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Welcome to the group, le!

This group has been trying out simple DC battery current on various

things and finding it useful. It started with a research project at

Einstein College of Medicine in NYC, in which HIV was inactivated by

simple DC current, just like we are doing here with plain old

batteries. We've lowered the viral load on some with this. It's

got a nice history of results without problems.

A wide variety of germs seem to go 'quiet' or inactive using this,

resulting in the infections clearing up without anti-biotics or with

minimal assistance from other things. It could be the ticket for

MRSA, since the infection is local (at first) and it can be found on

the body easily.

To use this, see the photos section and the files section. In

photos the Apprentic Godzilla device is simplest to make and can

just be applied to the area. You put an electrode on each side of

the infection and move them around to pass the current through the

area. If it is " too much " try adding a bit of wetted cloth between

the battery terminal and one wire to act as a resistance. Usually

that's not needed but some may be very sensitive to electrical

energy, so go easy. More cloth resistance will mean lower power.

20 minutes a couple times a day like this, and see if it helps. Let

us know how you do, since we want to know if this is helpful or not.

Thx,

bG

>

>

> Hey everyone, Im new to this group and would love to find out more

> about about the subject of the group. I have a son that has MRSA

and

> I also have a support group for people with MRSA and anyone with a

> loved one with mrsa. We are up to date on any and all news.

>

> le

> MRSA_SUPPORT/

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Welcome to the group, le!

This group has been trying out simple DC battery current on various

things and finding it useful. It started with a research project at

Einstein College of Medicine in NYC, in which HIV was inactivated by

simple DC current, just like we are doing here with plain old

batteries. We've lowered the viral load on some with this. It's

got a nice history of results without problems.

A wide variety of germs seem to go 'quiet' or inactive using this,

resulting in the infections clearing up without anti-biotics or with

minimal assistance from other things. It could be the ticket for

MRSA, since the infection is local (at first) and it can be found on

the body easily.

To use this, see the photos section and the files section. In

photos the Apprentic Godzilla device is simplest to make and can

just be applied to the area. You put an electrode on each side of

the infection and move them around to pass the current through the

area. If it is " too much " try adding a bit of wetted cloth between

the battery terminal and one wire to act as a resistance. Usually

that's not needed but some may be very sensitive to electrical

energy, so go easy. More cloth resistance will mean lower power.

20 minutes a couple times a day like this, and see if it helps. Let

us know how you do, since we want to know if this is helpful or not.

Thx,

bG

>

>

> Hey everyone, Im new to this group and would love to find out more

> about about the subject of the group. I have a son that has MRSA

and

> I also have a support group for people with MRSA and anyone with a

> loved one with mrsa. We are up to date on any and all news.

>

> le

> MRSA_SUPPORT/

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I should explain that the group has not proven anything, and the

simple devices are such that anyone can do this without depending on

someone else to make and market devices. That is a legal issue,

selling these, and someone has been jailed for doing so recently.

So, this design gives a self-solution that is every bit as good as

anything made by anyone. You can do this and find out for yourself

if it is helpful. My own opinion under the 1st amendment, is that

it will help--immensely. But I'm certainly no doctor, and not

giving advice of a medical quality to anyone here. I do hope you

try this out, though.. it could mean a lot for a whole lot of

people, both close and far away from us.

bG

> >

> >

> > Hey everyone, Im new to this group and would love to find out

more

> > about about the subject of the group. I have a son that has MRSA

> and

> > I also have a support group for people with MRSA and anyone with

a

> > loved one with mrsa. We are up to date on any and all news.

> >

> > le

> > MRSA_SUPPORT/

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I should explain that the group has not proven anything, and the

simple devices are such that anyone can do this without depending on

someone else to make and market devices. That is a legal issue,

selling these, and someone has been jailed for doing so recently.

So, this design gives a self-solution that is every bit as good as

anything made by anyone. You can do this and find out for yourself

if it is helpful. My own opinion under the 1st amendment, is that

it will help--immensely. But I'm certainly no doctor, and not

giving advice of a medical quality to anyone here. I do hope you

try this out, though.. it could mean a lot for a whole lot of

people, both close and far away from us.

bG

> >

> >

> > Hey everyone, Im new to this group and would love to find out

more

> > about about the subject of the group. I have a son that has MRSA

> and

> > I also have a support group for people with MRSA and anyone with

a

> > loved one with mrsa. We are up to date on any and all news.

