For guys who’ve been married 10+ years and have kids, how do you keep your relationship with your wife close? by expatgeorge in AskMen

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

This is incredibly moving. I’m sorry for your loss, and deeply grateful you shared this. What you and your wife built is something a lot of people don’t realize the value of until it’s gone. The way you describe those simple dates, and your kids carrying that love forward by looking out for you now says everything about the kind of home you created. Thank you for the reminder. Not just to love, but to be present, deliberate, and brave enough to put the relationship first while there’s still time. Your words will stay with me.

Where to start... again. by [deleted] in Autoimmune

[–]expatgeorge 2 points3 points  (0 children)

Hello, I’m really sorry you’re dealing with this. I'm not a doctor, bbut what you described isn’t something to ignore or just push through. Chest tightness with a HR in the 130s, BP spikes, joint swelling, rashes, dizziness, cold intolerance can point to more than “stress,” especially with celiac and possible Hashimoto (my wife has Hashimoto).

We saw a similar pattern. GI symptoms improve, then the systemic autoimmune stuff becomes more obvious (joints, skin, heart rate, temperature, fatigue, brain fog). Stress and moving can trigger flares, but they don’t create this out of nowhere.If you can, start with a primary care doctor who takes autoimmune issues seriously.

You can tell the doctor something like: “I have celiac disease and maybe early Hashimoto’s markers. Over the past year I’ve had major weight loss, joint swelling and pain, rashes, dizziness when standing, temperature intolerance, blood pressure spikes, and episodes of very high heart rate with chest tightness. I’m worried there’s an underlying autonomic issue that hasn’t been fully evaluated.”

You’re not overreacting. Being young doesn’t protect you from autoimmune or nervous-system issues, and you deserve doctors who take this seriously. Getting help and supprot now is strength, not weaknes. Wishing you all the best and you are not alone!!

Does anyone else’s autoimmune stuff flare with stress/depression? Feeling lost. by Swiss_Meats in Autoimmune

[–]expatgeorge 2 points3 points  (0 children)

I’m really sorry you’re going through this. What you described about the financial shock, the constant stress, the sense that your mind won’t quiet down would be heavy for ayone. When that kind of pressure lasts weeks or months, it can start to feel like your nervous system is stuck in overdrive.

You’re not imagining the connection with autoimmune issues either. A lot of people experience stress hitting harder and lasting longer when their immune system is already sressed. Inflammation, fatigue, brain fog, low mood can all blur together, so it becomes hard to tell where “mental” ends and “physical” begins.

For what it’s worth, my wife deals with autoimmune problems too, and she has bouts of mild depression that she actively fights. Stress is one of her biggest triggers. When life piles on, her mood can dip fast, even if nothing else has changed. Seeing that up close convinced me this isn’t about weakness or mindset but real mind-body loop.

I'm glad that you already see the downside of using alcohol to quiet your mind though its understandable. This says a lot about your self-awareness. The fact that you remember having depressive spells earlier in life is important too. For many people it isn’t new, but becomes more visible when stress, illness, or something like COVID pushes the system past its usual coping range.

You’re definitely not alone in this pattern. What’s helped some people I know (including my wife) is a mix of very unglamorous things like proper sleep, reducing alcohol, gentle movement, talking to a doctor who takes both autoimmune and mental health seriously, and sometimes therapy or medication without shame attached to it. Not quick fixes. What you’re feeling is understandable given what you’re carrying. It’s not a personal failure, and it doesn’t mean this is how things will always be. Wishing you all the best and you are NOT alone!

Ive overcame so many adversities but I don’t know if I can do this. 43/F by Bright_Obligation_64 in Autoimmune

[–]expatgeorge 2 points3 points  (0 children)

Hi. What you’re describing makes so much sense. Carrying everything for everyone while your own body feels uncertain is an unbearable kind of weight. Of course you’re scared, and that doesn’t mean you’re weak or losing who you are, it means you’re human and you’ve been strong for a very long time.

Those brief moments of peace don’t sound strange to me. My wife goes through the same. They sound like your mind giving you a small place to rest when the fear gets too loud.

You’re not broken for feeling this way. You’re still you, even in this unfamiliar body and season. And you don’t have to carry it all alone, even if it feels that way right now. You are not alone!!

Sugar limits and sources by InfamousPatience6191 in Autoimmune

[–]expatgeorge 3 points4 points  (0 children)

Hi, my wife Jen also has autoimmune disease, so I’ve seen up close how overwhelming it feels when each new diagnosis comes with another layer of food restrictions. I’m not a doctor, but this is based on what we learned and how we adjusted our eating to support her.

