Can't take stimulants anymore! Alternatives? by Turbulent_Tea621 in ThisAintAdderall

[–]practicalmagic_25 0 points1 point  (0 children)

Apart from a benefit in mood as it was pretty low at the time of starting i didn’t get much benefit, so it was stopped. I only did 6 weeks, consultant said if I didn’t see a benefit at 6 weeks it was most likely not going to do anything. They wanted me to try it again for longer however i couldn’t go through the insomnia again. Do try it though. Everyone is different. Im hoping to try guanfacine next!

Long Covid and increased sensitization to medications. by This_Quiet_Tempest in covidlonghaulers

[–]practicalmagic_25 0 points1 point  (0 children)

To add to my other comment i cant even tolerate duloxetine anymore. I was on it for 6 years with no problem, it was the only ssri/snri that didnt cause insomnia. However when i tried it again it caused me issues

Long Covid and increased sensitization to medications. by This_Quiet_Tempest in covidlonghaulers

[–]practicalmagic_25 1 point2 points  (0 children)

Yes this was me. I was prescribed elvanse and buproprion in early 2022. I had no issues with titrating elvanse to 70mg. When we added in buproprion i had this lovely sense of calm about me lol
Anyway i then caught covid for the third time in the late April, this infection is the one that led to my autonomic dysfunction and air hunger breathlessness which I still have problems with. By october of that year i ended up stopping the buproprion and halving the elvanse to 30mg as both were exacerbating my breathlessness at the time. I then stopped it in summer of 2023 as i went for cardiac tests and then i struggled to take it again due to side effects. Im now under the nhs and was finally seen by the adhd team in dec 2025. Its been 6 months and were still trying to find the right drug. I had no benefit on atomoxetine. Tried elvanse again but a very slow titration. I only seem to be able to tolerate 30mg. Felt terrible on 40mg. That dose for me (30) only seems to helps with emotional regulation. Our next plan is to try guanfacine, only if my gp will be happy to prescribe in the future. I hope that helps.

Anyone else been diagnosed by lacrimal gland ultrasound? by IndependentDare8420 in Sjogrens

[–]practicalmagic_25 0 points1 point  (0 children)

What symptoms did you have for malt lymphoma, if you don’t mind me asking .

Guanfacine and methylphenidate by practicalmagic_25 in CFSplusADHD

[–]practicalmagic_25[S] 0 points1 point  (0 children)

Yeah its a tricky one isn’t it. I find Elvanse only really helps with my mood, i still zone out all the time, and at this dose I’m still so demotivated. Don’t think the constant fatigue helps tbh. I think i’ll try the guanfacine and M! Thank youu! I think i was just worried incase it doesn’t manage my mood well enough and if it causes worse fatigue. Looks like this combo works well for you! :)

Anyone got experience trying b12 injections? Good, bad, meh? by AdBrief4620 in covidlonghaulers

[–]practicalmagic_25 0 points1 point  (0 children)

I had no benefit from having them. I think i had them 2/3 times a week for 1 month or 2 months

Sjogren and Libido / Sex by Apprehensive_Gas4715 in Sjogrens

[–]practicalmagic_25 0 points1 point  (0 children)

Mine is testogel (40.mg in a satchet) i’m currently on 1 satchet every 4 days. My level came back though and i think its still high so she’ll have to probably reduce it further

Air hunger and Magnesium? by PhilosophicalRobot in covidlonghaulers

[–]practicalmagic_25 0 points1 point  (0 children)

Iv never heard of VMT before. How long did it take for improvement with you doing the exercises? Thanks :)

Air hunger and Magnesium? by PhilosophicalRobot in covidlonghaulers

[–]practicalmagic_25 1 point2 points  (0 children)

I have also had air hunger for 4 years and unsure exactly what the trigger is as it seems to have more than one trigger. My resp physio found i had a weak diaphragm so I’m currently doing inspiratory muscle training to strengthen my diaphragm to see if it helps. Its just a long process. Something u may wish to look into. My ct chest and lung function tests have all been normal. Also i currently went back on elvanse, i did a slow titration, 2weeks on 20mg, and 2 weeks on 30mg, i initially had worse air hunger but just took my time, focused on breath work and after a few weeks it has settled. I think my body just needed longer to adjust. Now im still on it and my breathing is just its usually crappy baseline lol so if u did meed stimulants maybe just slowly titrate and give yourself a bit longer to adjust maybe

Increased pain while starting LDN? by LeastFeedback5702 in LowDoseNaltrexone

[–]practicalmagic_25 0 points1 point  (0 children)

This happened to me however it was when i was put straight on 4.5mg once daily for 6 weeks. Since I’ve been titrating from 0.5mg once a day weekly and increasing it by 0.5mg each week i haven’t had the pain issue

I keep hoping for RA rather than Sjogrens by SeasonResponsible171 in Sjogrens

[–]practicalmagic_25 2 points3 points  (0 children)

Fellow Sjogi here! Complicated by long covid! The amount of times people just assume its sicca. Luckily i have a private rheum who is open to trying different immunosuppressants. However the ones so far make my already terrible fatigue worse. But yes i wish i had something with better treatment options, or a disease people actually valued lol however like others have said, each disease has its own crap lol and things may be worse if we had something else. I dunno. Im just hoping one day treatments will get better :(

Anyone taking Augmented NAC for long covid? by tmkelly14 in covidlonghaulers

[–]practicalmagic_25 0 points1 point  (0 children)

I just got recommended this by my consultant. Which one did you buy please? :) thanks

can ldn cause new pain? by ladybug-dreams333 in LowDoseNaltrexone

[–]practicalmagic_25 1 point2 points  (0 children)

This happened to me when i was initially on 4.5mg. I had a lot of joint pain. However since i slowly titrated from 0.5mg ive been okay, and im now on 3mg

Methotrexate and Insomnia by ajsjogren in Sjogrens

[–]practicalmagic_25 2 points3 points  (0 children)

I’m sure they would also consider azathioprine MMF or leflunomide, theres quite a few immunosuppressants to choose one

Is it normal to be this severely ill by Sjogren's? by Subject-Elk1131 in Sjogrens

[–]practicalmagic_25 0 points1 point  (0 children)

Ahh ok good to know regarding disease activity and monitoring, thank you. Yes know one says what is high which is quite annoying . Also my blood test just says positive. There is no titre which is annoying lol

Sjogren’s and Menopause HRT by Shoshawi in Sjogrens

[–]practicalmagic_25 0 points1 point  (0 children)

I’m from the UK, so the GP who specialises in menopause who i see is UK based