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The Stress and Emotions behind SS Disability
This thread is for those who feel they just need to express some of the feelings they have while waiting for their SS decision.
I have helped a few people get Social Security Disability and I must admit it becomes so hard to hear how they are suffering. They have no money, how will they pay their bills? They are in pain and need to see their doctor, what can be done? All these questions seem to be addressed to me all the time. Unfortunately I cannot always answer their questions, so I'm hoping everyone who has questions and positive answers come together on this thread and maybe we can help each other. I'm looking for positive feedback, I know sometimes there is not a whole lot that can be done, but lets do out best for the ones who are waiting and need someone to talk to and give them a positive outlook even if it is just for enough time to give them a good nights rests, or even a good afternoon. So to all of you out there with a pending case, this thread is for you. I am also going to start a thread at the "social chat" on this site. |
The Stress and Emotion of SS Disability
The paper work alone is enough to stress you out. We're here to help those who are suffering with the Social Security Disability Administration and just need someone to talk to. Everyone is invited to join in. Whether you are trying to get approved or trying to help someone, I hope we can give positive reinforcement to those who are struggling right now. Your stories are welcomed and I hope in some small way we can help.
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((hugs)) I am glad you are willing to be helpful. :hug: I have a question tho. Do you charge a fee if you get involved in helping someone file for SSDI? Are you a legal office or just a friendly helper who does this for free?
I was rare, my SSDI was easy. The place I worked for retired me, and filed the paper work for me. My retirement is caculated based on what I get from SSDI so its cheaper for them to get me on it. I didnt have a single hiccup. I helped a friend file years later and the folks at the small town local office were extremely helpful. They provided a person to sit down with her to help her fill out the paperwork and help her understand the follow thru and next step needed. Many folks dont know that the SS office will assign someone to help you if you ask. |
well let me be the first to jump in and to say thanks to you:hug:this is a real tough time for me(us)in every sense of the word(financially,physically,emotionally,etc).not knowing the "Unknown".:( cant get answer's .always on "Hold".but want to say again is a big thanks to "LegalMania" and others here.we may not have the answer to everyone question or problem,but this is a good place for us to hear,listen or just talk to others.its real rough "OutHere"when you feel alone.cause the mind will play "games"with you,and unfortunately there all negative:(.You'll have time when its difficult to get a good night sleep,lost of appitite,hard to concentrate on other things.your whole life as you once knew/had is now different.but i think with this "socialChat" here that "LegalMania" is putting together will help some
hope all will partake and take advantage of this;):hug: |
benefits
While I was waiting for my benefits, I had five surgeries with no insurance. All my savings for my whole life was used up. I am on dissability, and sad that I can't work, mad at all the agiencies involved and sick of waiting to talk to them on the phone. I have found the whole proceedure very difficult, and alot of people do indeed suffer. If you have no resourses, there is little a person can do. I borrowed to exist from my family. I receive medicade also, and have now been informed that will no longer exist, it was just instated this past April 2010. Now Where did that coverage go? I am on the phone writing letters once again. fun fun fun ginnie:(
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thank you
Thank you for a place to vent about this subject. ginnie
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Let's do our best together!
