#lupus

MOST RECENT

Lol. I find it very hard to take photos - well be in photos - these days coz I dont feel pretty. Not a fan of tying my hair up like that coz I look like a bloody fish ball. But well with the chemo and hair loss, this is the nicest way to look presentable. Something that upset me recently and I like to talk about it here. So suddenly - like really suddenly - 90% of my friends are dating around or started new relationships - I felt really shitty about it I dont know why - maybe I felt left out or like everybody’s coupling up except me. I told this to my friend and we rationalised it together. I can go on any dating apps if I wanted to - but I promised myself that I will focus on my health until my chemo is done. Plus I don’t feel pretty and confident at the moment to go on any dates. I think also coz few months back before the infection, I did try to date but couldn’t get any 😭😭 but doesn’t matter. Anyway, I blame the hormones. I had a second round of hormone injected to stop my period to protect my eggs during this chemo treatment. So yeah. I’ll just keep looking like a fishball for now. But I am very happy to know my friends are starting to date - coz some had a dry spell if u know what I mean. #chemo #chemosucks #lupus

It makes me sad to hear the stories told about people they considered friends or even loved ones not being supportive or understanding what they are going through. I too have experienced this and it is upsetting because we confide in these people when we are at our lowest points. On the contrary, the AMAZING compassion I have seen come out of the #chronicillness community is second to none and beyond impressive. All of you should be so proud because you are the true example of compassionate human beings and in a world with so much b.s going on with humanity, it's a real inspiration that it's the #chronicallyill fighting through their battles and pains to still set this example and help comfort others. Kudos to all of you, and thank you.👏👏👏💪💪💪💪💜💚💙❤️🌸🎗️🎗️🎗️
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#EmPOWERThePATIENTS #invisibleillness #spooniesunited #fibromyalgia #thyroid #anxiety #autoimmunedisease #cancer #lupus #hashimotos #apoonie #warrior #gravesdiseaae#awareness #butyoudontlooksick #brainfog #invisibledisability #depression #hyperthyroidism#migraine #hypothyroidism

Very smug with my lunch, although I had to eat it with a knife and fork because it’s so bloody big! 😍 #f45challenge #lunch

Went to our annual lupus walk today with my girls fam out in SF #91Gang #FuckLupus #Support #AnnualWalk #Lupus #SF

do you know why you do what you do?

i sometimes forget... but this is the quote i see every morning i sit down at my 🖥 to work.
i thought that started my business @anchoreddesign to ensure i was raising my 👦🏼👧🏻 while bringing in a paycheck to help out my family.

fast forward a few years and it became the only paycheck for my kids and i as i went through a disturbingly awful divorce for many long years. then, being diagnosed with autoimmune junk, it became a way for me to stay home and protect myself from getting sick.

i know why i think i started, but i love how God intimately knows my heart, my needs and my desires and made it possible for me to be home and take care of my beautiful children, be financially secure and protect my health.

i worship an incredible God.
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#Christian #amen #praiseGod #qotd #quote #inspirationalquotes #inspiration #Godisgood #autoimmunedisease #autoimmuneprotocol #aip #hashimotosdisease #hashimotos #adrenalfatigue #lupus #chronicallyill #mom #smallbusiness #smallbusinessowner #igotthis #fitfam #jesusisking

Hello everyone writing this book has been a delightful; unfortunately, things will have to come to end soon everyone has been a great support and I have enjoyed writing this book bless all of you of your votes and comments. I will; however, willgive everyone another new poem Scars of the Past life can have challenges of the past but the real question how do we over come it? Here it is a brand new Scars of the Past by Lndscripts everyone
Next week will be my last poem everyone love you all of your support

#love #glory #lupusawareness #lupus #positivevibes #healing #mother #father #wattpad #wattworld #poems #church #change #grow #elevate #prosperity #bravery #beautiful #live #lifequotes #blessed #rhyme #balance #poetry #adventuretime #conquest #rising #antibullying #endbullying #poems
#poetry

