Meet your Posher, Carrie

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Hi I'm Carrie. I started selling in September of 2016 and have been blown away by how easy it is. Friends and family donate their items so that I can make a little extra money to help pay for my many medications. Lupus is an invisible disease where your white blood cells start to attack healthy parts of your body. I really enjoy selling on Posh as I am on disability for my illness. I just want to say thanks everyone for buying items or sharing them with your followers. Much Love 💕💕

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Women

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winstondunbar and 24 others like this

64 Comments

gypsyfeather Thanks, Carrie! You have a powerful story and community behind you! Plus, your closet rocks! Sending you good vibes😘❤️

Apr 22Reply

mrstomsha @gypsyfeather Thank you Caroline. I appreciate that you took time to comment. I am really not tryi g to get sympathy but, bring awareness of this disease❤❤

Apr 22Reply

ashleyquinn77 I was just diagnosed with fibromyalgia. Prayers and love to you!

May 02Reply

mrstomsha @ashleyquinn77 I'm so sorry ☹ Its a lot to process, the thought of there being no cure. But, remember you aren't alone. Their are others that know what it's like. I'm sure you're going to have bad days. But personally, I made a choice:

May 02Reply

mrstomsha @ashleyquinn77 either I can be sick and stay in bed and pull the covers over my head or I can be a warrior and fight through it and spend my time with my family. Don't get me wrong, I have days where I can't smile through the pain or that I'm too sick to get up, but I make a choice to keep living my life to the best of my abilities. You'll be in my thoughts and prayers.

May 02Reply

ashleyquinn77 @mrstomsha thank you! ❤❤🙏

May 02Reply

pineapple_coast Hello fellow Lupie! I can definitely understand the hardship of lupus, I was just diagnosed two years ago. Stay strong! Best wishes on your closet! ❤❤❤

May 03Reply

mrstomsha @pineapple_coast I'm sorry to hear that youb are battling too. I think the most frustrating thing is when someone says "you don't look sick" Thanks for leaving me a message. It's always nice to know I'm not fighting it alone.

May 03Reply

pineapple_coast @mrstomsha yes! So frustrating! And of course! It's comforting to know when I'm not the only dealing with this disease..and I wanted to let you know you're not alone!

May 03Reply

mrstomsha @pineapple_coast Thank you so much for that. I hope you are feeling okay right now. I'm in a flare that is causing my kidneys not to function correctly ugh! But, we try to just smile through the pain and I have the best primary care doctor who coordinates my care with all of the specialists and stays on top of everything for me, I'm so lucky to have her.

May 03Reply

pineapple_coast @mrstomsha I'm so sorry to hear that! I hope your flare subsides soon. It's challenging finding the right combo of medication to treat the various symptoms, but having a great team of doctors is definitely crucial! I just started infusions (Benlysta) and I'm hoping this works better than my copious amount of pills I'm taking. Best wishes!

May 03Reply

mrstomsha @pineapple_coast I have been on it for 6 months, I'm hoping I improve enough to get off the prednisone.

May 03Reply

pineapple_coast @mrstomsha girl yes! Prednisone is the worst! 😂😂😂

May 03Reply

mrstomsha @pineapple_coast Right? I've been on it solid for 5 years.

May 03Reply

lucksterlw @mrstomsha Hope this finds you feeling good! These autoimmune diseases are the pits! Good Luck to you every day and I will be thinking of you! LOL. BARB❤️❤️❤️❤️💋‼️

May 04Reply

mrstomsha @lucksterlw Thank you so much Barb! Auto-immune disease is the worst! With lupus I also have Chrons disease, neuropathy, epilepsy. But the best part is I'm a fighter... I wake up and decide to live my life. Are you diagnosed?

