Back in OCtober Kelly came for a respite weekend.
The morning after she arrived I found *gasp* an head lice in little Tyla’s hair. I was mortified. How could my little bubba have headlice. Then, I was brushing Bonnie’s hair and *gasp* found she had some too. What!? I went striaght to David and went through his hair. Nothing. What? Where had they come from? How did my gorgeous little girls get head lice?
Sitting at lunch I found the answer to my question.
Kelly had them. I could see them from across the table. How I didn’t see them Friday night I’ll never know. Her head was literally crawling with them. Thousands of them. It was the worst case of headlice I’ve ever seen. I took Kelly for a walk and we had a chat about the situation.
I was furious. Not with Kelly. By no means was this any of her fault.
But with her foster dad.
Kids get nits. It happens, but, how could he let them get this bad without proper treatment? How could he send her to respite without any consideration for us or more imortantly the other children in our care? How could he not bother to tell us in advance so we could decide if it was ok for her to come and also be prepared to deal with them.
Needless to say, EVERYONE in our house got nits. No one was spared. The following weeks were filled with hours of conditioning and combing the girls hair to remove the little critters and checking and rechecking everyone to make sure we were rid of them. Kelly wasn’t allowed back for respite until we were all clear and so was she.
It was 3 months before we saw Kelly again for respite.
3 weeks ago Kelly was here for respite and a few days later I found more head lice on the little ones. *Sigh* I couldn’t say for certain it was from Kelly, it could be from day care, but, I had a feeling it was Kelly.
I reported the nit problem to my support worker and we agreed that when Kelly was due again for repite I would check her hair, treat it if necessary, keep her the following day to comb those eggs out and send her home early Sunday morning, instead of the evening.
They haven’t been treated since she was here last, you can see that by the number of them. According to Kelly her dad knows she has them as he treated his bio-ddaughter during the week but told her to treat herself, which she can’t do because she has mobility issues. If that’s correct, and he knew, he sent her anyway, without checking to see if it would be ok, and again didn’t tell me at drop off.
We have on many occassions talked about stopping respite for Kelly because her foster dad is so difficult to deal with and has no consideration for our family. Knowing we have small children in our care he has sent her ( numerous times now) with head lice, a couple of times with gastro, and also with terrible head colds. It means we often cancel our plans for the weekend and then have sick small children to care for after Kelly has gone.
Kelly deserves so much better than the care she is recieving.
Our girls deserve so much more than the fallout from a Kelly visit.
This weekend the girls missed out on going to our foster agency Easter picnic and also to visit my parents. Why should Bonnie and Tyla miss out because of Kelly?
But, if we don’t provide respite for Kelly who will? Respite carers are in short supply. I know of carers who have waited years for respite, and being 15 makes it even harder to find someone to provie respite for her. If we don’t provide respite for Kelly, who is going to make sure she’s ok? Who’s going to advocate for her?
I’m torn between helping Kelly and keeping Bonnie and Tyla free of whatever bugs she brings with her.
My priority needs to be the little ones, but, how would we explain to Kelly we can’t provide respite for her anymore?