Any longhaulers successful getting Social Security Disability or SSI?
Any one here that has been diagnosed with long Covid been successful in getting SSI OR SSDI? I would like to hear about your journey... its been since the end of September, 2023 and I am still having problems with the after effect of LONGCOVID. I have been officially diagnosed with it so I am thinking in terms of applying for long covid disability. thoughts?
Interested in more discussions like this? Go to the Post-COVID Recovery & COVID-19 Support Group.
Just a couple of suggestions from a prior SSA employee: If your medical condition is not clear cut, write a journal of how your medical issues affect your daily life. Just a couple of day's worth should be sufficient. Start with when you get up in the morning and document all your activities and how your illness played a role.
For financial assistance provided to someone applying for SSI: Pay for things that are not required for daily life. For instance, pay the phone bill, internet bill, cablevision rather than pay the electric bill or the rent. Don't give cash on a regular basis. "Infrequent and irregular" financial assistance is generally acceptable.
The appeals process for SSA is a very long process. Too few administrative law judges to handle all the appeals.
I wish you all good luck. It's hard.
Donna
What are you doing now for work? I have been a long hauler since 11/2020 and I just can’t work I have changed jobs 3 times and never worked a full year. I wish a lawyer would take us all as a case for disability.
I am working as a grocery bagger/cart getter and at self checkout in a small grocery store. Town population of 16,000. 3 days a week, bagger shifts 4 hours, self checkout 6 hours. Minimum wage. After about 2-3 hours of each shift I am overheating, my internal thermometer is still broken. My legs, back and feet hurt. I am feeling tired, SOB and headache begins. Just trying to do this is exhausting. When more customers come up, my anxiety increases, head gets full feeling, ringing increases. My word finding and hearing gets muffled. I smile and banter with customers, inside I am not doing well.
It's been a month. I sleep poorly every night from the beginning of this PCS, my days off I am exhausted.
It has to be done. I can't trust myself to work in the medical field.
Reading, writing and concentrating is exhausting and I don't comprehend or remember a lot.
Sorry to ramble.
Going to try a nap before my 4 pm shift.
If you find that lawyer, let me know.
A malpractice suit would be good way to go.
I am not working. Last time I worked back on September 26, 2023, I picked up the Covid from a customer that had a high viral load and I have not been back since due to having Covid for 3 weeks, then pulmonary and fatigue and other problems that keep dragging on. I understand why you cant work, It is a lot! I am barely scraping by and I am living on cc's mostly.
It would be nice to see if a lawyer could help us.
I literally have tears bc I too did the same thing and had to file bankruptcy. I couldn’t keep up with payments bc the more you owe the higher the payment and that crept up on me. I have fatigue, fibromyalgia, sensory neuropathy (that’s is what they said when my toes turn a purple color), migraines, I’m sure more it’s hard to keep track. I’m sick now and this is the first time I’ve been sick since Covid however I’ve had Covid 5 times. I work in a healthcare facility and can’t escape all these germs with our immune system being compromised. If anyone else would like to chime in if they have approved disability and who they used let us know please!! I’m not giving up on this bc we need to be able to pace ourselves.