> >

> > le

> > MRSA_SUPPORT/

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  • 1 year later...

glad to have you join the group. i am sorry to hear about your mother. there are a bunch of very helpful people on this list i am sure you will find the support you are looking for. evelynterri <Nurse_Terri99@...> wrote: im a 39yr old mother who just over 5yrs lost my parnetal rights to my kids i lost all my rightts and just found out my mother has cancer just looking for a few friends i also suffer from depresion bipolar~~~~ *** ~~~ *** ~~~ *** ~~~~The Being Sick CommunityMessage Archives-/messagesChat:- Scheduled Chats at /chatBookmarks:-Add a website URL you have found useful./linksPersonal

Complaints or problems:-Please contact a moderator email: -owner Subscription Details:-1) Individual email - means that every email sent to the list you receive.2) Daily Digest - sends you 25 messages in one single email for you to browse. This is an excellent option if you receive alot of email.3) Web only/No mail - means that you can pop into groups at your convenience and receive no email.To modify your subscription settings please visit:- /joinTo subscribe or unsubscribe please email:--subscribe -unsubscribe This group is not intended to diagnose or treat illnesses. No one on this group is qualified to diagnose medical conditions. If you feel you need medical attention, seek the advice of a qualified physician.~~~~ *** ~~~ *** ~~~ *** ~~~~When nothing is sure, everything is possible.---

Margaret Drabble~~~~ *** ~~~ *** ~~~ *** ~~~~

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  • 9 months later...

Hi Verdaeni,

I think you will find this group to be helpful. No one

here will roll their eyes. Everyone here has chronic

problems themselves so they understand.

I've been here a little while and I don't know of any

rules except common courtesy. You probably got some

files when you joined. Scan through those. There are a

lot of resources here too.

I look forward to getting to know you.

; )

Willow

P.S.

Most of us have a 'signature' that summarizes our

ailments so we can each remember who's dealing with

what.

--- kate olachlan <Verdaeni@...> wrote:

> i am here looking for a support group, support for

> me and that i may

> possibly help others. its very difficult to talk

> about my life to

> non ill people without bumming them out. i hope i

> can share here

> without bringing anyone down.

>

> i have been sick for five years now with 90%

> paralyzation of my

> diaphram. i have about half my lungs left after the

> pneumonia that

> the paralyzed diaphram gave me, which is actually

> how we found the

> original problem of the diaphram. this disease,

> which comes vaguely

> under the term 'parsonage and turner syndrome'

> leaves me very tired

> all the time and also has nerve pain. its hard to

> get out, i live

> alone because i have no family, im 50 years old,

> female, and i hope

> to get to know you all better.

>

> my condition is permanent and im trying to build a

> new life. any

> help that you all can do for me would be greatly

> appreciated. please

> feel free to let me know if there are any common

> rules to this

> discussion that i might break until i find out what

> the common

> standards of behavior is.

>

>

> Verdaeni

>

>

>

My Challenges:

Scoliosis, Radiation Injury to my Brain, Ministrokes, Memory Problems, Cluster

Migraine Headaches, Osteoporosis with Multiple Broken Bones, Fibromyalgia,

Chronic Pain and Fatigue, Depression, PTSD, Bipolar Type II Rapid Cycling,

Anxiety, Chronic Insomnia, Sleep Apnea, Spinal Stenosis, TMJ injury, Thyroid

Cancer X3, Skin Cancer, Loss of Salivary Glands due to Thyroid Radiation Tx,

Teeth Destruction with Loss of Salivary Glands, Obesity, Restless Leg Syndrome,

Alpha Wave Intrusion on Delta Sleep plus many other Sleep Anomalies,

vonWillebrand's disease (genetic bleeding disorder), Hypertension, High

Cholesterol and Triglycerides, Chronic Allergies, Asthma, Peripheral Neuropathy,

Chronic Gastritis, GERD, Adult ADD, Overactive Bladder,

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thankyou for responding. is there a way to set the signature in here

so i dont have to copy/paste it out of a document, or have it show up

in other groups? i see a lot of things in common.. i have

allergies, sinus infections, acid reflux, water retention as well.

im realizing this group could help me out with some of my 'smaller'

problems as well.

