Closet Pays 4 My Lupus Meds💜

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I have Lupus. Thank you for stopping by & for shopping with me. Due to my condition this is my only source of income & is used for my Lupus medications. Please, no lowball offers. My prices are only a fraction above my cost & usually lower than other closets. I’m not trying to get rich, just pay for the medicine & treatment I need. I am so grateful for my wonderful customers & their amazing support. Thank you from the bottom of my heart 💜

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Seller Discount: 10% off 2+ Bundle
Ships to: United States
$7.97 Expedited (1-3 day) Shipping on all orders

stephyyeager67 and 129 others like this

147 Comments

bbargains3 Praying for you ...praying for better health my dear posh friend ❤️

Oct 27Reply

lolas_place @hopeh227 Thank you for the prayers & support! I appreciate it so much! 💕💜💕

Oct 27Reply

bbargains3 @lolas_place You’re very welcome ☺️

Oct 27Reply

chonka68 Hope you are feeling as great as your closet looks✌💃🌺Wishing the best---for everything💪🌹

Oct 27Reply

lolas_place @chonka68 Thank you my friend. The Lupus meds & whooping my booty but I’m plugging away! Thank you for your support! I truly appreciate it! 🥰💜

Oct 27Reply

chonka68 One day at a time--that's all we(you) can do..🌍Poshmark keeps ya connected--a good thing✌

Oct 27Reply

taylorfamily17 Stay Strong My Dear Friend! 💐 I’m praying for you 🙏 sending you lots of love and well wishes ❤️

Oct 27Reply

lolas_place @taylorfamily17 Thank you Doll 🙏🏻 That means so much to me! Have a wonderful rest of your weekend! Thank you for being so sweet! 🥰💜

Oct 27Reply

greatfinds111 Aww I'm sorry to hear that. I have some issues to and it's not always easy. I wish you all the best💝💗🌺

Oct 29Reply

lolas_place @greatfinds111 Tgank you my friend...my prayers are with you too! 💜🙏🏻🥰

Oct 29Reply

lynn2578 I feel your pain. On Plaqunil too. Retired now and loving posh! One day at a time. 💜💜💜💜💜💜. Remission will be a blessing!

Nov 10Reply

lolas_place @lynn2578 Bless you for sharing...I was just recently diagnosed & am just beginning the meds process. Bless you for reaching out. Have a wonderful day! 💜🥰💜

Nov 10Reply

lynn2578 @lolas_place If you can get into remission it will be great. I was in remission for 30 yrs. Then bingo. Systemic. SLE. This keeps me busy along with all my grandchildren. Lol This is a lot of my kids stuff I sell to help them with bills while they work. 💜💜💜

Nov 10Reply

lolas_place @lynn2578 That is so sweet of you to help. I’ve been on posh since Feb. hoping to sell enough to help with cost of meds. Thank you for reaching out. I hope you feel better soon. 💜🥰

Nov 10Reply

nikomy101 Wish you well... take a look into cole Robinson Snake diet..hope it helps. I’m praying for you much love

Nov 10Reply

nikomy101 Cole Robinson snake diet on YouTube The snake wizard check it out

Nov 10Reply

lolas_place @nikomy101 Thank you for reaching out & for the info. I’ll check it out! 💜🥰💜

Nov 10Reply

512glo Sending hugs 💜

Nov 14Reply

lolas_place @512glo Thank you so much for that! I needed it today! 💜

Nov 14Reply

512glo @lolas_place I can relate. I’m a fibro warrior taking it one day at a time as well. Trying to make money when I can since I can’t work a regular job. If you ever need to vent feel free to reach out. Fight on warrior 😉 💪🏽 💜

Nov 14Reply

lolas_place @512glo I feel your pain! I haven’t been able to work a 9-5 for years & that’s why I’m here! You do what you can on the good days. I’m here for you too! Keep fighting. One day at a time. 💜🥰💜

Nov 14Reply

512glo @lolas_place same! I haven’t worked since I was in my teens. Support grateful and excited to find poshmark. Good luck on sales doll! Happy holidays and happy poshing 💖

Nov 14Reply

lolas_place @512glo You too Hon! Lol...I always call people Doll too. I ❤️ your closet so you’ll get daily shares from me. Sell lots! We’ll stay in touch! 💜🥰💜

