Foundation Fighting Blindness
Region: US
Monday 12 October 2026 18:55:02 GMT
784739
1317
34
48
Music
Download
Comments
Martha Jackson :
What RP? Don’t assume we will all know this short form. I don’t.
2026-10-13 21:38:57
16
Angelfaust🇨🇦 :
Hey I have RP I’m very lucky to have remaining vision in my left eye but tell her she’s not alone. I know it’s an add but if the girl in the video sees this comment reach out
2026-10-15 17:36:43
0
user3181856781255 :
hi people love to judge too much stay bless
2026-10-14 21:31:28
0
Kim Armstrong LeBlanc :
This runs in my family. My grandfather, 3 aunts, 5 cousins and some 2nd cousins. I've grown up watching how this progresses and its an awful condition.
2026-10-15 03:44:54
0
France Charest :
I have RP and one of the most frustrating thing I have to deal with is explaining my vision and the way I see the world to others,
2026-10-14 01:09:16
4
user2923789499756 :
Thank you
2026-10-14 23:53:32
0
Peg :
You must walk in another’s shoes before you cast judgment 🥰🥰🥰
2026-10-14 23:36:58
1
M A E :
I see a lot of Canadians here, there’s a Canadian version of this organization!!: Fighting Blindness Canada
2026-10-15 01:19:45
2
Tbone :
Three of my siblings have RP Ushers syndrome. It was heartbreaking to grow up with.
2026-10-13 15:56:02
6
mathewtobin1 :
RP is also used for relapsing polychondritis. Abbreviations are never good for external communications.
2026-10-15 04:35:38
4
Triciadelicia🇨🇦 🇺🇦 :
I have juvenile macular dystrophy, day to day sucks
2026-10-13 08:14:03
4
scottie :
I can remember doing a RIDE FOR SIGHT ,motorcycle charity ride for RETINITUS PIGMENTOSA many years ago. we helped raise funds for the cause and went on a ride to Kelowna where we deposited the donations to.🤔 was a fun weekend.
2026-10-13 07:38:56
3
kathleenoshea2 :
My granddaughter was diagnosed 5 months ago
2026-10-13 11:54:11
0
user8816322356708 :
My daughter explains the the same feeling when I’m navigating and people are quick to judge‼️
2026-10-12 20:43:01
1
PM 🇨🇦 :
Runs in my family. So sad to see people’s world shrink as their site does.
2026-10-15 02:34:38
1
Julie Faye :
So sorry for RP sufferers. ❤️
2026-10-13 20:42:47
0
DD :
My husband has RP
2026-10-13 22:11:02
0
PaPa-paul :
I hate that my wife is going blind. She loves life and I can’t do anything to help her. I’ve seen her be injected in the eyes more than 40 times. We r so depressed and our life sucks for so many reasons. We need a change.
2026-10-14 09:33:25
0
Stylinguru 🇨🇦 :
I was never tested , so that leaves it up to my daughter to do the genetic testing . Really hard here in Manitoba . First Dr said she had never even heard of it 🤨? This one is making commmenta about her age and there is time sort of commmets !! 27 !! They are discussing children !! I didn’t test because I never would have gotten pregnant . Watching it happen slowly since toddler to my older brother . His horrid life . Nope . But I tell ya a bully better not even with me or mine . I have had much practice 😞
2026-10-13 20:03:56
0
coughslikeahorse🇨🇦 :
My brother has RP, but nobody else in our large family does
2026-10-13 14:05:15
0
tabletop485 :
💯! My grandpa and aunt had it .. your mom is lucky to have you!
2026-10-14 03:06:48
0
Tara Lovelace 🇨🇦 :
My dad and my uncle both have RP. We have grown up with their struggles. There are a lot of amazing people who see and help, but there are also a lot of others who refuse to. People just need to be more aware of others around them instead of just themselves.
2026-10-13 17:57:07
0
Tanja🇨🇦 :
My daughter is having vision issues from diabetes. She gets hemorrhages in her eyes and the blood pools reduces her bision
2026-10-13 16:56:34
0
DANIKA :
This is totally ai that tripped me out
2026-10-15 02:54:27
0
Rebecca🇨🇦 :
My dad has retinal pigmentosis. He struggles with acceptance due to his low vision. He started using a cane so people around him will know he is low vision and be more empathetic. He used to get yelled at a lot for being in the way and not reacting to peoples hand gestures and facial expressions.
2026-10-13 17:18:08
1
To see more videos from user @fightblindness, please go to the Tikwm
homepage.
