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I'm an MSer and a Librarian

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Underwear and pills, oh my!

by LornaNovember 6, 2017March 12, 2020

When I was first diagnosed, ATMs existed and there were 24-hour grocery stores. I remember thinking that of all the times in history to

Money tips for MSers

by LornaOctober 30, 2017March 12, 2020

Since your earning power is widely regarded as your greatest resource, for those of us with MS it is even more critical

How to Find an MS Doctor

How to Find an MS Doctor

by LornaOctober 23, 2017April 14, 2020

This is how you can look for an MS specialist.

Would you rather?

by LornaOctober 6, 2017March 12, 2020

Just two years after diagnosis, my friend has died. Ovarian cancer. Kinda ironic because she was the least girly-girl I knew, so

MSer in a heat wave

MSer in a heat wave

by LornaSeptember 4, 2017April 16, 2020

Many MSers experience a temporary worsening of symptoms when the weather is very hot, or really anytime their core body temperature rises

Our chronic inflammation

by LornaAugust 21, 2017March 12, 2020

Inflammation is one of the body's responses to injury. It is considered acute (temporary), when you get hurt in sports or have

The biotin protocol

The biotin protocol

by LornaAugust 7, 2017April 16, 2020

The protocol, created by the company MedDay Pharmaceuticals in France, tests high-doses of the vitamin Biotin. The trial aims to prove that

Where I live

by LornaJuly 31, 2017March 12, 2020

When I was diagnosed, I was counseled to go home and make plans to be in a wheelchair. Wow.

Wash but don’t rinse

by LornaJuly 17, 2017March 12, 2020

I discovered no-rinse laundry soap for hand-washing. Genius!

Play the cards you are dealt

by LornaJuly 10, 2017March 12, 2020

When you are first diagnosed with MS, and you suddenly feel like you are in free-fall, it's helpful to quickly assess your

Reluctant budgeter

by LornaJuly 3, 2017March 12, 2020

I've always seen making a budget as "more of a guideline".

Feed yourself

by LornaJune 26, 2017March 12, 2020

I work from home full-time as a "reasonable accommodation" for my MS (see the Americans with Disabilities Act, or ADA for description). Unfortunately, my office space

I celebrate a carepartner: my Dad

by LornaJune 18, 2017March 12, 2020

A poem I wrote to my dad for Father's Day.

All ‘flavors’ of MS

by LornaJune 12, 2017March 12, 2020

Last week I wrote a post about the new MS drug Ocrevus and used some acronyms that I didn't properly stop to

Jury still out on Ocrevus

by LornaJune 5, 2017March 12, 2020

The new MS treatment Ocrevus is showing a dramatic reduction in active relapses. But what about the rest of us?

When you have trouble falling asleep

by LornaMay 29, 2017March 12, 2020

Try these suggestions the next time you have trouble falling to sleep

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