little.lulu.love : Most liked Posts

Something hasn’t been sitting right with me, and I’ve just realised it’s Erin’s language in relation to Lu. It’s all about Erin. Examples in her recent post
- My non-verbal and disabled child
- I sat there with her privates exposed
- 2 catheters in my daughter
- without my consent
I feel like she very rarely touches on what it must be like for Lulu. It’s all about Erin.
Obviously, she is the parent and she is the one writing the posts. But it seems to me like her focus is wrong. Sometimes, it’s like she doesn’t see Lu as an independent person, but as an extension of herself. Even though Lu has a disability, she is still an individual.
I truly hope Luella recovers quickly

trish_allstar said:

Erin, I've made some corrections for you.
Now before you come as me, I am a mum of 3 with post natal depression/anxiety I know too well that life is not all sunshine and rainbows BUT you really are like a black cloud. Appreciate those children, appreciate the little things, enjoy time together, look at how incredible it is you all got out of the house together. Any mum will know and appreciate how difficult that is alot of days. Stop the negative narrative and maybe you'll enjoy life a little more.

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The post about Luella’s immune system sent me spare. Literally everyone BUT Erin understands that with her anti-science, anti-vaccine, taking that poor sick baby out and about literally hours after posting about her having gastro, or saying she’s been to the doctor and being checked for a UTI (which landed her in hospital for a week the last time, where she contracted Covid). Jesus this woman.

Does she not realise the older Lu gets the harder it’s going to be. The bigger she gets the harder to get her around. She should be relishing the time she has with her daughter while she is still young.

Erin is a miserable c*nt and it sickens me the way she treats her daughter. No wonder she lost all her friends.

I know many people with disabled children who would never even think about going on holidays without their disabled child.

EAA should be ashamed of having someone like her representing their organisation.