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To let go, you need to do the opposite of fighting and resisting. You need to

let go of your demands and expectations for how life should be and make peace

with the way life is.

~~Bill Ferguson~~

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To let go, you need to do the opposite of fighting and resisting. You need to

let go of your demands and expectations for how life should be and make peace

with the way life is.

~~Bill Ferguson~~

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To let go, you need to do the opposite of fighting and resisting. You need to

let go of your demands and expectations for how life should be and make peace

with the way life is.

~~Bill Ferguson~~

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  • 4 weeks later...
Guest guest

Janice,

I live alone too with one cat and one dog. It has it's ups and downs, this week it's mostly down.

corky

(no subject)

Thank you all you you on the group have already been a big help and now with the respounse from my email it is even better. Its nice to have some one to talk to. Living with 2 dogs and 1 cat they won't answer me. love to all janice Please visit our homepage at http://members.xoom.com/AChallengersYou will find information, recipes, before and after pictures.To contact the list owner please send mail to lindag@...Visit our 2000 Train Tour Site - http://www.brunnet.net/k & l/web_site_train_tour/actraintour.htm

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Guest guest

Janice,

I live alone too with one cat and one dog. It has it's ups and downs, this week it's mostly down.

corky

(no subject)

Thank you all you you on the group have already been a big help and now with the respounse from my email it is even better. Its nice to have some one to talk to. Living with 2 dogs and 1 cat they won't answer me. love to all janice Please visit our homepage at http://members.xoom.com/AChallengersYou will find information, recipes, before and after pictures.To contact the list owner please send mail to lindag@...Visit our 2000 Train Tour Site - http://www.brunnet.net/k & l/web_site_train_tour/actraintour.htm

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  • 1 year later...

My 9 year old son had his CI evaluation done at Boston Children's

Hospital in mid-July. We got their decision about 3 weeks later that

Ben was a good candidate for CI. Because the surgeon, Dr. Licameli

was away for a couple of weeks, Ben's surgery was scheduled for Oct.

18. We didn't want it in September because we wanted him to get a

good start at school before being out for 7 days. Ben's CI was

hooked up last week. He has Dr. Marilyn Neault for his audiologist.

She is incredible with Ben. It has been one week since the hook-up

and Ben is starting to make sense of what he is hearing. He said

that his brain is having an argument with his implant trying to make

sense of the sounds it is hearing.

Good luck.

> This is a qustion for anyone who has had an CI done at Childrens

Hosp in

> Boston. they feel it is time to proceed with a Ci for my 9yo

daughter. Being

> a bit overwhelmed I forgot to ask about how long it takes from

this inital

> decision to actually getting a surgery date. I would assume it will

be a

> while , but just wondering what any of you have experienced there.

> Thanks,

>

>

>

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My 9 year old son had his CI evaluation done at Boston Children's

Hospital in mid-July. We got their decision about 3 weeks later that

Ben was a good candidate for CI. Because the surgeon, Dr. Licameli

was away for a couple of weeks, Ben's surgery was scheduled for Oct.

18. We didn't want it in September because we wanted him to get a

good start at school before being out for 7 days. Ben's CI was

hooked up last week. He has Dr. Marilyn Neault for his audiologist.

She is incredible with Ben. It has been one week since the hook-up

and Ben is starting to make sense of what he is hearing. He said

that his brain is having an argument with his implant trying to make

sense of the sounds it is hearing.

Good luck.

> This is a qustion for anyone who has had an CI done at Childrens

Hosp in

> Boston. they feel it is time to proceed with a Ci for my 9yo

daughter. Being

> a bit overwhelmed I forgot to ask about how long it takes from

this inital

> decision to actually getting a surgery date. I would assume it will

be a

> while , but just wondering what any of you have experienced there.

> Thanks,

>

>

>

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  • 2 months later...

Hey

We have had much the same situation in the past just reverse the ears. We

are now in the process of talking to the C.I. center to implant her right

ear. However, should my daughter loose the rest of her hearing in her left

before the implant I have thought I would have to revert to a written form

of communication for the short term. Does your county offer CART (computer

assisted note taking) for the classroom. For a short term educational

solution that might work. At home, we have used Cued Speech in the past

when my daughter was unaided but she does not read it well at all now so we

have thought that we might have to revert to a lip reading and writing

system.

If I wanted something to happen quickly in my county, I would call the

Exceptional Children program facilitator and explain the situation and

request an IEP meeting ASAP.

