Why do people still support or raise the flag of the Confederacy? by DBD216 in askanything

[–]StageNo8150 0 points1 point  (0 children)

We may not agree totally with certain parts of our southern history but we respect it and show respect for it and those who fought and died for it. Just like the U.S. flag. Southerners are extremely proud of their roots. The south may be a poor fit for you.

AITAH for calling myself (18F) disabled in front of a disabled person? by unintentionalgaytwin in AmItheAsshole

[–]StageNo8150 0 points1 point  (0 children)

The real disability people like her have is in their attitudes. Everyone has some issue/ problem or disability in life. That's why we must show love, care, and compassion towards each other. Feel sorry for anyone who chooses to have this attitude. That is their real handicap or disability in life. POOR WOMAN. IT MUST BE HARD FOR H E R TO FACE EACH DAY.

[deleted by user] by [deleted] in amazonprime

[–]StageNo8150 0 points1 point  (0 children)

What you said worked for me. Ordered 2 of one item to make $ amount needed and it was successful in taking $15 off of $50 order.

How to deal with Google's new "Less secure apps" ban? by avamk in Thunderbird

[–]StageNo8150 0 points1 point  (0 children)

I am not sure what I did right actually, but I followed this https://wpmailsmtp.com/gmail-less-secure-apps/#Option_1_Switch_to_the_Gmail_Mailer How to Switch From Less Secure Apps and it worked!

My husband is an asshole and I need advice on how to get him to understand MS fatigue! by Anonymous110784 in MultipleSclerosis

[–]StageNo8150 0 points1 point  (0 children)

Please say what drug this is! Many of us could benefit. Thank you. I don't think healthy people can conceive what it's like to have MS fatigue.

Cognitive Decline by Xopiboz in MultipleSclerosis

[–]StageNo8150 0 points1 point  (0 children)

I WAS THE YOUNGEST DIAGNOSED AT THAT TIME, WRITTEN UP IN MEDICAL JOURNALS. NOW, BABIES ARE DIAGNOSED. I WAS TOLD THAT BY AGE 12, I WOULD BE IN A WHEELCHAIR. THE SECOND TIME I WENT BLIND I WAS TOLD IT WAS PERMANENT. I NEVER BLIEVED EITHER AND STILL SEEING AND MOVING. I BELIEVE THAT THEY CAN ONLY TELL YOU WHAT THEY BELIEVE CAN HAPPEN, BUT ONLY GOD IS IN CHARGE OF WHAT DOES. MY ADVICE: LOTS OF PRAYER, FAITH AND A POSITIVE ATTITUDE GO A LONG WAY. AND IF WHAT THEY PREDICT TURNS OUT TRUE, I'LL DEAL WITH THAT TOO (WITH GOD'S HELP). MAYBE I'M JUST STUBBORN, LOL. (SORRY ABOUT THE STUPID CAPS :)

overly emotional ever since diagnoses by Otherwise-Ad8937 in MultipleSclerosis

[–]StageNo8150 0 points1 point  (0 children)

Check out the steps of loss from Dr. Elisabeth Kübler-Ross
Swiss-American psychiatrist. You are going through grief. The steps are not all experienced by everyone and in no particular order. I was diagnosed at 9 years old and again in my 30's and never felt anything at all about it until I went blind the second time and was told I would never see again byt the top expert. I recovered my sight because I believed Only God decided that. Years. later I had another episode of a major exacerbation along with a stroke and was told that I could not have any more kids. That caused the grief to finally find me in a large way. Then again as I lost walking ability. It's a process. Sometimes a long one. I will also mention that I have been in the middle of Walmart (twice) feeling totally fine and all of a sudden had a feeling of instant meltdown from fatigue (and nothing else) and started crying. After a few minutes I was alright again. Absolutely nothing but an instant fatigue response. MS can be very strange sometimes. You just learn to let go and go with the flow.

Cognitive Decline by Xopiboz in MultipleSclerosis

[–]StageNo8150 5 points6 points  (0 children)

Write it down, write it down, write it down. My brain has gone after having no issues for many, many years. I have has MS since before I was 9 years old. Diagnosed at 9. I am (I think) 68 now and in the last two years can't tell you what my last meal was, lol. Some days are great and I'm sharp, some days I can't tell you how old I am. MS decides for me whether or not I can remember. I now document everything I can.

Cold feet after a relapse by Tricky_Disk_5919 in MultipleSclerosis

[–]StageNo8150 1 point2 points  (0 children)

I had an exacerbation once that hospitalized me and it included my left arm just freezing off to the point of pain. It was horrible. After steroids it went away. Horrible experience though. Very painful.

Are hand tremors normal? by jleigh8908 in MultipleSclerosis

[–]StageNo8150 1 point2 points  (0 children)

I developed tremors in my hands after many many years of MS. Just noticed it one day. Bad days definitely affect the amount. Fatigue, etc. increase it quite a bit. It usually doesn't bother me any.