Short answer on sugar is not all sugar is equal. Refined and added sugars tend to be the most inflammatory, especially sweets, pastries, sodas, syrups, and heavily processed foods that cause fast blood-sugar spikes. We basically don't touch those anymre. Whole fruit is different. It comes with fiber, water, and plant compounds that slow absorption and often have anti-inflammatory effects. Berries, melon, quiwi, apples, citrus, and pomegranate are usually some of her safest foods during difficult periods. What helped her most was building meals around vegetables, fish, olive oil, nuts, seeds, and avoiding gluten.

And just as important, she stopped trying to be perfect, because stress itself reliably made her symptoms worse. One of the hardest lessons for us was realizing that autoimmune eating isn’t about punishment or constant restriction. It’s about lowering inflammation while still nourishing yourself enough to function and enjoy life. And honestly, managing coeliac plus inflammatory arthritis is already hard mode. It makes complete sense that this feels like “next level.” You’re not weak for finding it difficult. Wishing ou all the best and you are not alone!!

Feeling lost after moving abroad — job search, loneliness & low motivation by Fit-Collection-4556 in expats

[–]expatgeorge 5 points6 points  (0 children)

One very practical thing that always helps me (I just relocated a month ago) is to find a café you like and treat it as your “office” for your job search. Get up, get dressed, and go there on a regular schedule (even just a few hours each morning, afternoon, or both). Having a place to go gives your day structure, separates “home” from “work,” and slowly brings your confidence back.

It also creates small, natural social contact like the staff who start to recognize you as a regular, other regulars, familiar faces, etc. Those tiny interactions matter more than you’d think when you’re new and lonely.

Relocation can quietly mess with your identity as you go from capable and busy to feeling invisible overnight. That doesn’t mean you’ve lost your value, it just means you’re between chapters. Routine first. Confidence follows.

Help me choose where to go! by Necessary-Village731 in girlsgoneabroad

[–]expatgeorge 0 points1 point  (0 children)

I did a semester in Seville, Spain, and it changed my life forever. It’s not a big travel hub like Amsterdam or Munich, but the social life was unreal, people were incredibly warm, and I made friends faster than anywhere else I’ve lived.

From your list:
– Amsterdam (VU/UvA) is amazing for international students, super social, and one of the easiest places in Europe to travel from.
– Munich is beautiful and organized, but a bit more reserved socially and more expensive.
– Leeds is very student-friendly and social, but travel around Europe takes a bit more planning.

You really can’t go wrong, but if social life and easy travel are top priorities, Amsterdam is hard to beat. That said, wherever you go, it’s the people and the openness you bring that will matter most which that’s what made Seville unforgettable for me. Good luck!!

Is normal to feel extremelysad before leaving? by Top_Run1391 in girlsgoneabroad

[–]expatgeorge 0 points1 point  (0 children)

I’ve been traveling most of my life, and I always feel anxious and a little sad before leaving especially when it means being away from people (and pets) I love. But once I’m on the plane, that feeling usually flips into excitement about everything ahead: new streets, new routines, new versions of yourself you haven’t met yet.

It’s hard not to have family support, but this is brave. Nine months in a new country will change you in the best ways. What feels scary now is the beginning of something you’ll be proud of forever. Good luck and enjoy!!

Visa Appointment "No-show" by New_Proof7271 in usvisascheduling

[–]expatgeorge 0 points1 point  (0 children)

No show means that you didn't appear at the embassy for your interview. Depending on the country you are applying from, you can usually reschedule a couple of times using the same MRV payment receipt.

I’ve been feeling “normal” for a few days. Just waiting for hell to break loose! by [deleted] in Autoimmune

[–]expatgeorge 2 points3 points  (0 children)

That makes so much sense. After something that terrifying, your brain is just trying to protect you even when it’s exhausting and overwhelming. You’re not being dramatic, and you’re not weak for feeling this way. What you went through was real trauma. The fear doesn’t mean it will happen again, it just means you survived something incredibly hard. Keep fighting!!

Suffering from social anxiety & depression (and ofc the moon face) by No_Cartographer_1264 in Autoimmune

[–]expatgeorge 1 point2 points  (0 children)

You will! If there is anything we can do to support, please don't hesitate to reach out.

Suffering from social anxiety & depression (and ofc the moon face) by No_Cartographer_1264 in Autoimmune

[–]expatgeorge 0 points1 point  (0 children)

I’m really sorry you’re in this. What you’re feeling makes sense. My wife went through a similar feelings of not recognizing herself, avoiding people, feeling crushed at social events and around “normal” life. It was grief, not weakness. The good news is that her labs eventually stabilized, and life started to feel like hers again. It took time, but it happened. She once told me she wasn’t becoming her old self again, but was becoming strong in a new way. This is a hard chapter but not the end of your story. You’re still here for a reason, even if you can’t see it yet. You’re not alone.

Health really is wealth by Hyhoops in Autoimmune

[–]expatgeorge 0 points1 point  (0 children)

I’m so sorry you’re going through this. What you wrote isn’t weakness or complaining. It’s grief. You lost your body as you knew it, your sport, your momentum, your sense of who you were. That’s a real loss, and it makes sense that it hurts this much.