Hope these thoughts help, we my be in your situation one day, but my

daughter is only 7 and as yet her reading skills could not support a written

system at school.

Regards

Martha Soltani

Sara's Mom severe/profound hl (Connexin 26) bi lat odicon digifocus II

superpower ha (

(no subject)

>

> I need some major help and suggestions. My 9yo daughter will be

> implanted in 2 weeks. She has a profound loss in the left and a

progressive

> loss in the rt, treated the past few months with prednisone with good

effect,

> but knew she couldn't stay on it forever. She was basically at 50-70 dbl

in

> the rt ear when we decided to implant her in Nov. Dec 18 she lost about 10

> dbl in most freq.( still on prednisone). Last week she lost 10-20 more

dbl

> now at 70-80 dbl and she came off the prednisone the next day to avoid any

> complications with the surgery.

> Well Tuesday we again noticed more problems with her hearing, a big

> change in just 1 weekend, she is mainstreamed in a reg 4th grade class

uses

> an fm system, knows very liitle ASL and is now having great dificulty

hearing

> the teacher even withthe fm, I am even noticing her having trouble hearing

me

> at home. Well her hearing has dropped another 5-10 dbl in a week. Now at

> 75-90 dbl, and they feel they have done just about everything they can

with

> her hearing aid.

> I know this is why she is getting an implant, but at this rate I don't

> know how much (if any) residual hearing she will have left in the next 6

> weeks when the implant is done and finally turned on. Also they were

going

> to implant the left ear that has never had any measurable hearing, but now

> are asking me about just doing the rt because it has the most recent

hearing.

> If so or if she looses it all in the next few weeks my question is How

do

> we communicate with her and what about school!! She has always been

totally

> oral and because this has occured in 1 year only lip reads a little.

What

> do I do with her?

> Any suggestions would be great because needless to say I think I am going

to

> loose my mind in all this. Oh one other thing how do you get the school

to

> get services in place VERY quickly if she is suddenly totally deaf or I go

> along with implanting her rt ear. We are thinking about an

i-communicator

> and/or a 1:1 aid for her.

> thank you for any help,

>

>

>

>

>

>

>

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Hey

We have had much the same situation in the past just reverse the ears. We

are now in the process of talking to the C.I. center to implant her right

ear. However, should my daughter loose the rest of her hearing in her left

before the implant I have thought I would have to revert to a written form

of communication for the short term. Does your county offer CART (computer

assisted note taking) for the classroom. For a short term educational

solution that might work. At home, we have used Cued Speech in the past

when my daughter was unaided but she does not read it well at all now so we

have thought that we might have to revert to a lip reading and writing

system.

If I wanted something to happen quickly in my county, I would call the

Exceptional Children program facilitator and explain the situation and

request an IEP meeting ASAP.

Hope these thoughts help, we my be in your situation one day, but my

daughter is only 7 and as yet her reading skills could not support a written

system at school.

Regards

Martha Soltani

Sara's Mom severe/profound hl (Connexin 26) bi lat odicon digifocus II

superpower ha (

(no subject)

>

> I need some major help and suggestions. My 9yo daughter will be

> implanted in 2 weeks. She has a profound loss in the left and a

progressive

> loss in the rt, treated the past few months with prednisone with good

effect,

> but knew she couldn't stay on it forever. She was basically at 50-70 dbl

in

> the rt ear when we decided to implant her in Nov. Dec 18 she lost about 10

> dbl in most freq.( still on prednisone). Last week she lost 10-20 more

dbl

> now at 70-80 dbl and she came off the prednisone the next day to avoid any

> complications with the surgery.

> Well Tuesday we again noticed more problems with her hearing, a big

> change in just 1 weekend, she is mainstreamed in a reg 4th grade class

uses

> an fm system, knows very liitle ASL and is now having great dificulty

hearing

> the teacher even withthe fm, I am even noticing her having trouble hearing

me

> at home. Well her hearing has dropped another 5-10 dbl in a week. Now at

> 75-90 dbl, and they feel they have done just about everything they can

with

> her hearing aid.

> I know this is why she is getting an implant, but at this rate I don't

> know how much (if any) residual hearing she will have left in the next 6

> weeks when the implant is done and finally turned on. Also they were

going

> to implant the left ear that has never had any measurable hearing, but now

> are asking me about just doing the rt because it has the most recent

hearing.

