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This board is for adults and teens to discuss issues relating to BPI since birth (OBPI).
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Baeta

New here,

Post by Baeta »

Hi, my name is beth and I suffer from OBPI. I found this place just browsing after I was explaining my injury to a client of mine and wasn't completely sure about everything with my injury. I really felt pretty alone until i started researching. A little bit about myself: I am 20 years old and my BPI is in my right arm. when i was a baby i used to pull my arm up so my elbow is locked and i cannot bend it. my pinky and ring finger are also locked and my wrist is paralyzed/ however, i have a minimum amount of numbness in the arm and have managed to learn and do things the doctors said i would never do. my parents refused to call me disabled. they never did surgery and stopped occupational therapy when i was 8 (the OT hurt me pretty bad) my mother kept pushing me to not label myself disabled and i am so grateful to her for it. I lead a pretty normal life because of it, i am in college and engaged to a wonderful man and i work with children with autism. there are a lot of things i cannot do. there are many things i can. i am questioning surgery or therapies but i'm not sure yet. it kind of scares me. i would like to move my wrist or unlock my arm. i have carpel tunnel in my other arm, which is making things a bit harder, but i deal with it. I am happy i found a site with so many resources.
rachelcasa
Posts: 729
Joined: Mon Apr 21, 2003 11:45 pm

Re: New here,

Post by rachelcasa »

Baeta,

You have defintely come to the right place and welcome to the boards. There are so many wonderful people with such great insight for people with bpi.

Finding this website and going to the camps has been a life changing experience for me. It's so great to have such wonderful, warm and carinng support here.

Please feel free to ask any questions and you will get many responses.

Rachel from MT
Carolyn J
Posts: 3424
Joined: Tue Apr 06, 2004 1:22 pm
Injury Description, Date, extent, surgical intervention etc: LOBPI. I am 77 yrs old and never had a name for my injuries until 2004 when I found UBPN at age 66.

My injuries are: LOBPI on upper body and Cerebrael Palsy on the lower left extremities. The only intervention I've had is a tendon transplant from my left leg to my left foot to enable flexing t age 24 in 1962. Before that, my foot would freeze without notice on the side when wearing heels AND I always did wear them at work "to fit in" I also stuttered until around age 18-19...just outgrew it...no therapy for it. Also suffered from very very low self esteem; severe Depression and Anxiety attacks started at menopause. I stuffed emotions and over-compensated in every thing I did to "fit in" and be "invisible". My injuries were Never addressed or talked about until age 66. I am a late bloomer!!!!!

I welcome any and all questions about "My Journey".
There is NO SUCH THING AS A DUMB QUESTION.
Sharing helps to Heal. HUGS do too.
Location: Tacoma WA
Contact:

Re: New here,

Post by Carolyn J »

WELCOME BETH! :)
I too,am glad you found us here. There is instant support and love, information as well as a healthy place Vent...we understand because we experience alot of the same things altho BPI injuries are individually diffent.

Also there is no dumb question and you are welcome on all Message Boards.

Please come back often. We continue to learn from each other too.

Carolyn J
LOBPI/69 and counting..;)


Message was edited by: Carolyn J
Carolyn J
Adult LOBPI
User avatar
hope16_05
Posts: 1670
Joined: Tue Jul 01, 2003 11:33 am
Injury Description, Date, extent, surgical intervention etc: 28 years old with a right obstetrical brachial plexus injury. 5 surgeries to date with pretty decent results. Last surgery resolved years of pain in my right arm however, I am beginning my journey with overuse in my left arm
Location: Minnesota
Contact:

Re: New here,

Post by hope16_05 »

Hi Beth! I am also 20 years old and in college. I too have my injust to my right arm. I have had 5 surgeries for it though with my most recent being last May, so I am not even a year post op.
So if you have any questions about therapy and surgery please feel free to ask me anything! I am still in therapy. I see an OT when I need to for evals or splints and am starting to see a PT on Friday for feldenkrais therapy. I also see a chiropractor and that has been amazing! So if you want any info or just want to talk feel free to post to me or email me any time!