My wattpad page

https://my.w.tt/XZBEFwrw1K

Todos los días que paso con él son únicos, pero los últimos han significado más porque me sanan el alma y me preparan para una semana más de hospital: hoy fuimos a estar con muchos perritos en un santuario, a comer marranadas de más a un buffette de carnes, a visitar a mi suegros y no es por acá, pero a ustedes su suegra no les prepara té de frutas ni les regala anillos de la temporada porque saben que son bien darks 😬 Estaba nerviosa porque era la primera vez que me vería totalmente calva y sin cejas por la quimio; pero al contrario, me recibió con mucho cariño y estuvimos platicando y riéndonos por hoooooooras :3 Basurín dice que siente bien bonito ver que las dos mujeres que más ama tengan tanta química y se lleven tan bien ❤ Fue un día tan tan tan bonito que me regresó la sonrisa a la cara :')
Mañana tengo hospital; veo a mi hematóloga y al ginecólogo. Sabré cómo salí de la sangre y pues a ver con qué nueva sorprecita me salen, pero por ahora no me importa pensar en eso. Estoy feliz porque esta familia que me ha adoptado como parte de ellos, me tratan, me apoyan y me quieren bien y bonito aun con todo mi pedo físico. Y yo amo llevarles postres hechos por mi, obvio.
#fucklupus🖕#LES #lupuslife #Lupus #trombocitopenia #desordensanguineo #enfermedadescrónicas #chronicillnesswarrior #enfermedadesinvisibles #lupussucks #plaquetas #spoonie #ilovemyself #quimioterapia #chemotherapy #MiVidaConLasMontoneras 💉💜

The Jaimi Leigh Jones Foundation for Dual Diagnosis of chronic illnesses is a nonprofit organization that thrives off the donations received. Please find it in your heart to donate to a worthy cause...
#thejljfoundation #autoimmune #awareness #lupus #ilivewithlupus #lupusnephritis #epilepsy #diabetes #chronicillness #support #speaker #consultant #mytestimony
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Testimoni : Lupus
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#lupus #lupusindonesia #magozai #nutrasetika #herbalsoho #unihealthjambi #unihealth

🐺🌙Wolf and crescent moon earrings in bronze, sawn from 20 gauge metal. 🐺🌙 30 dollars, delivered. #wolves #wolfmagic #howlingwolf #handcrafted #hollaatchagirl #bronzejewelry #bronzegoddess #wolflove #wolfandmoon #lupus #ulv #threewitches

I was definitely living on a prayer with this one 🙏 Last phase it felt like every workout worked the shoulders and this phase it’s like every day is leg day 😬 So happy tomorrow is rest day because my poor legs are dead 💀

Discoid lupus erythematosus is a chronic form of skin lupus that can present in the scalp as scaly red plaques that cause permanent hair loss. This patient was unfortunately only given a treatment to help with dandruff, but his hair loss continued. When he presented to me in clinic (top picture), I performed a scalp biopsy to diagnose his condition. With the correct treatment, the redness and scaling resolved (bottom picture). This is a scarring condition, so the hair loss that he had already incurred is permanent, but with the right treatment, progression can be halted.
For hair loss conditions, call 305-856-6555 for appointment availability with Dr. Z. #medicaldermatology #hairloss #alopecia #discoidlupus #lupus #dermatology #boardcertifieddermatologist #boardcertified #physician #doctor #skincare #diagnosis #diagnostic #biopsy #hair #scalp #miami #brickell #southflorida

HEYYY YALLL im Nay and I have #lupus and to this day I’ve gained 9 pounds since my last medical surgery ! My #nowandthen pics are lit (😛😛😛 ) and it’s only been almost two months. I’m so proud of myself and so blessed to have good doctors in my corner. I wanted to share this seemely very small thing that means a huge deal to me because people really take things for granted wayyyy toooo much. A lot don’t understand how hard it may be to gain weight for some people. I will never forget how I felt when I started losing my boobs 😪😢 as a female it was the worst thing for me. #lupus has really taken me on an emotional roller coaster ride and it’s nowhere near done but I’m not scared to put my hands up and enjoy the ride anymore. I had to fight for my body back. Every day I fight for it. I really hope after reading this caption and seeing these pictures you who’s reading this will have no more excuses. 😬🙏🏾🙌🏾🙌🏾💜💜💜💜💜 #fucklupus #teamlupus #gains #notstoppin #lupusbody #lupuswarrior

Have you had this tea? @kikoko_hq is such a wonderful cannabis tea with different ratios of thc to cbd.
After this long weekend of working this is life! #lupus #sympatea

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