> If so or if she looses it all in the next few weeks my question is How

do

> we communicate with her and what about school!! She has always been

totally

> oral and because this has occured in 1 year only lip reads a little.

What

> do I do with her?

> Any suggestions would be great because needless to say I think I am going

to

> loose my mind in all this. Oh one other thing how do you get the school

to

> get services in place VERY quickly if she is suddenly totally deaf or I go

> along with implanting her rt ear. We are thinking about an

i-communicator

> and/or a 1:1 aid for her.

> thank you for any help,

>

>

>

>

>

>

>

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Hey

We have had much the same situation in the past just reverse the ears. We

are now in the process of talking to the C.I. center to implant her right

ear. However, should my daughter loose the rest of her hearing in her left

before the implant I have thought I would have to revert to a written form

of communication for the short term. Does your county offer CART (computer

assisted note taking) for the classroom. For a short term educational

solution that might work. At home, we have used Cued Speech in the past

when my daughter was unaided but she does not read it well at all now so we

have thought that we might have to revert to a lip reading and writing

system.

If I wanted something to happen quickly in my county, I would call the

Exceptional Children program facilitator and explain the situation and

request an IEP meeting ASAP.

Hope these thoughts help, we my be in your situation one day, but my

daughter is only 7 and as yet her reading skills could not support a written

system at school.

Regards

Martha Soltani

Sara's Mom severe/profound hl (Connexin 26) bi lat odicon digifocus II

superpower ha (

(no subject)

>

> I need some major help and suggestions. My 9yo daughter will be

> implanted in 2 weeks. She has a profound loss in the left and a

progressive

> loss in the rt, treated the past few months with prednisone with good

effect,

> but knew she couldn't stay on it forever. She was basically at 50-70 dbl

in

> the rt ear when we decided to implant her in Nov. Dec 18 she lost about 10

> dbl in most freq.( still on prednisone). Last week she lost 10-20 more

dbl

> now at 70-80 dbl and she came off the prednisone the next day to avoid any

> complications with the surgery.

> Well Tuesday we again noticed more problems with her hearing, a big

> change in just 1 weekend, she is mainstreamed in a reg 4th grade class

uses

> an fm system, knows very liitle ASL and is now having great dificulty

hearing

> the teacher even withthe fm, I am even noticing her having trouble hearing

me

> at home. Well her hearing has dropped another 5-10 dbl in a week. Now at

> 75-90 dbl, and they feel they have done just about everything they can

with

> her hearing aid.

> I know this is why she is getting an implant, but at this rate I don't

> know how much (if any) residual hearing she will have left in the next 6

> weeks when the implant is done and finally turned on. Also they were

going

> to implant the left ear that has never had any measurable hearing, but now

> are asking me about just doing the rt because it has the most recent

hearing.

> If so or if she looses it all in the next few weeks my question is How

do

> we communicate with her and what about school!! She has always been

totally

> oral and because this has occured in 1 year only lip reads a little.

What

> do I do with her?

> Any suggestions would be great because needless to say I think I am going

to

> loose my mind in all this. Oh one other thing how do you get the school

to

> get services in place VERY quickly if she is suddenly totally deaf or I go

> along with implanting her rt ear. We are thinking about an

i-communicator

> and/or a 1:1 aid for her.

> thank you for any help,

>

>

>

>

>

>

>

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  • 2 years later...
  • 3 months later...

Hi I'm , new to this group. Last week, I had a severe bout of depression, followed by shortness of breath, and increased heartrate. After 4 days, I started to read some labels I hadn't read for a while, including by long-time used hair conditioner, some Kroger brand cooking oil, and Country Crock margarine. My conditioner had wheat germ oil in it, Kroger's oil is nothing but soybean, and the margarine had something in it too that I shouldn't have. I eliminated these things, and low and behold, I started to feel better. When I was first diagnosed with celiac, I was experiencing what I thought were panic attacks, shortness of breath, and chest pains. The Drs. never commented on my symptoms, connecting them to celiac, but after going GF, they disappeared. It just goes to show ME that, i need to read everything all the time, in order to stay GF. I also have to watch family members, so not to get any

crosscontamination at home.

My 2 cents

My mother gets that and she has mitral valve prolapse. I don't know if she has celiac.