Nov 14Reply

512glo @lolas_place lol 😆 😉 🥰

Nov 14Reply

yourpostal Hi, I have Lupus myself for about 3 years ( on top of psoriatic arthritis ).., I am sending Love and best wishes, hope you get relief and never be in pain again!!!! May New Year bring you much happiness!!!🌹💕🌹

Jan 14Reply

lolas_place @yourpostal Thank you so much for that! It took forever to finally get diagnosed but I’m starting to get some relief with meds. I hope you’re well & pain free too! 💜🥰💜

Jan 14Reply

barbirene2 @lolas_place Hi 🌹Like you I also have Lupus with Sjogren's and Fibro & RA. I am so happy to be following you. At the present time I just follow, share, I have had to limit myself to buying once a month as I think I am a Posh-a-holic 😉. I like your closet and have found several really cute items. So I WILL be back. Sending Positive Energy & Posh Blessings 💲🌹🧚🕊 Barbi 💜

Jan 24Reply

lolas_place @barbirene2 My ❤️goes out to you! I literally feel your pain. Here’s to more good days than bad! Have a wonderful evening & thanks for the compliments, support, & follow. Good vibes, prayers & thoughts back to you as well. 💜🥰💜

Jan 24Reply

demonhunters I have been living with lupus for many years. You never know what kind of day you have when you wake up. People can’t understand that it’s hard for me to plan ahead. I didn’t celebrate the holidays because I spent almost there months in bed with bronchitis, flu and now a virus. So I totally understand what you are going through.🌺🌺🌺🌺🌺

Jan 28Reply

lolas_place @808classysassy Oh honey...my ❤️goes out to you! I know exactly what you’re going through. I’m home 24/7 too. You can’t work a 9-5 with Lupus. I do some sewing for a friend who sells flags online so that’s part time & I found Posh to try to supplement that. People don’t understand the bad days & how terrifying it is to be out in public around sick people with a compromised immune system. I’m glad we found each other through a Miriam’s closet. 💜🥰💜

Jan 28Reply

demonhunters Did you get disability for your lupus? It took me 5 years to get approved, after hiring an attorney which only took a month and I didn't even have to go to court.

Jan 28Reply

lolas_place @808classysassy I had applied in 2009 prior to Lupus dx because I had other major health issues. I fought along with/my lawyer up & through all appeals & going to court where my judge was a 72 yr old blind judge...literally sightless & denied my claim 6 yrs later since he could work blind, I could find something. He said I could drive a bus or be a Walmart greeter. No joke. 😭

Jan 28Reply

lolas_place @808classysassy I need to get another attorney & start over now that I have the Lupus Dx...plus diabetes & neuropathy. It’s very frustrating. By the time I got my Dx I couldn’t lift my arms to wash my own hair! I’ll be 55 on Sunday & I couldn’t get any doctors to take me seriously. I have an amazing Rheumatologist now. He’s 1-1/2 hours away since there isn’t one in my town...crazy. Thanks for sharing! I’m thankful when others reach out & share. I don’t feel so alone.

Jan 28Reply

demonhunters @lolas_place What a dummy! Don't stop trying to get what you deserve, you just need another judge. As long as you have documentation from the doctors, you deserve it. Get an attorney that you don't pay anything until you win. Remember, when you every go to court, under dress with no makeup or anything dressy. Harrison and Harrison is who I had. An advocate got nowhere in five years....

Jan 28Reply

demonhunters I am 58. I gotten my disability when I turned 50. Go for it and don't stop fighting. I am in Las Vegas and it's hard to get anything. But I won in the end....

Jan 28Reply

lolas_place @808classysassy Thank you so much for that! I’m gonna jump back in. You’re the 2nd person that’s told me to do it. That’s a consensus! Thank you for sharing! 💜💜💜

Jan 28Reply

simplytsa Praying for you... I have the other horrible autoimmune that’s close to yours Multiple Sclerosis 🤦🏽‍♀️ I feel your pain! 💕💕💕

Feb 08Reply

lolas_place @wandaladawn Oh honey! I have 2 friends with MS... 1 is wheelchair bound now & the other is getting close. I see their struggles & don’t know how they do it. You have my heartfelt prayers & support. Bless you my dear. 💜🥰💜

Feb 08Reply

simplytsa I got diagnosed March 2017... who knew being a workout junkie would work so well to my benefit! 😶 I’ve been a extremist since 2010. I had no clue I had MS... every year I got a new diagnosis of something but the day I clean passed out after a workout my husband was like “oh hell no you need to go to the neurologist!” I went... got a MRI... and pow head and spine full of tiny spots! 😳🤦🏽‍♀️ My doctor says my MRI reads like I should be in a wheelchair but I keep fighting that!

