Support for
Patients and Caregivers

We are extremely grateful to caregivers and patient advocacy groups who help volunteers take part in clinical trials.

Pictured above: Hélène Bonnet, CSR Projects, France

Caregivers help volunteers in many ways, for example by:

  • driving them to and from a research facility, 
  • staying with them during evaluations,
  • filling out questionnaires on their behalf,
  • making sure their needs are understood and addressed, and
  • outside the research facility, ensuring their medications are administered correctly and on time.

This work, while rewarding, can be emotionally and physically fatiguing. Family caregivers may not have relevant training or assistance. Balancing work and other obligations can be challenging. The impact on mental and physical health cannot be ignored.

We do our best to provide accurate, reliable support services for caregivers. We provide information about health conditions, connect them with patient advocacy groups and support networks, and help them navigate questions that can be difficult to handle alone.

Support Resources

The following list provides links to patient advocacy groups with whom Sanofi currently partners. Please check back periodically as the list expands!

For people living with cancer:

Cancer Support Community 

GO2 for Lung Cancer 

Imerman Angels (matches Cancer patients with Cancer survivors for support)

LUNGevity (Lung Cancer)

HealthTree Foundation for Multiple Myeloma

Multiple Myeloma Research Foundation

Susan G. Komen (Breast Cancer)

Tigerlily Foundation (Breast Cancer)

For people living with immune diseases or inflammation:

AltogetherEczema (Atopic Dermatitis and Eczema)

For people living with Multiple Sclerosis:

International Progressive MS Alliance MS International Federation

For people living with Parkinson's disease:

The Michael J Fox Foundation for Parkinson's Research

For people living with rare blood disorders:

Cold Agglutinin Disease Foundation

Sickle Cell Disease Organization (ASCAA)

Hemophilia Federation of America

National Hemophilia Foundation 

For people living with rare diseases:

American Association of Kidney Patients (AAKP)

EveryLife Foundation for Rare Disease Europe (EURORDIS) Rare Disease UK

Gaucher Community Alliance 

Global Genes

National Fabry Disease Foundation

National MPS Society 

Polycystic Kidney Disease (PKDF)


MAT-GLB-2202355 v2.0 06/2023