Commentaires 11
Filtres:
Notation
La langue
Trier:
Le plus récent
S
6 il y a des mois

🌟⭐⭐⭐🌟

🌟⭐⭐⭐🌟

Just stumbled upon this charitable foundation's website and it left quite an impression! The website design is clean and simple, making it easy to navigate and find information. 👌 The organization's mission of supporting families affected by a particular condition is truly commendable. However, I did find that the website lacked detailed information about their programs, initiatives, and impact. It would have been great to see more stories or testimonials from the families they've helped. 💬 Additionally, the website seems to be static and could benefit from more frequent updates to keep visitors engaged and informed. 💻 Overall, while the foundation's efforts are laudable, I believe there is room for improvement in terms of transparency and engaging content. With some enhancements, I am confident this foundation can continue making a positive impact on families in need. 🤝💙

D
7 il y a des mois

I've had the privilege of working closely with the...

I've had the privilege of working closely with the A.l.s. family charitable foundation and have been consistently impressed by their dedication and compassion. Their commitment to helping those affected by ALS is truly remarkable. They provide invaluable resources and support to families facing this challenging disease. The impact they have made is undeniable, and I am proud to be associated with such an amazing organization.

S
8 il y a des mois

I have been following the work of the A.l.s. famil...

I have been following the work of the A.l.s. family charitable foundation for a while now, and I am continuously amazed by their impact. The support they provide to families facing ALS is invaluable, and their commitment to finding a cure is unwavering. I appreciate the effort they put into raising awareness and funding research. They are truly making a difference in the lives of so many.

C
8 il y a des mois

💙 I can't say enough good things about the A.l.s. ...

💙 I can't say enough good things about the A.l.s. family charitable foundation. They have been a source of support and comfort for my family during a difficult time. The resources they provide and the sense of community they foster is truly remarkable. I am incredibly grateful for their dedication to helping those affected by ALS. Thank you for all that you do!

J
10 il y a des mois

👍 The A.l.s. family charitable foundation is doing...

👍 The A.l.s. family charitable foundation is doing a fantastic job in supporting individuals and families affected by ALS. The services they provide are incredibly valuable and make a real difference. It's heartwarming to see an organization that truly cares and goes above and beyond to help those in need. Their dedication is inspiring, and I'm grateful for their work.

C
11 il y a des mois

I recently came across this organization and was i...

I recently came across this organization and was impressed by their commitment to making a difference in the lives of those affected by ALS. The A.l.s. family charitable foundation provides resources and support to families who are dealing with this challenging disease. I appreciate the efforts they make in raising awareness and funding research for finding a cure. It's great to see an organization so dedicated to making a positive impact.

M
Il y a 1 an

I came across this organization while searching fo...

I came across this organization while searching for resources for ALS support. I was pleasantly surprised by the wealth of information available on their website. The A.l.s. family charitable foundation provides comprehensive resources and a supportive community for individuals and families affected by ALS. The website is easy to navigate and offers a range of useful tools. I highly recommend checking them out if you or someone you know is dealing with ALS.

F
Il y a 1 an

💙 I cannot express enough how grateful I am for th...

💙 I cannot express enough how grateful I am for the support provided by the A.l.s. family charitable foundation. They have been a lifeline for me and my family as we navigate the challenges of ALS. The resources they offer, the sense of community they create, and the empathy they show is truly exceptional. I feel truly blessed to have found this organization in our time of need.

J
Il y a 1 an

The A.l.s. family charitable foundation is a truly...

The A.l.s. family charitable foundation is a truly remarkable organization! Their dedication and commitment to helping those affected by ALS is inspiring. The resources they provide and the support they offer to families is invaluable. I have personally seen the positive impact they have made on the lives of those struggling with this devastating disease. The work they do is truly amazing and I highly recommend supporting them. 💙

N
Il y a 1 an

😊 I've been involved with the A.l.s. family charit...

😊 I've been involved with the A.l.s. family charitable foundation for some time now, and I must say they are an incredible organization. The work they do in supporting families affected by ALS is outstanding. Their commitment to improving the lives of those touched by this disease is unwavering, and I am honored to be a part of their mission. Keep up the amazing work!