Thanks to legalmania for starting this thread. My father applied for social security disability June 2010 and was approved finally in Dec.2010 after months of sleepless nights and I want to share with others my family's story. My message to you all is to not let the worries get to you. Take time out to focus your energy on other things and let things be what they will be. I know it's easier said than done, but it's necessary for you and your family's well-being. We were so worried for the first three months that we were mentally exhausted asking ourselves "What if it get's denied..What if some info is missing..What if"
We got to the point where we said "That's it!We've done everything we can do so if it gets denied then it gets denied, all that would be left to do it to appeal..and if we have to appeal over and over again we'll do it if it comes down to it!" So we stopped worrying and let things run their course.. but ofcourse I do advise to be on top of the doctors/receptionists/nurses in charge of your case. Contact the medical examiner in charge of your case everytime you have to do a medical update(whether you have started taking new medicine, whether there's been a change in dosage quantity, whether you've seen a new doctor, whether you started taking therapy, anything). If you don't have a fax,get yourself one, it is a must. That way you have peace of mind that your info was received. Try to take all the right steps and remember to take things one step at a time. Paperwork is part of the process so don't get frustrated. Get all your things in order, ask many questions and you will have a better chance at getting approved. My advice would be to not leave everything up to others when it comes to your case. Take charge and have a positive outlook at the same time. Godbless and don't lose hope, even if you get denied just try and try again. You are not alone, so many people get denied the first time but you just have to re-strategize and just do it! Don't lose confidence in your case, only you know your condition, only you feel the pain so you must fight for it! and as a final note, always have god in your heart..he is the one fighting alongside with you and your loved ones. Big hugs and kisses to all of you going through this process. :grouphug: |
"Sakuranokaori"said something that i strongly agree with by having god in your heart.i got baptize on 10/10/10.i pray to him daily.and by joining a church it keeps me busy with there functions.good people and good fun:hug:;)
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I'm so glad to see people getting involved please let your stories become reality. Thank you for your time. Peace be with you.
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i filed back in august and am awaiting a reply. i am kind of worried that since i am not using a walker all the time now, i might be denied. but i am definitely not cured (MS) and basically get by on assistance, i don't think i could work more than a couple hours a day and that would depend on how the morning went.
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If you filed back in August then you should hear from the agency soon. Please let us know what happens we all care and want to give you all the support we can. http://www.ssa.gov/pubs/10029.html#part1 |
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To flip the coin a bit..........
I was very fortunate from most of the posters who post here when I applied for SSDI back in 2002. I had enough years at my job to fully retire, collect a pension and UE too boot! Prior to applying, I went to my local library & researched SSDI & SS attorney fees in my state. Therefore, I knew before hand the backlog length in my state (4-5 yrs) and I could do all the paperwork filing myself. Knew if necessary I could hire an attorney at the ALJ level if need be (which I ended up doing). I guess you could say, I was fully prepared of what to expect when I applied for SSDI. The only surprise for me was that I received a fully favorable decision based on the paperwork that I submitted from all my treating physicians with no help from any attorney. SS did not pay him the $5000+ as I did all the work. The only thing my attorney did, was show up at the ALJ hearing which I paid him OOP ($250). :D I really feel for all the people here who are not as fortunate as I was during their time of waiting. Trying to collect SSI & SSDI can be really financial draining for a lot of folks. :grouphug: http://img689.imageshack.us/img689/8072/148322.gif |
Dear Legal Mania
Hello, I vented the other day. You may know about this, I do not. I applied for and received medicade since last april 10. This has now been taken away starting this Jan. The exact sentance stated "You are not eligible for dcf Medicaid because ssa found you to be eligible for ssi medicaid." There was no explaination that I could understand nor do I know all processing. I am lost. I was dumped on the phone 3 times after a wait of 40 minutes each. I wrote back asking for my caseworker to call me RIGHT away. No answer, so I don't know whats happening. I feel sick in my stomach, as it has been such an effort up until this point. I thought my work was over and I could heal from my last surgery. I am fed up and tired. Help please people, legal aid,so I can rest. I need response so I can sleep. love to all and Yes I God in my heart as so many of your od:hug::hug::hug:ginnie
