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Re: Come in if you live in PA and benefitted from EI
I don't know wtf happened with all that weird text on the top (I guess Bump frowns upon typing something in Word and then copy/pasting it to the webform?)
And no, I don't know how to make a link clicky. Help!
Yes, I did also write a lengthy letter to my state rep. (I promise, I wrote it! This English teacher doesn't plagarize, tyvm).
I knew most other people who aren't directly affected by this issue wouldn't bother taking the time to do that, so sharing the simple petition (on facebook and here) seemed like a great way to still get the word out and encourage my friends to help in SOME way.
Yes, I did also write a lengthy letter to my state rep. (I promise, I wrote it! This English teacher doesn't plagarize, tyvm).
I knew most other people who aren't directly affected by this issue wouldn't bother taking the time to do that, so sharing the simple petition (on facebook and here) seemed like a great way to still get the word out and encourage my friends to help in SOME way.
I actually agree totally with your friend about the helpfulness of EI with Apraxia. It was "sort of useful" to us in that they first mentioned the possibility of Apraxia and pointed us in the right direction to get the "real" help (private PROMPT therapy) we needed. When it became apparent that our DD was more than just a "late talker", the only "help" we got from our pedi was to tell us to call EI. Unfortunately, I think that is often the norm in Pediatrics around here with developmental issues. She didn't ever suggest an eval from a private SLP, or seeing a dev pedi (as we finally did when DD turned 3). If we had just called EI as our pedi instructed, only to be told DD didn't qualify, I probably would have gone on thinking DD must be "fine" for a good many more months or a year!
Each speech therapist we had through EI was truly subpar - and I really did my homework to try to get the best ones available. Even the "best" one we had cancelled at the last minute for just about every other session. So yeah, I definitely have my complaints about EI. However, there are other people out there who A) don't have private insurance that will help pay for private therapy (our does not whatsoever),
cannot afford to pay for private therapy out of pocket, and C) don't have the knowledge/time to seek out other methods for funding, i.e. grants, medical assisance. The EI program is critical for these apraxic kiddos, as obviously some therapy would be better than nothing... which is what they'd get if these proposed changes are passed.
I've posted on this board before, although very infrequently, and you have answered my questions before - and almost always with a pessimistic outlook. (Obviously I don't remember the exact words, but you didn't seem to think I had any chance of winning a fair hearing against Gateway Health Plan [MA] last February, but I did - twice! You then were less than enthusiastic/congratulatory when I posted that I'd won. I'm not looking to pick a fight, but just know that that's how I've remembered you.) I was, quite frankly, offended to be accused of plagiarism, and I really think you owed me an apology for the questioning of my authenticity. However, I *get* that as a frequent poster and mod, you would see that kind of thing here often, and that you wouldn't remember me. You've obviously had a long road and are a wealth of knowledge for the posters on this board... but how about a little more seeing the glass as half full?
Again, not looking for a net battle here. Best of luck to you!