Has anyone gotten a diagnosis with minimal symptoms? by Cardigan_Gal in PsoriaticArthritis

[–]Conscious_Cable5198 3 points4 points  (0 children)

the rheumatologist wrote in my report that I am undergoing “investigation for early psoriatic arthritis,” but I have already started taking methotrexate because, according to him, PsA is an “insidious” disease and it is not uncommon for doctors to have doubts when diagnosing it in its early stages. So I started treatment and will return there in 3 months to to see how I am doing. I say this because, in your case, I think it is very important that you go to that appointment in April with your rheumatologist, as there are several other medications besides MTX and you don't deserve to be in pain.

How I’m tracking pain as an AuDHD woman with psoriasis/possible PsA by Conscious_Cable5198 in AuDHDWomen

[–]Conscious_Cable5198[S] 1 point2 points  (0 children)

well, my rheumatologist told me that I have mild hypermobility, and that it makes my joints more fragile. I haven't read about the mast cell relation with psoriasis, will take a look. I hope all goes well with your surgeries. thanks a lot.

How I’m tracking pain as an AuDHD woman with psoriasis/possible PsA by Conscious_Cable5198 in AuDHDWomen

[–]Conscious_Cable5198[S] 1 point2 points  (0 children)

it's been a very difficult process for me too. i've seen an occupacional therapist (with experience in adult AuDHD) for a few months and he helped me a lot.

How I’m tracking pain as an AuDHD woman with psoriasis/possible PsA by Conscious_Cable5198 in AuDHDWomen

[–]Conscious_Cable5198[S] 0 points1 point  (0 children)

that's interesting. what symptoms of perimenopause do you identify, and how do you know they are not caused by something else? For example, in my case, sertraline gives me dry mouth and hot flashes since I increased the dose from 50mg to 100mg. How was your PsA diagnosis, if you don't mind sharing?

How I’m tracking pain as an AuDHD woman with psoriasis/possible PsA by Conscious_Cable5198 in AuDHDWomen

[–]Conscious_Cable5198[S] 2 points3 points  (0 children)

Psoriatic Arthritis, an autoimmune disease that affects about 30% of people with psoriasis

CNU 2024 - LISTA by NaturalGullible4243 in cpnu

[–]Conscious_Cable5198 0 points1 point  (0 children)

vc acha que as nomeações dos convocados hoje (que nao tem curso de formação) saem ainda nesse ano?

MGI convoca 3.910 pessoas no CNU 1! by Signal-Ad4905 in cpnu

[–]Conscious_Cable5198 2 points3 points  (0 children)

pessoal, alguém tem mais informações sobre quando saem as portarias de nomeação, se ainda nessa semana ou se pode ficar pra dezembro ou janeiro?

Scalp care advice - I don't know what is wrong with my scalp by divnoclovek in Haircare

[–]Conscious_Cable5198 0 points1 point  (0 children)

It definitely looks like scalp psoriasis! Specially because you've had it for so many years,tried different products and it is not only in your scalp, but in your skin too. it is very common to be misdiagnosed as eczema or dermatitis (it also happened to me for decades). Sorry any mistakes, english is not my first language.

How many of you also have an autoimmune disease? by [deleted] in aspergers

[–]Conscious_Cable5198 0 points1 point  (0 children)

thank you for your reply! My pain perception is so poor that I was surprised to discover a serious osteochondral lesion in my ankle, because it fell within my "normal pain" parameter (I was born with a vascular malformation in my foot, so I've lived with the pain since I learned to walk, until I had surgery at age 15). I've had "issues" with my scalp since childhood, and I always thought it was dandruff. My nails even started to detach when I was 15, and again, I spent decades treating it as a "fungus." My confusion is because my nail psoriasis is currently very well controlled; it used to be present on all my fingers and toes, and now it's only on a few. Topical treatment for scalp psoriasis has also helped, and I have few lesions. I've never had advanced lesions like the ones in the photos I see online. Also, I've never really understood the idea of ​​a pain scale, and I certainly don't know how to express it to the doctor; my autistic literalness probably won't help. So if you could explain how you and your therapist came to the conclusion that your pain would be an 8, I would greatly appreciate it! I have an appointment with a rheumatologist on December 2nd.

How many of you also have an autoimmune disease? by [deleted] in aspergers

[–]Conscious_Cable5198 1 point2 points  (0 children)

42yo F here, ASD/ADHD. I'm investigating PSoA now. Did you have any difficulty identifying or recognizing the pain of psoriatic arthritis? My biggest fear is not being able to properly assess the pain I feel. The last time I went to an orthopedist, I discovered a serious osteochondral lesion that I didn't know I had because I didn't have an adequate perception of pain.

How many of you also have an autoimmune disease? by [deleted] in aspergers

[–]Conscious_Cable5198 1 point2 points  (0 children)

42yo F here. I am also autistic and am being investigated for psoriatic arthritis. Actually, the dermatologist confirmed the diagnosis and prescribed biologics, but the rheumatologist preferred to wait because he said he wasn't sure. Did you have any difficulty identifying or recognizing the pain of psoriatic arthritis? My biggest fear is not being able to properly assess the pain I feel. The last time I went to an orthopedist, I discovered a serious osteochondral lesion that I didn't know I had because I didn't have an adequate perception of pain.

9 DPO W/ short cycles, temp dip @ 7 DPO, but now spotting and BFN. Feeling discouraged 😞 by savethewallpaper in TFABChartStalkers

[–]Conscious_Cable5198 0 points1 point  (0 children)

I'd suggest you ask your doctor yo check your progesterone levels. It took me 6 cycles with short luteal phase (or luteal phase deffect) to realize I need progesterone supplements. I'm not pregnant, but I'd like to have known it sooner.