Feb 08Reply

lolas_place @wandaladawn you keep fighting it Sista! That’s crazy. It blows my mind how long it takes to get these things correctly diagnosed. Glad you’re on the right path. Thank you for reaching out! 💜🥰💜

Feb 08Reply

simplytsa @lolas_place I fight everyday... apparently so well people give me the double look once they find out I have MS. “ You don’t look sick” is what they tell me but I’m like “how does a sick person supposed to look?” I feel blessed everyday I wake up and still high functioning! Thank you for your profile! Somehow I feel like we all have to stick together and bring positive vibes to each other! I am on IG as wandaladawn if you want to see. 💕💕💕😘

Feb 08Reply

lolas_place @wandaladawn I agree...what does someone with a compromised immune system look like? Yes...we have to stick together & continue to lift each other up & support each other. No one knows what we go through other than another going through the same thing. 💜🥰💜🥰💜

Feb 08Reply

bentleychick I'm also dealing with lupus. your in my prayers 🙏

Feb 09Reply

lolas_place @bentleychick My Heart ❤️ goes out to you you’re in my thoughts and prayers as well.

Feb 09Reply

bentleychick @lolas_place ♥️

Feb 09Reply

popachei I hope you are able to find more good health days than bad and that you’re able to find relief through the pain 💜 My daughter is an MCTD warrior and started struggling with her autoimmune issues a year ago, at 24. Despite it showing up in her tests, her PCP never told us so it took us a year and switching specialists to get the correct diagnosis. We are still new to Poshmark so our closet is a work in progress, but we are happy to have found your account 😊💜

Mar 05Reply

so_intofashion Came across your page. Stay positive & keep going. I've been living with Lupus for over 13yrs. There are going to be some good days & bad. Always believe & push through. You got this!

Mar 05Reply

lolas_place @popachei Thank you so much for sharing. Getting a correct dx is 1/2 the battle. It took me years of Drs telling me it was all in my head & tons of anti-depressants & meds that made things worse. I’m so glad your daughter finally got a correct dx. I will keep you all in my thoughts & wish her many good days. There are so many awesome people here on PM. Feel free to ask me any questions you have & thanks for stopping by. 💜🥰💜

Mar 05Reply

lolas_place @sointofashion Thank you so much for that! I’m struggling through a flare now. Just lost my Dad & trying to help my mom as much as physically possible but I get up every day & push through the pain. Dr took me off Prednisone...I feel better on it but understand the negatives. Thank you so much for the support! 💜👍💜

Mar 05Reply

auntnann @lolas_place thinking about you...take care! 😘

Mar 15Reply

lolas_place @auntnann Thank you so much for that. I hope you’re feeling well & doing great. Have a great weekend 💜🥰💜

Mar 15Reply

tawandaog fibromyalgia warrior here,prayers for your recovery 🤟💕🤗

Mar 31Reply

lolas_place @kellieingram72 Thank you so much for that & right back atcha. Stay safe out there. 💜🥰💜😷💖🤟💜

Mar 31Reply

lolas_place @patriciaposh06 Thank you so much for your sweet comment. My prayers for your healing & strength as well. Stay strong & be safe. It’s definitely scary out there. 💜🥰💜

Apr 09Reply

godizgracious Prayers for you ❤️❤️ !

May 06Reply

lolas_place @janabg_24 Thank you so much for your sweet comment. 💜🥰💜

May 06Reply

ginad2018 ❤️❤️❤️

Jun 19Reply

lolas_place @ginad2018 Thank you so much ☺️ 💜🥰💜

Jun 19Reply

poo1moo8 Sending you good vibes. 💫💫

Aug 25Reply

catpvaughn You have a wonderful closet! Wishing you all the best and thinking of you... I battle chronic health issues as well. ❤️

Aug 25Reply

lolas_place @catpvaughn Thank you so much. I appreciate your message. My thoughts are with you as well as you battle through your issues! 💜🥰💜

Aug 25Reply

lolas_place @poo1moo8 Thank you so much! 💜🥰💜

Aug 25Reply

kayjun_girl Prayers for you!! Mine pays for MS 🧡💜

Aug 25Reply

rrranda oh I feel for you as I used to work in surgery and one of the nurses had Lupus. God bless u and may you feel well and do well with your sales. I have EDS so know what it's like to struggle with a serious illness. Hugs from Randa.

