Guest guest Posted August 23, 2000 Report Share Posted August 23, 2000 Dear All: Please take this in the manner it was written. I in no way mean to hurt anyone's feeling and hope you all see the humor in this...otherwise it is totally unbelievable. I have finally figured out the Social Security Administration. Due to the ADA they have to hire Disabled Individuals also. That is great, everyone deserves a chance at a job, but you would think they would think twice about the position they give them...apparently the ones deciding who is disabled and who is not were hired under the ADA (mentally challenged). This is how I came to my conclusion. I received a letter today from the SSI. Now was awarded his initial SSI, beginning at birth, in an unbelievable 22 days. We applied Feb. 4 and received our approval letter on Feb. 26th. However the following is the first three paragraphs of a letter accompanied by a 10 page questionnaire << " E. 's Social Security Disability Case file has been sent to the Federal Disability Determination Services in Baltimore, land for medical development and evaluation. After reviewing the claim, we find that we need more information about daily activities and/or pain allegations. Please attempt to answer all the questions on the enclosed form in as much detail as possible and avoid single word answers. The information you provide will help our agency make a final decision on the case. This form should be returned within 10 calendar days from the date of this letter, in the self-addressed, postage paid envelope provided. Failure to do so may result in a determination being made based on the evidence in file. " >> Now believe it or not I sent in the other routine papers a month ago explaining how is paralyzed from the waist down, 24 hour a day humidified oxygen dependent, is G-Tube fed, and has had his trachea and esophagus surgically separated to prevent aspiration pneumonias and bacterial respiratory infections. This surgery has left him Non-vocal, and with the trache as the only airway (he cannot breathe thru his nose or mouth) he requires constant suctioning to keep this airway clear. All these situations are permanent (Unless God intervenes). WHAT else could they possible need to determine that is disabled. Even a child could figure it out with what I sent already and just looking at his medical records they got. Any one with any sense or smarts knows that spinal cord damage is irreversible, that a cure has yet to be found. You know I have to find some humor in this or the ignorance and stupidity level at which the Government agencies function would really PISS me off. Hope everyone is having a much better day!!! Love, huggs, and prayers, Haydee (Nana to , 8 years old w/Spina Bifida, ACM II, Hydrocephalus w/VP Shunt, Tethered Cord, Syringomyelia w/Syrinx @ c1-c2, G-Tube fed, (totally NPO), Swallowing Coordination Disorder, Neurogenic Bladder, ARDS (Lung Failure 3/30/97, 33 days on ECMO (total lung bypass), 50 days in a Coma, 60 days on life support, 24 HR-Humidified Oxygen Dependent, Radical Tracheostomy w/total loss of Vocal Cord Use, Resistant Pseudomonas, Paralyzed from the Waist Down, 18 Surgeries, Asthma, Severe Latex Allergy, Allergy to many Medications, Adhesives, and tons of other stuff, Posterior Fossa Decompression, Opening of the Dura, No Graft, c1-c2 Laminectomy, March 2, 1999, so far so good and getting better and stronger every day!!! With Such a Wonderful Love of Life and one crazzzzzy Nana (dx'd so far with Lupus, Hypothyroidism, GERDS, IBS, Sleep Apnea, Severe Edema) living right outside Baton Rouge, Louisiana) 's Web Page~~~~> The Story http://www.pressenter.com/~chip/joshua.htm Quote Link to comment Share on other sites More sharing options...
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