Yesterday I spent a couple of hours
collecting for Arthritis New Zealand. It was
far more tiring, but also far more enjoyable than I thought it was going to be.
So many people stopped and told me their
stories. People of all ages either had a form of arthritis themselves, or had
loved ones who did. They all gave so generously, donating handfuls of coins and
a huge number of people gave $5, $10 or even $20 dollar notes. Many people were
apologetic over not being able to give more, but every little bit makes a
difference. By the time I dropped the bucket off at the bank, it was almost too
heavy for me to carry.
One of the stories that really stuck with
me was a young mother who showed me her very painful-looking wrist, and said
that she was in the process of getting a diagnosis of Scleroderma. She said
that Arthritis New Zealand had been incredibly helpful to her, which was great
to hear.
Many other people who were not affected by
arthritis themselves, stopped and asked me my story. Though many still asked what
I’d done to my leg, others realised straight away my reason for having
Molly-Stick and for collecting for Arthritis New Zealand.
It was interesting to note that everyone had heard of lupus (possibly from
watching House!) but no-one had ever come across Psoriatic Arthritis before.
One man asked me how they treat arthritis in young people, and when I said
chemotherapy he said “But that’s only for lupus, not for other types, isn’t
it?” so I think it turned into quite an awareness raising exercise as well.
I ran into a few people I know, and one
woman gave me a coin because she thought she’d recognised me as Mike’s daughter
(I did tell her he’s not my dad.) I did have to laugh, as a couple of people I
know avoided eye contact and quickly walked away (it’s okay, I wouldn’t have
guilt tripped you!)
My tremors and joints were not a huge fan
of the standing still for so long, so I did get rather shaky and probably
looked like I was doing the needs-to-pee dance, as I shifted around trying to
keep my joints from locking up. The bucket did end up on the floor at one
point, as my hands decided they weren’t having any more of it, but some lovely
ladies helped me out picking it up and reclaiming the coins that had made a
break for freedom. Another very nice guy offered me an energy drink, to keep me
going, however I decided that would probably not be the best idea seeing as I
was already shaking!
As I said, the day was quite tiring. I was
supposed to be collecting from 1pm-2pm but it wasn’t until about 2.30pm that I
realised the time. As there was no-one available to collect after me, I decided
to stay until 3pm as there were still many people donating. In fact, it became
rather hard to leave as people were still coming up to me with coins as I was
packing up to leave. I had to go into town to get a blood test straight after,
then managed to fall asleep sitting upright in a café!
Thank you so much to everyone who donated,
or came up and talked to me. Thank you too, to all the staff at New World
Thorndon and Arthritis New Zealand who did
such as great job of organising all of the collectors.
Little Miss Autoimmune