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Foundation in Waadt (Region)

: 2,139 Entries
 Closed until Dienstag um 08:00 Uhr
Schweizerische Hämophilie-Gesellschaft

Rating 5 of 5 stars from 2 ratings

Schweizerische Hämophilie-Gesellschaft

Scheidgasse 48, 3800 Unterseen

The Swiss Haemophilia Society The Swiss Haemophilia Society (SHG) was founded in 1965. It is a self-help organization that supports people with haemophilia and other congenital bleeding disorders, as well as their families. Professionally, it is supported by the Swiss Haemophilia Network (SHN) , which consists of treating physicians from haemophilia centers. The SHG represents the interests of those affected both publicly and vis-à-vis insurers and pharmaceutical companies. Like many other Swiss patient organizations, the SHG is a member of AGILE , the umbrella organization for disability self-help. Through AGILE.CH , the SHG also influences political processes and public opinion, for example regarding disability pensions (IV-Renten) or equality for people with disabilities. As a member of the World Federation of Hemophilia , the SHG maintains contact with international haemophilia societies. It manages a solidarity fund for individuals in financial need and provides information on insurance and legal matters. Our Activities Journée Romande This event takes place every two years in Western Switzerland. The event is alternately organized by one of the haemophilia centers in the region. In addition to lectures on medical topics related to haemophilia, participants have the opportunity to network and engage in personal discussions with other affected individuals and physicians. Berne Conference The annual Berne Conference focuses on families with children who have haemophilia and their surroundings. Medical and psychosocial aspects are addressed to help participants manage everyday life better. Topics include possible sports activities, siblings of children with haemophilia, correct dosing of medications, and more. The event provides ample opportunity for questions and exchange among family members. Organized by specialists from the Haemophilia Center at Inselspital Bern. SHG Summer Camp Each year, the SHG organizes a summer camp for children with haemophilia. This program allows young people with haemophilia to exchange experiences with peers. It promotes independence and responsibility in managing haemophilia, offers physical activities within their capabilities, and provides relief to parents caring for chronically ill children. Autumn Conference Organized by specialists from the pediatric and adult haemophilia centers of the SHN Eastern Region. The event begins in the morning with a shared brunch. Lectures focus on one or two current topics related to haemophilia, often featuring guest speakers who provide insights into complementary therapies supporting conventional medicine. The conference also offers opportunities to reconnect with old acquaintances and establish new contacts with other affected individuals. Workshop Every two years, the SHG organizes a two-day workshop weekend. The goal is to provide members with the opportunity for extensive exchange in a pleasant atmosphere. Specialized knowledge and entertainment are also part of the program, ensuring a balanced and informative experience.

CharitableFoundation
Schweizerische Hämophilie-Gesellschaft

Schweizerische Hämophilie-Gesellschaft

Scheidgasse 48, 3800 Unterseen
CharitableFoundation

The Swiss Haemophilia Society The Swiss Haemophilia Society (SHG) was founded in 1965. It is a self-help organization that supports people with haemophilia and other congenital bleeding disorders, as well as their families. Professionally, it is supported by the Swiss Haemophilia Network (SHN) , which consists of treating physicians from haemophilia centers. The SHG represents the interests of those affected both publicly and vis-à-vis insurers and pharmaceutical companies. Like many other Swiss patient organizations, the SHG is a member of AGILE , the umbrella organization for disability self-help. Through AGILE.CH , the SHG also influences political processes and public opinion, for example regarding disability pensions (IV-Renten) or equality for people with disabilities. As a member of the World Federation of Hemophilia , the SHG maintains contact with international haemophilia societies. It manages a solidarity fund for individuals in financial need and provides information on insurance and legal matters. Our Activities Journée Romande This event takes place every two years in Western Switzerland. The event is alternately organized by one of the haemophilia centers in the region. In addition to lectures on medical topics related to haemophilia, participants have the opportunity to network and engage in personal discussions with other affected individuals and physicians. Berne Conference The annual Berne Conference focuses on families with children who have haemophilia and their surroundings. Medical and psychosocial aspects are addressed to help participants manage everyday life better. Topics include possible sports activities, siblings of children with haemophilia, correct dosing of medications, and more. The event provides ample opportunity for questions and exchange among family members. Organized by specialists from the Haemophilia Center at Inselspital Bern. SHG Summer Camp Each year, the SHG organizes a summer camp for children with haemophilia. This program allows young people with haemophilia to exchange experiences with peers. It promotes independence and responsibility in managing haemophilia, offers physical activities within their capabilities, and provides relief to parents caring for chronically ill children. Autumn Conference Organized by specialists from the pediatric and adult haemophilia centers of the SHN Eastern Region. The event begins in the morning with a shared brunch. Lectures focus on one or two current topics related to haemophilia, often featuring guest speakers who provide insights into complementary therapies supporting conventional medicine. The conference also offers opportunities to reconnect with old acquaintances and establish new contacts with other affected individuals. Workshop Every two years, the SHG organizes a two-day workshop weekend. The goal is to provide members with the opportunity for extensive exchange in a pleasant atmosphere. Specialized knowledge and entertainment are also part of the program, ensuring a balanced and informative experience.