May 04Reply

lucksterlw @mrstomsha Yes unfortunately. Fibromyalgia, Crohns, Arthritis, Nerve pain. Every day is a challenge. I need a gizillion spoons! I will send you some when I find them😜😜😜😆😃🤗😘‼️

May 04Reply

mrstomsha @lucksterlw 😂😂😂 that would be much appreciated! I always seem to run out lol

May 04Reply

lucksterlw @mrstomsha Take care of yourself and pace is the magic word for today💫🙏🏻💫‼️

May 04Reply

mrstomsha @lucksterlw Amen!

May 04Reply

kysmother I FULLY understand YOU and I are in the same category. I was diagnosed and have a Rare Condition Called Behect's Disease which is in the Lupus Family. There is no cure it attacks overtime your lungs which Mine has already effected a Main Valve in my Right Lung to the point I have to carry a Rescue inhaler. Stay Strong Keep Pushing forward and remember as my Doctor once told me Don't let Your Condition Define who you are and control you you control it . Many Blessings 🌺🌺🌺🌺🌺

May 24Reply

mrstomsha @kysmother Thanks so much for sharing your story with me, it can definitely be frustrating when your body has a war going on inside and so it's hard for people to understand how sick you are. I've lost friends because they think I "don't look sick". But, I try to focus on the positives today. If I focus on what is coming next with my illness I miss what is happening with my family. I'm on a steroid inhaler and have a rescue too. You keep fighting to because life is worth it! Lots of love ❤️❤️

May 24Reply

temptingpieces I too am doing posh because of disability and need the cash to pay for meds. Love your page. Good luck!!

May 25Reply

mrstomsha @temptingpieces Thank you. It's a rough road. I hope you are successful too. I am happy you shared with me. I hope you can stay on your meds and you don't have too many bad side effects.

May 25Reply

aslodzinski Thanks for sharing your story ♡

Jun 03Reply

mrstomsha @aslodzinski Thank you for taking the time to read it and comment. It means more than you know to have support from you.

Jun 03Reply

bmjmatheson 💖

Jun 25Reply

sharonreifel Hey! I know this is SO random, but I can imagine how hard lupus is, I know several people though who have benefited from NeoLife. Have you heard of it? My friend healed from fybromialgia through equipping her body with the right nutritions that these product give you. I hope you can research it.

Aug 01Reply

sharonreifel or if you have questions please let me know. (I know that this sounds like a sales pitch, but I don't care if you'd end up buying from me; its health and well being we are talking about and that is awe full when you struggle) I'll give you my email if you end up caring even a bit. ☺️ prayers are up for you and your struggles!

Aug 01Reply

mrstomsha @sharonreifel Thanks so much. I will definitely check into it, I actually just started a nutritional program and an herbal supplement made for people with lupus. I'm hoping to start seeing some results soon.

Aug 01Reply

sharonreifel @mrstomsha I hope it will work! I'll be praying :)

Aug 01Reply

lilroxie30 AMAZING CLOSET!!! LOVE EVERYTHING!! ❤

Aug 02Reply

mrstomsha @lilroxie30 Awww, you are so sweet. Thank you so much 💕

Aug 02Reply

hoppy777 Hugs to you, Carrie💕. I have fibromyalgia & a TON of other debilitating conditions - so I can empathize your situation. You are a warrior! Best of luck & hope you are able to keep the Lupus from flaring up better now 🌸🌸

Aug 05Reply

mrstomsha @hoppy777 Thank you so much. And hugs right back to you💕 I also have more than one, with the lupus I have small fiber neuropathy, crohn's, epilepsy and rheumatoid arthritis. I can certainly understand fighting more than one. I hope your conditions are not flaring too bad. I know how tough it can be and what a warrior you are for fighting these invisible diseases. Stay strong sister!

Aug 05Reply

cruella24 😊💐💕

Aug 10Reply

mrstomsha @cruella24 Thank you 💕

Aug 10Reply

snave Hi Lupie Sister! I hope this finds you feeling better. Yes, I too have Lupus SLE, and I've been home with swollen red hot knees. It's one day post Benlysta infusion for me, so I'm exhausted and having flu symptoms. I'm an R.N. and i worked for 32 yrs., but had to give it all up in 2012 and file for disability. Feel better!