Aug 25Reply

karenpont Hi, I have lupus also. I was diagnosed 20 years ago at age 40. Even though I was symptomatic since age 16. I took plaqueniI, prednisone, methotrexate & anything else my dr thought would help. I was able to go on Benlysta infusions which a foundation paid for. My Drs nurse found it. I will try to find for you. I still have symptoms but it took away that constant fatigue which was really awful. Have you tried applying for social security disability? It would get you Medicare.

Aug 26Reply

karenpont @patriciaposh06 What a warrior you are! And extending yourself to others too. I pray your health is improving.❤️

Aug 26Reply

karlensclassics I pray daily for a cure, I have too many friends trying to cope with this disease. 🙏💜

Aug 26Reply

mariposacloset 🙋🏼‍♀️ Same!💜

Aug 27Reply

donnacorless Omg! 😳 Sending you positive energy and healing energies and prayers.🙏❤ I wish you much success from the sales from your closet. 🙂

Aug 28Reply

lolas_place @donnacorless Thank you so much! That means so much to me. My husband just had a heart attack Last Friday & 2 stents placed & is off work for 2 months minimum...so we’ll take all the prayers we can get! I hope you & yours are all safe & healthy out there & know we’re praying for you also. 💜🥰💜

Aug 28Reply

lolas_place @kayjun_girl my prayers back to you also hon. I have a friend with MS. Thank You so much for the sweet message. 💜🥰💜

Aug 28Reply

lolas_place @rrranda Randa bless your ❤️ & thank you for the sweet message. Prayers back at you too! 💜🥰💜

Aug 28Reply

lolas_place @karenpont you’re a sweetheart. Thank You so much for that. Yes, I had applied 4 years prior to my dx due to all my other health problems & was denied & got a lawyer & fought to the final denial in 2017. It took so much out of me, then I was Dx’d in late 2018 & here I am. Lol. My husband just had a ❤️ attack this past Friday & will be off min 2 months. No stress there!!! 🤣

Aug 28Reply

lolas_place @karenpont I’m at the prednisone, methotrexate stage now, with diabetes & thyroid disease but disability judge said I could be a Walmart greeter or a bus 🚌 driver. Lol...not! So glad you’re doing well & that gives me hope so thank you again so much for messaging me. You’re awesome! 💜💜💜

Aug 28Reply

lolas_place @karlensclassics Thank you so much for that! Bless you right back! 💜🥰💜

Aug 28Reply

lolas_place @mariposacloset Bless your 💜! Thank you! 💜🥰💜

Aug 28Reply

lolas_place @ginad2018 💜💜💜 back at ya hon!

Aug 28Reply

mariposacloset @lolas_place Lupus Warriors need to stick together. It’s no joke... so many are clueless to what we go thru. Monthly chemo and handful of meds daily. Gotcha girl!💜

Aug 28Reply

lolas_place @mariposacloset Right back atcha! Praying for you too! 💜💜💜🥰💜💜💜

Aug 28Reply

donnacorless @lolas_place Wow! Sending your husband prayers and well wishes too.

Aug 28Reply

lolas_place @donnacorless Thank you so much Donna! I pray for your health, happiness & prosperity 💜

Aug 28Reply

karenpont @lolas_place I’m so sorry about your husband. Right no stress which is our worst enemy. I hope he gets well & comes home soon.

Aug 30Reply

mariettaberry I have lupus too. I'm fortunate to still be working. It's not easy. Fatigue, lupus fog, and muscle weakness make it hard.

Sep 03Reply

lolas_place @mariettaberry My 💜goes out to you. Thank you for stopping by & commenting. It means so much. Hoping for better health days for you! 💜🥰💜

Sep 03Reply

jenimadedesigns I hope you’re doing well! I happen to know a few people who have Lupus & know it’s a daily struggle for many! I hope you continue to make progress each day! 💜 Jeni

Oct 03Reply

seretaisthebest I am also a Lupus Warrior. I will be praying for you.