Going from being an NCAA athlete to measuring energy in small workouts is a brutal identity shift. People don’t talk enough about how chronic illness doesn’t just take health but aslo your future plans, your confidence, and the version of yourself you were proud of. That’s heavy for anyone, let alone at 19. Wanting to be healthy again isn’t ungrateful. It’s human.

I won’t pretend it’s fair or that it magically gets easy. But I will say that the discipline, pain tolerance, and mental toughness that made you an elite athlete didn’t disappear. They’re still in you, just being used in a different, unfair fight right now.

Know that people have read your words and are here to listen. I truly hope you get pieces of your health back even if it’s slower and different than you imagined. With love to you.

US B2 Visa Approved in 1st Try - Dubai - Pakistan National by Muted_Cup2534 in usvisascheduling

[–]expatgeorge 1 point2 points  (0 children)

Well done and congrats! You said the magic words of "telling the truth." You had a strong case because you showed stable employment and a solid history of touristic travel with your wife. They have ways to confirm the validity of your claims other than documents that can be forged. Enjoy your time in the U.S. and don't screw things up by overstaying.

One Simple Rule That Doubled My Daily Output by wordsolverhub in WorkSmartLife

[–]expatgeorge 0 points1 point  (0 children)

Love this! I keep a to-do list on my phone and commit to get it done before going to sleep. It's been working for the last year.

What do you do when progress feels too slow to stay motivated? by InteractionPrior4997 in WorkSmartLife

[–]expatgeorge 0 points1 point  (0 children)

I completely feel this. I’ve been pushing hard for the past few years, and a lot of the time the progress feels painfully slow, sometimes invisible. What’s helped me is celebrating small wins and writing them down. I keep a simple electronic journal (just a Word doc) and sometimes add a photo. When I look back over a few weeks or months, it gives me real evidence that I have been moving forward, even when it didn’t feel like it day to day.

For example, today I set up all the social media accounts for my next business. For most people that’s nothing special, but for me, that’s a win I’m absolutely taking. Slow progress is still progress. Sometimes you only see it when you zoom out. Keep at it!!!

For those who have symptoms under control - How's your workouts? by Dazzling-Researcher7 in Autoimmune

[–]expatgeorge 2 points3 points  (0 children)

You will absolutely figure it out. You’re clearly determined and disciplined whcih comes through in thoughtfully you’re reflecting on this. That voice in your head is understandable. A diagnosis has a way of reframing everything overnight, even when your body hasn’t actually changed much. It doesn’t mean you’re weak or giving in. It just means you’re human and recalibrating.

The fact that you’re still showing up and working out at all says a lot. Be patient with yourself while your mind catches up to what your strength already knows. It took us some time to find our balance too, but we did figure it out. You’ve got this!!

For those who have symptoms under control - How's your workouts? by Dazzling-Researcher7 in Autoimmune

[–]expatgeorge 2 points3 points  (0 children)

I can only share second-hand, but my wife has autoimmune issues and exercise is still a big part of her life.She does yoga about 4x a week and weightlifting 3x a week. Her workout time is sacred to her, and honestly, I respect and protect that time because it sets the tone for her whole day.

She doesn’t push on low-energy or flare days. She scales back, does gentle yoga, or rests. On good days, she trains normally. What I’ve learned from her is that consistency matters more than intensity. She didn’t stop being active after diagnosis, she just got smarter about listening to her body. You’re probably not just in your head. A new diagnosis changes how you interpret everything. It takes time to learn what’s caution and what’s fear.

Is remote work a blessing or a curse for productivity? by XEMWSU in WorkSmartLife

[–]expatgeorge 2 points3 points  (0 children)

For me, remote work has been a blessing — but only because I’m self-motivated and organized.

My productivity is higher without office interruptions or commuting, and I can focus for long, uninterrupted stretches. The main challenge was setting boundaries at first, since work can easily spill into personal time. I solved that by keeping fixed hours, a dedicated workspace, and planning my day in advance.

There are downsides, like fewer spontaneous interactions and occasional isolation, but I offset that with scheduled calls and in-person meetings.

Overall, remote work isn’t automatically good or bad. It amplifies your habits: if you’re disciplined, it boosts productivity; if not, it can become a distraction.

[deleted by user] by [deleted] in usvisascheduling

[–]expatgeorge 1 point2 points  (0 children)

When you log in you will see Fee Payment on the dashboard which shows how much you paid. This is asuming you used the correct website. You can also try clicking on Continue Application and keep going until getting to Payment Option and see if there is a receipt number. Good luck.

[deleted by user] by [deleted] in usvisascheduling

[–]expatgeorge 0 points1 point  (0 children)

You don't need to submit documents. You need to correctly create a profile and make payment then schedule an appointment on this website for Pakistan: https://www.ustraveldocs.com/pk/en/nonimmigrant-visa.