Our Function

The function of the Association can be defined by three areas of activity:

Support, Education and Information

Support

Postnatally depressed women may feel unable to go out of their house, and meeting people may cause them a great deal of stress, therefore contact made on the phone or by e-mail can be ideal.

Women often find that talking, or writing to someone, who has had the illness and recovered, allows them to discuss the most distressing symptoms of the illness. The phone and e-mail volunteers also give women hope that they will eventually recover.  This service is also available to women who would prefer to be supported by post.

The Association has a countrywide network of phone and e-mail volunteers, who have had, and recovered from post-natal illness. The volunteers are carefully vetted to ensure that they are completely well, that they have had no previous mental illness and that they are not opposed to drug therapy.

Depressed mothers are contacted at regular intervals throughout their illness and the recovery period. The relationship between the volunteer and depressed mother is regularly monitored. Most women find it a great relief to talk to someone who really understands how they feel. Depressed mothers are always advised to seek medical help and constantly assured that they will recover.

The Association runs a support service for husbands and families of the depressed woman. Many of the volunteer husbands  will to talk to husbands of sufferers and offer help and advice if necessary.

If you have been diagnosed with postnatal illness we do advise you to try talking to one of our volunteers. You can call our helpline on 0207 386 0868 (Monday to Friday) or email us at [email protected] and we will gladly answer any enquiries that you may have.

Education

The Association has produced a leaflet which is available to maternity units, ante-natal clinics, etc. The leaflet describes the Baby Blues and Post-natal Depression. It seeks to make women more aware of this illness without alarming them. It is hoped that women who do suffer from post-natal depression will seek medical advice at an earlier time in the course of the illness if they are educated about it.  See Leaflets on PNI

The  Association has worked hard over many years to persuade the media to more accurately  describe post-natal illness and its effects. The Association is frequently asked to comment on news items and  we work hard to reduce sensational and alarming stories.

It is a matter of great sadness that some of the stigma of  suffering from post-natal depression still persists but we work continuously to give accurate information to members of the press who contact us.

All those individuals who contact the Association can do so in the utmost confidence.

All matters are considered confidential within our organisation and APNI continues to follow GDPR policies and guidance, our Privacy Policy is located on the home page.

Information

The Association has a publication called “Post-natal Depression. This explains the symptoms of the illness and gives some idea of the treatment available, and ways in which sufferers can help themselves.

It is constantly being revised and expanded. The Association is able to advise correspondents on a wide range of issues concerning the management and treatment of postnatal illness.

You are not alone, get in touch for some friendly advice, or just to talk through how you're feeling.

APNI is here to help you.

How to Donate

To make an online donation please click on the button below. This will take you through to our Just Giving page or our Virgin Money Giving page . All donations are appreciated however large or small.

Company Donations

If your company donates to charity, would you be able to put our association forward?


We exist solely on donations so any help or sponsorship would be hugely appreciated! Thank you.

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