hello
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Janet&joseph
- Posts: 7
- Joined: Sun May 31, 2009 4:13 pm
hello
hello,
I am a new user and just wanted to introduce myself.
My name is Janet (23) and I am a new single mom to a beautiful baby boy as of 9/9/08 . He does have a severe ( from what I was told) case Of EP.
He is a few days shy of 9m. Ive seen few drs but they dont really give me information. Just tell me to file a law suite or not to file. I was recently told he needs surgery asap. Any moms that have any experience with a law suite and/ or surgery at this age? any input would be great! thanks.
[IMG]http://i42.tinypic.com/2w50zkz.jpg[/IMG]
Message was edited by: Janet&joseph
I am a new user and just wanted to introduce myself.
My name is Janet (23) and I am a new single mom to a beautiful baby boy as of 9/9/08 . He does have a severe ( from what I was told) case Of EP.
He is a few days shy of 9m. Ive seen few drs but they dont really give me information. Just tell me to file a law suite or not to file. I was recently told he needs surgery asap. Any moms that have any experience with a law suite and/ or surgery at this age? any input would be great! thanks.
[IMG]http://i42.tinypic.com/2w50zkz.jpg[/IMG]
Message was edited by: Janet&joseph
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DianaLB1999
- Posts: 22
- Joined: Tue Nov 04, 2008 10:38 pm
Re: hello
It would help if I knew what state you live in so that I can give you some good suggestions...Thanks!
Diana
Madison 1 year ROBPI
Diana
Madison 1 year ROBPI
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ironmansmom
- Posts: 92
- Joined: Sun Jul 27, 2008 7:15 pm
Re: hello
Unfortunately, the window for nerve reconstruction is before 1 year old. I am sorry that your child and family has to go through this, but welcome to this site. My child is 11 1/2 years old with ROBPI. We have always seen Dr Nath in Houston, but there are many other great specialists out there. You can check out the medical resources page on this site.
Good luck!!
ironmansmom
Good luck!!
ironmansmom
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DianaLB1999
- Posts: 22
- Joined: Tue Nov 04, 2008 10:38 pm
Re: hello
Ok so time is of the essence! This is VERY important! You need to see a BPI specialist. You can check out the list of doctors on this site by state, but I would recommend that you seek multiple opinions. If you need anymore information, or anything please e-mail me at DianaLB1999@aol.com.
Diana
Diana
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tkirkland
- Posts: 55
- Joined: Tue Mar 31, 2009 9:46 am
- Injury Description, Date, extent, surgical intervention etc: My daughter suffered a ROBPI at birth on 10/7/2000. She has had no surgeries as of yet but we are currently seeking surgical intervention. She is a continous source of strength and encouragement for as she absolutely amazing!!!
- Location: Rockland County, New York
Re: hello
Please see a specialist as soon as possible. By six months most specialists will begin to recommend surgery (if needed). There is only a small window (and you are just about there) you really need to get in with a specialist as soon as possible. Like people before me have already said there is a list of specialists on this website. My daughter has seen Nath in Texas and Kozin in Philadelphia, PA. Both great Docs!
Re: hello
It is so frustrating that families still aren't getting good information about how to treat this challenge!
Please come to the San Diego Brachial Plexus Network picnic on July 12:
http://www.scbpn.org/familyevents.html
Dr. Nath from Houston will be there and gives free evaluations. You need to register at his site:
http://www.drnathclinics.com/
And you should check out his whole site. He has a ton of helpful information. You can also email him directly on his site and give him all of your son's info and he will reply amazingly quickly.
But, as others said, you will probably want to get a few opinions.
Rady Children's Hospital in San Diego also has specialists:
http://www.chsd.org/body.cfm?id=2316
It is overwhelming, but you will find amazing information and support on this site and hopefully make some California connections at the picnic.
Please come to the San Diego Brachial Plexus Network picnic on July 12:
http://www.scbpn.org/familyevents.html
Dr. Nath from Houston will be there and gives free evaluations. You need to register at his site:
http://www.drnathclinics.com/
And you should check out his whole site. He has a ton of helpful information. You can also email him directly on his site and give him all of your son's info and he will reply amazingly quickly.
But, as others said, you will probably want to get a few opinions.
Rady Children's Hospital in San Diego also has specialists:
http://www.chsd.org/body.cfm?id=2316
It is overwhelming, but you will find amazing information and support on this site and hopefully make some California connections at the picnic.
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Janet&joseph
- Posts: 7
- Joined: Sun May 31, 2009 4:13 pm
Re: hello
thanks ladies, I have seen a few people but I really want to go to Philly. I was referred to them by 2 doters and every where I look his name pops up. Anyone have any info on how to contact them? and any programs that would help me get there?
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Janet&joseph
- Posts: 7
- Joined: Sun May 31, 2009 4:13 pm
Re: hello
(PSMom)
I was just looking into this and I am planing to attend. (just have to get some one to take me) Are there any meet ups in the Los Angeles area?
Message was edited by: Janet&joseph
I was just looking into this and I am planing to attend. (just have to get some one to take me) Are there any meet ups in the Los Angeles area?
Message was edited by: Janet&joseph
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marieke
- Posts: 1627
- Joined: Fri Apr 01, 2005 6:00 pm
- Injury Description, Date, extent, surgical intervention etc: LOBPI
no external rotation against gravity, can only go to 90 degree fwd flexion, no hand-to-mouth
1 surgery at age 14 (latissimus dorsi transfer). In 2004, at age 28 I was struck with Transverse Myelitis which paralyzed me from the chest down. I recovered movement to my right leg, but need a KAFO to walk on my left leg. I became an RN in 2008. - Location: Montreal, Qc, Canada
- Contact:
Re: hello
Just wanted to welcome you!
Marieke 33, LOBPI
Marieke 33, LOBPI