Aug 12Reply

mrstomsha @snave Hi, I too am on disability and did my Benlysta infusion yesterday too. I get the flu and cold type symptoms every time. I hope you feel better soon. It's nice to find others that can understand what life can be like with SLE. Thank you for your well wishes.

Aug 12Reply

snave Oh wow! I've never met anyone who has the same treatment and side effects as me! So wonderful you qualified for Benlysta too! I totally understand, and I talk to several women on Facebook with Lupus trouble. Love to talk more. You can find me under Lynn (Burrows) Evans and I'm from Tucson, AZ. :))

Aug 12Reply

mrstomsha @snave Just added you on Facebook 💕

Aug 12Reply

snave Great! Thx!!

Aug 12Reply

punanamous Hey...You could be a fashion stylist. Live the outfits.

Aug 21Reply

mrstomsha @punanamous Oh, wow. Thank you so much. That is really nice of you. I'm glad you like them 😊 gives me something to do.

Aug 21Reply

mrstomsha @punanamous Love the picture of your puppy. I have a blue nose too.

Aug 21Reply

misskrissss Love your closet! Your flat-lays are on point!

Aug 26Reply

mrstomsha @misskrissss Oh my gosh! That's so sweet! I really appreciate it 💕💕

Aug 26Reply

misskrissss 💖

Aug 26Reply

fann96 @misskrissss love your closet! Do you mind putting some out fits together for me and tagging me in them?

Aug 30Reply

mrstomsha @fann96 not at all... what size and price range are you looking for?

Aug 30Reply

fann96 @mrstomsha jeans size 24 or small, shirts size small or medium depending on they way they fit.

Aug 30Reply

fann96 And my price range is nothing over $50 please, thanks!

Aug 30Reply

mrstomsha @fann96 Perfect. I will put some stuff together for you. I'm headed to my daughters volleyball tournament but, will try and get some stuff put together and take pictures tomorrow.

Aug 30Reply

fann96 @mrstomsha okay that's fine! Thankyou!

Aug 30Reply

makushe Hi! Just came across your closet- wanted to share a link with you that may give you some hope of living a healthy long happy life ... https://www.forksoverknives.com/stroke-doctor-reversed-lupus-plant-based-diet/#gs.izJztmE I have been eating a Whole Foods plant-based diet since April and I've lost over 30 pounds and feel amazing. Currently enrolled in a plant based nutrition course thru ecornell. Wishing you the best!

Sep 03Reply

mrstomsha @starfire8 That's cool. Hello Carrie 2 😊

Sep 17Reply

tatertot3 Prayers out to you! MS and EDS for me, and most recently Crohns diagnosis after a long hospital stay.. It is difficult. We ARE Warriors!!! Take care

Oct 24Reply

mrstomsha @tatertot3 I’m so sorry to hear that I have Crohn’s too. I know how rough it can be.

Oct 24Reply

kaleidokloset Happy Sunday! Thank you for the like! If you’re interested, I always consider offers, discount bundles, and ship next day! Let me know if you have any questions! Hope to hear from you soon. ❤️👗💃🏽🎉

Mar 18Reply

wrforrest Greetings Warrior! Bless you! Great outfit layouts! What if I like an outfit do you have different sizes? Or just the sizes in the layout? Does that make sense?

Jun 15Reply

wrforrest I have a warrior friend like you!! I use to take her in for her treatments!

Jun 15Reply

pancakesinlove Right there with you .. most people are unaware and think it’s contagious 😷.. and unless u have it.. no one knows the pain.. and struggles

Sep 14Reply

mrstomsha @pancakesinlove it’s tough for sure. But always nice when someone that can truly understand reaches out and lets you know that you aren’t alone in this.

Sep 14Reply

mrstomsha @wrforrest Thanks for reaching out. I hope your friend is doing okay.

Sep 14Reply