Primary progressive MS (PPMS)
Any suggestion how to come with it
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
Any suggestion how to come with it
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
@hansa, I see from your previous post in the Multiple Sclerosis (MS) - please introduce yourself discussion that you are looking for any suggestions on how to cope with extreme fatigue and numbness in toes and fingers from the PPMS. While we wait for other members with PPMS to share their experience and what helps, I thought I would share this information from the National MS Society in case you haven't already seen it.
--- Numbness or Tingling: https://stage.nationalmssociety.org/Symptoms-Diagnosis/MS-Symptoms/Numbness
--- Fatigue: https://stage.nationalmssociety.org/Symptoms-Diagnosis/MS-Symptoms/Fatigue
--- Other symptoms: https://stage.nationalmssociety.org/Symptoms-Diagnosis/MS-Symptoms.