Dean had to do the show alone at Ciro's. Dean was nervous but got through it without Jerry. He refernced him often and after the second show rushed to Jerry's home.
August 21, 1954
Dean brings him gag gifts.
"Dean comes over every day."
September, 1954
Guess Dean wanted to go with him. I think he missed him.🥰
August 1954
They got an award for 'Citizens of the year' by the 'Guardians of the Jewish homes for the aged' Jack Benny accepted for them and director Norman Taurog took it directly to Jerry.
"Martin is sticking close to his bedside"
Found these while looking for articles about Dean and Jeanne for @vipercats. It just shows the strong feelings that Dean had for Jerry, even though they had fought earlier in the year. Actions speak louder than words.
For those of you who don't know what we are talking about, we have finally approached that time to begin writing the actual first year fic itself. Which means it is time to begin looking for beta readers.
We are looking for anyone who really wants to, but a few specific groups as well. Here is a list for some of the general things we're covering and we cannot represent as realistically since they do not apply to us.
This is a fanfiction, and both authors are broke, so anyone completing this form must understand they are volunteering to help and will not be paid.
Groups of people and google form link below!
For first year specifically:
Irish
Scottish
Black British/English
Generally people who grew up in the British isles in the 90s
People with knowledge or experiences with refeeding syndrome
Ones we have covered but are welcomed as betas anyways:
General beta readers for the plot/vibes
C-PTSD
Pagan witches
Autistic folk
ADHD
Transmasc folk (for Ron)
General lung capacity problems (for Harry)
For the future (these are the ones we know we need to help represent specific groups but will not be doing much until we start writing those books):
Transfeminine folk (pref. from the 90s)
Punjabi
Diné people
Argentinian
Brazilian
French
Bulgarian
Ukrainian
Independent Samoan
Burmese
Moroccans
Malagasy people
Tajiks
Taiwanese
Egyptian
Indian
Members from the Apache, Ute, and/or Pueblo tribes
Russian
Filipino
Ugandan
People from Pophnpei Island or are from Micronesia
Chinese
If you would like to join us, here is the google form to sign up!
This is the sign-up to be recruited as a beta reader for The Wix World! We are finally here at the point of writing, and we need people LIKE
Out of curiosity, what kind of masks do you use to avoid potters lung?
I stick to my vogmask for pretty much everything. it’s covid safe, and me and my spouse still mask whenever we’re around people so I’ve always got it on me
I know they’re not NIOSH approved but they filter 95% of particles
(but mostly I just do my best to avoid kicking up any dust. and I’ve got an air filter next to my desk)
Results from a study in China suggest that some COVID-19 patients will be left with long-term lung problems.
Among patients who have recovered from COVID-19 in China comes the first evidence that some may suffer long-term lung damage from the disease.
In 70 patients who survived COVID-19 pneumonia, 66 had some level of lung damage visible in CT scans taken before hospital discharge, researchers report March 19 in Radiology. The damage ranged from dense clumps of hardened tissue blocking blood vessels within the tiny air sacs called alveoli, which absorb oxygen, to tissue lesions around the alveoli, Yuhui Wang, a radiologist at Huazhong University of Science and Technology in Wuhan, China, and colleagues found.
The tissue lesions can be a sign of chronic lung disease. Similar damage has been documented in survivors of SARS and MERS, respiratory diseases caused by coronaviruses similar to the SARS-CoV-2 virus behind COVID-19. Long-term studies of SARS patients have shown that roughly a third of people who recovered from severe bouts were left with permanent lung damage. In the case of MERS, one study found about a third of people who recovered from a serious infection still had signs of lung damage about seven months later.
But while initial lung images indicate that SARS and MARS typically set into just one lung, COVID-19 appears to be more likely to afflict both lungs right away. In 75 of the 90 patients admitted to Huazhong University Hospital with COVID-19 pneumonia from January 16 to February 17, damage was seen across both lungs, Wang and colleagues report. CT scans taken before hospital discharge revealed that 42 out of 70 patients displayed the type of lesions around the alveoli that are more likely to develop into scars.
