Still fighting for PLS/ALS claim. Going on 16 months now. I need to hear from anyone who has been approved for PLS and to see how it was worded. I would love a copy of someone's award letter and what office granted the claim. My paperwork is all over the map - predominantly upper motor neuron als, PLS/Lou Gehrigs disease. I definitely do not have classical but a variant there of.
Please help - I am in desperate need of help. Just a couple people who have been successful would be of grat benefit here.
Please help - I am in desperate need of help. Just a couple people who have been successful would be of grat benefit here.