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Sarcoidosis and depression

Can Sarcoidosis cause depression? Could it affect your mood? Find out how Sarcoidosis can affect your mood.

Sarcoidosis and depression
6 answers
Yes. Pain and feeling alone and getting worse

Posted Mar 31, 2018 by Cathleen 1900
Being diagnosed with any long-term disease can be depressing and frightening. One of the most difficult things is not knowing what to expect, and not knowing where to turn for help. Seek support. Whether it's through online support groups, your local resources such as hospitals or churches, and Friends Are Family. Know that you don't need to go through this alone!

Posted Jul 4, 2018 by msinky 2550
It can cause but its always up to the individual. You have to try to stay positive. Stay around strong people

Posted Oct 8, 2019 by Lashawn 2500
Yes sarcoidosis Can cause depression due to the fact that there is no cure at this time and some people go through physical changes And emotional changes due to feeling so sick and tired. Plan for a lots of doctors appointments. But tried to sit in the Sun every change to get to change your mood and make yourself feel better

Posted Mar 8, 2020 by Elizabeth 4800
I have read that it can cause depression. I do not have depression but I do have days where I get angry with how my life is. I was an avid runner (25 plus miles a week) and now I am a maybe 1 mile walker (slow paced).

Posted Jan 18, 2021 by Althea 4550
Sarcoidosis do not cause depression. However not able to do the things you use to do. Not feeling like you. I feel that I live only to take medicine. While I can't get out of the bed or move without taking my steroids daily, the side effects for taking them, i.e. weight gain, irritable and joint bands become loose are the things that can make you depressed.

Posted Sep 14, 2023 by Emma Johnson 2500

Sarcoidosis and depression

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World map of Sarcoidosis

Find people with Sarcoidosis through the map. Connect with them and share experiences. Join the Sarcoidosis community.

Stories of Sarcoidosis

SARCOIDOSIS STORIES
Sarcoidosis stories
My story continues and I wonder how and why I go through what I do... Then there is that one person that calls me or sees me and either thanks me or just gives me that Hug that just means I am doing something right!!! I have been going through some r...
Sarcoidosis stories
Who I'm I- My name is Madeline, 50yrs old, born in NY raised in Puerto Rico. Living in Massachusetts. Single mom of two amazing son's, a 30 yr old and a 23 yr old US Marine. My illnesses are-Cancer survivor, Hodgkins Lymphoma diagnosed in 1992 while...
Sarcoidosis stories
My name is Barbara Weber and I suffer from this disease called Sarcoidosis. It affects your body’s organs for example skin, heart, kidneys, but mainly the lungs. In people who have Sarcoidosis, the inflammation doesn't go away. Instead, some of the...
Sarcoidosis stories
My dr diagnosed me with COPD in 2013 but my cough was dry and breathing treatments weren't helping much.  She did blood work and said I needed vitamin d. So I began taking it and a lump came up on my wrist and kept growing.  She referred me to s su...
Sarcoidosis stories
_I WAS DXD AFTER I HAD A BAD TICKLE IN MY THROAT THAT WOULDN'T GO AWAY, I COUGHED SO MUCH THAT I CRACKED A RIB THAT LEAD TO SHINGLES, I THOUGHT I HAD PNEUMONIA & WENT TO SEE MY PCP, HE ORDERED A CHEST X-RAY WHICH SHOWED THE GRANDULOMAS, THE DR ASSIST...

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Sarcoidosis forum

SARCOIDOSIS FORUM
Sarcoidosis forum
#Teamandreafight will be hosting a sarcoidosis awareness Day. April 30,2016. Games. Raffles. Guest speakers. Holistic remedies. We're even selling inflammation reducing lemonade! Bake sale and more. JOIN US!! Survivors please visit our facebook page ...
Sarcoidosis forum
I am looking for other with Neurosarcoidosis, my Dr.s have all told me its a rare type of Sarcoidosis and my also being a white male Im very more a rare bird, are there any others, I am also open to talk to anyone

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