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Are you talking about the battery that is implanted? The one that I have is

rechargeable. I recharge it with a disk that you get when you have the implant.

Eventually it will go dead and it will have to be replaced surgically.. Only the

battery will have to be replaced, not the wires. The company says it should last

from 5-7, maybe 7-l0 years. The life of the battery will depend on how high you

keep the stimulation. You get a remote to control the intensity of the

stimulation. Hope this helps.

Sue C

________________________________

From: Tinkler <tinklerjoshua@...>

Stimulator

Sent: Friday, August 14, 2009 11:35:58 PM

Subject: Re: Re: Welcome new members

 

THIS IS JOSHS WIFE AND I JUST WOULD LIKE TO KNOW ABOUT THE BATTERY DOES IT GO

DEAD AND IF SO HOW DO YOU CHANGE IT

____________ _________ _________ __

From: Corn <butterfliesrfree309 @>

Stimulator@gro ups.com

Sent: Friday, August 14, 2009 4:10:21 PM

Subject: Re: Re: Welcome new members

 

You're welcome. I hope you are able to get the appointment for the counselor and

then the trial ASAP. If you have any questions or need any information, please

contact us.

Sue C

____________ _________ _________ __

From: Tinkler <tinklerjoshua>

Stimulator@gro ups.com

Sent: Friday, August 14, 2009 4:40:14 PM

Subject: Re: Re: Welcome new members

 

THANK YOU I WILL BE DOING THE TRIAL AS SOON AS I GET DONE WITH THE COUNSELING

THAT THEY SAY I HAVE TO GO TOO. THANX FOR YOUR INPUT AND I WILL KEEP YOU (THE

GROUP) INFORMED

____________ _________ _________ __

From: Corn <butterfliesrfree30 9 @>

Stimulator@gro ups.com

Sent: Friday, August 14, 2009 12:22:49 PM

Subject: Re: Re: Welcome new members

 

Hi Josh. As I have stated before, I have 2 stims. I have a cervical and a lumbar

spinal cord stimulator as well as a pain pump. The stims have helped me a great

deal. They have helped me with my mobility. The lumbar stim kept me out of a

wheelchair. The cervical stim gave me back the mobility of my arm. The stim does

not cure your problem, but it does hopefully give you back your quality of life.

The stim will not take away all of your pain, but will hopefully reduce your

pain by about half. The stim makes it possible for you to have more good days

than bad days. You can't overdo things, or your pain level will increase, but

you should be able to do more with the implant. You go for a trial before the

implant to see if the stimulator will help you. I suggest you try the trial. If

it helps, and you get enough relief, then you know it's worth going for another

surgery. Good luck. Keep us posted.

Sue C

____________ _________ _________ __

From: Tinkler <tinklerjoshua>

Stimulator@gro ups.com

Sent: Friday, August 14, 2009 12:53:32 PM

Subject: Re: Re: Welcome new members

 

HI MY NAME IS JOSH AND I HAVE CHRO NIC BACK PAIN EVEN AFTER MY SURGARY. I HAVE 2

TITANIUM RODS IN MY BACK. I AM LOOKING INTO THIS STIMULATOR IMPLANT AND WOULD

LIKE SOME INPUT ON IT. SO IF ANYONE WHO HAS IT WOULD PLEASE LET ME KNOW SOME

INFO ON IT. LIKE HAS IT HELPED AND IF SO HOW MUCH AND IS IT WORTH ANOTHER

SURGARY. THANK YOU FOR YOUR TIME

____________ _________ _________ __

From: Deanna Ramsey <Photobug33777@ sbcglobal. net>

SCS support group <Stimulator@ gro ups.com>

Sent: Friday, August 14, 2009 10:45:15 AM

Subject: Re: Re: Welcome new members

 

One day would never be enough to gain understanding of our pain. Pretty much

anyone can get thru a day or two cause they know it's gonna end...light at the

end of the tunnel syndrome. Give them a few weeks thinking it's never going away

would be much better! Not that I wish chronic pain on anyone...I'm just saying!

Deanna

Sent from my iPhone

On Aug 14, 2009, at 8:47 AM, Corn <butterfliesrfree30 9 @> wrote:

Hi Mike. I'm glad that you are getting relief from your pain. What works for one

person might not work, or be right for someone else.