Rating 5 of 5 stars from 2 ratings

 Closed until Dienstag um 08:00 Uhr
 Closed until Montag um 08:30 Uhr
Stiftung Märtplatz

Rating 5 of 5 stars from 3 ratings

Stiftung Märtplatz

Othmar Blumer-Strasse 1, 8427 Freienstein
Welcome – The Märtplatz Foundation!

The Märtplatz Foundation is a training institution for young people facing psychological and social challenges. Around 45 individuals are trained in eleven workshops and studios, usually aged between 16 and 25. Vocational training takes place in a protected environment, with subsequent integration into the primary job market. Most trainees are referred by the disability insurance authority, in some cases by the juvenile court or a social services agency. The focus of the training is on the individual – their talents, interests, and abilities: strengths are nurtured, and manual, technical, and professional skills are learned and deepened. The training process takes into account specific difficulties and deficits. In this way, we offer all trainees a personalized education – in manual, creative, culinary, and technical professions. The goal is successful training and sustainable integration into the workforce. The following qualifications are offered: Federal Diploma of Vocational Education and Training (EFZ), Federal Vocational Certificate (EBA), and Practical Training according to INSOS (PrA). The Märtplatz Foundation was established in 1985 and is based in Freienstein, Zurich. The workshops and studios are located on the grounds of a former cotton spinning mill. Two shops are located in Embrach, and one in Rorbas.

FoundationYouth workAssisted livingPrivate schoolWorkshop for the handicappedTraining instituteInstitutions for people with disabilities
Stiftung Märtplatz

Stiftung Märtplatz

Othmar Blumer-Strasse 1, 8427 Freienstein
FoundationYouth workAssisted livingPrivate schoolWorkshop for the handicappedTraining instituteInstitutions for people with disabilities
Welcome – The Märtplatz Foundation!

The Märtplatz Foundation is a training institution for young people facing psychological and social challenges. Around 45 individuals are trained in eleven workshops and studios, usually aged between 16 and 25. Vocational training takes place in a protected environment, with subsequent integration into the primary job market. Most trainees are referred by the disability insurance authority, in some cases by the juvenile court or a social services agency. The focus of the training is on the individual – their talents, interests, and abilities: strengths are nurtured, and manual, technical, and professional skills are learned and deepened. The training process takes into account specific difficulties and deficits. In this way, we offer all trainees a personalized education – in manual, creative, culinary, and technical professions. The goal is successful training and sustainable integration into the workforce. The following qualifications are offered: Federal Diploma of Vocational Education and Training (EFZ), Federal Vocational Certificate (EBA), and Practical Training according to INSOS (PrA). The Märtplatz Foundation was established in 1985 and is based in Freienstein, Zurich. The workshops and studios are located on the grounds of a former cotton spinning mill. Two shops are located in Embrach, and one in Rorbas.

