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Welcome! I'm a new member, too. The group seems to welcome us very

quickly and there doesn't seem to be a right or wrong way to

negotiate things. I think some people jump in writing messages or

asking questions, others sit back and read for a while, others strike

up personal friendships with members and share anything from

frustrations about medical care to details of their dating life. I

get overwhelmed by the number of messages, but I'm also getting great

feedback when I have questions and I feel less alone with this site --

it gets tough to explain to friends what this disease is about.

I'm also a parent (father in my case) to three children, though mine

are just 8, 4, and 1. I was diagnosed in '94 w/ PSC and I've been

itching fairly persistently since '93. I didn't have many other

symptoms until this past April. The itching can be quite annoying,

but I'm having good luck with a combination of actigall and

naltrexone, an opiate antagonist. For several years, rifampin helped

me a lot. Others I've talked to had luck with atarax, but that did

nothing for me. My most frustrating/embarrassing experiences with

itching have been when I'm around others and suddenly realize my hand

is in my shirt or inside my sock scratching. When I was dating my

wife to be her sister even commented to my wife that I seemed to have

an obsession with scratching -- I think she thought I did it because

I was really nervous about something. I hadn't been diagnosed then

and thought I just had allergies. When I had a bout with more severe

symptoms in April and May of this year, I had trouble concentrating

because of the itching. I practiced a lot of distraction, relaxation,

and sometimes meditation techniques then. What do others do?

Again, welcome to the group. Hope grad school is treating you well.

I'm in grad school, too. I hope to finish my coursework and

dissertation for my PhD next spring and then I'll just have a one

year intership left.

Philip

> I am a new member and am wondering how to negotiate this site. Do I

> just start sending messages? I have been dianosed with PSC /UC 3

> years. I take Actigol and Asachol. Other than a few episodes of

> Cholangitis I have been doing pretty well. I am a graduate student

and

> a nurse and an artist. I have 3 children 25, 24, and 20 and a

> wonderful husband. I'm also a grandmother. I really want to know

how

> others deal with this itching thing and the fatigue

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  • 1 year later...

Bernie-

Hello and welcome to you and Josh. My daughter, Aubrie, is nearly 7 yrs

old and attending our neighborhood school in regular 1st grade with an

aide. She mild-mod hearing loss, some visual impairment, submucous

cleft palate, motor issues, etc. No trach or Gtube. We're in IL so I

can't help with CA-specific questions.

Good luck- Schooling is a challenge to say the least -

Michele W

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Bernie,

I strongly recommend you contact Jackie Kenley and Brown who work in

San Francisco for CA deafblind services. Even if does not have

vision impairment also, these folks are the best at understanding CHARGE and

may be of help with the school issues. Jackie has an adult daughter who has

CHARGE as well. There are other families on the list in the bay area, I am

sure you will be hearing from them.

There is comfort in finally having an answer as to what Syndrome our child

has, at least then information can be gained and action taken. Not knowing

was hard for me and it was only for 3 weeks, 5 years and I might have gone

nuts. Glad you have answers.

Kim L

>

>

> Hello All,

>

> My name is Bernie Hill, I'm the mom of a 5 year old names who

> was just diagnosed with CHARGE last week. I can't believe it has

> taken this long. has a cleft lip and palate, hearing loss,

> Trach, g-tube, he is missing a kidney and testicle, he just started

> walking this year (without his walker) and is going to

> Kindergarten. The appropriate school is the challenge right now and

> I'm not sure if he's in the right place, more meetings to come. I

> was wondering if anyone was from California, specifically the Bay

> Area. I hope to get to know you all over time. Thanks for being

> out there.

>

> Bernie, mom of Josh

>

>

>

>

>

>

> Membership of this email support groups does not constitute membership in the

> CHARGE Syndrome Foundation.

> For information about the CHARGE Syndrome

> Foundation or to become a member (and get the newsletter)

> please contact marion@... or visit

> the CHARGE Syndrome Foundation web page

> at http://www.chargesyndrome.org

> 7th International

> CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005.

> Information will be available at our website

> www.chargesyndrome.org or by calling 1-. In Canada, you may

> contact CHARGE Syndrome Canada at 1- (families), visit

> www.chargesyndrome.ca, or email info@.... Thank you!

>

>

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Bernie,

Welcome to the list, there are a lot of knowledgable professionals involved with

CHARGE out in CA, I'm sure you'll be pointed towards them from the members of

this list. Brown sticks out in my mind as someone you should contact.

You can email me privately lisaweir@... and I will give you his contact

info.

Weir

Mom to Kennedy, 6 yr old with CHARGE, 15, 13 and wife to Graeme

New Brunswick, CANADA

Visit our family on the web - http://ca.geocities.com/weirfamilyrogers

Email: lisaweir@...

Bernadine Hill wrote:

Hello All,

My name is Bernie Hill, I'm the mom of a 5 year old names who

was just diagnosed with CHARGE last week. I can't believe it has

taken this long. has a cleft lip and palate, hearing loss,

Trach, g-tube, he is missing a kidney and testicle, he just started

walking this year (without his walker) and is going to

Kindergarten. The appropriate school is the challenge right now and

I'm not sure if he's in the right place, more meetings to come. I

was wondering if anyone was from California, specifically the Bay

Area. I hope to get to know you all over time. Thanks for being

out there.

Bernie, mom of Josh

Membership of this email support groups does not constitute membership in the

CHARGE Syndrome Foundation.

For information about the CHARGE Syndrome

Foundation or to become a member (and get the newsletter)

please contact marion@... or visit

the CHARGE Syndrome Foundation web page

at http://www.chargesyndrome.org

7th International

CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005. Information

will be available at our website

www.chargesyndrome.org or by calling 1-. In Canada, you may contact

CHARGE Syndrome Canada at 1- (families), visit

www.chargesyndrome.ca, or email info@.... Thank you!

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Hello Bernie and welcome.

Kay

50 yr old CHARGEr

New Member

>

>

> Hello All,

>

> My name is Bernie Hill, I'm the mom of a 5 year old names who

> was just diagnosed with CHARGE last week. I can't believe it has

> taken this long. has a cleft lip and palate, hearing loss,

> Trach, g-tube, he is missing a kidney and testicle, he just started

> walking this year (without his walker) and is going to

> Kindergarten. The appropriate school is the challenge right now and

> I'm not sure if he's in the right place, more meetings to come. I

> was wondering if anyone was from California, specifically the Bay

> Area. I hope to get to know you all over time. Thanks for being

> out there.

>

> Bernie, mom of Josh

>

>

>

>

>

>

> Membership of this email support groups does not constitute membership in

> the CHARGE Syndrome Foundation.

> For information about the CHARGE Syndrome

> Foundation or to become a member (and get the newsletter)

> please contact marion@... or visit

> the CHARGE Syndrome Foundation web page

> at http://www.chargesyndrome.org

> 7th International

> CHARGE Syndrome Conference, Miami Beach, Florida, July 22-24, 2005.

> Information will be available at our website

> www.chargesyndrome.org or by calling 1-. In Canada, you may

> contact CHARGE Syndrome Canada at 1- (families), visit

> www.chargesyndrome.ca, or email info@.... Thank you!

>

>

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