The Aphasia Caregiver Guide: Advice for navigating aphasia and your love ones care without losing yourself on the journey.,Used
The Aphasia Caregiver Guide: Advice for navigating aphasia and your love ones care without losing yourself on the journey.,Used

The Aphasia Caregiver Guide: Advice for navigating aphasia and your love ones care without losing yourself on the journey.,Used

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It is with great pleasure that the National Aphasia Association makes this book on caregiving available to the aphasia community. It is our mission to serve families living with aphasia, with an emphasis on the word family. We know that aphasia affects the whole family, indeed, the person? whole sphere of influence. When an individual experiences a stroke or other brain trauma that leads to aphasia, life changes in an instant.We recognize that the road to a future with aphasia can be a rocky one, with many twists and turns. Aphasia is a lifelong condition. No one is prepared for all the adaptations that will need to be made. It is our intent that this book will provide some help navigating the path which leads to a ?ew normal.?This document was prepared by the NAA team and reviewed by caregivers who gave us their expert input. Not all the information will apply to every family and not every family will be in a position to use all of the suggestions. Take from it what you find most helpful and what makes the most sense foryour situation.Most importantly, this should be a dynamic book. We?e compiled our thoughts, but you?l see in the final chapter that we welcome your thoughts. Please use the linked form in the final chapter to give us your helpful hints and suggestions. If you share what worked best for you, we can include the information in the next version to provide a much more comprehensive guide for all caregivers.The NAA has a proud history of service to the aphasia community. We hope you enjoy this latest initiative, we hope you share the information, and we hope you continue to engage with and support the NAA.

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We ship your order within 2–3 business days for USA deliveries and 5–8 business days for international shipments. Once your package has been dispatched from our warehouse, you'll receive an email confirmation with a tracking number, allowing you to track the status of your delivery.

Returns
To facilitate a smooth return process, a Return Authorization (RA) Number is required for all returns. Returns without a valid RA number will be declined and may incur additional fees. You can request an RA number within 15 days of the original delivery date. For more details, please refer to our Return & Refund Policy page.

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We provide a 2-year limited warranty, from the date of purchase for all our products.

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This warranty strictly does not cover damages that arose from negligence, misuse, wear and tear, or not in accordance with product instructions (dropping the product, etc.).

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Frequently Asked Questions

  • Q: What is the main purpose of The Aphasia Caregiver Guide? A: The Aphasia Caregiver Guide aims to assist families navigating the challenges of caregiving for loved ones with aphasia, providing advice and insights to help them adjust to their new normal.
  • Q: Who authored The Aphasia Caregiver Guide? A: The guide is authored by the National Aphasia Association, which has a history of supporting the aphasia community.
  • Q: How many pages does The Aphasia Caregiver Guide have? A: The guide contains 78 pages of valuable information and support for caregivers.
  • Q: What type of binding does The Aphasia Caregiver Guide have? A: The Aphasia Caregiver Guide is available in a paperback binding.
  • Q: When was The Aphasia Caregiver Guide published? A: The guide was published on February 13, 2020.
  • Q: Is The Aphasia Caregiver Guide suitable for all families? A: While the guide provides helpful suggestions, not all information may apply to every family, and caregivers are encouraged to adapt the advice to their unique situations.
  • Q: Does The Aphasia Caregiver Guide include contributions from caregivers? A: Yes, the guide includes insights and suggestions from caregivers, ensuring the content is relevant and practical.
  • Q: Can readers contribute their own suggestions for future editions of The Aphasia Caregiver Guide? A: Yes, the guide encourages readers to share their experiences and tips through a linked form in the final chapter for potential inclusion in future editions.
  • Q: Is there a focus on family support in The Aphasia Caregiver Guide? A: Yes, the guide emphasizes the importance of family support, acknowledging that aphasia affects the entire family and community.
  • Q: What challenges does The Aphasia Caregiver Guide address for caregivers? A: The guide addresses the various challenges caregivers face, including emotional adjustments and practical caregiving strategies for individuals with aphasia.