Oct 19Reply

lolas_place @seretaisthebest Thank you so much. Prayers right back to you my dear...💜🥰💜

Oct 20Reply

erinmevans Just here to send you some love because I can relate to your story... I have over 10 chronic illnesses myself and much of your journey sounds like mine. It took 5 years for them to believe me, to get diagnosed, and to finally get the state to believe me too. Took another 2 years to get insurance... fighting that battle now. My heart goes out to everyone who lives with chronic illness- our lives are forever changed. Prayers and love your way 🙏🏻💜💖🌹

Apr 29Reply

lolas_place @erinmevans Thank you so much Hon. My heart goes out to you as well. We gotta stick together & boost each other through the down times & bad days. It makes me feel less alone in my trials. Not that I want anyone to have to go through these things. But friends help to endure them better. Thanks for sharing your struggles with me. Have a wonderful day & thank you for sharing my closet. You’re awesome 😎! 💜🥰

Apr 29Reply

erinmevans @lolas_place I agree 💜 It’s hard to find others who understand how isolating this all can be. It was hard enough before covid... Thank you for your kindness, support and for sharing your story too. You will be in my prayers, as well 🙏🏻💖 And as always, thank you for sharing my closet too! May much healing and many blessing come to you ❤️💖💜

Apr 30Reply

lolas_place @erinmevans My absolute pleasure. I share yours when I share mine. Not as often as I want but as often as I can. Love & prayers to you too hon! I’m here for you anytime...just a message away. Hoping for more good days than bad for you. Have a good night 😴😘 💜🥰💜

Apr 30Reply

dmg4050 Thinking of you🙏Praying for you🙏Wishing you many sales to help you in your time of need💕🦋Dee

Jun 02Reply

mangoann Sending you prayers and well wishes. My cousin has lupus and I know how challenging it can be. 💗

Jun 03Reply

psu1976 Stay well, take care of yourself. Marcey

Jul 02Reply

lolas_place @dmg4050 Thank you so much Dee. You’re so kind. Happy 4th of July! ❤️🤍💙

Jul 03Reply

lolas_place @mangoann Thank you so much for your kindness & lovely message. I appreciate it so much. Happy 4th of July ❤️🤍💙

Jul 03Reply

dmg4050 @lolas_place Happy July 4th to you⭐️

Jul 03Reply

lolas_place @psu1976 Marcey Thank you so much for the kind words & thoughts. Happy 4th of July! ❤️🤍💙

Jul 03Reply

mangoann @lolas_place same to you!!

Jul 03Reply

shopwithceee Praying for you and wishing you success💜💜✨!!!!

Aug 14Reply

lolas_place @shopwithceee Thank you so much for your support & kindness. 💜🥰💜

Aug 14Reply

letamaykilgore Hello sweet lady and God Bless you. I know first hand what it is like to have Lupus and so many other things also. The struggle is great. Know that you have others out here that share your story. From this day forward I ask God to keep you, protect you and keep you safe from harm. I know anything is possible through God. Take care and if you ever need to talk please do not hesitate to let me know. Christine

Sep 01Reply

elizabethand201 I am so sorry. Unfortunately, medical are ridiculous. I know all about that. I have epilepsy. I understand. I hope you feel better soon. I'll take a peak to see what you got! God is good, even when it doesn't make sense! 🥰😇

Sep 01Reply

elizabethand201 meds,*

Sep 01Reply

lolas_place @elizabethand201 Elizabeth Thank you so much for the kind words & thoughts. I truly appreciate it from the bottom of my 💜 Thoughts & prayers back to you also. I have an aunt with epilepsy…seizures are awful 😢 Have a wonderful day. 💜🥰💜

Sep 01Reply

elizabethand201 @lolas_place I'm so excited for my purchase. I love crafts. I think your page will certainly be looked at by me daily. So much peace & love your way. 💝

Sep 01Reply

lolas_place @elizabethand201 💜💜💜

Sep 01Reply

lolas_place @letamaykilgore Thank you so much from the bottom of my 💜 I feel so blessed to have this community and for all the wonderful people like you that share kind words & thoughts. My thoughts & prayers right back to you as well as you fight the fight. Have a wonderful day! 💜🥰💜

Sep 01Reply

elizabethand201 @lolas_place Real quick, you, the way you are honest about your situation just made me not feel the shame about mine. Silent diseases. Never suffer alone. Thanks for making me feel BRAVE! YES WE CAN!