Verdaeni

>

> Hi Verdaeni,

>

> I think you will find this group to be helpful. No one

> here will roll their eyes. Everyone here has chronic

> problems themselves so they understand.

>

> I've been here a little while and I don't know of any

> rules except common courtesy. You probably got some

> files when you joined. Scan through those. There are a

> lot of resources here too.

>

> I look forward to getting to know you.

>

> ; )

>

> Willow

>

> P.S.

> Most of us have a 'signature' that summarizes our

> ailments so we can each remember who's dealing with

> what.

>

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Kate,

Welcome first of all..

I am saddened to hear of all you suffer with, it must be hard to get by day to day...

I found this group to be great.. I had to leave for a bit because I burned myself out working and basically crashed in a ball of pain..

But now I have given up working, am on disability and have lost about 35% use of my back and 25% of legs and I just couldnt cope even though it was a work at home job in front of the computer...

I am Heidi and suffer from epilepsy, fibromyalgia, rheumatoid arthritis, ankylosing spondylitis, shoulder impingement, bursitis, plantar faciitis, mentally I suffer from DID, BPD, PTSD, BP and Schizoid..

This group is great that is why I came back, everyone is so supportive and you never feel like a newbie, you just walk on in and become part of the group, not many groups are like that...

Some of the members are sure to be able to point you in the right direction, I live in Australia so the rules are a bit different here.

I am 33 and on disability and live with 63, we have a big age difference but it does not bother us...

Gentle Hugs

Heidi

DUNGEON MIZTREZZ aka Heidiwww.geocities.com/heidijayesplace/http://blog.360./kookaburradezignsLook, Listen, but most of all Believe.+=<^^>=++=<^^>=++=<^^>=++=<^^>=+

hello im new

i am here looking for a support group, support for me and that i may possibly help others. its very difficult to talk about my life to non ill people without bumming them out. i hope i can share here without bringing anyone down.i have been sick for five years now with 90% paralyzation of my diaphram. i have about half my lungs left after the pneumonia that the paralyzed diaphram gave me, which is actually how we found the original problem of the diaphram. this disease, which comes vaguely under the term 'parsonage and turner syndrome' leaves me very tired all the time and also has nerve pain. its hard to get out, i live alone because i have no family, im 50 years old, female, and i hope to get to know you all better.my condition is permanent and im trying to build a new life. any help that you all can do for me would be greatly appreciated. please feel free to let me know if there are any common rules to this discussion that i might break until i find out what the common standards of behavior is.Verdaeni

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welcome to the group. everyone is welcome here. there are ill people, people who are care givers or family members of someone who is ill. my son has cystic fibrosis and asthma and i am newly diagnosed with fibromyalgia. this is a very welcoming group that gives tons of support to all. hope to hear from you again soon. evelynkate olachlan <Verdaeni@...> wrote: i am here looking for a support group, support for me and that i may possibly help others. its very

difficult to talk about my life to non ill people without bumming them out. i hope i can share here without bringing anyone down.i have been sick for five years now with 90% paralyzation of my diaphram. i have about half my lungs left after the pneumonia that the paralyzed diaphram gave me, which is actually how we found the original problem of the diaphram. this disease, which comes vaguely under the term 'parsonage and turner syndrome' leaves me very tired all the time and also has nerve pain. its hard to get out, i live alone because i have no family, im 50 years old, female, and i hope to get to know you all better.my condition is permanent and im trying to build a new life. any help that you all can do for me would be greatly appreciated. please feel free to let me know if there are any common rules to this discussion that i might break until i find out what the common standards of behavior

is.Verdaeni

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Answers.

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Someone with AOL know how to do the signature?

makes it easy. You have your signature typed out

and it only goes on the email when you check a box

unless you have it set to always go on the email. I

just don't know AOL, but I'll bet someone here does.

