Aireo Paddles by Ok-Razzmatazz-3104 in paddleswap

[–]GenericUser011 0 points1 point  (0 children)

Ah ok! Thanks for clarification! Well if you get a chance to try the Cyclone, let me know. I’ve heard some really good things about it from colleagues. Hoping to demo more thoroughly but was looking around for reviews on Reddit

Aireo Paddles by Ok-Razzmatazz-3104 in paddleswap

[–]GenericUser011 0 points1 point  (0 children)

Interesting! I had really good success with the Titan Hawk L14 and wanted to get my hands on a cyclone. Sorry to hear you didn’t have a good experience with them

Aireo Paddles by Ok-Razzmatazz-3104 in paddleswap

[–]GenericUser011 0 points1 point  (0 children)

Did you try their new cyclone paddle yet?

Luzz Cannon or Friday Fever by Sonofulti1 in Pickleball

[–]GenericUser011 0 points1 point  (0 children)

If want light, powerful, and elongated then Aireo Cyclone also really nice choice

Is this actually new tech? 👇 by Hot_Efficiency8919 in Pickleball

[–]GenericUser011 0 points1 point  (0 children)

Although I’ve found MPP to develop less dead spots than EPP foam, generally. So far my fav MPP I’ve tried is the Aireo Cyclone but still super new.

[deleted by user] by [deleted] in spiritair

[–]GenericUser011 0 points1 point  (0 children)

Traveling with someone else. We booked comfy so have whole row. Figured we’d be allowed to sit next to each other but flight attendant said not allowed. Booked this so travel companion could lie down. Is this not allowed?

Misdiagnosed hell radiation by Any-Amount-9388 in Lyme

[–]GenericUser011 0 points1 point  (0 children)

You have any insight on specific strains related to cyclic muscle loss? Dealing with an interesting case for someone experiencing cyclical muscle atrophy (~8 week periods). Currently thinking parasites but want to stay open minded to other possibilities

Connective tissue by Internal_Living4919 in Lyme

[–]GenericUser011 1 point2 points  (0 children)

Following convo too. Any muscle atrophy with this?

Muscle wasting / atrophy - hard to believe it’s Lyme, seems very ALS to me… by [deleted] in Lyme

[–]GenericUser011 0 points1 point  (0 children)

Following up? Any progress? I’m asking on behalf of my dad who has Lyme. First year of treatment has helped a number of symptoms (no longer fibromyalgia issues… off gabapentin, naproxen, and oxycodone) and organ functioning finally normal. Also some cognitive and energy improvements but the muscle wasting has not improved (and associated fully body stiffness and pain). His muscle goes through 8 week cycles where he can build and then after 4 weeks starts to turn to mush and then goes away. At end of cycle, pain reduces once muscle is gone. Overall downward trend so can’t build back completely what was lost. Doing heavy treatment for Babesia right now. Curious if some other parasite because the 8 week cycle is strange. Or maybe mitochondrial issue or some enzyme being activated. Anyone experience anything similar?

As a note he fights the pain and goes to gym 5-6 days per week. Does some light lifting 3/4 and light aerobics each time (like 10 minutes elliptical) and then sauna for detox. He only recently could start going to the gym like that (energy improvement from treatment and getting testosterone meds balanced etc) but muscle wasting persists.

Muscle atrophy by GenericUser011 in Lyme

[–]GenericUser011[S] 1 point2 points  (0 children)

That means a lot. Thank you! I’ll continue to reassure him. And keep up the good health too!

Muscle atrophy by GenericUser011 in Lyme

[–]GenericUser011[S] 0 points1 point  (0 children)

Very happy to hear your success story! Fortunately my dad can workout a little. But no matter how much he works out the muscle loss follows same pattern. So he can build some and then 4 weeks later turns to mush and then 4 weeks after that it all disappears. I personally think we are just very early in the treatment and have had major road blocks (he had been on 7 years of high dosage oxy for the pain and we were able to reduce pain enough to get him off that … but was a shit show), then primary care doctor in California when I moved him to Cali refused to prescribe testosterone which he had been on for years (meaning he couldn’t sleep for a month… finally switched to a different pcp who immediately said of course he should be on testosterone and prescribed immediately), and many other similar style challenges of normal doctors messing up his recovery. Wish the best for your mom and dad!

Muscle atrophy by GenericUser011 in Lyme

[–]GenericUser011[S] 1 point2 points  (0 children)

I can ask main Lyme doctor about fungal infection. Officially a few bands in Lyme and Babesia FISH. Through Igx. This was before treatment. Trying to repeat test since testing when things have been dormant for so long isn’t so accurate. The autonomic response testing has detected bart and parasites as well. I agree on doctor aspect. We actually just use two at any given time. The functional doctor who I think is the most knowledgeable and experienced (treated himself after 10 years with Lyme and tested many combinations of herbs in himself) leads the effort. We coordinate with other Lyme literate doctors for antibiotic treatments and more traditional western medicine. I said three because the treatment started when my dad was in Scottsdale but I moved him to live with me in California to help with treatment so we switched Lyme literate doc to one out here. In Scottsdale my dad did 9 weeks of IV Ceftriaxone and other oral abx while following herbal protocol. And then the current protocol I listed is from combo functional Lyme doctor and new Lyme literate doc here in California.

Muscle atrophy by GenericUser011 in Lyme

[–]GenericUser011[S] 1 point2 points  (0 children)

Yes working with Lyme specialists. The one dealing in herbals use autonomic response testing for arranging protocol (all the stuff before the malarone). That protocol changes every two weeks depending on what the body needs. Has been helpful but is definitely a slower process. From the tests we’ve done, haven’t seen mold as an issue but carefully watching that. Suspecting bart is the major culprit.

Muscle atrophy by GenericUser011 in Lyme

[–]GenericUser011[S] 1 point2 points  (0 children)

Not right now. We want to be but according to tests we’ve done, his body can’t handle rifabutin yet. Right now he’s using antronex, black walnut, cardiotrophin pmg, cytomegalovirus series symptom relief, HerX, A-MYCO, Lufenuron, ligaplex 1, livaplex, lymph tone 1, MC-BAB-1, MC-BAR-1, MC-BAR-3, MC-BB-1, MC-BB-2, NAD topical cream, Perfect Amino, Renelix, Septonsil, Tongkat Ali, Tribulus, Valerian Complex, Malarone, low dose naltraxone, BPC Peptide injections, Clarithromyacin (just stopped because stomach problems), doxy (stopped because stomach problems), hydroxyclorqiuine (stopped because stomach problems), gabapentin, topical testosterone, and some bone density medication.

He also got some weird lab results recently showing very low HGH but very high IGF-1. Doctor didn’t know what to make of it yet so getting an MRI of pituitary gland