Welcome to the boards!
Hugs,
Amy 20 years old ROBPI from MN
Amy 28 years old ROBPI from MN
Baeta

Re: New here,

Post by Baeta »

thanks for such a warm welcome! its nice to meet someone my age as well going those this. i have never met anyone with my injury and when i came here i felt good meeting others who understand (though uniquely different). tell me about your sugery, i dont know what is available because i never have had surgery. i would like to straighten my arm but i havent thought about an OT you think they casn help? thanks!
beth
Baeta

Re: New here,

Post by Baeta »

thank you all for being so welcoming to me. I don't know much about my injury, or no anyone who has gone through it so this is very comforting!
Thanks!
Beth
Kath
Posts: 3242
Joined: Mon Nov 18, 2002 4:11 pm
Injury Description, Date, extent, surgical intervention etc: I am ROBPI, global injury, Horner's Syndrome. No surgery but PT started at 2 weeks old under the direction of New York Hospital. I wore a brace 24/7 for the first 11 months of my life. I've never let my injury be used as an excuse not to do something. I've approach all things, in life, as a challenge. I approach anything new wondering if I can do it. I tried so many things I might never have tried, if I were not obpi. Being OBPI has made me strong, creative, more determined and persistent. I believe that being obpi has given me a very strong sense of humor and compassion for others.
Location: New York

Re: New here,

Post by Kath »

Hi Beth
Welcome to the Club...
It is a strange feeling when you find out that you are not the only one with a rare birth injury.

Most of us here were never treated disabled and have been able to live full productive lives.

One of the things I never realize was that it's possible to injury your unaffected arm from overuse.
When I first found UBPN I was so shocked when I read about all the newborns on the General Board.
I was happy to meet a few adult/obpi posting and we shared so much of our common experiences. It was very healing for me and helpful.
As one of the older obpi I try to warn the young people of secondary injuries. Because we compensate so well for the loss of our limbs we actually began to wear out our healthy arm.
As you can see that you are beginning to have problems now with carpal tunnel. If you read some of the older posts you will see that most of us began to have problems with our unaffected arms in our twenties.
Now is the time to stop the progression of secondary injuries by protecting your unaffected arm. Overuse is a real problem as you get older.
Proper use of your body to function (OT instructions would help) and good equipment for Acts of Daily living will really help you to prevent some secondary injuries.
I was over sixty before I could admit I was disabled.
That was way to late to help with overuse and secondary injuries.

It was thrilling the first time I met another OBPI. We were comparing arms and talking freely to people who really understand. When I am with another obpi, I don't have to say a word when something happens... we both just GET IT! If I am frustrated by the outside world who truly do not understand our limitations. I simply post or e-mail one of my buddies on this board. Frustration can be our constant companion with this injury but as you will see most of the obpi here seem to have a great sense of humor.

Welcome again

Kath robpi/adult
Kath robpi/adult

Kathleen Mallozzi
smith24s1
Posts: 3
Joined: Fri Apr 18, 2008 11:38 pm

Re: New here,

Post by smith24s1 »

I am new to this site. My injuries are from birth, and by the sounds of it, not as severe as some here. I have a winged out shoulder blade and my shoulder turns towards the front of my body. I am not able to fully extend my elbow and I have problems pronating my arm. This is all on the right side.

What kinds of surgeries have you had, and what is your recovery like? I suffer from new and unexplained pain. Any ideas?

Thanks!
Baeta

Re: New here,

Post by Baeta »

Actually, my parents were offered the opportunity to seek surgery with my arm when i was a baby but they decided to wait. I had a lot of function in my arm so they didn't want to risk it. I have about 90% of full feeling in my arm, my wrist is paralyzed but never really got in the way. and my elbow is locked so i can't extend my elbow at all only up. a lot of people on this board have has excellent things come from surgery, but i'm not one to ask. I have carpal tunnel in my good arm from over use and some time pain in my effected shoulder. I haven't figured it out either.
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