Many speech pathologists only work on the good work done by neurologists after they have made the diagnosis. My friend had misdiagnosed myastenia and numerous speech pathologists in rehab failed continously over a number of months to pick up or recognise the symptoms of myastenia. He then had a crisis and passed away. Speech pathologists very rarely think outside the square.
There is hope for MG, my son was 6 years old when he got really sick with Myasthenia Gravis, and he had the Thymectomy in 2006 since than he has been ok. Read his story on squidoo.com it's called "Bradley's Myasthenia Gravis", it will give you hope!
I urge everyone with mg to take a look at this woman blog and then you will have an understanding of what you are up agains Google her name and see for yourself. Freya ross .
Excellent Video. I am an SLP and just picked up a patient with this.....you really confirmed what I had suggested. Thank you! We need more of these(ideos) in practice.
Also have this. Was diagnosed about 8 weeks ago. First noticed Double Vision then slurring of my speech. Went to Dr. and he found or diagnosed it in a few luckydays. I did have a "Crisis" about two weeks ago and had to be air flighted to a much larger hosp. in NW PA. I was almost DOA due to respiratory failure.
I'm now under controlled meds and seem to be getting well from this last attack but also know this is a controlled disease and no real cure for it. Good Luck. :)
Many speech pathologists only work on the good work done by neurologists after they have made the diagnosis. My friend had misdiagnosed myastenia and numerous speech pathologists in rehab failed continously over a number of months to pick up or recognise the symptoms of myastenia. He then had a crisis and passed away. Speech pathologists very rarely think outside the square.
gollymutt 5 months ago
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There is hope for MG, my son was 6 years old when he got really sick with Myasthenia Gravis, and he had the Thymectomy in 2006 since than he has been ok. Read his story on squidoo.com it's called "Bradley's Myasthenia Gravis", it will give you hope!
ftuley 1 year ago
I urge everyone with mg to take a look at this woman blog and then you will have an understanding of what you are up agains Google her name and see for yourself. Freya ross .
ecobra169 1 year ago
Excellent Video. I am an SLP and just picked up a patient with this.....you really confirmed what I had suggested. Thank you! We need more of these(ideos) in practice.
Csteele814 1 year ago
okay. i have this condtion...
it really sucks.
i just started high school sounding like i need help.
and i do.
help?
haileybrew88 1 year ago
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Greetings,
Also have this. Was diagnosed about 8 weeks ago. First noticed Double Vision then slurring of my speech. Went to Dr. and he found or diagnosed it in a few luckydays. I did have a "Crisis" about two weeks ago and had to be air flighted to a much larger hosp. in NW PA. I was almost DOA due to respiratory failure.
I'm now under controlled meds and seem to be getting well from this last attack but also know this is a controlled disease and no real cure for it. Good Luck. :)
TheKaneGuy
thekaneguy 1 year ago
Excellent Video!!!
thekaneguy 1 year ago
I have this condition. I say condition because I hate the word DISEASE . it is so outdated .
rambohs 2 years ago 2
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OMG !!! hey is that you ?
I've been on video chat with this chick
I have a link to her dating profile @ DateHerSafe(`)com/profile?=0385
Howard3486 2 years ago