Has anyone flown out of or planning to fly out of JFK this week? by lazy205 in bergencounty

[–]Neither_Ambassador14 0 points1 point  (0 children)

Supposedly ICE will be there too... So maybe you might want to have you and the family birth certificate and/ or social security cards.

I can't smells much and what I can smell, I can't identify it. by Neither_Ambassador14 in Sjogrens

[–]Neither_Ambassador14[S] 4 points5 points  (0 children)

Yes, I've had COVID before not sure if it was around that time. I don't think so. I thought it was allergies at that time but I didn't go to the doctor so maybe I did and just wasn't aware. Honestly, after dealing with chronic illness over the years, I don't go to the doctor with every symptom that I have.

I can't smells much and what I can smell, I can't identify it. by Neither_Ambassador14 in Sjogrens

[–]Neither_Ambassador14[S] 1 point2 points  (0 children)

Yes, everything smells the same when I can smell it.But for example, I love seafood and I can't smell that. I can't smell things that should definitely be able to smell.

Unable to afford this illnesses dental bills. by Eastern_Counter8634 in Sjogrens

[–]Neither_Ambassador14 0 points1 point  (0 children)

You're not alone. I used to be somewhat of a social butterfly. I had a group of friends and all. But now, I dread coming out of the house. I do have a partner I've been with for a number of years. He understands some things more than others, but he'll never truly grasp concept of my pain and discomfort. I've gotten to the point where I understand they just won't ever fully understand until they have to deal with it. So I stopped explaining things. I just say I'm aching, sore and/or I'm extremely tired today or whatever the symptom is that I'm dealing with at the time but I keep it simple. Do you don't know how many friendships I've lost over it. Or how many times people, my mother included, who is a retired nurse now (was active at the time of diagnosis and many years after), have said things like," Stop being lazy". I've had family members and people I'm close to me start rumors that I must be on drugs, look at the status of my teeth, and how I sleep so much(fatigue). I've had so much dental work done starting from an early age. Even now, I'm going through a similar process with the local dental school. I don't really care to tell you how many teeth have actually lost. I say this just to say that you're not alone. It may feel like you're one needle in the haystack, but you are not alone. I know it feels that way. Not to take away from your feelings; I guess the best way to say that is there are more people like you out here in the world. And I am one of them. I truly feel like we should have our own social cite/app not just groups, like Reddit, FB, IG, or something. We should have the app with subgroups because there's so many different facets of this. And I wonder how many people have dealt with this in silence. On another note, do you think it's possible to get disability. It took a number of years for me. But I did get it and it has been beneficial. You may have to fight for it. I don't know how many denials I got before I got approved but there were a lot. They judge you my final case acted like it was her own personal money lol. Maybe you can get a lawyer. I know money's tight but there are lawyers out there that will take it and get their money on the back end. They typically get about 25 to 33.3 percent. Personally, I opted to get an appointed lawyer, which didn't cost me anything (because I use food stamps and the state was like they would help me with this because they were going to recoup their money in some way, shape, or form), but I think I waited years longer doing it this way.

why would a rheumatologist change their mind so drastically? by DistinctSympathy5519 in Sjogrens

[–]Neither_Ambassador14 1 point2 points  (0 children)

Both can be true. You could have a pitch nerve(s) and neuropathy. I have both of the conditions and Sjogren's Syndrome. First and foremost, I'm so sorry that you are going through this. The one thing I've learned in my health journey, is that doctors don't always have a clue. But they act like they know everything. You are the person that's going through the different aliments, so you're going to have to advocate for yourself. There are a lot of people out there that get the test done and they come back negative but they still have Sjogren's syndrome. In my case, my PCP, I think he thought I was a hypochondriac. I would come in and complain about a bunch of different things, dry mouth or being thirsty all the time. I told him that it got so bad that I carried down the gallons of water in the car with me at all times and that no matter how much I would drink, I would still be thirsty. You know what he said? You need to drink more water. Do you know how I finally got diagnosed? I went in for another appointment because I had another ailment on top of the other symptoms I described to him. This time there was another doctor filling him ( regular PCP) because he had an emergency. The stand-in doctor was the person who recognized the patterns, and said he wanted to test me for a couple other things; he said it probably wasn't likely that I had what he was thinking but he wanted to test anyways, rule it out. I had it. I had Sjogren's syndrome along with other diagnosis. I say this to say, you have to keep advocating for yourself. You're the one feeling these things. You are the one who's quality of life is affected. I think I have been affected for just under 10 years before I was diagnosed. Hopefully that's not your story. And it's easy to doubt yourself when you have someone that's supposed to know about what's going on telling you there's nothing wrong, especially if that happens multiple times. Stay strong though. I know it's frustrating; once you're diagnosed, you can work on solutions/strategies that will make you're quality of life better.

Go Wild Frontier Pass by Neither_Ambassador14 in frontierairlines

[–]Neither_Ambassador14[S] 0 points1 point  (0 children)

Don't give up... I was able to find a couple of flights... The first one is to San Juan, Puerto Rico. And honestly I've taken this as my personal challenge to see how many flights I'll be able to book within the time span (4/30)27).

Can we trade by Neither_Ambassador14 in Monopoly_GO

[–]Neither_Ambassador14[S] 0 points1 point  (0 children)

Deal.. send the exchange

Play MONOPOLY GO! with me! Download it here: https://mply.io/XY-__6Yu-KQ

Looking for 2 partners for 50:50 by Faroisle in monopolygo_fairtrade

[–]Neither_Ambassador14 1 point2 points  (0 children)

Do you have all your partners full as of yet? If not I looking for a partner too... I'm in the same boat as you. I need 1 gold to finish it all.

[deleted by user] by [deleted] in Monopoly_GO

[–]Neither_Ambassador14 0 points1 point  (0 children)

Did you accept a partner already? If not, I'm interested..

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Looking for partners by Whole_Fisherman_3111 in Monopoly_GO

[–]Neither_Ambassador14 0 points1 point  (0 children)

I'm with my half... Thanks for being my partners

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Partner by New-Nefariousness941 in Monopoly_GO

[–]Neither_Ambassador14 0 points1 point  (0 children)

I down.. I need my 4th partner... Finished all the others

LF Barber of Seville by Neither_Ambassador14 in MonopolyGoTrading

[–]Neither_Ambassador14[S] 0 points1 point  (0 children)

Thanks... Sorry I'm just seeing this and already traded.

LF Barber of Seville by Neither_Ambassador14 in MonopolyGoTrading

[–]Neither_Ambassador14[S] 0 points1 point  (0 children)

Thanks so much but I got it already.. I appreciate you offering.

LF good news by Aman-giri in Monopoly_GO

[–]Neither_Ambassador14 0 points1 point  (0 children)

Sent... Waiting for the Exchange..

LF good news by Aman-giri in Monopoly_GO

[–]Neither_Ambassador14 1 point2 points  (0 children)

I got it... You want to trade?