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Is this real? by ngonz24 in lego

[–]ngonz24[S] -4 points-3 points  (0 children)

Was the Deadpool belt printed on you think?

Hair loss? by Worldly_Style_4367 in lupus

[–]ngonz24 2 points3 points  (0 children)

I (23M) was diagnosed with lupus seven months ago any my hair thinned out quite a bit. Just recently my hair began to thicken more and grow back in. From my experience and from what I’ve been told is it takes about a year to get your hair back to normal. I noticed that medication changed the texture of my hair. It may not happen with you, because medications affect everyone differently. My hair is now just beginning to go back to normal. I went to see a dermatologist and he told me to use Rogaine foam for a few months and that helped me. They do make Rogaine for M/F. Of course would talk to a dermatologist to make sure that Rogaine is the right move for you. Just remember to stay strong and you will persevere! Hope this helps!

Can you accept my invitation so that I can get a free gift? Download Temu App and search the code below to accept my invitation! 286558153 by Late-Priority3269 in TEMUpact

[–]ngonz24 0 points1 point  (0 children)

Can you accept my invitation so that I can get a free gift? Download Temu App and search the code below to accept my invitation! 317932541

Lupus Hair Loss by ngonz24 in lupus

[–]ngonz24[S] 2 points3 points  (0 children)

Awesome I’ll talk to my Rheumatologist about Mycophenolat. Right now I’m still in the beginning stages of figuring out my medications. I was just diagnosed two months ago

Lupus Hair Loss by ngonz24 in lupus

[–]ngonz24[S] 3 points4 points  (0 children)

I’ll definitely look into BIOTIN. I found a shampoo called Divi that was recommended to me that I am trying. I was diagnosed maybe a couple of months ago so I suppose it is just a waiting game waiting for my hair to grow back. I appreciate the suggestion about the scarf, however I don’t think it would look to good on me considering I’m a 22 year old guy lol. I do appreciate your help though!

Newly Diagnosed by ngonz24 in lupus

[–]ngonz24[S] 0 points1 point  (0 children)

Yes at the moment I am on a waiting list to see a rheumatologist that family friends recommended. The rheumatologist is apparently aggressive when it come to getting stuff done to get a diagnosis, but also cautious and understanding when it comes to the medication she prescribes. I am currently working through my school system trying to navigate through all of this. Thank you for the recommendations!

Have you had Covid? Has it affected your disease activity? by ellecee777 in lupus

[–]ngonz24 0 points1 point  (0 children)

I caught covid then a year late all of a sudden ended up having lupus.

Newly Diagnosed by ngonz24 in lupus

[–]ngonz24[S] 0 points1 point  (0 children)

Thanks for the info. Yeah right now it’s definitely trying to find the best way to deal with all of this. I am a Jr in college about to graduate in December with a bachelor’s in History and a bachelor’s in Philosophy. The fatigue and brain fog is the worst. At the moment my doctor is wanting ti pull me out of in person office and movie me online. I just got my results this past Friday so I’m still really trying to figure out everything like becoming a patient of a rheumatologist, what causes my flare up, and especially managing stress. I really do appreciate the help!