We must stand up and advocate for ourselves. You are so right when you say that

we want our quality of life back. It's not right that other people (drs,

insurance cos, politicitians, etc) make the decisions that effect our lives.. We

are the ones living in pain, we are the ones who can't function, and they are

the ones who dictate what can and cannot be done. If only they trade places with

us for one day!! We must take a more active role in our own lives. We must do

what we can to take back whatever control we can. We must move our bodies. Some

form of excersie is important. Immobility makes the body stiff and increases the

pain.

Sue C

____________ _________ _________ __

From: oldstylemike1 <oldstylemike1@ ...com>

Stimulator@gro ups.com

Sent: Friday, August 14, 2009 7:19:41 AM

Subject: Re: Welcome new members

>

> I want to welcome all the new members to the group. My name is Sue. I have RSD

along with several other medical conditions. I have 2 spinal cord stimulators

and a pain pump.

>

> The stims and pump have made it possible for me to be able to function

> again. Yes, there are still things that I cannot do, yes, I still have pain,

but I am able to function. The stim is not a cure, but a means of giving you

your life back. The key is doing things in moderation.

>

> Everyone in the group knows what everyone else is going through. We are all

going through, or have gone through the same thing. Only someone who lives in

chronic pain can understand what it is like to be in pain each day, every minute

of the day. We are here to support each other. If you have any questions, or

need any information, please contact us.

>

> Sue C

>

>hey sue, its a pleasure to talk. my name is mike graham, i'm a 46 year old

disabled man. i have suffered from a degenerative condition in my spine. i

currently have a spinal cord stimulator and a morphine pump installed inside my

body. back during my first spinal fusion, i was prescribed very large doses of

medication to battle some of the pain i was in. the oral opiates almost killed

me, i was bedridden and had lost over seventy pounds. if not for the

recommendation of a hospice nurse, i wouldn't be here writing letters on this

issue, i would have died. i'll leave that as the reader's digest version.

there are too many people that are suffering needlessly. is marijuana the answer

to everything, obviously no, but it works for me, and many others, so why

shouldn't a doctor have the ability to alleviate pain and suffering in some, if

they can? it doesn't make sense. i was taking more prescribed medications for

the side effects i was having from the opiates i was taking.

in 2009, we made great strides towards making a difference in the lives of many,

and that is why i got involved, to make a difference. many folks have put in

countless hours to get where we are, and it will take more to get this job

complete. state senator haine led the fight through the SENATE and state

representative lou lang has gained the support of fellow state congresspersons

across the state. we were proud that 30 SENATORS had the courage, compassion and

common sense to allow patients access to something that has been used as

medicine in CHINA for over 5000 years. when the " powers that be " down in

springfield get all the votes counted, they will bring it before the HOUSE for a

vote and then on to the GOVERNOR. we want a system that will be " patient

focused " & one that will be used as a model when other states work on their own

legislation. we need more patient's to help educate those members of the HOUSE

that may " not have had any idea the issue

affected so many " (honest answer).. we need to make it well known, we want some

quality of life back!!!

sue, this is my " form " letter i send to my local politicians, along with a

little tweaking, it truly has saved my life.

>

>

>

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  • 2 months later...

Thank you for the welcome !!!  I look forward to learning more from

everyone here and to being a support to those that need it.

~ Utah

________________________________

From: <radiant.salubrity@...>

Stimulator

Sent: Mon, October 19, 2009 6:00:40 AM

Subject: Welcome New Members

 

Welcome to all the new members. Things have been a little quite around here of

late. Don't let that worry you though. There are quite a few people on board

that can help with any query you might have, or anything you would like help

with.

Don't be shy, jump on in and let us know how we can help you. Or if you just

want to introduce yourself that's ok too.

Not everyone has had the same procedures done. We've all had something different

and varied. If we can't help you, we'll pass you on to someone who can.

Cheers & welcome Aboard.

__________________________________________________

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Welcome , wow you have been through alot, you poor thing! I am hoping

that everything goes smooth for you. I have to be somewhere in 20min but will

respond to your questions when I get home if nobody has. everyone here is so

nice and I am sure you will get all the anwers you need. take care and you are

in my thoughts

melissa

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,

Thank you so much for the kind and warm welcome and wishes.  I look forward to

learning more about you!  Have a wonderful day!