; )

Willow

--- kate olachlan <Verdaeni@...> wrote:

> thankyou for responding. is there a way to set the

> signature in here

> so i dont have to copy/paste it out of a document,

> or have it show up

> in other groups? i see a lot of things in common..

> i have

> allergies, sinus infections, acid reflux, water

> retention as well.

> im realizing this group could help me out with some

> of my 'smaller'

> problems as well.

>

> Verdaeni

>

>

> >

> > Hi Verdaeni,

> >

> > I think you will find this group to be helpful. No

> one

> > here will roll their eyes. Everyone here has

> chronic

> > problems themselves so they understand.

> >

> > I've been here a little while and I don't know of

> any

> > rules except common courtesy. You probably got

> some

> > files when you joined. Scan through those. There

> are a

> > lot of resources here too.

> >

> > I look forward to getting to know you.

> >

> > ; )

> >

> > Willow

> >

> > P.S.

> > Most of us have a 'signature' that summarizes our

> > ailments so we can each remember who's dealing

> with

> > what.

> >

>

>

>

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  • 1 year later...

Hi my name is ,

I have 2 children, Jordon is 8 and is 7, we live in Utah.

In June 2007 my son Jordon got a sceptic knee. It was very swollen and

infected, he had to have 3 surgeries and a PICC line to fix this, we

were in the hospital for 2 weeks.

The Rhumatology team came in and said that they would be keeping an

eye on Jordon for the next 6mths to see if anything else would swell

up. They put him on naproxn

5mths later his other knee swelled up, very large. So then they Dx'd

Jordon with JRA. Then our doctor had us go see our optho to check his

eyes. Which are fine so far, we see the optho every 3mths now.

2mths later his ankles swelled up and Dr. Zeft had us do steroid

injections in both knees and both ankles.

In May we changed meds to Meloxicam.

His legs and ankles are in pain almost every day, and they are

slightly swollen. And whenever it gets cold here he gets worse.

Jordon also has Type 1 Diabetes Mellitus, Epilepsy, Sensory

integration disorder, and developmental delay. His sister has a Cleft

mitral valve, severe epilepsy, and developmental delay.

Do you guys have any suggestions for me on how to lessen my son's

pain? this med doesn't seem to be working.

, Bryon, Jordon 8, 6

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Hello-

Sounds like you have a lot of challenges going on. Is sensory integration

disorder along the Autistic Spectrum? I only ask because there is a

connection between Pervasive Developmental Disorders and Autoimmune diseases

like JRA. Not like knowing that actually does anything to Help you

personally but just something interesting.

Anyways, they might need to treat his JRA more aggressively but in the mean

time, one thing that helps a lot is warm baths... swimming... water

therapy.... really helps with range of motion, and relaxing the joints,

etc.... Baths in the morning, and before bed can really help with stiffness

and sleep.

Massage is really great too and many people like ice or heat packs too.

I hope that can help some...

Issadora

On Wed, Oct 15, 2008 at 8:03 PM, myshel1_01 <Mathena@...>wrote:

> Hi my name is ,

> I have 2 children, Jordon is 8 and is 7, we live in Utah.

> In June 2007 my son Jordon got a sceptic knee. It was very swollen and

> infected, he had to have 3 surgeries and a PICC line to fix this, we

> were in the hospital for 2 weeks.

> The Rhumatology team came in and said that they would be keeping an

> eye on Jordon for the next 6mths to see if anything else would swell

> up. They put him on naproxn

> 5mths later his other knee swelled up, very large. So then they Dx'd

> Jordon with JRA. Then our doctor had us go see our optho to check his

> eyes. Which are fine so far, we see the optho every 3mths now.

> 2mths later his ankles swelled up and Dr. Zeft had us do steroid

> injections in both knees and both ankles.

> In May we changed meds to Meloxicam.

> His legs and ankles are in pain almost every day, and they are

> slightly swollen. And whenever it gets cold here he gets worse.

> Jordon also has Type 1 Diabetes Mellitus, Epilepsy, Sensory

> integration disorder, and developmental delay. His sister has a Cleft

> mitral valve, severe epilepsy, and developmental delay.

