Your questions about disability benefits for Hidradenitis Suppurativa, answered!
Tune in on Facebook live on Tuesday, April 24th at 7:00 PM Eastern to view our presentation on disability benefits for Hidradenitis Suppurativa from attorneys at the law firm of Benjamin Levine – disability specialists based in Michigan but serving clients nation wide.
If you have any questions for the attorneys before the presentation begins, comment here or e-mail them to detroit@hopeforhs.org.
Hannah Gittings-Hamilton
For some reason no matter what I attempt to play the recorded session on I get almost no volume whatsoever. I can vaguely hear someone’s voice but I don’t know what they’re saying. Is it possible to get a subtitled version or a transcript of this event? Or perhaps someone could just tell me something I may not know about fixing the volume issue! Any suggestions would be happily accepted!
Hope for HS
There were some technical difficulties during the broadcast and the sound didn’t come through for the first few minutes. Try skipping ahead in the broadcast about 5 minutes and see if you can hear then.
tanya holcolm
i wish i could of been there, i would of had a lot of other questions. i wish i would of found this website or organization years ago! im sooooo over my hs. im always in a lot of pain!
NA
Please leave this video up for reference and individuals who might stumble across it. Minus the technical difficulties at beginning, it was very helpful and informative!
Jimanique Wilson
I have condition always in pain get very depressed don’t want to get out of bed. Trying to seek advice on applying for disability. I live in Detroit, Mi. Ty.
Amanda
Jimanique, I feel the same way and not that far from you ,I’m in Warren. May as well be a million miles today tho because I just can’t get myself to do anything and I’m going through a flare up of ha this time mainly my arm pits..hurts so bad. I’m tired of pcp just giving me same ol antibiotics, but I don’t know where else I can go with Medicaid. And I’m scared to death of that humira crap I see on tv, not worth all the risks I’ve heard and read about that drug. Nice to no I’m not alone but I wish no one had deal with this b.s or other diseases.