Appreciation Y'all!: I can't express my appreciation... - NRAS

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Appreciation Y'all!

kellymomcars profile image
31 Replies

I can't express my appreciation for the information and joy that y'all bring to my day! I am a newbee to NRAS and Beyond Psoriasis, and feel so grateful to have my thirst for information satisfied any time I have a question -- I can usually find real answers on HealthUnlocked (not much help in reading predictable pharmaceutical pamphlets - "blah, blah, blah").

And special thanks to the frequent posting people in NRAS! There aren't many days that go by without someone posting a hilarious take on a difficult day -- some of you really are very naughty... my kind of people!

Just a little background about me. I am an almost 60 year old female living in the great state of Texas. I have been diagnosed with psoriatic arthritis as of December 2020. I'm on my 3rd biologic -- Cimzia and Humira gave me horrible hives, and I have just finished my loading doses of Cosentyx with luck so far.

I have been so very fortunate to have been health issue free my whole life until this diagnosis. It has been a quick learning curve with so many health issues added to my plate -- mixed incontinence, cervical radiculopathy, erythrocytosis, to name a few. Now waiting to see a Neurologist because the bottom of my feet tingle all the time -- what's up with that?

I find it very frustrating the lack of knowledge that doctors (outside of Rheumatologists) have about RA and PsA. There are so very many affects chronic inflammation can have on a body, and each problem is treated as it's own issue without thought about the treatment of the cause -- just test, medicate and operate away. Enough of my soapbox...

So, I felt the need to let you know that I appreciate y'all. You are my peeps!

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kellymomcars profile image
kellymomcars
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31 Replies
Neonkittie17 profile image
Neonkittie17

Sending smiles from this side of the pond 💗😀

kellymomcars profile image
kellymomcars in reply to Neonkittie17

One of the things I like the most is finding out where everyone live. It makes me feel like beyond all the media noise, we are still just a bunch of people that belong together as a community. Smiles back atcha!

Neonkittie17 profile image
Neonkittie17 in reply to kellymomcars

We have a strong bond 😍

It’s definitely a God send this sight. I get tingling feet . Some of it caused by medication or active disease but I’ve recently been diagnosed with fibromyalgia which has answered a lot of questions. A lot of us have multiple problems.. bloody RA. Yep and medics are useless often feel like I give a lecture on meds and side effects 🙄 keep in touch and do join in the naughty chats it keeps us going x

kellymomcars profile image
kellymomcars in reply to

One of my favorite quotes I tell myself is to be "bloody bold and audacious". This has not been my norm, but I definitely am learning.

in reply to kellymomcars

Good one!

Mmrr profile image
Mmrr

Welcome ! I love it 'bloody bold and audacious' , you will find a few of us fit into this category on the forum 😎

kellymomcars profile image
kellymomcars in reply to Mmrr

I know there is! Y'all are great.

sylvi profile image
sylvi

Welcome to the club of RAers darling.xxxx

kellymomcars profile image
kellymomcars in reply to sylvi

I finally decided to introduce myself after others here were worried because you hadn't posted for a bit. How wonderful to find out that you mattered to people.

sylvi profile image
sylvi in reply to kellymomcars

It is true darling we are a very caring bunch here. xxxx

stbernhard profile image
stbernhard

Well, you sound like my kinda girl. Positive! Welcome 😊

kellymomcars profile image
kellymomcars in reply to stbernhard

Oh my gosh, and your recent post about being stubborn and stupid...! If you don't mind, I am going to add that to my collection of mantras 🤗

sylvi profile image
sylvi in reply to kellymomcars

We all have mantras like that, i am stupid before i am always over doing it and paying for it. Some of the things i get up to are just plain stupid, but at the end of the day we all laugh about it. xxxxx

Bless your heart 😁

Did I get this right ? Meant it the nice way not the sarcastic way 😘

kellymomcars profile image
kellymomcars in reply to Marionfromhappydays

Oh course you got it right. Here in the South, "bless your heart" is more often than not meant sarcastically. It's still a blessing (and those folks need all the blessings they can get) 😇

Gladders profile image
Gladders

What I like about this site is people tell how it "really is" living with RD.

kellymomcars profile image
kellymomcars in reply to Gladders

Me too. Can't get this kind of advice anywhere else

Sheila_G profile image
Sheila_G

It is good to welcome you to the site from across the Atlantic. Stay posted.

kellymomcars profile image
kellymomcars in reply to Sheila_G

I will. I don't post to any social media anywhere else -- y'all make this feel so safe

Sheila_G profile image
Sheila_G in reply to kellymomcars

I don't do any either. This is totally different.

Green230461 profile image
Green230461

Texas- well if you have to be ill with RA at least you are in a wonderful part of the world I have visions of John Wayne and Audy Murphy as my RA consultants on a horse each with the pink horizon behind them…. And up comes nurse Yul Brenner…….yehaw

kellymomcars profile image
kellymomcars in reply to Green230461

Oh yeah! My favorite cowboy is my husband (corny but true). Although Tom Selleck makes a pretty picture on a horse !

Green230461 profile image
Green230461 in reply to kellymomcars

They both have great teeth!

Kags1068 profile image
Kags1068

Welcome!👋👋😊xx

kellymomcars profile image
kellymomcars in reply to Kags1068

Thank you so much!🤗

Ritaritis profile image
Ritaritis

Hi Kellymomcars, this site has, as with you, been of enormous help to me. I would be lost without it. Their helpline is brilliant and supportive too. I wish you good health.🐕🐕

kellymomcars profile image
kellymomcars in reply to Ritaritis

Hi backatcha Ritaritis. Thanks for the wishes too.

Lovetodanceto profile image
Lovetodanceto

Welcome the folk are lovely here 😀

kellymomcars profile image
kellymomcars

Love love love your name. Hoping you still get to dance like no one is watching!

Oshgosh profile image
Oshgosh

Looks greatI know what you mean about medics not having knowledge of. RA.

I had a medication review this week with the pharmacist.I had to explain the benefits of taking immunosuppressant drugs,also side effects,also had to explain why I’ve been on steroids for nearly 3 years ( when they try to reduce the steroids,I get to 8 MGM’s,I start to feel unwell,spir( lung function detioriates on testing.

I had a similar conversation with the palliative care consultant.again had to justify why I was on the drugs. I’m on.

One thing the pharmacist asked me was do you get confused with your medication ?

I replied that I always check at least twice.

My main problem with medication is when they change manafacturers ,then the tablets look different.

He didn’t reply to this comment.

I’m sure that M not the only person who has issues with thus

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