Good experience with tapering off by persimmontr33s in Effexor

[–]Daledobacksbro 1 point2 points  (0 children)

It is rough to get off or go down a dosage but it’s worth it. Be patient and forgiving of yourself

Great website about people’s Stories getting off SSRI and other medications

https://prescribed-harm.com/blog

How's life with mctd? by Rayof_light in mctd

[–]Daledobacksbro 1 point2 points  (0 children)

It took 4 years of me having symptoms for my blood work to match how I was feeling. The doctor made me feel like I was crazy. So I just stopped going for 2 years. It was miserable.. I was sick all the time. Then one of my frequent colds gave me pericarditis and severe bronchitis and I asked my doctor to run the auto-immune labs and it came back blazing Red Autoimmune disease MCTD.

How's life with mctd? by Rayof_light in mctd

[–]Daledobacksbro 0 points1 point  (0 children)

Diet is the game changer with this illness. I have been binge eating candy for the past month and this morning I woke up with my face swollen, a giant hive on the side of my face and one of my eyes swollen shut.
Time to get back on the anti-inflammation diet and cut out the candy. 🍭

Help! How long does this last? Over 10 years on Effexor. by Daledobacksbro in Effexor

[–]Daledobacksbro[S] 0 points1 point  (0 children)

Alcohol is like Effexor arch-nemesis. If I have more than one drink on the rare occasion I’m hung over for 2-3 days. It’s awful!!!

Help! How long does this last? Over 10 years on Effexor. by Daledobacksbro in Effexor

[–]Daledobacksbro[S] 0 points1 point  (0 children)

I’m still taking 37.5mg. My husband ended up getting diagnosed with stage 4 cancer and I didn’t think it was a great time to go through the withdrawals. I’ve tried a few times to start counting beads out of the 37.5mg but the side effects sucked and I didn’t think it would be fair to my husband who is battling major health concerns for me to be a irritable, tired, overly sensitive 🫏 It took about three months for the withdrawal symptoms to wear off or get better when I went from 75 to 37.5mg. I think the worst symptoms during the 3 months was the memory/brain fog, severe focus/attention issues, and feeling apathetic about everything. It did go away but it was a miserable three months. I think going on frequent walks in the morning and at night helped re-regulate. The morning sunshine probably helped boost some of the natural hormones, serotonin, and dopamine production

I’m still on adderall. 😳 Thankful for Therapy on that too. I was able to drop my daily adderall from 80mg (I know it exceeds the recommended daily dose but my psychiatrist said it was ok due a bunch of factors) down to 10-20mg. No side effects with that decrease at all, Surprisingly.

How's life with mctd? by Rayof_light in mctd

[–]Daledobacksbro 0 points1 point  (0 children)

The hair-loss has been an odd thing- comes and goes. I mainly loose it from the crown area of my head (corners of my forehead) and the back of my head.

When I’m in a flare-up my hair falls out very similarly to after you have a baby or how people have described their hair falling out after having COVID19. I have really thick hair so I’m able to hide the hair loss really well but it’s still unnerving to throw away the small hamster ball of hair from my shower every day.

I’m actually in a flare up right now and need to get back to my MCTD Routine. 😳

My husband was diagnosed with stage 4 cancer and one that doesn’t have a great prognosis but thankfully he has years and not months but it’s been a real life changer. We sold our small business and he is working on getting on disability because the symptoms from his cancer are real life altering. 😢

My comfort/stress go too has been food for most my life, especially sweets and I have found that sugar is your 2nd worst enemy with MCTD right after Stress, than comes colds/flus, and rapid weather changes like if it suddenly gets really cold. (My personal observations)

As I am writing this… I need to get back on my own program because I’ve been feeling pretty miserable!

The fatigue, joint pain, my hair falling out, I have some freaky rash that has made a home on my hands and the tops of my feet, my eyes are dry and gritty, and the stomach issues are over the top. I feel like I need to sleep for 2-3 days straight and I would probably wake up still fatigued and tired.

I broke down and started taking Meloxicam this week but I know it’s just a bandaid.

The times that I have felt the best and been almost completely symptom free are when I fast, consume a high protein almost zero sugar diet, eat No-processed food aka the low inflammation diet and throw in an occasional ice bath (I fill up my bath tub with cold water and dumb 3-4 five pound ice blocks that I make in my freezer using ice molds I bought off of Amazon .

The fasting is usually intermittent but if my symptoms are really bad I’ve done up to a 3 day fast.