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I literally left work on Xmas eve in 09 knowing I wasent coming back, my neuropathy had gotten to the point that I was dangerous to myself and my co-workers, I was a electrician, I did talk to my employer about trying something different but was pretty much told I was a electrician and that was that, I was not upset about it becasue I knew my body was giving out
I applied for SSDI, had all the functional papers sent to my doctors, called them to make sure they were filled out, and new testing I had done I faxed it to my caseworker, literally flooded her with it, five months later I got the award letter, am I glad I go it?, yes I am, but I wish I were still able to work instead of spending my days sitting at home not being able to drive and being in pain, but for all those still trying,,stay the course, keep trying, |
dear mz
no I was not lucky to recieve a favorable decision the first few rounds. I was not able to do any of the paperwork on my own, even though I wanted to. There was a trust from my mother that played hell with what the agencies had for its rules. I had to spend the money for the attorney, as this trust existed at the time. I do not think after this experience I would advise any parent to leave a trust to a child having medical issues. My mother tried to help me as she knew before she died that I was having medical problems. This trust complicated all matters in the tens of degrees. I was not allowed to keep my familys' trust. I was required to use all assets and go broke before I was able to receive my benefits. All my parents savings were required to be used and that was not hard to do with 7 surgeries. The whole process is lousy to go through lawyer or not. People who are sick and injured have so much more on their plate to deal with. When you are in pain it is hard to do anything at all much less have to yak with all these agencies. Even when you have a real case, real dissability, it is not easy. Just venting again to day, since I am writing letters and sending certified mail again. ginnie:(
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thinking of you
Don I was the one who spoke out about the test. That EMG you have to do soon. Are you sure your doctor said there was no other test you could do?. Some how I did manage to get through all these surgeries without having that test. There are others that can be done maybe. I just hate to think of anyone going through that unless there was no other option. I choose another doctor and changed directions mid stride because I am so stubborn. I did't like shots as a kid. I hid behind the couch, and hid behind the chairs. I held on to the furnature while they dragged me away. Nope not for me, I just don't want to. The good lord knows me quite well. I am asigned an extra guardian angel, just to let the other one take a break from me. I do not think my doctors were prepared for me! Good luck in which every decision you make, and I hope the results turn out with your best interest at heart. :hug:g:hug:innie
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Here is the neurological listing on the Soc. Security website for MS:
http://www.ssa.gov/disability/profes...dult.htm#11.09 Multiple sclerosis Note: you will have to scroll back and forth to find all of this info. IF you "meet" these requirements and it "shows" in your medical records, you automatically qualify for disability. The KEY is.................your doctor MUST make sure that it accurately states this in your medical records -- OR a Social Security doctor can ascertain this from an examination. |
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Hi don
Hi and I got your post through the e-mail, got lost again on which post. I understand about you wanting to put your faith in your doctors, that they know best for you. I don't know about that sometimes. Each doctor approachs problems differently. I still would run for the hills and check to see what other solutions may present with another opinion. I have been through alot and delt with all those needles like we all do. I still turned down this test. God bless you don, I will pray for you. ginnie:hug:
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Dejibo was very clear in the post.......already approved for SSDI |
"Ginnie" that little bit what you said just made my night:Wave-Hello:its not how much you say as to "whatYousaid" .now im getting another good night sleep:wink::Thanx:
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Someone that I helped get benefits a few years back, called me very upset. She told me her benefits were being stopped in March because she no longer was available for SSI. I told here to call the SSI local office and find out why, there was no explanation in the letter. The SSI administration said they had nothing in their system that showed her benefits were stopping. So I asked her if she could fax me the letter. In receiving the letter, I noticed my name at the top with her address and SS#. Because I was the representative someone put my name as the claimant. Even though they made this error she still has to file an appeal so her benefits won't stop, until we straighten this out. This is just some of the emotions and stress of the SS administration. So when you get a letter make sure you keep it make copies and don't ignore it if it's a mistake, because even though it is totally their fault she still has to prove they made that mistake.
