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Is This Normal?

10/27/2013

3 Comments

 
Things have changed drastically for me in the past six weeks.  After contracting some sort of mono-like virus my life has begun to take on a new look.  Gone are the days of zipping around the grocery store or taking the spot at the far reaches of the parking lot because “it’s only 15 seconds farther away.” I’m now walking so slowly with my cane that the World War II vets are asking me “Do you need help?”

It has been more than six weeks since my run in with the virus and my return to “normal” is taking much longer than it has in the past, so I’m now asking myself “is this my new normal?” If so it is going to take some getting used to. At my last neuro appointment my doc filled out the paperwork for a handicap parking pass and recommended that I not work until the New Year. After doing the timed walk that took a grand total of 30 seconds I needed to sit in a chair to catch my breath before heading into the exam room.

All of this is coming pretty fast and is all very overwhelming to me, so I’m asking you my fellow MSers “What do I need to do to keep from getting down on myself and remain positive?” “How do I end my current streak of bad news?”
 

--Blogger Donn
3 Comments
Jessica
10/29/2013 01:02:45 am

I'll be honest, there's probably no one who can stop your streak of bad news, however having people to talk to is a good start for coping.

A good support system of people with AND without MS is also good. Sometimes it's nice to talk to others who share the same strife's, but after awhile it becomes (at least in my experiences) a competition of symptoms, severities, losses, needs... etc. And having some people around who don't have MS but can let you vent your frustrations, who can lend an ear or a shoulder helps quite a bit.

A dog (or a really cuddly cat). Sitting and petting one (or several) can sometimes be more therapeutic than the aforementioned social needs.

A forum, website or chat group- for those days when you need to talk, but don't really want to be around people.

Reply
Donn
10/29/2013 05:26:42 am

Jessica,

Thanks for all of the information all are great suggestions.

Thanks, for posting.

Reply
Donn
10/29/2013 02:18:50 pm

Jessica,
thank you for the advice, I'm always working on my support system I just feel like I've hit a rough patch here lately. Thanks for posting.

Reply

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  • About Us
  • Home
  • 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