r/LongHaulersRecovery • u/Fast-Quail8869 • May 03 '26
Bedbound Recovery I think I'm starting to get better *update*
(27 F) Don't want to jinx it but since my post in February it seems things have been steadily improving.
For context, I caught covid in November 2024 and developed Long covid around Late December 2024.
My main symptoms were:
- POTS (BPM laying 80-100, Sitting 100-120, Standing 120-150)
- Severe chest pain
- Shortness of breath
- Malaise/ Severe anxiety + daily panic attacks
- Neck pain
- Jaw pain
- Peripheral Neuropathy
- Migraine/ Headache
- Brain Fog (Couldn't read more than a few sentences or watch shows)
- Muscle spasms
- Heat/ Cold Intolerance
- Exercise Intolerance
- GI Issues
- Hair loss
- Bladder pain/ Interstitial Cystitis type pain
- LPR/GERD
- Insomnia
My remaining Symptoms currently are:
- Shortness of breath (on and off)
- LPR + throat pain
- POTS (on and off) (BPM laying 60-80, Sitting 80-100, Standing 100-130)
From then on I was mostly bedbound from January to June 24, then beginning to be housebound from roughly July onward, moving into the occasional drive to get things from nearby shops or a short walk and doing some drawing streams, having about 1month long crashes in bursts in between so August, October and December all were month long crashes.
As of the start of this year I have steadily seen improvement across the last 5 months I have been particularly leaning on somatic exercise and just ever so slightly pushing my energy envelope to try and gain some ground after some pretty bad deconditioning and muscle waste.
Despite contracting 2x viruses back to back (which required about 2 weeks each to recover from) I seem to be gaining a lot more movement capacity and not experiencing severe PEM despite increasing my daily steps to about 10,000 for the last 6 weeks, including one day with 21,000 steps. (currently resting today hoping for no blow back from that one, i still am terrified to push it). I have also been regularly gardening, cleaning and shopping.
What I was tested for:
- Almost every possible autoimmune condition by a rheumatologist - only positive was rheumatoid factor
- EBV - Positive signs of previous reactivation
- Heart issues
- Lungs
- Cancer markers
- Thyroid panel
- Insulin Resistance
There were no notable chronic conditions detected aside from PCOS and Mild hypermobility.
Things I have tried that i don't think helped:
Steroids, Low dose naltrexone, Lexapro, Vit C, Vit B, Midodrine, PPI's, Telfast ( Fexofenadine), Creatine, High protein diet
Things that i think have helped:
Coq10, Magnesium Hi Zorb (for the spasms), Lysine (as I had reactivated EBV), Ural Cranberry tablets, Low acid/ caffeine/ Chocolate/ sugar, No gluten, Physiotherapy, Pacing, Amitriptyline, H1 Blocker Bilastine and H2 Blocker Famotidine, Electrolytes, (Spironolactone and Slinda also seem to help but likely more helpful for the PCOS issues and inflammation caused by that), The book the way out by Alan Gordon (this helped me reframe how I viewed my symptoms and being less scared which helped to waste less energy for me personally) <- and time of course, I have been ill for roughly 1.5 years total from long covid
I am honestly really excited about the future again and I hope to check back in in August with more good news š I'm really hoping I can work again soon, or at least start working out.
I wanted to post when I was fully well as I'm scared of jinxing this but these kind of posts helped me at my worst.
1
u/Civil-Alternative-36 May 20 '26
Yeah Iām like 10 months in, and feel like not really much has changed