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I know this has been said before probably. I don't understand why SSA, SSDI, SSI and most any other so called public assistance program whether it is state funded or federally funded has to fight tooth and nail to keep people from getting help. They don't give a hoot if you are loosing everything you worked for all your life or can't afford to eat. They don't care if your lights are going to be cut off. They don't seem to realize that when a person becomes disabled, that persons bills are not put on hold. They keep coming and coming and a person has got to survive somehow. Take SSDI, that money is not theirs. It was paid in by the person applying for it and they are bound and determined that the person is not going to get it without a long drawn out battle royal and sometimes not even then. All the so called "lawmakers" in Washington who were elected by these people to help them and protect their rights and property. But yet and still, these elected officials let one of their own organizations cause this terrible nightmare for the people who gave them their cushy job in the first place. It just don't make sense.
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because politicians are part of the elite and serve them and we are the common swill who should accede to their wisdom. in other words they are bought and paid for by corporate america and every dollar you get is one less dollar for them. they want it all.
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I got a phone call today from my clients District Manager. She apologized for the error. She said it was corrected and that my client should get a letter from the agency, within a couple of weeks. So it pays to go over peoples heads. It's the way I have always gotten things done, when I couldn't get anywhere with an agent. Thank you AJS for your quick response. I told her about this site and she said she would check it out. It will be good to have a good DM on the site.
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back and witchy again
So This past week I had to get a lawyer for my benefits again. This past week I was denied food stamps because I did not have $2,700.00 for this home that is in trust to me. I ran out of money in 09 and applied and recieved medicaid and months later a resonable amout of food stamps. The rules of medicaid state you may not have that much money in your possesson, no can I work to earn it. If I could earn it I would pay it. My son paid my taxes and they cut out my food stamps because I do not have the money for taxes. Well I don't have the money for food eithor. I am being treated like SH__. I worked 30 years. I can't help what happened to me regarding my finances. My health cost all that two generations had. This same gov. does not give me enough to live in my current home Now I have to fight one part of my family to let me move from here. I have to take my family to court over this same trust. One funny....On friday, I got some mail from DCF. I refused to open it and ruin my super bowl sunday. I am giving it to the lawyer on monday. DCF want to do this by phone with two of their agents and just me, no way....I want help with an attoney on my side. Why am I having to do all this anyway, somebody remind me...ginnie:mad:
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Hi Legal Mania
I did put in a new squack today, thank you for replying to me directly in your post. I Did indeed go to both offices in person and waited in long lines, and neithor agency would pull my information up on their PC, to find out was going on in my case. Each agency sent me to the other agency, so I am driving repetedly back and for between SS office and medicaid office. The both of them refused me help. So I got :mad::mad::mad:and got my former attorney to help me. He was the good soul who helped me to get before a judge. My families trust confused all three acencies. I cannot tell you how many copies I have made of this document that they cannot keep track of. Evidently neithor agency talks to the other. I am also having to go to court over this same trust with my family. I do not receive enough in benefits to keep a paid for home. This home is in trust to me, only while I live in it. It is a long icky story. I could not pay my taxes, flat out. My son had to and they took my food stamps away. I had less money so they took my food away. What is going on? Ginnie :(:confused::mad:
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hi gennie,sorry i dont have any advice but just to let you know that someone here is listening.as you have read from my post and how you responed to my, you to know what and how my situation is very similar to yours.just met a lady in my church who asked for our prayers.when she began to tell her story it was what we all are going thru .its her knee she having problem with but all the red tape she going thru and being denied this and that .she worried about her finances.now checks or money coming in.how many of us are out there who are hurting and have no one to turn to:confused::( who can help us:(.....all i have is "the good lord" my faith and the good people here.like "Gennie",Rlj1959,and of course "LegalMania":hug:
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Hi legal mania
Thank you for your response, I will be back in the attorneys office today. DCF wants an interview by phone with two of them against me. NO WAY. I will have the law in front of me through my attorney. I know that right now, I cannot do the research this would require. My BP soared, 225/100 with dealing with it. I had to get the help or go crazy. My son will pay my fee. In changing from DCF to SSID something went wrong. I will find out for sure just what can be done. thanks ginnie
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