I get the lightening strike shocks, but i get mine in my shoulder around my scapula. sometimes this BPI just gets frusterating no matter how positive i try to be about it.

<t>Okay thanks for the replies. My whole scapula area is what gives me the most problems. Also another question...does anybody understand why i would feel numbness or a funny feeling in my pinky finger? it feels funny to me. <br/> and you know what i just realized. when i was younger and was learnin...

<t>Hi Nila,<br/> I am also very new to this. I just joined this site about a week ago so I would like to welcome you here. The people here all seem so wonderful and I felt kind of awkward coming here but now that im here i feel soo welcome!!!! I hope this site gives you the same feeling. I would lov...

<t>Do a lot of others experience a popping around their scapula area and a winging out of the scapula? i was just wondering because these are two things i experience, and since ive never talked with anybody else with this, i was just wondering what all people experience. <br/> thank you!<br/> Britta...

<t>I actually live in the Coral Gables area of Miami and know of some cheaper hotels in this area. I would suggest looking closer to the Coral Gables area for a cheaper hotel if you cant find anything near the hospital and then if you do decide to go closer to Coral Gables let me know and Ill give y...

<t>Hi im Kat's daughter and i just want to say you hit the nail on the head. My parents did a wonderful job raising me to live with my BPI. Before I found this site I didnt even realize it was a disability, it was just one more thing I had to live with. I am very lucky my parents were so dedicated t...

<r>Hi Kristen,<br/> My mom is Kat the one who posted right above me. I do attend the University of Miami so if you have any questions feel free to contact me at <EMAIL email="bvasum@hotmail.com">bvasum@hotmail.com</EMAIL> and i will answer them. also if you are planning on a visit to the university ...

<t>Hey Marieke,<br/> Thank you for welcoming me to this site. I have only been a part of it for a few days but everybody who has responded to me has made me feel sooo welcome. I am very excited about this site. I cant wait to meet other people who share my same disability and who can possibly help m...

<t>Hey guys,<br/> Thanks for the replies!!! It makes me excited that I get to be a part of something like this. Im really going to try to make it to the camp, but that is right around when I start up with school again.<br/> By the way, to answer Joanie's question, I'm 20 years old.<br/> <br/> Glad t...

<t>Hi my name is Brittany and I just recently found this site. I have lived with LOBPI (I guess thats how you write it?) since birth. I have never heard of it called Brachial Plexus Injury, my parents have always called it Erb's Palsy. So as you can tell Im very new to this. I have never met anybody...