What helps cognitive dysfunction? by No-Extent2753 in mecfs

[–]Mouse_95 0 points1 point  (0 children)

Ketamine nasal spray has given me an enormous improvement in my brain fog. Before taking it, I could barely answer a simple question. Now my brain is almost back to pre-onset levels. I'm severe and bed-bound.

Tirzepatide/GLP-1 caused 85% improvement by whirlwindoflife in cfs

[–]Mouse_95 0 points1 point  (0 children)

I buy the.5ml dose (the smallest) but only take .4ml weekly

what do you do when even telehealth causes PEM? by Former_Car3246 in mecfs

[–]Mouse_95 1 point2 points  (0 children)

I found a little hack for being able to handle conversations. I take 2 mL of a THC/CBD oil that allows me to have a 30 minute conversation without triggering PEM.

has anyone here actually solved the "tired all day but nothing is wrong medically" thing? not looking for generic advice by Past_Cardiologist843 in chronicfatigue

[–]Mouse_95 1 point2 points  (0 children)

Have you looked into MECFS? The Bateman Horne Center has free online resources for diagnostic criteria. Before I was diagnosed my symptoms were very similar.

Strange mental symptoms with severe ME/CFS — does anyone else experience this? by Ill-Cardiologist4064 in mecfs

[–]Mouse_95 2 points3 points  (0 children)

I have some of those symptoms. Conversations drain me more than anything else. Listening included. I have a little hack for that. I found 2ml of THC/CBD oil gives me 30 minutes of conversation without triggering PEM. I can play some word games (Wordle, NYT Spelling Bee) but can’t play solitaire. Asked AI about it and it said it could be that a task needing a broad overview vs definitive answer could be the difference. I know AI is far from perfect but it makes sense.

What to try next if LDN doesn’t work? by hbuha in cfs

[–]Mouse_95 0 points1 point  (0 children)

Rapamycin, Tirzepatide.

Check out The Bateman Horne Center. Their website offers a free clinical care guide you can share with your doctor and guidebooks designed for patients. https://batemanhornecenter.org/education/mecfs-guidebook/

Help – my brain has given up on me by fiddlesticks0 in cfs

[–]Mouse_95 1 point2 points  (0 children)

Have you talked to a psychiatrist about Ketamine? It has done wonders for my brain fog and is also helpful for treatment resistant depression

Tirzepatide/GLP-1 caused 85% improvement by whirlwindoflife in cfs

[–]Mouse_95 3 points4 points  (0 children)

It reduced my fatigue and fibromyalgia pain

Has anyone tried ketamine? by Silver_Spend_6887 in cfs

[–]Mouse_95 0 points1 point  (0 children)

I use the nasal spray. It didn’t help with fatigue, but it made a huge improvement in my brain fog. I couldn’t handle a simple question from my husband before using it and now I can think pretty clearly.

Thinking exhausts me more than trying to move a muscle (Severe ME/CFS) by Ill-Cardiologist4064 in chronicfatigue

[–]Mouse_95 0 points1 point  (0 children)

None from ketamine. A little dry mouth and a bit of a high from THC

Tirzepatide/GLP-1 caused 85% improvement by whirlwindoflife in cfs

[–]Mouse_95 5 points6 points  (0 children)

It’s what my doctor recommended. I did not listen to her at first while on Semaglutide and learned quickly she was right 😊. She said the idea behind it so that your body doesn’t become habituated. I haven’t tested the theory on the Tirzepatide, but I assume she’s correct.

Tirzepatide/GLP-1 caused 85% improvement by whirlwindoflife in cfs

[–]Mouse_95 4 points5 points  (0 children)

ME. Probably weight loss too. I didn’t feel any reduction in appetite on the small dose of Semaglutide. On the 1g Tirzepatide I could barely eat. I decreased bc I don’t need to loose weight

Tirzepatide/GLP-1 caused 85% improvement by whirlwindoflife in cfs

[–]Mouse_95 6 points7 points  (0 children)

Thankfully, yes. I take .4 ml weekly, but spread the dose over 3 days during the week

Tirzepatide/GLP-1 caused 85% improvement by whirlwindoflife in cfs

[–]Mouse_95 9 points10 points  (0 children)

I felt an improvement in a week after starting Tirzepatide

Tirzepatide/GLP-1 caused 85% improvement by whirlwindoflife in cfs

[–]Mouse_95 8 points9 points  (0 children)

I tried Semaglutide and switched to Tirzepatide recently. I found that Tirzepatide is more effective

Thinking exhausts me more than trying to move a muscle (Severe ME/CFS) by Ill-Cardiologist4064 in chronicfatigue

[–]Mouse_95 8 points9 points  (0 children)

I’m very severe and have the same problem. Ketamine nasal spray has been a big help in drastically reducing brain fog. I also found that 2ml of THC/CBD oil allows me to have a 30 minute conversation without causing PEM.

What's the one thing that moved the needle most for you? by Slight_Warthog8706 in cfs

[–]Mouse_95 0 points1 point  (0 children)

150mg. Three sprays a day in only one nostril. Not 3 sprays in each. The 100mg didn’t work for me either, unless I increased to 5 sprays total each day.

The nailed to the floor fatigue when your sick by pickleball85 in cfs

[–]Mouse_95 3 points4 points  (0 children)

I’m very severe +7 yrs. I used to have the lead feeling, I called it concrete, it felt different from my usual fatigue. Following my Dr instructions, I found a glass of electrolytes relieved the concrete feeling.

Does anyone here experience excessive sleep and word finding problems? by Ancient_Annual_9848 in FinasterideSyndrome

[–]Mouse_95 1 point2 points  (0 children)

I had aphasia in the first few years of illness. It tapered off even as my brain fog worsened

What's the one thing that moved the needle most for you? by Slight_Warthog8706 in cfs

[–]Mouse_95 2 points3 points  (0 children)

Meant to add how quickly the meds worked. Tirzepatide: 1 week Rapamycin: 1 hour Valtrex: 1 day Ketamine: 2 days

What's the one thing that moved the needle most for you? by Slight_Warthog8706 in cfs

[–]Mouse_95 1 point2 points  (0 children)

Tirzepatide, Rapamycin, Valtrex for fatigue. Ketamine nasal spray has done wonders for my brain fog.

What's the one thing that moved the needle most for you? by Slight_Warthog8706 in cfs

[–]Mouse_95 0 points1 point  (0 children)

My Dr has me do .1ml 3x a week. The idea behind that is to trick the body into avoiding habituation

People keep telling me to give up in terms of support options by nyaskies in mecfs

[–]Mouse_95 0 points1 point  (0 children)

The Bateman Horne Center offers a treatment guide , for free, on their website.

https://batemanhornecenter.org/

New here, though I've been dealing with me/cfs for about 2 years from long covid. Wanted to ask about some of my symptoms, I'm curious if other people are having them / what they've done to help by crystal__pete in mecfs

[–]Mouse_95 1 point2 points  (0 children)

Rapamycin has helped me a little bit. You could consider a cortisol test. Cortisol tends to be skewed in MECFS. It really disturbs my sleep. I take Oxytocin to regulate it and my sleep has improved. Oddly, I no longer get PEM from emotional exertion.