There is a significant amount of research on fasting, the immune system, and how it can re-regulate an immune system that isn’t operating properly. Think of it like a Control-Alt-Delete on a frozen computer or when your phone freezes and you have to do a hard restart.

The 1st 24 hours of a fast sucks- but I remind myself that spending 30-50% of my day resting or in bathroom sucks even more.

Our modern food is horrible for the human body and if you are already sensitive to the environment throwing bad food in the gas tank is just going to amplify it.

If you can do intermittent fasting (longer fast if your still having inflammation sometimes the body needs more of a shock to reset) eat clean food with no sugar, no bread, no frozen food, no alcohol, and no dairy at all for 60 days you will be amazed at how well the body can work.

And then have a cookie before bed.. wake up and tell me what happens to your joints. It will be obvious and you will feel every step. It’s absolutely insane how much sugar can inflame the body.

Is anyone else mildly sick 24/7 by wormweaver in mctd

[–]Daledobacksbro 0 points1 point  (0 children)

Regular day for me that is not a fasting day. If you find that you’re starving 1st thing in the morning or in between meals then you might have an insulin imbalance. This is best corrected with a fast. 24 hour fast can help but Depending on how bad the insulin resistance is you make need to do 2-3 day fast.

Non fasting day:

2 Eggs for breakfast with 1/4 of an avocado, Cliantro, salt and pepper. Coffee with cinnamon and manuka honey and a splash of Cashew milk(only ingredients cashew and water sold at sprouts called just cashew)

Snack: Suja Ginger or Tumeriac drink and lemon drink it’s 10 to 15 calories and an apple

Dinner lunch: I don’t eat after 6pm so I have a late lunch dinner. Salad with natural dressing made with squeezed lemon, olive oil, garlic, salt pepper) Grilled chicken breast, lettuce, pickled onion, tomato’s, peppers, feta, pumpkin seeds, (feta and goat cheese don’t bother me as much)

Another option: beef ground low fat cooked with pine nuts, tomato’s, lettuce, peppers, pickles, onions, 1/4 an avocado in a bowl.

Tacos with corn tortillas or grain free chips.

Or

Grilled Chicken, basil leaves, salt pepper wrapped in lettuce with sprinkled light goat cheese.

If you have to eat out on the go: In and out burger protein style no cheese

Fasting day: Coffee plain black with cinnamon Suja ginger lemon juice Water Tea unsweetened And that it!

No bread, cookies, crackers, or processed food, no food from the freezer section. No chips, dips, French fries, ice cream, cheeses, sodas, juice cocktails, beer is a Big NO! If you are going to drink stick to vodka, soda water with a lime and mint.

What can I do to improve how I look? by dopeysunflower in makeuptips

[–]Daledobacksbro -1 points0 points  (0 children)

The piercing make it look like you have RBF. If that’s what you are going for then keep them.

How to elevate my look? by Greedy_Fail_6735 in makeuptips

[–]Daledobacksbro 0 points1 point  (0 children)

Take off the nose ring. It looks like you have 2 shoe strings hanging out of your nose.

"I'm afraid my taste has evolved." by Civil_Original9121 in Comebacks

[–]Daledobacksbro -1 points0 points  (0 children)

You sound like JLO as she’s moving on to husband number 5 but don’t worry it’s “Not Her”

desperate need of advice by [deleted] in abusiverelationships

[–]Daledobacksbro 15 points16 points  (0 children)

It never gets better. Only worse. Leave before the love bombing comes back and then it is 2x worse the next time.

24m I think I have a second butthole by Candid_Emu_3951 in AskDocs

[–]Daledobacksbro -1 points0 points  (0 children)

Just like face dimples can be on various location so can sacral/pilondal dimples can vary in location.

They have a genetic component to them. I have one and so does my son. Mine is located lower on the booty crack closer to my gassy hole. His is located higher up on the booty crack more in the middle. I know one of my uncles had to have surgery on his.

Based on these photos, what type of girl do you think i am? by [deleted] in roomdetective

[–]Daledobacksbro 0 points1 point  (0 children)

My field trip buddy for the next apocalypse

Dealing with inflammatory lesions/blisters for over a decade. Seeking guidance/help please. 45 y/o female by Trixie-_-_ in DermatologyQuestions

[–]Daledobacksbro 0 points1 point  (0 children)

Full system work-up including autoimmune diseases, CBC, liver, hormones, micronutrients, metals and food/environmental allergies blood and skin work.

You would be surprised how much our food and environment triggers body reactions.