IHaveAFunnyName 2 points 6y ago
Oh goodness. Well, I totally understand about Facebook politics (yuck) but perhaps a vision only no friends type of a profile might be helpful, I know I've found the resources there invaluable. If not there are a few websites: national federation for the blind, Perkins school for the blind, and wonderbaby which has great articles. My son has cortical visual impairment (cvi) from brain bleeds and hydrocephalus caused by prematurity (cvi is when the brain doesn't process what the eyes see very well. He sees bright toys best when they are against a solid background and when there is some movement involved, if you think her blindness may be from cvi I highly recommend you look up Dr. Christine Roman in Pennsylvania, she is the leading expert in the US and cvi is still relatively unknown by some eye doctors. Also the fb groups for cvi are great and I am happy to help in any way I can. But I digress.) He also has optic nerve atrophy from hydrocephalus where the nerve appears pale.
As my son is under three, we have early intervention helping us and they found us a TVI consultant from the local school for the blind who comes and works with us. You should look into finding a TVI or OM to come work with your daughter, perhaps by contacting the EI program nearest you and asking for resources even if they can't provide you services they should be able to direct you to help. If she is behind in motor skills you may also need to seek out physical or occupational therapy and finding one who is familiar with children who are blind would be a wonderful thing. (Edit: I just realized you're not in the US so....that may not work in your country, sorry!) An OM would help her with her cane, too, if she uses one.
I believe there are annual conferences for families who have a child or parent who is blind...we have never been but it sounds great. (Again, US)
For us, we wanted toys that have good texture and sounds, light especially for his cvi. I would mostly recommend calling all blind resources near you and asking where you should be looking, or if there are families with similar aged children you can connect with. Having support from others is huge for us, even if it is through messages.
Label everything and describe where she is, what is going on around her. If you walk in or out of a room tell her. Movies and shows can have audio descriptors so she can enjoy movies with you. I have been reminded by others as well to always push him and not restrict his activities because of blindness, you may just have to adapt. Best wishes and please let me know if I can help in any way. :)