John Connor

Hi ZA,
Welcome – as you’re new to MS sure you’ll first look at the
‘Newly Diagnosed Forum’. As one of the
‘Patient Columnists’ here I wrote one, a while back, sparked by the
post ‘An Open Letter to a Newly Diagnosed
Patient’. Mind u, it only relates to Relapsing Remitting MS (RRMS)
https://mu…[Read more]

Hi Cynthia,
Didn’t know you could move from primary progressive to secondary progressive. I’m now SPMS also. Is it the same? Before I was RRMS.
Anyways, welcome – loads of info, research & experiences
on here.
You can also start topics – my fellow
moderator Ed Tobias explains ‘Posting Items’ at
the top of each Forum.
Cheers John

Hi S.M.,
My world still turns upside down when I drive too aggressively in my powered wheelchair! Hey-ho.
Anyways, welcome – loads of info, research & experiences
on here.
You can also start topics – my fellow
moderator Ed Tobias explains ‘Posting Items’ at
the top of each Forum.
Cheers John

Hi Anthony,
Welcome – loads of info, research & experiences
on here.
You can also start topics – my fellow
moderator Ed Tobias explains ‘Posting Items’ at
the top of each Forum.
Cheers John
PS BTW how old is your daughter?

Hi Deb,
Welcome – loads of info, research & experiences
on here.
You can also start topics – my fellow
moderator Ed Tobias explains ‘Posting Items’ at
the top of each Forum.
Cheers John

Hi Dennis,
Welcome – loads of info, research & experiences
on here.
You can also start topics – my fellow
moderator Ed Tobias explains ‘Posting Items’ at
the top of each Forum.
Cheers John

Hi Self,
It seems that recent studies indicate that Fibromyalgia is probably an autoimmune disease. MS most definitely is. Many of us are also severely affected by fatigue.
So there are some similarities.
Anyhoo, welcome – loads of info, research & experiences
on here.
You can also start topics – my fellow
moderator Ed Tobias explains ‘Po…[Read more]

Hi Laura,
Your not alone. There so many of us with MS that we don’t even count as a rare disease. Latest estimates for 2022 is there are million MS patients in the USA.
Try joining the MS Society and seeking out your nearest chapter. Indeed, do it the other way around.
Anyway welcome – as you’re new to MS sure you’ll first look at the
‘…[Read more]

Hi Ricardo,
Welcome – as you’re new to MS sure you’ll first look at the
‘Newly Diagnosed Forum’. As one of the
‘Patient Columnists’ here I wrote one, a while back, sparked by the
post ‘An Open Letter to a Newly Diagnosed
Patient’. Mind u, it only relates to Relapsing Remitting MS (RRMS)
https://mu…[Read more]

Hi Patrick,
Congrats on already posting a topic.
U’ve also rendered my welcoming spiel redundant!
So just welcome it is then.
The other moderator around these here parts is
Ed Tobias.
Cheers John

Hi Rita,
No cure but loads of new Disease Modifying Therapies (DMT’s) but even if it does work, it only leaves you as you are with some recovery. Destroyed areas of the brain remain destroyed..
Anyways, on that sombre, note welcome – loads of info, research & experiences on here.
You can also start topics – my fellow
moderator Ed Tobias exp…[Read more]

Hi Melody,
Welcome – loads of info, research & experiences
on here.
You can also start topics – my fellow
moderator Ed Tobias explains ‘Posting Items’ at
the top of each Forum.
Check out the Forum, ‘Treatments and Trials’, for the latest breakthroughs. Though a lot are on mice which rarely works on us humans. Also the Home page of our sites main…[Read more]

Hi Gloria,
Welcome – loads of info, research & experiences
on here.
You can also start topics – my fellow
moderator Ed Tobias explains ‘Posting Items’ at
the top of each Forum.
Cheers John