Retinitis pigmentosa

[IronMaidenMan1]

I have recently started a Retinitis Pigmentosa Awareness Page on Facebook. If anyone is interested in spreading awareness and helping support finding a cure for RP, please visit my site and hit the "Like" button. It should be one of the first sites that pop-up if you type it in the search bar on Facebook. The picture is of a purple ribbon. Feel free to post personal stories on the wall also. Thank you for your time reading this short paragraph.

[jepie15]

I retines pigmentosa and it is not so nice,

so I do not think you should put some music underneath

[esteban666ful]

basuraaaaaaaa

[MrWoodage]

THIS HAS GOT TO BE MY FAVOURITE SONG ,,, EVER ,,, LOVE IT TO PIECES ,, WHO DONE IT ?? ,, PLEASE TELL ....

[MrWoodage]

ANY OF YOU R,P"ERS OUT THERE WANT A FRIEND OR A MOAN THEN FACEBOOK ME BRADLEY WOODAGE ,......... AND SOMEONE INVENT RUBBER BOLLARDS AND FOAM SIGN POSTS FOR GOD SAKE I"M BEGINNING TO LOOK LIKE A SCARRED UP BRAWLER ,,,

[MrWoodage]

HEY MASTEROF PUPPETS DO LIKE THE REST OF DO PINBALL YA WAY THROUGH LIFE BOUNCEING OFF EVERYTHING THAT GETS IN YA WAY ,, A WARNING "YOU COULD BE YOUR BIGGEST DISABILITY" I JUST SMILE COS I DON"T KNOW HOW LONG IT WILL BE TILL A LAMPOST KNOCKS MY FRONT TEETH OUT ,, LMAO ,, "ENJOY IT WHILE YOU"VE GOT IT BEFOR IT DISSAPEARS "

[pantyflash]

Like, wonderful way to recycle the core from a roll of buttwipes. Way to go, babe!

[chadc0613]

My RP never looks like I'm riding a bike with a used toilet paper tube held up to my eye. This video reminds me of one of the opening credits for a James Bond film. 8)

[Masterofpuppets07]

I have rp and im only 17

i just am praying for some treatment

life really isnt worth living, if it gets worse, i dont know what i would do.

its really depressing but yeah, need to look on bright side if any, and just hope

[Healery1978]

Hey :) I have RP too and I know what do you feel. But dont give your depression a chance its not worth it. Have fun with all the things you will do in your life. Learn to play an instrument it helps. You have to learn to live with it. Dont fight it !! Accept your RP as a part of you. Bye :)

[Masterofpuppets07]

I do play an instrument and Hmm, i will always resent it and fight it.. its just me lol

Cheers for advice anyways

Cya

[samlong38]

@Masterofpuppets07

im 19 and yes it is a bitch but mine has gotten worse this year quite a bit but you adapt. im at uni and living with friends the worst thing to do is to let it rule your life

good luck

[Ailoex]

@Masterofpuppets07 i can´t speak good english, but i think we can do something to heal this Illnes ;)!!!

[Batavian187]

RP is a collection of genetic disorders which cause the rods and cone cells of ones retina to slowly get destroyed.

Usually it starts with nightblindness (the inability to see in dark or dimly lit places) and as it progresses one starts to see less and less side vision (the tunnel vision) and eventually total blindness.

I have this condition as well..it's especially troublesome in busy streets with lots of traffic and crossing streets.

You simply miss things and people and they just appear.

[RPInternational1972]

Check out RP International's Channel and join its "Fight Against Blindness"

[HARIER416]

i think u cud explain it a bit.....give more info on rp....i think rp is genetically transmitted disease....it runs in my family.....

[nacianell219]

I have RP and it is similar to this. Especially as how it seems when you look to the distance that you seem to see more area, but things close up you see less.

[hijaabiforlife]

i like it but would like more info. cuz i'm doing a researuch paper

[Yarnaguide]

Love it. I have RP and it is a good way of people seeing what it is like. Not exactly like this as you can imagine