> Do you guys have any suggestions for me on how to lessen my son's

> pain? this med doesn't seem to be working.

>

> , Bryon, Jordon 8, 6

>

>

>

--

" Life- Like the flutter of wings... feel your hollow wings rushing... " (AFI-

Silver and Cold).

my Flight in life is a metamorphosis of growth and this flutter of wings is

within me awaiting to find a space to find it's flow...

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Hello,

I trick that I learned this year that seems to help a lot with the

morning stiffness and pain is an electric banket. We plugged it into

a timer and it is set to come on one hour before my son gets up in the

morning. The heat helps relax his joints and make the mornings a

little more bearable.

(, 5-Pauci)

On Oct 16, 2008, at 1:44 AM, Issadora wrote:

> Hello-

>

> Sounds like you have a lot of challenges going on. Is sensory

> integration

> disorder along the Autistic Spectrum? I only ask because there is a

> connection between Pervasive Developmental Disorders and Autoimmune

> diseases

> like JRA. Not like knowing that actually does anything to Help you

> personally but just something interesting.

>

> Anyways, they might need to treat his JRA more aggressively but in

> the mean

> time, one thing that helps a lot is warm baths... swimming... water

> therapy.... really helps with range of motion, and relaxing the

> joints,

> etc.... Baths in the morning, and before bed can really help with

> stiffness

> and sleep.

>

> Massage is really great too and many people like ice or heat packs

> too.

>

> I hope that can help some...

>

> Issadora

>

> On Wed, Oct 15, 2008 at 8:03 PM, myshel1_01

> <Mathena@...>wrote:

>

> > Hi my name is ,

> > I have 2 children, Jordon is 8 and is 7, we live in Utah.

> > In June 2007 my son Jordon got a sceptic knee. It was very swollen

> and

> > infected, he had to have 3 surgeries and a PICC line to fix this, we

> > were in the hospital for 2 weeks.

> > The Rhumatology team came in and said that they would be keeping an

> > eye on Jordon for the next 6mths to see if anything else would swell

> > up. They put him on naproxn

> > 5mths later his other knee swelled up, very large. So then they Dx'd

> > Jordon with JRA. Then our doctor had us go see our optho to check

> his

> > eyes. Which are fine so far, we see the optho every 3mths now.

> > 2mths later his ankles swelled up and Dr. Zeft had us do steroid

> > injections in both knees and both ankles.

> > In May we changed meds to Meloxicam.

> > His legs and ankles are in pain almost every day, and they are

> > slightly swollen. And whenever it gets cold here he gets worse.

> > Jordon also has Type 1 Diabetes Mellitus, Epilepsy, Sensory

> > integration disorder, and developmental delay. His sister has a

> Cleft

> > mitral valve, severe epilepsy, and developmental delay.

> > Do you guys have any suggestions for me on how to lessen my son's

> > pain? this med doesn't seem to be working.

> >

> > , Bryon, Jordon 8, 6

> >

> >

> >

>

> --

> " Life- Like the flutter of wings... feel your hollow wings

> rushing... " (AFI-

> Silver and Cold).

>

> my Flight in life is a metamorphosis of growth and this flutter of

> wings is

> within me awaiting to find a space to find it's flow...

>

>

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I'm so sorry to hear how much your kids have gone through. It's hard

on a mom to have to see their child in pain and particularly cruel

when there's little you can do to take that pain away. Then to add in

the other issues....well..I can only imagine. My daughter had

seizures for a year and a half and then " poof " , they were gone. It

was right around the same time as her JRA dx. and they never did find

a reason behind it.

Sounds like the injections aren't doing enough for Jordon and I agree

with Issadora that you may need to ask for more aggressive

medications. My daughter is on Methotrexate but there are many other

children that do well with Enbrel or another biologic; ask about

other options. The baths are essential and maybe even several per

day. We did this with Isabelle for a long time when her Naprosyn

wasn't working and both her knees and ankles were affected too.

Also, ask for the time being whether it's safe to give your son

Ibuprofen in conjunction with his other medication????`

Cheers to you and I sincerely hope that your son finds relief soon.