Rating 5 of 5 stars from 3 ratings

 Closed until Montag um 08:30 Uhr
* No advertising material

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Foundation in Waadt (Region)

: 2,139 Entries
 Closed until Dienstag um 08:00 Uhr
Schweizerische Hämophilie-Gesellschaft

Rating 5 of 5 stars from 2 ratings

Schweizerische Hämophilie-Gesellschaft

Scheidgasse 48, 3800 Unterseen

The Swiss Haemophilia Society The Swiss Haemophilia Society (SHG) was founded in 1965. It is a self-help organization that supports people with haemophilia and other congenital bleeding disorders, as well as their families. Professionally, it is supported by the Swiss Haemophilia Network (SHN) , which consists of treating physicians from haemophilia centers. The SHG represents the interests of those affected both publicly and vis-à-vis insurers and pharmaceutical companies. Like many other Swiss patient organizations, the SHG is a member of AGILE , the umbrella organization for disability self-help. Through AGILE.CH , the SHG also influences political processes and public opinion, for example regarding disability pensions (IV-Renten) or equality for people with disabilities. As a member of the World Federation of Hemophilia , the SHG maintains contact with international haemophilia societies. It manages a solidarity fund for individuals in financial need and provides information on insurance and legal matters. Our Activities Journée Romande This event takes place every two years in Western Switzerland. The event is alternately organized by one of the haemophilia centers in the region. In addition to lectures on medical topics related to haemophilia, participants have the opportunity to network and engage in personal discussions with other affected individuals and physicians. Berne Conference The annual Berne Conference focuses on families with children who have haemophilia and their surroundings. Medical and psychosocial aspects are addressed to help participants manage everyday life better. Topics include possible sports activities, siblings of children with haemophilia, correct dosing of medications, and more. The event provides ample opportunity for questions and exchange among family members. Organized by specialists from the Haemophilia Center at Inselspital Bern. SHG Summer Camp Each year, the SHG organizes a summer camp for children with haemophilia. This program allows young people with haemophilia to exchange experiences with peers. It promotes independence and responsibility in managing haemophilia, offers physical activities within their capabilities, and provides relief to parents caring for chronically ill children. Autumn Conference Organized by specialists from the pediatric and adult haemophilia centers of the SHN Eastern Region. The event begins in the morning with a shared brunch. Lectures focus on one or two current topics related to haemophilia, often featuring guest speakers who provide insights into complementary therapies supporting conventional medicine. The conference also offers opportunities to reconnect with old acquaintances and establish new contacts with other affected individuals. Workshop Every two years, the SHG organizes a two-day workshop weekend. The goal is to provide members with the opportunity for extensive exchange in a pleasant atmosphere. Specialized knowledge and entertainment are also part of the program, ensuring a balanced and informative experience.

CharitableFoundation
Schweizerische Hämophilie-Gesellschaft

Schweizerische Hämophilie-Gesellschaft

Scheidgasse 48, 3800 Unterseen
CharitableFoundation

The Swiss Haemophilia Society The Swiss Haemophilia Society (SHG) was founded in 1965. It is a self-help organization that supports people with haemophilia and other congenital bleeding disorders, as well as their families. Professionally, it is supported by the Swiss Haemophilia Network (SHN) , which consists of treating physicians from haemophilia centers. The SHG represents the interests of those affected both publicly and vis-à-vis insurers and pharmaceutical companies. Like many other Swiss patient organizations, the SHG is a member of AGILE , the umbrella organization for disability self-help. Through AGILE.CH , the SHG also influences political processes and public opinion, for example regarding disability pensions (IV-Renten) or equality for people with disabilities. As a member of the World Federation of Hemophilia , the SHG maintains contact with international haemophilia societies. It manages a solidarity fund for individuals in financial need and provides information on insurance and legal matters. Our Activities Journée Romande This event takes place every two years in Western Switzerland. The event is alternately organized by one of the haemophilia centers in the region. In addition to lectures on medical topics related to haemophilia, participants have the opportunity to network and engage in personal discussions with other affected individuals and physicians. Berne Conference The annual Berne Conference focuses on families with children who have haemophilia and their surroundings. Medical and psychosocial aspects are addressed to help participants manage everyday life better. Topics include possible sports activities, siblings of children with haemophilia, correct dosing of medications, and more. The event provides ample opportunity for questions and exchange among family members. Organized by specialists from the Haemophilia Center at Inselspital Bern. SHG Summer Camp Each year, the SHG organizes a summer camp for children with haemophilia. This program allows young people with haemophilia to exchange experiences with peers. It promotes independence and responsibility in managing haemophilia, offers physical activities within their capabilities, and provides relief to parents caring for chronically ill children. Autumn Conference Organized by specialists from the pediatric and adult haemophilia centers of the SHN Eastern Region. The event begins in the morning with a shared brunch. Lectures focus on one or two current topics related to haemophilia, often featuring guest speakers who provide insights into complementary therapies supporting conventional medicine. The conference also offers opportunities to reconnect with old acquaintances and establish new contacts with other affected individuals. Workshop Every two years, the SHG organizes a two-day workshop weekend. The goal is to provide members with the opportunity for extensive exchange in a pleasant atmosphere. Specialized knowledge and entertainment are also part of the program, ensuring a balanced and informative experience.