O
Il y a 1 an

The A.l.s. family charitable foundation has been a...

The A.l.s. family charitable foundation has been a lifeline for me and my family throughout our journey with ALS. Their resources, support, and sense of community have been invaluable. It's difficult to put into words how grateful I am for the help they have provided. Their dedication is truly commendable, and I highly recommend their services to anyone in need.

À propos de A.l.s. family charitable foundation

L'A.L.S. Family Charitable Foundation est une organisation à but non lucratif qui fournit un soutien et des ressources aux personnes et aux familles touchées par la sclérose latérale amyotrophique (SLA), également connue sous le nom de maladie de Lou Gehrig. La fondation est basée à Cape Cod, Massachusetts, et est au service de la communauté SLA depuis 1998.

La SLA est une maladie neurodégénérative progressive qui affecte les cellules nerveuses du cerveau et de la moelle épinière, entraînant une faiblesse musculaire, une paralysie et éventuellement la mort. Il n'existe actuellement aucun remède contre la SLA, mais l'A.L.S. La Family Charitable Foundation se consacre au financement des efforts de recherche visant à trouver un remède à cette maladie dévastatrice.

La fondation a été fondée par Steve Saling, qui a reçu un diagnostic de SLA en 2006 à l'âge de 38 ans. Malgré son diagnostic, Steve est resté déterminé à vivre pleinement sa vie et à faire une différence dans la vie des autres personnes atteintes de la SLA. Il a fondé l'A.L.S. Family Charitable Foundation comme moyen de fournir un soutien et des ressources aux personnes touchées par cette maladie.

La fondation offre une vaste gamme de services aux personnes vivant avec la SLA et à leurs familles. Ces services comprennent une aide financière pour les dépenses médicales non couvertes par l'assurance, les modifications du domicile telles que les rampes ou les ascenseurs pour fauteuils roulants, l'aide au transport pour les rendez-vous ou les traitements médicaux, les soins de relève pour les soignants qui ont besoin de s'absenter de leurs fonctions de soins, le soutien émotionnel par le biais de services de conseil ou de soutien. groupes.

En plus de fournir des services de soutien direct aux personnes vivant avec la SLA et à leurs familles, l'A.L.S. Family Charitable Foundation finance également des efforts de recherche visant à trouver de nouveaux traitements ou même un remède à cette maladie. La fondation a financé de nombreux projets de recherche au fil des ans visant à mieux comprendre comment la SLA se développe et progresse.

L'un des projets de recherche les plus remarquables financés par l'A.L.S. Family Charitable Foundation est Project Revoice - une technologie innovante qui permet aux personnes atteintes de SLA qui ont perdu leur capacité de parler en raison d'une faiblesse musculaire de retrouver leur voix en utilisant une parole synthétique générée à partir de leur propre voix enregistrée. Cette technologie révolutionnaire a changé la donne pour de nombreuses personnes vivant avec la SLA, leur permettant de communiquer plus efficacement avec leurs proches et leurs soignants.

L'A.L.S. La Family Charitable Foundation s'est également engagée à sensibiliser le public à la SLA et à plaider pour un financement accru des efforts de recherche. La fondation organise de nombreux événements tout au long de l'année, y compris une marche annuelle pour collecter des fonds et faire connaître la recherche sur la SLA.

En conclusion, l'A.L.S. Family Charitable Foundation est une ressource vitale pour les personnes et les familles touchées par la SLA. Grâce à ses services de soutien direct, au financement de projets de recherche et à ses efforts de plaidoyer, la fondation a un impact significatif dans la lutte contre cette maladie dévastatrice. Si vous ou quelqu'un que vous connaissez vivez avec la SLA, veuillez visiter le site Web de l'A.L.S. Site Web de la Family Charitable Foundation pour en savoir plus sur la façon dont ils peuvent vous aider à naviguer dans ce voyage difficile.

Traduit
A.l.s. family charitable foundation

A.l.s. family charitable foundation

4