Trudy in CA

-------------- Original message --------------

hello i am jennie and i am wondering if anyone has ever experienced increased heart rate with fatigue as part of reaction thanks for anyone who can help

jennie in NC__________________________________________________

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Hi I'm , new to this group. Last week, I had a severe bout of depression, followed by shortness of breath, and increased heartrate. After 4 days, I started to read some labels I hadn't read for a while, including by long-time used hair conditioner, some Kroger brand cooking oil, and Country Crock margarine. My conditioner had wheat germ oil in it, Kroger's oil is nothing but soybean, and the margarine had something in it too that I shouldn't have. I eliminated these things, and low and behold, I started to feel better. When I was first diagnosed with celiac, I was experiencing what I thought were panic attacks, shortness of breath, and chest pains. The Drs. never commented on my symptoms, connecting them to celiac, but after going GF, they disappeared. It just goes to show ME that, i need to read everything all the time, in order to stay GF. I also have to watch family members, so not to get any

crosscontamination at home.

My 2 cents

My mother gets that and she has mitral valve prolapse. I don't know if she has celiac.

Trudy in CA

-------------- Original message --------------

hello i am jennie and i am wondering if anyone has ever experienced increased heart rate with fatigue as part of reaction thanks for anyone who can help

jennie in NC__________________________________________________

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Maybe it's the name?!?!?  :)

(too - with almost the exact same symptoms!)

On Wed, 21 Sep 2005 07:03:36 -0700 (PDT), lisa you wrote

> Hi  I'm , new to this group.  Last week, I had a severe bout of depression, followed by shortness of breath, and increased heartrate. After 4 days, I started to read some labels I hadn't read for a while, including by long-time used hair conditioner, some Kroger brand cooking oil, and Country Crock margarine.  My conditioner had wheat germ oil in it, Kroger's oil is nothing but soybean, and the margarine had something in it too that I shouldn't have.  I eliminated these things, and low and behold, I started to feel  better.  When I was first diagnosed with celiac, I was experiencing what I thought were panic attacks, shortness of breath, and chest pains.  The Drs. never commented on my symptoms,  connecting them to celiac, but after going GF, they disappeared.   It just goes to show ME that, i need to read everything all the time, in order to stay GF.  I also have to watch family members, so not to get any crosscontamination at home.  >   > My 2 cents >

> >

> My mother gets that and she has mitral valve prolapse.  I don't know if she has celiac. >   > Trudy in CA >   -------------- Original message -------------- >

>  hello   i am jennie  and i am wondering if anyone has ever experienced increased heart rate   with fatigue as part of reaction    thanks for anyone who can help    >   > jennie   in NC

> __________________________________________________

>

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Maybe it's the name?!?!?  :)

(too - with almost the exact same symptoms!)

On Wed, 21 Sep 2005 07:03:36 -0700 (PDT), lisa you wrote

> Hi  I'm , new to this group.  Last week, I had a severe bout of depression, followed by shortness of breath, and increased heartrate. After 4 days, I started to read some labels I hadn't read for a while, including by long-time used hair conditioner, some Kroger brand cooking oil, and Country Crock margarine.  My conditioner had wheat germ oil in it, Kroger's oil is nothing but soybean, and the margarine had something in it too that I shouldn't have.  I eliminated these things, and low and behold, I started to feel  better.  When I was first diagnosed with celiac, I was experiencing what I thought were panic attacks, shortness of breath, and chest pains.  The Drs. never commented on my symptoms,  connecting them to celiac, but after going GF, they disappeared.   It just goes to show ME that, i need to read everything all the time, in order to stay GF.  I also have to watch family members, so not to get any crosscontamination at home.  >   > My 2 cents >

> >

> My mother gets that and she has mitral valve prolapse.  I don't know if she has celiac. >   > Trudy in CA >   -------------- Original message -------------- >

>  hello   i am jennie  and i am wondering if anyone has ever experienced increased heart rate   with fatigue as part of reaction    thanks for anyone who can help    >   > jennie   in NC

> __________________________________________________

>

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  • 4 years later...

Hi These are my sisters Vara results from over 6 weeks ago. I am adding the reverse t3. Can someone tell me her ratio. She is already treating ferritin, vitd and b12.TSH 2.1 mU/L (0.40-4.00)> Free T4 16 pmol/L (10-20)> Free T3 5.4 pmol/L (2.6-6.8)> Anti-Thyroglobilin Ab 26 U/mL (< 60) Anti- Thyroid Peroxidase Ab 74 U/mL (< 60)Reverse T3 567 pmol/L (170-450)Sky

Win 1 of 4 Sony home entertainment packs thanks to Yahoo!7. Enter now.

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