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Amen!

> Thank You

>

> To all:

>  

> I've only been a member for a short time and I find myself looking forward

> to reading your messages each and every day.  Some I relate to others I

> appreciate...I just want to say thank you in advance for your time,

> thoughts and concerns.. What I  like is the feeling that I can express

> myself .. that your listening...This is the best thing that could have

> possibly happen to me...

>  

> Lynn

> _____

>

>

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  • 6 months later...

Debbie,

I never found anything that relieved the itching. I tried

atarax, with a break after several months. I couldn't tell the

difference. I took Questran for a month, since I noticed no

effect and it was more of a bother than popping a pill, I

stopped without giving it a long term chance (at that point I

didn't believe it would work for me).

My itching seemed to subside when my bilirubin got high (>4).

Early on, as my bilirubin crept above 1.5 the itching bothered

me a lot, and especially at night as you say. Later, at higher

bili levels I don't recall much of a problem. My brother-in-law

who is a GP commented on seeing the high bili levels that I must

be really bothered by itching and I had to admit it wasn't a big

problem at that point. I don't know if anyone else has had a

similar experience. My theory is the nerve receptors get

saturated and stop sending signals or my brain just started to

ignore the itching signals. Similar to the was you get used to

strong smells. Very noticeable when you enter a room, but less

intense after a few minutes.

Tim

--- J & D Lynch wrote:

> Thank you to those who suggested the Questran and

> cholestyramine for my itching. The itching has become

> unbearable especially at night so I phoned my study nurse and

> asked for the She spoke to my GI who agreed. It is

> perfectly safe while nursing and pregnant because it is not

> absorbed by the body but merely binds itself to the bile and

> then excretes it. I've had two doses so far and no change so

> I hope it kicks in soon.

>

> Those of you who have used Questran, how long does it normally

> take before it begins working??

>

> Debbie

__________________________________________________

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  • 4 years later...

Answer in the way you think it relates to your Child. Also, we are here to

answer any of your Questions about your Child.

Me :)

Nebraska, USA

mymocha@...

> I am not sure how to answer most of these as I a parent to a TSC child

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  • 2 years later...

They didn't not numb me when they did my spinal taps.

-- Re: thank you

I have had several epidurals and blocks in my back and neck. they are not

back at all. most of the time they kinda sedate you and they do numb the

area good. and all of the one's I have had except for one have worked really

good. and when it has been long enough I will get another one. but because I

have a problem with the vertebrae's in my backs I have to wait longer in

between than most people.

Jena

~:~Jena~:~

My Home Page

My E-mail

Re: thank you

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  • 1 year later...

Annemie

Thank you for all the little stories that you have posted. I've read

them, but haven't responded to them directly. Just wanted to say thank

you and I appreciate them. They do brighten up my day. Hope you don't

mind, but I wanted to pass some of them on to my family.

I also suffer from neuropathy - Autonomic neuropathy caused by an auto

immune disorder brought on possibly from the flu. I just started with

a new Dr. a couple of weeks ago. She was the first one that was

willing to try a different pain med other than tylenol #3. I've been

on the new med now for almost 2 weeks. It's taken a while for me to

get used to how it works, but I have noticed a slight improvement in my

pain level during the night.

Hugs

Diane-Minnesota

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Hello Diane

You are welcome and I hope to be able to continue sending stuff , at the

moment I have pc problems so if it takes longer then you know what the

reason is ,..

And surely you can send whatever I send to your friends and family I dont

have a problem with that at all,..

I also got a :(((( email of a lady that has neuropathy and it did scare me ,

I will send it to you , so be prepaired and if you dont want to see it then

delete it please,..

I know that I deal with neuropathy and it is bad enough you do too:(((

liefs

Annemie

Thank you

> Annemie

>

> Thank you for all the little stories that you have posted. I've read

> them, but haven't responded to them directly. Just wanted to say thank

> you and I appreciate them. They do brighten up my day. Hope you don't

> mind, but I wanted to pass some of them on to my family.

>

> I also suffer from neuropathy - Autonomic neuropathy caused by an auto

> immune disorder brought on possibly from the flu. I just started with

> a new Dr. a couple of weeks ago. She was the first one that was

> willing to try a different pain med other than tylenol #3. I've been

> on the new med now for almost 2 weeks. It's taken a while for me to

> get used to how it works, but I have noticed a slight improvement in my

> pain level during the night.

>

> Hugs

> Diane-Minnesota

>

>

>

> To read these messages on the Hugs web site go to:

> http://groups.yahoo.com/group/Hugs-N-Pain

> you can contact me privately at starlyin@...

> Rose

> Owner/ Moderator Hugs N Pain

> God Bless our Troops

> Please Pray for them

>

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