~ Utah

________________________________

From: <kenya@...>

Stimulator

Sent: Mon, October 19, 2009 9:21:15 AM

Subject: Re: Welcome New Members

 

Welcome , wow you have been through alot, you poor thing! I am hoping that

everything goes smooth for you. I have to be somewhere in 20min but will respond

to your questions when I get home if nobody has. everyone here is so nice and I

am sure you will get all the anwers you need. take care and you are in my

thoughts

melissa

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  • 1 year later...

Sorry to hear about your father's demise. May his soul rest in peace.

Nandini K. Kumar

Former Deputy Director General Sr. Grade

Co-investigator NIH project

National Institute of Epidemiology

R 127, 3rd Avenue,

TNHB, Ayapakkam,

Chennai 600077

Ph : +91 44 26136214

Telefax : +91 44 26820891

netrum From: drvijaythawani@...Date: Fri, 28 Jan 2011 16:50:32 +0000Subject: Welcome new members

Welcome to NetRUM.I am sorry for not taking you in the fold during the last few days, due to preoccupation with rituals associated with my father's death.Pardon me.VijayGroupie

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  • 3 months later...
Guest guest

...and please, if you're waiting on a new Vitamix, take the time to become very familiar with all of the instructional material, including the DVD, that arrives with your machine BEFORE you start blending. This sounds trivial but you'll save yourself possible frustration by acquiring "book smarts" first.

WELCOME New Members

Hello and WELCOME!

(We've recently had a noticeable influx of new members)

I would like to encourage you to review our files, links, and photos - just visit: http://www..com (or click on the link at the bottom of this email that says, "visit your group"). You can also search the archives of past messages here: /messages

Two links that I think are important for new members are:

1) this can be a really busy list and hopefully this information might help you manage your Vitamix Enthusiasts email:

/message/9810

2) and this might inspire you to see ALL of the ways a Vitamix can be used…

/message/9684

Hope this is helpful and we'd love to hear from you - got any questions? :-)

Blessings,

Lea Ann Savage

Satellite Beach, FL

(321) 773-7088 (home)

(321-961-9219 (cell)

www.VitamixLady.com

www..com

<:)))><

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Guest guest

Recently got mine...and I did read and read and went to VE site etc. before I tried to use it. Great advise...as there's a lot to know before you turn it on. DH is a diabetic, so it will be important for me to know how to make things he can enjoy and not just my delicious smoothies. I'm taking my time getting to know my Vitamix and sure have enjoyed it so far. Kare

From: <kareningotham@...> Sent: Wed, May 11, 2011 6:21:30 AMSubject: Re: WELCOME New Members

....and please, if you're waiting on a new Vitamix, take the time to become very familiar with all of the instructional material, including the DVD, that arrives with your machine BEFORE you start blending. This sounds trivial but you'll save yourself possible frustration by acquiring "book smarts" first.

WELCOME New Members

Hello and WELCOME!

(We've recently had a noticeable influx of new members)

I would like to encourage you to review our files, links, and photos - just visit: http://www..com (or click on the link at the bottom of this email that says, "visit your group"). You can also search the archives of past messages here: /messages

Two links that I think are important for new members are:

1) this can be a really busy list and hopefully this information might help you manage your Vitamix Enthusiasts email:

/message/9810

2) and this might inspire you to see ALL of the ways a Vitamix can be used…

/message/9684

Hope this is helpful and we'd love to hear from you - got any questions? :-)

Blessings,Lea Ann SavageSatellite Beach, FL(321) 773-7088 (home)(321-961-9219 (cell)))><'>www.VitamixLady.comwww..com<:)))><

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  • 3 weeks later...
Guest guest

I would like to welcome our newest members to the group:

Shaukat

Thank you for joining us.

Please say hi so we can all say hi back.

If you feel comfortable sharing a bit about your HCV journey, please do so.

By everyone sharing their experiances, we can all compare notes, and maybe find some answers.

love

don in ks

To post on forum:

<--- click here

- or -

< >

Links Library:

http://health.dir./group/ /links <--- click here

Our Sponcer:

http://www.healthyhepper.com/ <--- click here

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