Sep 01Reply

lolas_place @elizabethand201 you’re so sweet! There is strength in numbers & every kind word from someone struggling with similar issues as I am just makes my day & helps me not feel so alone! YES WE CAN! 😉🥰💜

Sep 01Reply

kellee99 Praying for you. My daughter and I both have lupus.

Sep 09Reply

lolas_place @kellee99 Oh honey, my 💜goes out to you both. Prayers your way for better days. 💜🥰💜

Sep 09Reply

handmedownhaven fellow chronic pain sufferer........ hugs. Going through life with invisible pain and the "but you don't look sick" (that's a website...look up the "Spoon Theory"!) stigma! Putting you in my prayers. 🙏💜

Sep 25Reply

lolas_place @handmedownhaven Thank you so much for stopping by & your encouragement & prayers. You’re so sweet. Directing all the positive vibes & 💜 back to you as well. 💜🥰💜

Sep 25Reply

atmyshop Praying for You💜🙏💜 I have SLE, Discoid Lupus (skin) DLE, Drug Induced Lupus and Lupus Nephritis (kidneys/CKD). I have been battling mine since 1978. It also effects my lungs (decreased lung function. The fatigue is unbearable. Doctor's gave me 10 years tops to live in 1983 but I am still here. May the Lord put his healing hands upon you.🙏

Oct 16Reply

lolas_place @atmyshop oh my goodness…bless your heart 💜 Thank you so much & prayers back to you as well. We’re all here to support each other. Thank you for the sweet message & here’s to better days! 💜🌻💜

Oct 16Reply

elleness Hi and thank you for sharing. I was diagnosed 5 years ago. I am thankful that I have no organ issues and can still work. I have had days where I could not lift my arms to comb or wash my hair. I had to cut my hair just to be able to manage it. No one understands our daily struggle. I push myself daily to go to work so that I can keep my health insurance. I take Plaquenil and Benlysta. Without the copay program and my insurance, there is no way I could afford $4,000 monthly.

Oct 18Reply

lolas_place @elleness Thank you for sharing. Praying for better days. I shaved my head during Covid. Couldn’t lift my arms or wash my hair. I don’t look like my pics anymore & have the butterfly rash. Taking max of MTX & Gabapentin & still can barely walk. I feel your pain & will keep you in my thoughts. We’re stronger together. Thank you for the message 💜

Oct 18Reply

jojo8427 Me too! I’m in the same boat as you! I was diagnosed about 15 years ago!

Oct 21Reply

lolas_place @jojo8427 Do you at least have your pain managed so you can do things? I’m going on almost 2 years since dx but 20 years of pain & Drs pushing antidepressants & opioids. Finally have a good Rheumatologist but still in pain while we play drug roulette. I hope you have more good days than bad. 💜☺️💜

Oct 21Reply

hopeschest910 I have Lupus too. I’m sorry you are having to deal with the financial side as well. Praying that you are very successful and are pain free.

Nov 03Reply

redbarnranch 🙏🙏🙏

Jan 17Reply

lolas_place @hopeschest910 Thank you so much for your kindness. Prayers back to you & hopes for pain free days. 💜🥰💜

Jan 17Reply

lolas_place @redbarnranch bless you. 💜🥰💜

Jan 17Reply

enchantingstar 💜💜 Nice to meet a fellow Lupie Posher! Lots of blessings and good sales! For sure get it

Jan 19Reply

lolas_place @enchantingstar Thank you for the message. Right back atcha. We’re all in this together! Have a wonderful day 💜🥰💜

Jan 19Reply

eg_ggsbtq @lolas_place I have Crohn’s disease and was diagnosed at the age of 22, now 23 years later it’s been getting harder and harder to just stay healthy and survive. I’ve also had lupus as well so I feel your pain. I’ve also received Ssdi about 4 years ago and that’s only helped a little. My thoughts and prayers are with you my friend! Hang in there! ❤️💜💙🦋🦋

Feb 16Reply

lolas_place @eg_ggsbtq Thank you so much for your sweet comments. My 💜 goes out to you. I fought to the end for my disability but was turned down & depleted all my appeals. The judge was legally blind & said if nothing else I could be a bus driver. 😳 I hope you have a great day. 💜💜💜

Feb 16Reply

eg_ggsbtq @lolas_place oh that’s terrible! I guess I got lucky somehow or it was my lawyer. My neighbor had tried to get Ssdi. She’s been denied 10 times.There’s so many problems with people who have autoimmune diseases that healthy people don’t realize that suffering we go through I had a ton of workplace harassment because of my illness. That’s a huge problem I wish could be more addressed so that we don’t have to go through that kind of suffering too.

