Список из самых популярных хештегов по теме #LIVINGWITHMS

I met Brian in 2014 when I turned 30. It was meant to be. We got engaged 3 years later and got married last year. This picture was taken on our #honeymoon in #Santorini - everything was just perfect. But I started seeing a therapist because I couldn’t explain the fear and anxiety I was having. I had this crazy feeling that something bad is going to happen. Few weeks later I got diagnosed with #MS - it was insane. Fast forward few months, I’m #pregnant and back to being positive. Life is very unpredictable and you never know what’s coming next. All we can do is hope for the best! #cheerstothefuture #bepositive #tomorrowisanewday #livingwithms #mylifewithms #beatingmyms #positivemindset #onlygoodvibes #positiveenergy #positiveattitude #positivelife #personalgrowth #goodthoughts #positiveliving #positivemood #positivevibesonly #selfgrowth #thinkhappythoughts #msfighter #msstrong #mssucks #mstreatment #mswarrior #multiplesclerosis #multiplesclerosisfighter #nevergiveup

What you're seeing is how a person with Multiple Sclerosis would normally view his or her surroundings... Blurred, disoriented and dizzy. This is what the disease can do when it affects the nerves in the brain. Not only that, Multiple Sclerosis is so rare that people think that the fatigue, or vision problems are related to vertigo. Sadly it is incurable. This World MS Day, I am raising awareness of MS by posting this #Blurfie to honor the people fighting this disease and trying to carry on their life as normally as possible. You can also be part of the movement. . . . im tagging @yasir.hussain131 @saheefajabbarkhattak @hinaaltaf to take the #Blurfie challenge with me‼️ Here’s what you need to do: Step 1: Take a picture while shaking your phone lightly Step 2: Apply the Facebook picture filter Step 3: Upload it on your social profiles Step 4: Use the hashtags #Blurfie #LetsBeatMS #WorldMSDay @letsbeatms #IntezaarNaKaro #Blurfie #WorldMSDay #LivingWithMS

I’m sorry (no I’m not) MS, but you just won’t win. I’m going to always fight you. You say I’m fatigued even though I slept 12 hours? Too bad. You want my feet and hands to fall asleep randomly? I’ll push through it. You want to debilitate me, attack my nerves, cause numbness, take my sight, knock me down, make me talk like I’m drunk even when I haven’t had a sip of alcohol (even though I wish I had )? Well too freakin bad. You messed with the wrong woman! You can try all you want, but you can’t shake me. Sure there are times I’ll think negatively, but let those thoughts be fleeting and replaced with positive/beautiful ones. Even at my darkest times, I will continue to fight. Even when you think you’ve broken me, think again. I will always fight you. You won’t ever win. #spreadpositivity #thisisms

I’m here to show a different side of this disease, Multiple Sclerosis, and how the attacks on the body differ in every single person diagnosed. What shouldn’t differ is our attitudes towards it. YES, it’s normal to be upset and fear the future (I’ve been there!) However, those thoughts should be fleeting. Get them out of your head as quickly as they popped in‍♀️ We mustn’t dwell on what we CAN’T control. You know what we can control?! We CAN control our positivity. Our mindset. We shouldn’t compare our symptoms or how well everyone is doing/not doing- what we should do is hold each other accountable. Spread positivity and hope instead of doubt and fear. Hold each other up when we start to get down. Keep each other positive and hopeful for a future free of MS. Keep fighting #mswarriors together we got this ✨ #namaste

I promised I’d take them on a holiday if they promised they’d sort their malfunctioning hearts out ❤️ • Manifesting or bribery at its best? • Where shall we go? It needs to be warm! ☀️ #manifest

Seeing a very blurred photo of me? Well, it’s to grab your attention and talk about Multiple Sclerosis. On 30th May, the world celebrates World MS Day, an initiative to raise awareness about a rare disease which is slowly impacting lives in Pakistan. One of the most common symptoms is blurred vision. This is why I have uploaded a #Blurfie to show my support for the people living with MS and to get the conversation started. Join me and be a part of the Blurfie Campaign! #LivingWithMS #WorldMSDay #LetsBeatMS #IntezaarNaKaro @LetsBeatMS . . Here’s what you need to do Step 1: Take a picture while shaking your phone lightly Step 2: Apply the Facebook picture filter Step 3: Upload it on your social profiles Step 4: Use the hashtags #Blurfie #LetsBeatMS I’m tagging @maazm.khan_ @khawarabedi @huzaifakhan_9 to take part in this #blurfie challenge with me.

Your eyesight isn’t weak, I’ve posted a #Blurfie in honor of people living with Multiple Sclerosis. Multiple Sclerosis is a neurological disease, it affects the central nervous system, which results in blurred vision as one of the most common symptoms. Multiple Sclerosis stays with the person for the rest of their life, I’m celebrating the warriors who are living with this disease. #LivingWithMS #WorldMSDay #LetsBeatMS #IntezaarNaKaro @LetsBeatMS. I’m tagging @uzmamubeen_02 @sarahislam11 @maazm.khan_ to take a part in this #BlurFie challenge with me.

This was our #pregnancyannouncement - a gift for Brian’s family and my mom. The first 3 months was rocky. Lots of emotional moods swing, crazy dreams about past that I thought I moved on from, sadness and worry. I tried to be positive but it’s hard when your hormones are going crazy and your brain is telling you different things. The #misscarriage last year and the #MS diagnosis this year was a lot to take in. But things turned around and the #secondtrimester feels bright with full of hope and joy!! I’m in a much better mood and ready to enjoy every second of #myfirstpregnancy #multiplesclerosis #pregnant #pregnant_world #msmom #livingwithms #dealingwithautoimmunedieases #msawareness #msstrong #positivevibes #thisisms #howmsfeels #howtoeatduringpregnancy #invisibleillness #msfighter #chronicillness #autoimmunedisease #msstrong #beatingmyms #momtobe2019 #grateful

For so long I kept my struggle to myself. I didn’t want to come off as “seeking attention” or “being overdramatic.” A few years back, way before I even knew a single thing about MS, I got extremely sick at work. (For those wondering- it was an attack of migraines almost daily.) Day after day I would either leave sick, have to leave for doctor appointments, call out etc. I didn’t share what I was going through because I thought keeping to myself was better. I was wrong. It caused resentment from my coworkers who didn’t understand why. Granted it was absolutely none of their business, but if I had faced my obstacle openly perhaps I would’ve gained support and understanding instead of isolation and resentment. In hindsight I wish I was more open and honest. To be honest I had no idea how to even vocalize what I was going through without sounding whiny- I would try to sugarcoat it, diminish my symptoms so it didn’t sound like a “big deal.” Now I 10000% realize that it doesn’t matter how I sound. As long as I’m speaking my truth- however others choose to perceive it speaks volumes about themselves more than it does about me. People are going to disagree, not sympathize, judge, but that’s none of our business. Again, as long as you speak your truth, your soul can rest easy. You can go about your day finding happiness and peace. Just a little letter to those who are afraid to speak openly about their struggles. Because I was there once and if I can get to the place I’m currently in, so can all of you! #thisisms #invisibleillnessawareness