# The test!

**URL:** <https://forum.mssociety.org.uk/t/the-test/37350>\
**Category:** Primary progressive MS\
**Created:** [12 September 2016 19:53 UTC](https://forum.mssociety.org.uk/t/the-test/37350 "2016-09-12T19:53:25Z")\
**Posts on this page:** 3\
**Page:** 1

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**Author:** ![Inactive\_User](https://avatars.discourse-cdn.com/v4/letter/i/3e96dc/32.png) [@Inactive\_User](https://forum.mssociety.org.uk/u/Inactive_User)\
**Post date:** [12 September 2016 19:53 UTC](https://forum.mssociety.org.uk/t/the-test/37350/1 "2016-09-12T19:53:25Z")

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Evening all!

Incase some of you might not see my post on EL, today I saw my neuro and asked for genetic testing. It was back in 2011 that my diagnosis of.PPMS was changed to HSP.

There is no exact test for HSP, but once the neuro decided i didn’t have PPMS , it seems all that was left after everything else was eliminated , was HSP.

Like with MS, there is no cure, so it just has to be lived with!

But you know, a tiny part of me still wonders if I do have PPMS in a different form!

Pollx

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**Author:** ![skippysprite](https://dub1.discourse-cdn.com/mssociety/user_avatar/forum.mssociety.org.uk/skippysprite/32/912_2.png) [@skippysprite](https://forum.mssociety.org.uk/u/skippysprite)\
**Post date:** [14 September 2016 17:35 UTC](https://forum.mssociety.org.uk/t/the-test/37350/2 "2016-09-14T17:35:11Z")

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Hi Poll

Best of luck with the test, and please let us know the outcome.

Pam x

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**Author:** ![Snow\_Leopard](https://avatars.discourse-cdn.com/v4/letter/s/e79b87/32.png) [@Snow\_Leopard](https://forum.mssociety.org.uk/u/Snow_Leopard)\
**Post date:** [15 September 2016 08:16 UTC](https://forum.mssociety.org.uk/t/the-test/37350/3 "2016-09-15T08:16:32Z")

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All the best with the test Poll.

Thinking of you hon,

Pat xx