As of
late, I haven’t been blogging. It’s not so much that I haven’t had things to
say as much as it has been a struggle about whether or not I should say it. I
hesitate to express feelings I’ve held for quite some time. But, here goes…
I have
made great friends through social media, blogging, and the chronic illness
community, and I am forever grateful for that. However, I feel like so often it
turns into a competition of who has it worse.
So, when I’ve
been doing relatively well, I hesitate to share it. In the last two years, I’ve
bought a house, gotten engaged, and gotten married. And while I know that the
friends I’ve made through this community are happy for me, it’s hard to
confront the larger community when so many others are struggling.
And it’s
not that I don’t struggle with lupus and RA. I definitely do. It’s just that the
suffering is no longer constant for me.
I’ve
wanted to share everything that’s been happening, both the good and the bad, but
it’s hard. It’s hard when you’re happy and want to celebrate it. It’s easier to
rail against the bad stuff – medications not working, doctors not listening,
struggling to stay above water when you feel like everything is closing in
around you – because you know that others can relate. You’ve heard it all
before, over and over again. You hear less of the good things.
And it
diminishes everyone to not allow the sun to shine through the clouds. It diminishes
all of us, because we are not just these illnesses. We are wives, husbands,
sisters, brothers, daughters, sons, friends, and so much more.
We are who
we are, and we should never have to apologize for that, or fear that having a
good day and sharing that, is going to anger those who aren’t in the same
place.
I think
that as a community, in order to be cohesive, we need to celebrate our triumphs
and our tragedies, our highs along and our lows, whether medical or otherwise.
We need to support each other, not tear each other down.
It starts
with a simple question: How are you? That’s pretty basic, right? But what’s not
so basic is to actually listen to the answer to the question, and to
enthusiastically respond, regardless of what the other person’s response is. If
someone’s doing well, be their cheerleader. If someone’s struggling, encourage
them.
We’re
stronger together. We’re stronger when we display a unified front, when we
fight as sisters and brothers in the struggle, no matter what stage of disease
we are in. We must acknowledge our shared experience. Our shared experience is
what brought us together in the first place, and our shared experience is what
will keep the community going.
In a world
filled with so much divisiveness and strife, we need to be part of the solution
rather than part of the problem.
The sooner
we stop fighting with each other, and start fighting for each other, the better
off we will be.
So true Leslie. The race to the most impacted is one we all lose because guess what, only one can be most impacted, and that leaves all 99% of us out.
ReplyDeleteThe sun ☀️ is shining on you. No judgement from the sun. Put it out there. Ship it. All you need is 3 people to read it. There’s me. Now 2 more. Got em. Go on the the next post. Thank you that you’ve got it as good as you do.
ReplyDeleteYes,we should fight for ourselves and for others, although it should not be necessary. After telling me that I had to go through hoops to get my antidepressant, my primary doctor says she will prescribe it just for the rest of the year, which is all I was asking for. Why do they have to make it so unnecessarily hard?
ReplyDeleteI am new to this. My sister has advanced ra, lupus and chrohns plus colon cancer. I appreciate the positive tone of these msgs. Thanks
ReplyDelete