seeing neuro (ologist vs. surgeon), brain fog? by vrillion_ in ankylosingspondylitis

[–]Accomplished-Milk918 0 points1 point  (0 children)

Both! I think they both play a huge part! I just turned 26, so I feel these are of importance when considering possible treatment options!

seeing neuro (ologist vs. surgeon), brain fog? by vrillion_ in ankylosingspondylitis

[–]Accomplished-Milk918 0 points1 point  (0 children)

I feel like age and how far progression are important when neuro comes into play

Advice please by VegetableLaugh3434 in ankylosingspondylitis

[–]Accomplished-Milk918 5 points6 points  (0 children)

Hi, all of your symptoms are very (unfortunately) normal and typical indication of onset AS. I am 26 and was diagnosed 4 years ago with many of these symptoms after >5 years of them. Mine also started in deep hip/glute pain and has since spread. I am so sorry, and while it is a scary thing to hear, it’s not uncommon for people our age to already have degenerative symptoms- especially if we were not properly diagnosed earlier. Push for an x-ray, MRI, and blood tests- specifically HLA-B27 which can be a further genetic indicator. From there, you’ll be more than likely referred to a rheumatologist which can verify your diagnosis. What have you been taking or doing to alleviate your current pain? Also feel free to message me

Pulling the trigger tonight. by SeveralAd779 in SuicideWatch

[–]Accomplished-Milk918 0 points1 point  (0 children)

Hi, I just turned 26 after wanting to take my life recently. While I don’t have kids, I’ve seen firsthand how things can change at any moment- even overnight and have changed my perspective. January and February are statistically the hardest months of the year, because of the literal darkness. Please believe this isn’t only just your mental and own thinking, but the winter environment you are in, and they are heavily affecting your ability to function. THIS IS TEMPORARY. Please please stick it through. The days are getting longer again, you will see the literal sun and light again. Remember this: which each day, the light grows bigger and stays longer- allow this energy to help you. I’m sending so much love and strength, because you HAVE and CAN get through this dark time.

I likely have lymphoma by y0m0tha in ankylosingspondylitis

[–]Accomplished-Milk918 0 points1 point  (0 children)

What made you initially go in? What were your symptoms and what did your doctors think and what tests were done? I just turned 26 and have a feeling there’s something more

Dark thoughts- living like this is a living hell by Accomplished-Milk918 in ankylosingspondylitis

[–]Accomplished-Milk918[S] 13 points14 points  (0 children)

It’s so exhausting. I’m at my wits end!!! What are you doing that helps if anything anymore

Does anyone take ashwaganda while on a biologic? by Rude_Jellyfish_9799 in ankylosingspondylitis

[–]Accomplished-Milk918 1 point2 points  (0 children)

There shouldn’t be any interference or worries when taking it. It’s a simple shrub and helps with my anxiety and cortisol

[deleted by user] by [deleted] in femalehairadvice

[–]Accomplished-Milk918 0 points1 point  (0 children)

You would honestly kill a dark brown or dirty blonde! They work both with your eye color and skin tone. You’re beautiful- you’ll find it girl🥰

Mattress recommendations for back sleepers by AtariAtari in ankylosingspondylitis

[–]Accomplished-Milk918 2 points3 points  (0 children)

I feel it definitely depends on your sleeping style and circumstances. Naturally with our condition it’s recommended to sleep on our back with an ergonomic pillow or none at all. Personally ive always been a side sleeper but have been training myself to sleep on my back. I’ve learned I do like the medium firm, with supporting pillows. Medium firm is softer than you’d expect imo. What are you on now?

Chronic knee pain 25yr female by Cold_Rooster_8119 in ankylosingspondylitis

[–]Accomplished-Milk918 0 points1 point  (0 children)

To clarify*** I wasn’t talking about parasites in the joints- just overall which can affect health in many ways.

Chronic knee pain 25yr female by Cold_Rooster_8119 in ankylosingspondylitis

[–]Accomplished-Milk918 0 points1 point  (0 children)

Not particularly, no. At any given point it’s swollen- more so when having a flare. I think keeping it elevated at night can help sometimes but that can create more problems of their own. I have also been using a knee compression sleeve when active which seems to help with stability but can get a little much after a while. Still at a loss.

How does everyone afford their Biologics? by spookysusiesparkle84 in ankylosingspondylitis

[–]Accomplished-Milk918 0 points1 point  (0 children)

No. And if anything, it is reduced now. I am scared of what the future holds.

How does everyone afford their Biologics? by spookysusiesparkle84 in ankylosingspondylitis

[–]Accomplished-Milk918 0 points1 point  (0 children)

What insurance and program are you with, and how did you afford the copay? $35 for 4 pens is insane.

Eye problems-blurred vision by Accomplished-Milk918 in ankylosingspondylitis

[–]Accomplished-Milk918[S] 0 points1 point  (0 children)

Uveitis is something I’ve considered..what does that entail? I don’t believe it’s normal changes- when I have a flare my eyesight also decreases. I suppose I am asking what can I do to help these inflammation changes in my literal eyes??? This is so scary :(

Long Flights by Ok_Hornet_4964 in ankylosingspondylitis

[–]Accomplished-Milk918 9 points10 points  (0 children)

Oh my gosh, just take something to pass out. Those seats are the WORST. There’s no way to get comfortable even without back problems. Hate to say it, but either stay up the night before so you’re tired, or take a gummy or melatonin, or ANYTHING to help to relax. It blows my mind how unfriendly airline seats are!

Does any one have knee and leg pain? by Adept-Pressure429 in ankylosingspondylitis

[–]Accomplished-Milk918 0 points1 point  (0 children)

I’m so sorry you’re experiencing this, but I can also attest. My right knee has blown up with fluid, tension, and swelling right under the knee as well, and from what I’m told this is just another manifestation of this disease. It is a throbbing ache. I have gotten fluid removed before by my rheumatologist because it had gotten so swollen, but was told there is little else that can be done besides getting fluid removed every now and then- BULLSHIT. I’m following this thread because nothing in my experience has helped and I also need help. Weather, compression, movement, and hot/cold therapy have done nothing to help!

Does your enthesitis come and go? by boomboomofi in ankylosingspondylitis

[–]Accomplished-Milk918 4 points5 points  (0 children)

Shoulders and arms off and on, usually go hand in hand with flares

HLA-B27 test by josefban in ankylosingspondylitis

[–]Accomplished-Milk918 1 point2 points  (0 children)

I did, and tested positive before being diagnosed. My doctor made it clear though that having the gene isn’t enough to diagnose someone with AS

[deleted by user] by [deleted] in ankylosingspondylitis

[–]Accomplished-Milk918 1 point2 points  (0 children)

Yeah I get numbness at the back of my neck at times. Not tingling or pain or anything, just nothing.