When I’m becoming depressed I usually start off eating a lot of junk food, staring at the TV for hours, avoiding all phone calls, people and situations. I sleep 15-20 hours a day and don’t care. I don’t take care of my hygiene or eat or drink enough. I self medicate with benzodiazepines. And I obsess about everything in my past and worry constantly about the future. I get extremely irritable and anxious and sometimes quite agitated. I often think of overdosing several times a day.
I do see a physiatrist but we can not seem to find the right meds since last year when my Paxil stopped working. My depression always gets worse in the winter from having S.A.D, but I also suffer from bipolar depression, PTSD, and borderline personality disorder mood swings, plus have a chronic illness. It all adds up!! How does your depression affect you?
It seems a lot of my current symptoms turned out to be related to my Addison’s, not my CFS or depression alone. I increased my hydrocortisone from 20 mg to 40 mg and feel completely different. Normally this is the ‘stress’ dose used when the body has an infection, Injury etc., but I’m staying on it for awhile, until my adrenals recover.
When my cortisol is too low, it means my adrenals are not producing enough. The most common symptoms are severe fatigue, loss of appetite, weight loss, nausea, vomiting, diarrhea, muscle weakness, irritability, and depression. These are the exact things I’ve been having but I just thought it was my CFS acting up, an infection, seasonal depression and a stomach flu. Now all my symptoms are gone.
I’ll be seeing my endocrinologist in March. We need to get my dose straightened out so this doesn’t happen again. What a waste I didn’t realize sooner.
Ive touched on the subject of depression in a couple of previous posts but i think now is such a relevant time to explain to people how depression can affect my life/my family/my friends.
When I was 17 I was diagnosed with depression and put on various medication to stabilise my moods which did help yes, until i made the worst decision to come off them without any sort of help. On and off over the years Ive been back on them and then when i thought i was ‘better’ i came off them(when really the medication was just doing its job).
I have seen councillors to help me deal with it and to find ways to cope and learn to enjoy my life again. Up until only a few months ago I took part in a 6 week CBT course which focused on strategies to find positives in negative…
Having an invisible illness brings a lot of judgement and opinions from others and a lot of time it’s negative and hurtful. Living with Depression and Chronic Fatigue is hard enough as it is without other people making me feel worse about something I cannot change.
Before my Fiancé met me, he had never met someone affected by depression and anxiety and I think it shocked him to see how much it affected me. He didn’t understand Depression and it took a while for him to get used to the condition but he made the effort to learn about it and support me as much as possible. The anxiety was hard for him to deal with because he is such an outgoing person who loves to socialise and it caused a lot of stress in the relationship but we both eventually learned how to compromise and he learned my boundaries and…
I’m not having an easy time lately. My mental health is iffy with a lot of anxiety, for months now, and depression setting in pretty hard this week. I’m in constant pain because of my back and something is going on with my CFS/ME. I’m completely drained and mostly bedridden. Because of this I missed three physiotherapy sessions, plus one of my DBT coping skills classes.
I’m so very, very frustrated . I have no answers. I just have to try to hold on, rest, get to physiotherapy and class when I’m able, and wait till January 10th to see my psychiatrist for possible solutions to lessen this gnawing anxiety and boost my mood a bit. Having my paxil poop out on me after 10 years has created a real disruption in my mood and trying all these new drugs has been a year long, not to successful trial.
My suicidal idealisation is becoming stronger each day as I feel I’m just too worn out to keep trying. If the thoughts get too strong I’ll have to go to the hospital, but I really don’t even have the motivation to deal with all that shit. Hours and hours waiting and I’m usually told there is no space, so they just increase my meds and tell me to go home. I’m just so tired of it all. I only keep going for my family. I’ll end this on a note of gratitude for them, the support they give me, the love and understanding .
I have not been well the last 2 weeks and only managed 3 walks (6 min) per week. I feel completely drained. I think it’s from the very busy days I have on Thursdays. I go to physiotherapy, have a 2 hour class and drive 1 1/2 hours plus usually run an errand, like picking up my mail, after weeks unattended.
Anyway, I am bedridden 3 day’s after, not able to cook or even get enough fluids down me. I feel extremely weak. I don’t know if the severe fatigue is from having such a busy day on Thursday or the core building exercises the physiotherapist gave me, or a combination of both.
I HAVE to do the exercises though. My back has been so bad since January, and the pain is not helping my fatigue or overall mood. They would be easy exercises for most, but they are difficult and tiring for me because of my severe deconditioning. I do still do them almost every day, even if it’s the only thing I can do.
I’m really worried about this week as I have physiotherapy tomorrow and Thursday plus class. Wish me luck.
Update: missed Tuesday physiotherapy session as too exhausted. Am becoming increasingly depressed, agitated and anxious. I have no motivation and barely care about anything. I don’t see my psychiatrist till mid January. I don’t know if this is S.A.D, my my dad’s recent death or medication related. Sucks.
My CFS has left me so deconditioned. I need to reverse this as I’m getting older and need to be as strong as possible for the journey ahead. I figure it might prevent some of the many problems that come with old age, especially loss of muscle mass. I’m hoping it will also improve my balance so I don’t end up falling, breaking a hip, and then in a nursing home.
I’m 50 but I desperately need to improve my overall physical condition now, no matter how long it takes, so I can have a better quality of life as I age. If I walk daily, and keep adding a minute a week, in one year, hopefully, I’ll be able to walk an hour a day. Then maybe I’ll add in some gentle strength training or tai chi etc. I just hope my body cooperates with me.
#ActuallyAutistic - An Aspie obsessed with writing. This site is intend to inspire through sharing stories & experiences. The opinions of the writers are their own. I am just an Autistic woman - NOT a medical professional.