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Taking Care of the Caregiver

11/19/2014

2 Comments

 
Being a caregiver to a MS patient doesn’t mean you are immune from your own health issues.  I was diagnosed with a seizure disorder 22 years ago, but have been seizure free for over 7 years with the help of medications. I had always thought my family would be well prepared to take care of my daughter if for some reason I was not around, either  for medical reasons or a much needed vacation.  I did experience a seizure a couple of days ago, recovered relatively quickly, but long enough to bring a dose of reality to my family.

I had always thought it was understood that my daughter’s daily medications were handily available for whomever needed to step into my place.  You can imagine my surprise when I was asked to write a list of her daily needs in case this happened again. This was a reminder that I should not be in sole care of my daughter and I need to make sure others know of her daily needs on a regular basis.

2 Comments
A.C.
6/29/2018 06:30:46 am

Hi there, you said you had made a list of needs i'm currently doing research on Ms and how it affects caregivers would you mind sharing this list with me? thanks a lot and great blog!

Reply
Johan
9/21/2020 11:54:05 am

After my Multiple Sclerosis diagnosis, my primary care provider introduced me to RichHerbs Foundation and i immediately started on their MS Formula protocol, the herbal treatment has made a tremendous difference for me. My symptoms including numbness and muscle weakness all disappeared after the recommended 5 months treatment! Their website is w w w. richherbsfoundation. c o m. Its just amazing

Reply



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  • Home
  • About Us
  • Virtual MS Center
    • Q & A for Virtual MS Center
    • Read About Our Virtual MS Center Staff
  • News & Resources
  • Seminar Registration
  • Health & Wellness
  • Blogs
    • Physician Blog >
      • Healthcare Provider Blog
    • Physical Therapy Blog
    • Patient Blog
    • Caregiver Blog
    • Research Blogs >
      • "Ask Dr. Debbie" Research Blog
      • Multiple Perspectives In Multiple Sclerosis Research Blog
  • About MS
    • What is MS?
    • Diagnosis
    • Treatment
    • MS Tips
  • Symptoms
    • Balance and Walking Issues
    • Breathing/Respiratory
    • Bowel Dysfunction
    • Cognitive Dysfunction
    • Crying/Laughing Uncontrollably (PBA)
    • Depression and Anxiety
    • Dizziness/Vertigo
    • Dysphagia
    • Fatigue
    • Foot Drop
    • Hearing or Smell or Taste Changes
    • Heat Sensitivity
    • Leg Weakness
    • Loss of Hand Dexterity and Coordination
    • Memory and Mutliple Sclerosis
    • Migraines
    • Numbness/Tingling/Altered Sensation
    • Nystagmus and Oscillopsia
    • Pain
    • Sexual Dysfunction
    • Sleep Issues
    • Spasticity/Spasms/Cramps
    • Speech/Swallowing
    • Urination/Bowel Problems
    • Vision
  • MS Clinics
  • MS Topics
    • Pregnancy and Infertility
    • Caregivers and Family Members
    • Employment and MS
    • Medical Costs and Insurance
    • Pediatric Multiple Sclerosis
  • Register With Us
  • Terms of Use/Privacy/HIPAA
  • MS HealthCare Journey