Connecting. Relating. Laughing. Crying. Life of a woman with Retinitis Pigmentosa.
I recall in my early days of Retinitis Pigmentosa we had and still do have many dear friends where the man has RP. Lately, I have been connecting with some amazing women with Retinitis Pigmentosa. Let me introduce some of them that are bloggers.
Lacey. Her blog is private, but love her. Such a blessing to be her friend and watch her family grow.
Oh how I can relate to her. Brings back many memories of earlier days.
She brings me laughter as I remember my days of training at the blind center and share the journeys of raising her two kids.
A friend from across the world inspires me.
A warm, gentle friend who I hope someday to attend one of her yoga classes.
Retinitis Pigmentosa does not define us. It is the commonality that has brought us together through blogging, and I hope one day in person!
The journeys of Becky, blind from retinitis pigmentosa, and her beauitiful guide dogs.
7 comments:
I'm so honoured to be included in this list. Love having you in my life. xx
Hello my name is fabio and 38 years are affected by retinitis pigmentosa, I am Italian, I still see well but I do not know for how long, but 'I can say the same here life goes on' in Italy there are many studies to defeat this disease But 'I think that the road is still long, a hug to all of you fabio
I want to write for those who can 'do it to my e-mail fabioprivato@alice.it hello to all
A very thought provoking post!
Made us pause and reflect.
Thank you.
Fiona
Becky, you are awesome. So supportive and kind. I am so excited about the links, and have been loving reading all the blogs.
Aawww...you are so sweet!! Thank you!! It is I who am so lucky to have you for a friend!
Thank you for including me! I absolutely love knowing you exist. Next time I'm in Utah, visiting family, we may need to make it a point to connect over a bowl of ice cream or something!
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