-hadley (Isabelle, 4.5 yrs, JRA)

-- In , " myshel1_01 " <Mathena@...>

wrote:

>

> Hi my name is ,

> I have 2 children, Jordon is 8 and is 7, we live in Utah.

> In June 2007 my son Jordon got a sceptic knee. It was very swollen

and

> infected, he had to have 3 surgeries and a PICC line to fix this, we

> were in the hospital for 2 weeks.

> The Rhumatology team came in and said that they would be keeping an

> eye on Jordon for the next 6mths to see if anything else would swell

> up. They put him on naproxn

> 5mths later his other knee swelled up, very large. So then they Dx'd

> Jordon with JRA. Then our doctor had us go see our optho to check

his

> eyes. Which are fine so far, we see the optho every 3mths now.

> 2mths later his ankles swelled up and Dr. Zeft had us do steroid

> injections in both knees and both ankles.

> In May we changed meds to Meloxicam.

> His legs and ankles are in pain almost every day, and they are

> slightly swollen. And whenever it gets cold here he gets worse.

> Jordon also has Type 1 Diabetes Mellitus, Epilepsy, Sensory

> integration disorder, and developmental delay. His sister has a

Cleft

> mitral valve, severe epilepsy, and developmental delay.

> Do you guys have any suggestions for me on how to lessen my son's

> pain? this med doesn't seem to be working.

>

> , Bryon, Jordon 8, 6

>

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Issadora

No one has ever mentioned Autistic Spectrum, ill have to check on that.

I'll have to try massaging him, and I'll have to work on the warm baths because

he can't stand anything warm due to his SID.

I think ill call our rec center and see if they do some water therapy and how

warm their water is.

tyvm.

, Bryon, Jordon 8, 7

From: Issadora

Sent: Wednesday, October 15, 2008 11:44 PM

Subject: Re: Hello Im new

Hello-

Sounds like you have a lot of challenges going on. Is sensory integration

disorder along the Autistic Spectrum? I only ask because there is a

connection between Pervasive Developmental Disorders and Autoimmune diseases

like JRA. Not like knowing that actually does anything to Help you

personally but just something interesting.

Anyways, they might need to treat his JRA more aggressively but in the mean

time, one thing that helps a lot is warm baths... swimming... water

therapy.... really helps with range of motion, and relaxing the joints,

etc.... Baths in the morning, and before bed can really help with stiffness

and sleep.

Massage is really great too and many people like ice or heat packs too.

I hope that can help some...

Issadora

On Wed, Oct 15, 2008 at 8:03 PM, myshel1_01 <Mathena@...>wrote:

> Hi my name is ,

> I have 2 children, Jordon is 8 and is 7, we live in Utah.

> In June 2007 my son Jordon got a sceptic knee. It was very swollen and

> infected, he had to have 3 surgeries and a PICC line to fix this, we

> were in the hospital for 2 weeks.

> The Rhumatology team came in and said that they would be keeping an

> eye on Jordon for the next 6mths to see if anything else would swell

> up. They put him on naproxn

> 5mths later his other knee swelled up, very large. So then they Dx'd

> Jordon with JRA. Then our doctor had us go see our optho to check his

> eyes. Which are fine so far, we see the optho every 3mths now.

> 2mths later his ankles swelled up and Dr. Zeft had us do steroid

> injections in both knees and both ankles.

> In May we changed meds to Meloxicam.

> His legs and ankles are in pain almost every day, and they are

> slightly swollen. And whenever it gets cold here he gets worse.

> Jordon also has Type 1 Diabetes Mellitus, Epilepsy, Sensory

> integration disorder, and developmental delay. His sister has a Cleft

> mitral valve, severe epilepsy, and developmental delay.

> Do you guys have any suggestions for me on how to lessen my son's

> pain? this med doesn't seem to be working.

>

> , Bryon, Jordon 8, 6

>

>

>

--

" Life- Like the flutter of wings... feel your hollow wings rushing... " (AFI-

Silver and Cold).

my Flight in life is a metamorphosis of growth and this flutter of wings is

within me awaiting to find a space to find it's flow...

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