral can help decrease your risk of osteoporosis. If you don’t like drinking milk – or want some variety – try consuming more milk products, such as yogurt, cheese and ice cream. Or add powdered milk to puddings, gravies, shakes and other recipes. Other good sources of calcium: broccoli, salmon (with the bones) and kale.

    • Do drugs – the right way

    Take your medication just as your doctor prescribes. If you’re tempted to stop because you feel it’s not working or you believe it’s causing side effects, call your doctor first. It can take weeks – or even months – for the full benefits of a medication to become apparent, and some side effects ease over time. Stopping a medication abruptly may not only cause you to miss out on its benefits – in some cases it can be downright dangerous.

    • Begin with breakfast

    Put up the pastry and grab some fruit, fiber (like oatmeal) and a tall glass of water instead of coffee. Like you’ve always heard, a healthful breakfast is a great way to start the day. Our free brochure on diet and arthritis can tell you more about healthier eating.
    

    • Try this on for size

    It’s time to toss those fashionable, yet oh, so uncomfortable pumps that cramp your toes, rub your heels and squeeze your bunions. A well padded, well fitting shoe with plenty of room for your toes – and their imperfections – can make a world of difference in the way your feet (and the rest of you) feel.

    • Take a hike

    Choose your favorite spots (indoors and out) and make plans to walk them at least once a week. Walking is the ideal exercise for most people with arthritis. It burns calories, strengthens muscles and builds denser bones – all without jarring fragile joints. Want to know more about walking as exercise? Try our Walk with Ease II program.

    • Sit, soak and soothe

    A warm bath before bed can relieve muscle tension, ease aching joints and help you get a good night’s sleep. Try our free brochure on ways to manage your pain for more ideas.

    • Treat your muscles

    Find a certified massage therapist and treat yourself to a good rub down. The benefits vary from person to person but may include decreased pain and increased circulation, energy and flexibility. And besides, it just feels good.

    • Work smarter

    Do something that will make your job easier — check into working flex hours, telecommuting or working part-time. No matter where or when you work, take frequent breaks to stretch stiff joints and sore muscles. Visit the arthritis in the workplace section for more insights.

    • Fess up

    Be sure to tell your doctor about the medications you’re taking, both prescription and over the counter. Don’t forget to mention any nutritional supplements you’re taking, too. All medications – even natural ones – have the potential to cause side effects or to react adversely with each other.

    • Write away

    Keeping a journal is fun and therapeutic. Best of all, there are no rules. Write about your feelings, fears, frustrations and fun times. Write about things you’d never tell another living soul. Write about anything – or nothing in particular. Just write. Try our Wellness Journal for starters

    • Stretch your legs

    Stretching is a simple way to keep joints and muscles flexible. It relieves stress and can help enable you to maintain your daily activities. Try this to keep your calf muscles strong and flexible: Stand two feet from a wall, with your toes pointed inward palms against the wall. Keeping your knees straight and feet flat, lean forward onto your hands without bending at the waist. Feel your calf muscles pull and extend. Hold this position for 10 seconds, then gently push away from the wall. Repeat. There’s even more in our free brochures on exercise and arthritis.

    • Take the plunge

    Exercising in the water can build strength and increase range of motion, while the water’s buoyancy reduces wear and tear on sore joints. Check the local YMCA or call your local Arthritis Foundation office for an aquatic exercise program in your area.

    • Make a pack

    When joints are hot and inflamed, applying something cold can decrease pain and swelling by constricting blood vessels and preventing fluids from leaking into surrounding tissues. Our favorite ice pack: a bag of frozen peas or corn that can be molded to the shape of your body. Get more ideas in our free brochure on managing your pain.

    • Kick butt

    If only for a day, and then another … and another. Smoking can increase your risk of complications from lupus and rheumatoid arthritis. It can predispose you to osteoporosis. Also, if you have to undergo joint surgery, smoking can prolong your recovery.

    • Open your heart

    Select a group that holds a special place in your heart — the elderly, the homeless, animals — and volunteer with an organization that helps them. Or raise money for a cause you believe in. Helping others can be a great way to help you forget your own problems – or at least put them into perspective.

    • Enjoy Your Exercise

    Take the work out of working out. Sign up for a class that makes exercise fun – country line dancing, ballroom dancing, swimming, yoga or tai chi.

    • Play 20 questions

    Well, maybe not 20, but write down questions about your condition or your medications as you think of them. Prioritize them and slip them into your purse or wallet before your next doctor’s visit. When you see the doctor, you’ll have your top concerns at your fingertips.

    • Appeal to a higher power

    No one knows exactly how, but research is showing that spiritual belief and prayer can help people feel better physically and emotionally.

    • Turn the other cheek

    Looking good helps you feel good. If an arthritis-related condition or its treatment has caused a rash on or tightening or swelling of your face, check at the cosmetics counter of your local department store for tips or special products to camouflage these problems and give your cheeks a healthy looking glow.
    

  • Blog post
  • 1 year ago
  • Views: 127