Given how widely the pandemic has spread, chronic lung conditions from COVID-19 could challenge many thousands of people in years to come. As of April 27, more than 2.9 million people worldwide have been diagnosed with the disease. In comparison, SARS, or severe acute respiratory syndrome, sickened about 8,000 people during its 2003–2004 outbreak. MERS, or Middle East respiratory syndrome, has infected more than 2,500 people (SN: 1/24/20). While an estimated 80 percent of COVID-19 cases are mild, the rest display problems ranging from breathing difficulties to respiratory failure (SN: 2/25/20).
Hey y’all, long time no update from me here on Tumblr.
So most of you may know that since late 2018 I have been disabled after a work ‘accident’ where I was not provided the proper safety equipment. I have been in the worker’s compensation process since then, trying to get a diagnosis and treatment so I can return to work and my previous quality of life. As you all may have noticed, I no longer post any personal fitness content because I can not physically do more than walk for a couple minutes at a time.
Unfortunately, the worker’s compensation Dr’s have thrown their hands in the air and said they do not know whats wrong with me, so I have been declared at “Maximum Medical Improvement” with a 0% disability rating and my disability checked have been stopped. I live in Texas, which is extremely bad for worker’s rights in this regard.
Thankfully I have a very hardworking and loving wife that is here to support me, and I do have some savings to pay my share of the bills for a little while, but I have been left to continue seeking a diagnosis and treatment on my own.
I’m not writing this to ask for any money help, but I am writing this to see if anyone can find any of my symptoms familiar so I can have a better chance at getting a diagnosis. Please share or send this to anyone with any knowledge on health, especially the lung/heart systems. I am only asking for help in trying to get a diagnosis and a treatment plan going.
I worked on an insect farm and during an experiment I was subjected to breathing in clouds of insect poop/pee, powdered food product, molds from water+food touching, bacteria, fungus, in a hot, humid, closed room for 3+ hours. I was the only person out of 4 people who was not provided a respirator mask to work in these conditions.
Immediately after this exposure I began feeling flu-like symptoms such as body aches, overheating, fatigue, headaches. I also began to experience breathing attacks where I would become confused and lethargic while forcefully breathing out rapidly.
The other 3 people also experience flu-like symptoms, but recovered after 2 weeks, but I was also the only person of the 4 who had to continue working with the insects and continued smaller daily exposures for the next 3 months.
I took a week of steroid and antibiotics which stopped the breathing attacks, but introduced chest pains to my symptoms, which I have continued to deal with over a year later.
I took a pulmonary function test 5 months after the accident and my results came back better than average, so no treatment was provided. I sought a second opinion and had a bronchoscopy done 7 months after the accident, which found chronic bronchitis damage in my lungs, as well as STAPH bacteria. 1 years and 3 months from the accident, my chest x-rays still show inflammation in my lungs.
I’ve taken one lupus blood test which tested negative, but lupus does run in my family. I have had an echocardiogram which found a minor unspecified cardiac murmur (tricuspid regurgitation). I am trying to get bronchial provocation test done to see if I have asthma now, as well as some sort of stress test since movement makes my symptoms worse. A huge issue is that none of the tests I have taken have proven anything so far, and despite the bronchoscopy finding bronchitis damage, that still does not diagnose me with anything.
My symptoms:
Upper chest pain (under the clavicle but above the breasts) that feels like tight strings being pulled, which physically makes me lean forward when I walk or sit. Movement affects this pain and laying down relieves it.
Center chest pain (which I describe as lung area) which feels like a hollow burning or needle pain. Breathing in things like smoke, humidity, perfume scents, cooking gas, etc, affects this pain and laying down does not relieve it. Basically if I can smell something, I hurt.
Lower chest pain (diaphragm region) which feels like a runner stitch that I get from movement. Eating can also bring this pain on. Laying down relieves this pain.
Shortness of breath, which I get from taking warm showers, talking too much, or from walking. My heart rate is often in the 150+ BPM range when I am having shortness of breath/air hunger.
Fatigue/lethargy. I have to sit to wash dishes, and sit to take my showers because I do not have the energy to stand for too long. Getting out of the shower has become very difficult.
Headaches that are resistant to medication. I’ve taken over 2000mg of Tylenol at a time trying to relieve these.
Loss of appetite/inability to eat full meals.
Random dizziness while laying down.
Constant dreams of choking.
Dry cough. This symptom has been getting worse with the cold weather.
Please, if any of this seems familiar to you then let me know. I just want to be able to live my life again. I do not accept that there is not treatment out there for me to take that will let me work and do fitness again.
