Love the funny’s on here since I write so much negative
Gotta laugh: Love the funny’s on here... - My MSAA Community
Gotta laugh
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This is the funniest one yet!
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Too Funny, agapepilgrim Do you think that they can fly INSIDE my house? Hmmm
They fly around putting out fires. Wish they could fly around and kill virus but unfortunately stubborn asymptotic carriers refuse to wear masks and continue to spread it to others. Until those people wear masks it is here to stay and kill or leave residual lung or heart scars for life. May daughter who is a Reapiratory Therapist and deals with it closer than anyone explains to me in detail what happens more so than the media even begins to, and tells me not to even think of going anywhere because I already have lots of lung scar tissue from very numerous bouts of pneumonia. Corona can scar tissue in lungs or heart or brain due to cutting off oxygen supplies in these areas or drastically reducing them, in any organ depending on where it is mutating (as with children). Please stay home or wear filtered mask for your protection or cloth mask for protection of others. And exam gloves, and social distance and hand washing and sanitizing. I think I should stick with posting funnies. I talk too much. I ruin my on funny posts 🥵😩
No, you do NOT get too negative! You are very pragmatic and a realist. I like it! This virus is nothing to mess with. I was tested twice, and while both tests came back negative, my pcp is still convinced I had a “ mild” case of it. Twice my cough went on for 14 hours constantly 2 separate days and I had it for over 8 weeks, still having some residual affects from it. Having wheezing, like I said nothing to mess with. I often think of your daughter and pray she is doing good. My doctor said the rate of inaccurate test results is about 30%. That is frightening. So I stay put unless I absolutely have to go do a pick up order of food. I wear a mask, I keep my house sanitized, and most of all I wash my hands! By the way, love the funny! And you! Kelly xx
My daughter said tests aren’t always true. Some doctors must resort to sputum test to get true results. Don’t know why they don’t do that in first place then. I think not enough of them. But my bronchitis is bad. Having to use meds in my home nebulizer for breathing treatments and some wheezing and lots of coughing and strange sounding voice. But I’ve had this off/on for about 40 years so I take it in stride. Along with pneumonia off/0n about 30 years. I didn’t know I had MS for 56 yrs. I was told it was fibromyalgia and Chtinic Fatigue and Arthritis and Anxiety and Bipolar and Stress Asthma and Eye Nerve Migraines (started at 17) and spastic stomach spasms (started at 8). Only when my tongue started burning all the time did a doctor send to neurologist for MRI. Lesions galore. Took medical history, vision and nerve damage, etc etc etc, started me on Aubagio that day. Since my cousin died at 55 of MS and I was 67 I started planning my funeral. But, here I am laughing, talking, crying, angry, cooking, breaking things, tearing up pictures of those who never cared, realizing a few who did, and making a collection of crosses and ocean paintings in my walls. The joy of my soul and the the happy place of my body.
I have told you before that we have much in common. In 1990 I could not walk. Had 7 small children at that point, including new twin boys. My eyes were strange. I had mono in high school all three years. Later learned that can be associated with MS. My dear husband took me to between 25-35 doctors. Not one tested me for MS! Got the same diagnoses you did. Not until 2006 did a great neurologist have a positive diagnosis in24 hours! Like you, loads of lesions and lots of cells in my spinal fluid. Really made me angry. But it was a relief to have an answer.
Hallelujah! Live on!
No, I like your posts!
The information you are relaying is correct
Thanks for sharing
Have you MS?
Yes I have RRMS for 56 years, with numerous other diseases and conditions.
How in the world have you coped for 56 years? I know we have chatted, but that is such a long time to deal with this disease. Also, I had read Corrie ten Boom books before, but am rereading all of them again. Thank you for reminding me! 😊
I commented on wrong place (above) MS brain. 🤣 so many inspiring writers who suffered so much more than we do. I read a poem “why do caged birds sing?” And was curious who wrote such a thoughtful poem. Maya Angelou. I bough a little bird cage with stuffed bird and flowers and hung it over my sink in kitchen to remind den just because I’m in the cage of MS is no reason not to sing. Caged birds still sing. Through Gates of Splendor is another biographical story I could never have the courage to live. And Joni Earickson. I fill my library with these stories and think who am I to complain (even though I do quite loudly😡) but repent every night hopefully. I love you Kelly. Thanks for sharing.
Good analogy
“Caged birds, still sing”
Love that
I will take that and keep it in my ❤️
Thanks
Perfect! We are supposed to have a fighter jet fly-over tomorrow. I’ll put in a request for this.
luv it
Good one 👍
had i known,i wouldn't be so concerned about finding it in the store!
😍 I wish those who think this virus is nothing would step into a healthcare worker’s shoes for a day. Their mind would change immediately!
Please thank your daughter as I have several family members who are in healthcare and are still showing up everyday scared as $hit that they don’t get it & bring it home to THEIR families.
Never mind all that they see/experience while at work.
I wish they could do that since we have such a "dense" population. If everyone would just follow simple sanitation and wear a mask we could all get back to running our own lives rather than letting the government run it for us.
In a information about MS said that MS people had a side dark, like bipolar persons.
Maybe we have a face happy but after we show a face negative.
I think that in the evening the people with MS is tired in the evening, and so we are more negative. I think is only to feel tired at the end of the day, not bipolar.
Happen to me that I am more tired at the end of the day because of doing many things all the day, and so I am tired and negative and fed up of all.
And when I am more tired more things I want to do.
My only daughter just informed me after I had a bad vet poor cognitive day and wondering what would happen to me in future when I couldn’t take care of myself that maybe Ben, her son, would. I just started bawling and hung up shortly. Means she doesn’t want me. My only child. That hurts. She said Ben will love to take care of me. Wonder why she wouldn’t? Hurts so very very deeply. My mother lived to be 95. I’m 73. I don’t want to live 22 years longer if I can’t take care of myself. I am doing sooo many stupid things nowadays. But to have her say that broke a big part of my heart forever. My husband didn’t want but one child because he had 2 children of previous marriage. After our 47 yrs of marriage he admits he should have yielded to my longing for 4 children. Maybe one of them would have wanted me in my old age. I will try to trust God for the future like I always have. It just cut deeply.