Rating 5 of 5 stars from 2 ratings

 Closed until Dienstag um 08:00 Uhr
 Closed until Montag um 08:30 Uhr
Stiftung Märtplatz

Rating 5 of 5 stars from 3 ratings

Stiftung Märtplatz

Othmar Blumer-Strasse 1, 8427 Freienstein
Welcome – The Märtplatz Foundation!

The Märtplatz Foundation is a training institution for young people facing psychological and social challenges. Around 45 individuals are trained in eleven workshops and studios, usually aged between 16 and 25. Vocational training takes place in a protected environment, with subsequent integration into the primary job market. Most trainees are referred by the disability insurance authority, in some cases by the juvenile court or a social services agency. The focus of the training is on the individual – their talents, interests, and abilities: strengths are nurtured, and manual, technical, and professional skills are learned and deepened. The training process takes into account specific difficulties and deficits. In this way, we offer all trainees a personalized education – in manual, creative, culinary, and technical professions. The goal is successful training and sustainable integration into the workforce. The following qualifications are offered: Federal Diploma of Vocational Education and Training (EFZ), Federal Vocational Certificate (EBA), and Practical Training according to INSOS (PrA). The Märtplatz Foundation was established in 1985 and is based in Freienstein, Zurich. The workshops and studios are located on the grounds of a former cotton spinning mill. Two shops are located in Embrach, and one in Rorbas.

FoundationYouth workAssisted livingPrivate schoolWorkshop for the handicappedTraining instituteInstitutions for people with disabilities
Stiftung Märtplatz

Stiftung Märtplatz

Othmar Blumer-Strasse 1, 8427 Freienstein
FoundationYouth workAssisted livingPrivate schoolWorkshop for the handicappedTraining instituteInstitutions for people with disabilities
Welcome – The Märtplatz Foundation!

The Märtplatz Foundation is a training institution for young people facing psychological and social challenges. Around 45 individuals are trained in eleven workshops and studios, usually aged between 16 and 25. Vocational training takes place in a protected environment, with subsequent integration into the primary job market. Most trainees are referred by the disability insurance authority, in some cases by the juvenile court or a social services agency. The focus of the training is on the individual – their talents, interests, and abilities: strengths are nurtured, and manual, technical, and professional skills are learned and deepened. The training process takes into account specific difficulties and deficits. In this way, we offer all trainees a personalized education – in manual, creative, culinary, and technical professions. The goal is successful training and sustainable integration into the workforce. The following qualifications are offered: Federal Diploma of Vocational Education and Training (EFZ), Federal Vocational Certificate (EBA), and Practical Training according to INSOS (PrA). The Märtplatz Foundation was established in 1985 and is based in Freienstein, Zurich. The workshops and studios are located on the grounds of a former cotton spinning mill. Two shops are located in Embrach, and one in Rorbas.

Rating 5 of 5 stars from 3 ratings

 Closed until Montag um 08:30 Uhr
* No advertising material