Living With PPMS

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1. 

   ShayDee Member

   <p>I know the feeling. I&#39;m pretty sure I have PPMS but no one will call it that. Like you, by the time I was diagnosed, it was a few years that I went from one cane to two canes to walker/rollator to scooter/wheelchair. I just started using hand controls so I&#39;m driving again. That&#39;s made me feel a bit freer.</p>

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   1. 

      Lori Foster Member

      <p>How wonderful that you can drive again, <inline-mention username="ShayDee" user-id="4082506"/>. That bit of independence must be such a relief. Wishing you the best. - Lori (Team Member) </p>

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2. 

   Lori Foster Member

   <p>My heart goes out to you, <inline-mention username="cindyj" user-id="3966826"/> . It must be difficult to be unable to help your mother, but it sounds like you still did the right thing by encouraging her to move there, close to both you and your sister. I hope her treatments are successful. I am glad you have so much support from family and friends. That must make all the difference in the world. Sending lots of gentle hugs your way. - Lori (Team Member)</p>

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3. 

   cindyj Member

   <p>It would be nice to drive again but I can&#39;t get around to well so it may be a mote point. I have the best friends and am so thankful for my congregation of family. There are many who have stepped up to help my mother also. I thank Jehovah everyday for them.</p>

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