February 8, 2012 at 3:44 pm #144857BushMember
Hi dylly, and welcome to the site,
I’m sorry to hear about your son, it must be so difficult for you. Unfortunately I don’t have any children and I started pulling when I was 17, so I don’t really have any advice, but I wanted you to know that you’re not alone.
Most parents I’ve spoken to find that rewards help, but as you say, being 4 it’s hard to stick to a reward scheme. Especially as pulling is its own reward for us.
As your son has trichophagia, I hope your doctors are taking it very seriously, because ingested hair can cause so many problems.
Is your son always/ever aware of his pulling? Many people don’t notice when they pull, which makes it difficult to consciously stop. For girls/women I recommend a jangly, noisy bracelet so they hear their hand move. Is there anything similar you could do for your son? Something noisy (but not a girly bracelet!) to attach to his wrist or arm so he hears it move? Just an idea. Other than that, the best thing is to make sure he has lots of toys etc, to fiddle and play with to keep his hands busy.
I hope you find something which will help your son, and I hope your doctor can help as well. Keep us updated. Hopefully another parent will see your post and reply, as I am aware that I am not very helpful!
Love and hugs,
KayFebruary 8, 2012 at 5:29 pm #144858dyllyMember
Hi, thanks so much for your message of support, it really means an awful lot to have someone who understands. I will keep you updated on how he is doing and in answer to your question he is becoming more aware of when he is pulling since we started therapy.
Thanks again, Dylly.February 10, 2012 at 3:54 pm #144875JayaMember
thanks for posting dylly, have you tried sending an enquiry to the website via contact us or filling out a questionnaire yet? they can send you some advice for parents. it’s really hard to see your child pulling. At least you have noticed and are getting help for him.
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