Feb 16Reply

lolas_place @eg_ggsbtq I agree 1000%! I tried to start the process over & was told by 3 different lawyers where I live that there was no point. Even with the mountain of documentation from my Drs. It’s incredibly frustrating. I SO appreciate you stopping by & leaving messages. You’re so sweet. We’re all in this together & it helps to not feel so alone. Thank you! 💜🥰💜

Feb 16Reply

hwalton322 @lolas_place I have Multiple Sclerosis. I feel your pain!!! I was diagnosed in 2014. I’ve learned that I am bigger than the disease. I push forward. I am patient with myself as my body literally eats itself (myelin sheath), every single day. Keep your head up. Keep shining! My info in my bio for Posh says the same thing; my closet is to pay for medical bills, particularly a hospital bill from 11/19-11/21 of last year. You are amazing! Don’t ever stop kicking girl 🧡🙏🏼🥰

Feb 19Reply

charliesvintage Right here with you. All of my sales go directly towards my medical treatments and my blind/senior horse rescue. I am so sorry that you too are fighting a medical fight. Its tough but we are survivors and warriors or else we wouldn't be here fighting so hard.

Apr 11Reply

lolas_place @mrsmazur Thank you. Keep fighting the good fight! Thoughts & prayers back to you. 💜💜💜

Apr 11Reply

aliadri30 thank you for the awareness

Jul 30Reply

lolas_place @aliadri30 Thank you for stopping by 💜🥰💜

Jul 30Reply

momofnina I’m a posher with Lupus too!

Sep 12Reply

lolas_place @momofnina Thanks for stopping by Jody. I feel your pain. My thoughts are for more good days than bad ahead for you. 💜🥰

Sep 12Reply

momofnina @lolas_place same to you! We cherish the good days right?

Sep 12Reply

lolas_place @momofnina absolutely! 💜

Sep 12Reply

lindseylind88 Hello fellow Warrior. We have a lot in common (read my “about me” section). People don’t understand how expensive of a disease this is! I’m finally on disability, but my Medicaid doesn’t cover $750/mo of my 23 meds….it’s crazy. Posh isn’t easy with SLE, also. I just got out of the hospital, and have 5 people emailing because their packages are 4 days behind. Oh well…. Keep fighting the fight! Lindsey

Jun 28Reply

stephyyeager67 I am so sorry. I can relate to your struggles. Myositis patient I am. Not fun stuff either one. Sending you a huge hug💜💙

Jul 01Reply

lolas_place @lindseylind88 I’m sorry to hear that. I understand about the lack of sales. I had 1 small (under $15) sale in June. 😱 I spent most of this year in a huge flare that put me out. And I keep falling for some reason??? It’s an unpredictable disease & my heart 💜 goes out to you Hon. Stay strong! 💪🏻 keep moving forward & know you’re not alone! 💜😘💜

Jul 01Reply

lolas_place @stephseuf811 Oh my gosh. I’m so sorry you’re going through that. No fun is an understatement. I’m so glad you stopped by to say hi. Stay strong 💪🏻 & know you’re not alone out there. 💜😘💜

Jul 01Reply

stephyyeager67 @lolas_place you’re in my prayers. My IVIG and chemo (yep, Myositis just keeps on giving🥴) are covered. Special help for the IVIG, chemo is from the manufacturer. I am on hold with the chemo. Not sure if I want to continue. Keep fighting the good fight for us all, you’re an inspiration!!! 💜🥰💙

Jul 01Reply

lolas_place @stephseuf811 You are the inspiration! Keep going! You got this! 🤗🤗🤗big hugs back to you as well. You’re in my thoughts! 💜😘💜

Jul 02Reply

mollys3 I’m so sorry that you’re having to deal with such a horrible disease! I, too have lupus and understand how difficult it can be! I pray you’re doing well! Molly 💕🩵

Aug 22Reply

lolas_place @mollys3 My 💜goes out to you. I hope you are well & your Lupus is under control. We’ve got to stick together and help lift each other up. Thank you for lifting me up today by stopping by & saying hi. Have a wonderful evening. 💜💜💜

Aug 23Reply