Most people today have heard the term ‘baby blues’ used to describe a mild, short, period of depression which many women experience after childbirth.
Fewer people are aware that as many as 10% of all recently delivered women develop postnatal depression. You are not alone in suffering.
The Association for Post-Natal Illness is the leading organisation in its field. It is a Registered Charity (No. 280510) and it was established in 1979 to:
– Provide support to mothers suffering from post-natal illness
– Increase public awareness of the illness
– Encourage research into its cause/nature
Question by Wera Hobhouse MP
3rd October 2019
Wera Hobhouse put a question to the Department of Health asking that as they are negotiating new contracts with GP’s that part of the new contract should be a fee for a proper mental and physical check of all new mothers 6 weeks after they have given birth.
Ms Hobhouse said that as Post-natal Depression affected many women after birth it was an opportunity for this illness to be identified.
Two other MP’s spoke adding their support to this question
The Association for Post-natal Illness gratefully acknowledges the very generous financial support of Mr and Mrs J. A. Pye’s Charitable Settlement since 1985. This support has enabled our organisation to continue through difficult financial times where otherwise we would have had to close. The funding given to APNI has enabled us to offer our services to thousands more sufferers.
The Association was founded in 1979 and we know that we would not be reaching our 40th Anniversary without the generous support given by the Pye Charitable Settlement.
We remember with gratitude and affection the late Mrs Mary Pye, and her son Mr Graham Pye, both of whom took a particular interest in our work.
Many of us feel much worse when shops are noisy and bright so this quiet hour will be a welcome blessing.
Apni have started a Youtube channel. If you find any Youtube links that you feel would benefit those suffering from postnatal depression or their families please email them to us through our contact form.
The Association provides a telephone helpline, information leaflets for sufferers and healthcare professionals as well as a network of volunteers (telephone and postal), who have themselves experienced postnatal illness. For a printed information pack send a s.a.e. to:- 145 Dawes Road, Fulham, London, UK, SW6 7EB or click on Leaflets on PNI for more information about PNI.
The work of the Association is essential as post-natal illness affects between 70,000 and 100,000 women and their babies in the UK every year. It is rightly called ‘the silent epidemic’.
Hi all, can any of our working mums or dads out there (or anyone you know) help raise much needed funds for APNI?
If your company donates to charity, would you be able to put our association forward.
We exist solely on donations so any help would be hugely appreciated! : THANK-YOU.
The Association has produced a number of leaflets relating to PNI, both for mothers and the medical profession. Below are the two leaflets that we send to mothers or individuals who need information on the subject:-
Click here for The Baby Blues and PND (This leaflet is available in the following languages on request:- Bengali, Gujarti, Hindi, Urdu, Punjabi).
The Association also has a ‘GUIDE TO PROGESTERONE FOR POSTNATAL DEPRESSION’ booklet. This is available on request.
We urgently need to recruit women who have suffered post-natal depression and who are now better, to support mothers who are currently ill by phone or by e-mail. Please click here to request information about becoming a volunteer.
We are truly grateful to the Friends of St Mary’s Barnes for choosing APNI as one of the beneficiaries of their 2019 Charity Ball and their very generous donation of £7,500.00. The Arabian-themed event was attended by our Chairman, David Wilson Clarke and Liz Wise, who is one of our Trustees. Truly a magical evening. (Photo credits to Andy Tyler Photography).
From sponsored walks to motorcycle rides across the Arctic we appreciate everything you can do. MORE
Lucie Holland has raised over £5,000 on her Just Giving page set up in 2012 in memory of her sister Emma Cadywould. Emma’s family, in particular her sister Lucie, and her parents Mr and Mrs Holland have been very generous contributors to the work of the Association and our profound thanks go to the whole family for their donations and fundraising efforts. Emma’s friends have also been busy raising money in her memory.