Call us between 10.00am and 2.00pm on: 0207 386 0868 or chat with us using the chat box on the bottom left of the website.
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
Many of us feel much worse when shops are noisy and bright so this quiet hour will be a welcome blessing.
Monday 8 October 2018
De Vere West One Conference Centre, London
This National Perinatal Mental Health Summit focuses specifically on implementing the 2018 National Perinatal Mental Health Care Pathways. The five pathways announced in May 2018 focus on Preconception advice, Specialist assessment, Emergency assessment, Psychological interventions and Inpatient care.
For further information and to book your place visit
www.healthcareconferencesuk.co.uk/perinatal-mental-health-services-conference or email [email protected]
or email [email protected]
To receive 25% discount quote HCUK25APNI
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.
The Association gratefully acknowledges the very generous support of Mr and Mrs J. A. Pye’s Charitable Settlement over the past 28 years. This support has enabled the Association to offer its services to many more sufferers, who otherwise we might not have been able to reach.The support of the Mr and Mrs J.A. Pye’s Charitable Settlement has enabled APNI to offer help to thousands of women over 28 busy years.
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.
APNI would like to say huge thanks to Tessa for raising £872 by completing the Hackney Half Marathon. Tessa said: “For those that know me well, running a half-marathon is totally out of my comfort zone and is something I have on my ‘things to do before I’m 40’ list. MORE>
From sponsored walks to motorcycle rides across the Arctic we appreciate everything you can do. MORE
Lucie Holland has raised over £4,000 during the past two years on her Just Giving page set up in memory of her sister Emma Cadywould. Emma’s family, in particular Lucie, and her parents Mr and Mrs Holland and have been very generous contributors to the work of the Association and our profound thanks go to the whole family for their generous donations and fundraising efforts. Emmsie’s friends have also been busy raising money in her memory.