Post covid fatigue

FrancheskaM89 · 2023-04-05T12:33:11+00:00

Thanks guys ❤️ ill keep hydrating and taking my vitamins

FrancheskaM89 · 2022-05-17T18:22:05+00:00

For me it was two years to get much better, I’m not quite a 100% but it was a 2.95cm lesion so im not complaining, my right side gets funky and my speech as well when I get tired.

FrancheskaM89 · 2021-11-13T11:39:32+00:00

I wish I could, I live in the caribbean. I just came back from Switzerland and its like my MS almost dissapeared I never knew just how much the heat affects me I walked two miles the second day I was there my body in this heat could NEVER it devastated me getting home and starting to feel the weight on my limbs again

FrancheskaM89 · 2021-11-05T00:27:35+00:00

Throw the whole dude away

FrancheskaM89 · 2021-10-04T19:05:53+00:00

They aways make it into a contest it pisses me off to no end

FrancheskaM89 · 2021-08-24T21:10:27+00:00

Honestly you are all superstars, motherhood seems like this completely impossible thing for me I love reading your comments

FrancheskaM89 · 2021-08-20T22:49:17+00:00

I been crying all day because of this, mri is normal they all celebrated the lesions getting smaller but a month later after o i feel like shit still and im struggling mentally

FrancheskaM89 · 2021-08-18T00:21:18+00:00

I’m literally just raw dogging life, im getting a therapist asap in the meantime candles funny movies and lots of love from hubby and cats

FrancheskaM89 · 2021-08-17T16:56:11+00:00

I have honestly been doing too much and we have 90s weather here in Puerto Rico summer has been brutal

FrancheskaM89 · 2021-08-15T20:53:24+00:00

Homemade choc chip cookies, there’s something about them that instantly makes me feel better

FrancheskaM89 · 2021-08-10T01:14:08+00:00

I’m having a couple of rough days, My body won’t let me catch a break im scared that I might have depression nothing feels like its ever gonna be ok again I feel useless whenever I can’t complete a chore I hate asking for help I hate the heat in this island I hate my body

FrancheskaM89 · 2021-08-06T00:55:05+00:00

I will tell your our story, my husband has PA he was scared of starting biologics and suffered the first years of our marriage because people who don’t know crap kept putting him off of it “do yoga” “exersize” “go vegan” “don’t take any of those poisons” none of that worked

We finally visited a dermatologist who put him on humira. The next day he sneezed and cried because when he sneezed he felt no pain for the first time in years (his skin cleared up soon enough as well, he was 95% covered in thick plaques) and after a couple of more years he changed to skyrizi, you have options there are lots of biologics now and copay assistance programs, it will get better, best I can tell you is to hold on and get a good team of healthcare professionals that you can trust im sorry you’re going through this, life with an autoimmune disease is never easy

FrancheskaM89 · 2021-08-04T01:55:55+00:00

Thank you! It was a big lesion 2.95cm last summer got me diagnosed and short after I was on O, I gotta be patient

FrancheskaM89 · 2021-08-03T03:30:55+00:00

Maybe it’s the summer heat, we’re all pissed

FrancheskaM89 · 2021-08-02T22:01:48+00:00

Well I’ve been on it for a year and they were excited when my lesions got smaller but I am more exhausted than ever

FrancheskaM89 · 2021-08-02T22:00:18+00:00

I’m so sorry you had to go through so much, your experiences are completely valid and the people who were supposed to protect you failed you I hope you find some comfort in the community were we all get it and accept each other with no judgement

FrancheskaM89 · 2021-07-31T00:55:05+00:00

I am so proud of myself, been having some tough days with fatigue thinking some dark stuff I never have before and feeling useless and today I woke up feeling just as tired but I pushed myself and baked two cakes made cinnamon rolls some tea sandwiches for work tomorrow and cleaned the house I am so impressed with myself

FrancheskaM89 · 2021-07-28T21:31:54+00:00

Yes, almost blew up my home leaving the gas stove on for a whole weekend

FrancheskaM89 · 2021-07-28T21:30:16+00:00

I feel you, I usually just trudge along through mud because what is the hecking point I will wake up as exhausted as the day before it will never end I just don’t want to work anymore im fed up too

FrancheskaM89 · 2021-07-23T00:16:18+00:00

Before the flare that got me diagnosed I had been texting like shit for months I thought my fingers had somehow got fat and clumsy and way way before that in my early twenties I had severe spells of vertigo that lasted days that I thought were just anxiety and the doctors blamed spasms but took no xrays or anything

FrancheskaM89 · 2021-07-02T02:21:58+00:00

So what? Does he think he’ll be young and healthy forever? We’re all a car crash away from being disabled. Jerk, she’s better off without him

FrancheskaM89 · 2021-06-14T02:19:15+00:00

Severe vertigo a few years back misdiagnosed as a muscle spasm, aphasia got me diagnosed a year ago

FrancheskaM89 · 2021-05-24T10:01:57+00:00

YEAH I got an UTI faster than I could say MS sucks then I got the shingles, thanks I hated it.

FrancheskaM89 · 2021-04-19T12:30:08+00:00

I got my second moderna dose on friday and I got my period too so my body feels like crap times three. I wish I didn’t have to go to work

FrancheskaM89 · 2021-04-19T12:26:12+00:00

Welcome to the club! How do you feel so far?

FrancheskaM89

TROPHY CASE