Let’s Talk, Caregiver to Caregiver
I’m Jaime, son and caregiver of my mother, Martha Yrene, who lived with Progressive Supranuclear Palsy (PSP). I know how lonely this road can feel. If you need to vent, share your story or ask about day-to-day caregiving, write to me. I read every message myself.
Fast, private and no forms.
Prefer Email?
If you don’t use WhatsApp or want to send something longer, email me at:
What Can You Write About?
🤝 Support
If you care for someone with PSP and need to talk with someone who has been there.
If you care for someone with PSP and need to talk with someone who has been there.
📖 Your Story
If you’d like to share your caregiving experience to help other families.
If you’d like to share your caregiving experience to help other families.
📚 Books & Resources
Orders for my books, journals and logbooks, or questions about using them.
Orders for my books, journals and logbooks, or questions about using them.
🔬 Collaborations
Doctors, researchers, associations or media who want to help raise awareness of PSP.
Doctors, researchers, associations or media who want to help raise awareness of PSP.
⚕️ Important: I’m not a doctor. I share my experience as a family caregiver and I’m happy to listen, but I don’t give diagnoses, treatments or doses. Any health decision should be discussed with your loved one’s doctor or therapist.
🚨 In an emergency, don’t write here: call your local emergency number (911 in the U.S.).
🔒 Your message is private. I don’t share your information with anyone. Read more in our Privacy Policy.
In the meantime, visit the PSP Caregiver Shop with my books and the home care products we used with my mother.