Starting a family
MS is most often diagnosed between the ages of 20-40, the age at which many people may be thinking of having a family. Deciding whether to start or add to a family is often a complicated process, and MS raises a host of other questions to consider.
MS Trust links
- Pregnancy and parenthood factsheet
- Summarises the research into the health aspects of MS and becoming a parent, and helps people discuss issues and concerns with the health professionals they see
- MS pregnancy and parenthood
- Article from Open Door, the MS Trust's quarterly newsletter
- Baby, MS and me
- A blog written by a woman with MS, following her through her pregnancy and beyond.
Other sources of information
- NCT (National Childbirth Trust)
- Provides information, publications and networks. There are branches throughout the country. NCT also provides ante and post natal groups
- Home Start
- A charity that provides supports for families dealing with illness, disability or social isolation. Operates through a network of trained parent volunteers
- DPPi (Disability, Pregnancy & Parenthood international)
- National organisation of disabled parents and people who hope to become pregnant. Offers a network with other disabled parents, practical helpline, a newsletter, backing for parents who are having difficulties, and training for professionals
- Disabled Parents Network
- Nationwide network of disabled parents, aiming to build up local and national networks of peer support, increase public awareness, and work for improvement in services
- Parents with Disabilities online
- As well as information on parenting, this website also hosts international peer support and email network of disabled parents
- Breastfeeding Network
- An independent source of support and information for breastfeeding women and those involved in their care
- La Leche League
- An organisation that aims to help mothers to breastfeed through mother-to-mother support, information and education