goodness!

A few of my friends have suggested that I should go to Gallaudet after I finish my undergraduate. We'll see :)
Did you do your undergrad in Deaf Education also?

No...got my BA in Special Education from Arizona State University. You dont have to get two Deaf Ed degrees. I suggest to get a degree in a different field of education for your Master's so you can have more options to select when looking for jobs since NCLB requires teachers to be highly qualified in certain areas of education. I am highly qualified in three areas of education..general Special Ed, Elementary Ed and Deaf education.
 
No...got my BA in Special Education from Arizona State University. You dont have to get two Deaf Ed degrees. I suggest to get a degree in a different field of education for your Master's so you can have more options to select when looking for jobs since NCLB requires teachers to be highly qualified in certain areas of education. I am highly qualified in three areas of education..general Special Ed, Elementary Ed and Deaf education.

Thank you very much for your insight!
By doing my undergrad this way, I'll be getting two Bachelors...one in Deaf Ed and one in Art Ed...plus I'll get my certification in Elementary Ed...
I still have a good 4 years (or more!) to go...so I'm sure I'll start figuring out what I want to do for my masters when the time comes lol!
 
what is the cause of your hearing loss?
i go back this friday to see the specialist again...is it possible to have an autoimmune disorder without testing positive?
how did you cope with all of this? i'm finding myself retreating into a shell rather quickly...

There is no "this is it" answer for me, it is more a combination of things. I have been diagnosed with Meneire's disease, a catchall type of disease that is given when everything else is eliminated. It comes with vertigo, dizziness, tinnitus, hearing loss in varying degrees. I also seem to have a genetic link to early hearing loss. They seem to have given me a double whammy, at least that is what my ENT guy thinks.
I have also wondered about the autoimmune thing. I was tested and it came back negative. But, I have chronic iritis (inflammation of the iris) that my eye doctor swears is due to "something hinky" in the immune system. If you were to ask him, yes, it is possible. It could be at a stage where it does not register in the tests. But who knows?
As for coping? It ain't easy... Honestly, I am usually an upbeat person and don't let things get me down for long. I always try to look for the good things. All in all, there are just days that I will cry for no reason (yes, there is, I know that..but..). I call them my "pity parties" and they are needed.
What helps me the most is telling myself that it could be worse. Ok, so I am deaf when I take my ha off and speech sucks when I do have it on. There are others that deal with being deaf every day and have dealt with it for far longer. They don't sit around and mope about it..they get up and live. That is why I joined this forum. To help balance my life and learn. I could be dealing with a life threatening condition, be in constant pain, any number of things.
But, at the same time, for a person that has heard "normally" for half a century, it does suck..which is why I have opted for CI implantation. At this stage of the game, I don't really care if music sounds good anymore. I just want to be able to understand speech again. :Oops: mini pity party snuck in for a sec. I too, sometimes, crawl into a shell. In large crowds, more often than not and I think that is normal too. It lets go of the stress trying to speech read causes when so many people are around.
It all comes with the territory..you just have to learn to make the best of it as you don't really have a choice. As long as you have a support system and someone to talk to, you will do just fine. If a therapist helps, use one. A close friend can do wonders too. I am glad you are becoming more fluent with ASL, that will help too since you are around those that share that language. It all sounds like your life choices have been made for a reason, though you didn't know it at the time.
 
OK- to answer your question many autoimmune diseases are detected in a serum protein electrophoresis test or AB.

Coriticosteroids are "first line" of treatment for MANY AI diseases because of both the antiinflammatory and immunosuppression properties. If MD put you on them so see if it would help hamper acute episode of an AI disease it will help rule in, or rule out many.

Long term use of these only used when benefits outweight the risks, because of long term side effects of them. IE imunosuppression, water retention, insulin resistance, weakened strength of bones, cataracts. But there are those with relentless AI disorders or especially Organ Transplant patients that have to always take Corticosteroids.
 
There is no "this is it" answer for me, it is more a combination of things. I have been diagnosed with Meneire's disease, a catchall type of disease that is given when everything else is eliminated. It comes with vertigo, dizziness, tinnitus, hearing loss in varying degrees. I also seem to have a genetic link to early hearing loss. They seem to have given me a double whammy, at least that is what my ENT guy thinks.
I have also wondered about the autoimmune thing. I was tested and it came back negative. But, I have chronic iritis (inflammation of the iris) that my eye doctor swears is due to "something hinky" in the immune system. If you were to ask him, yes, it is possible. It could be at a stage where it does not register in the tests. But who knows?
As for coping? It ain't easy... Honestly, I am usually an upbeat person and don't let things get me down for long. I always try to look for the good things. All in all, there are just days that I will cry for no reason (yes, there is, I know that..but..). I call them my "pity parties" and they are needed.
What helps me the most is telling myself that it could be worse. Ok, so I am deaf when I take my ha off and speech sucks when I do have it on. There are others that deal with being deaf every day and have dealt with it for far longer. They don't sit around and mope about it..they get up and live. That is why I joined this forum. To help balance my life and learn. I could be dealing with a life threatening condition, be in constant pain, any number of things.
But, at the same time, for a person that has heard "normally" for half a century, it does suck..which is why I have opted for CI implantation. At this stage of the game, I don't really care if music sounds good anymore. I just want to be able to understand speech again. :Oops: mini pity party snuck in for a sec. I too, sometimes, crawl into a shell. In large crowds, more often than not and I think that is normal too. It lets go of the stress trying to speech read causes when so many people are around.
It all comes with the territory..you just have to learn to make the best of it as you don't really have a choice. As long as you have a support system and someone to talk to, you will do just fine. If a therapist helps, use one. A close friend can do wonders too. I am glad you are becoming more fluent with ASL, that will help too since you are around those that share that language. It all sounds like your life choices have been made for a reason, though you didn't know it at the time.

thats interesting you mentioned your iris...my otologist commented on the fact my pupils are really big...they react to light but not in the right way...like they remain really big...theyll shrink slightly, but not much.
anyway...i just want them to figure it out so i know what to expect...or to fix it. if i can expect it to get worse...then perhaps it won't be as much of a crush each time i go and find out that something else has happened lol...
thank you for the encouragement...i definitely agree with what you said...i needed to hear that from someone :) Thank you.
 
OK- to answer your question many autoimmune diseases are detected in a serum protein electrophoresis test or AB.

Coriticosteroids are "first line" of treatment for MANY AI diseases because of both the antiinflammatory and immunosuppression properties. If MD put you on them so see if it would help hamper acute episode of an AI disease it will help rule in, or rule out many.

Long term use of these only used when benefits outweight the risks, because of long term side effects of them. IE imunosuppression, water retention, insulin resistance, weakened strength of bones, cataracts. But there are those with relentless AI disorders or especially Organ Transplant patients that have to always take Corticosteroids.

would he put me on them (the steroids) even if all the tests come back negative? i mean i'm 22 years old...
what should i expect this friday if my hearing has gone down more...or even if it is staying put at the moment? what do you think he'll do? can he call it AI even if the tests are negative? what else could it be if it's not AI?
 
He might. It wouldn't do any harm if he tried like 4 week taper of prednisone. I do not know other pertinent medical history of yours to say 'no' to the idea. PM me if you wanna privately discuss medical info, k.
 
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