r/ADHDMedsUK

Image 1 — Can Amfexa cause eczema or am I allergic?
Image 2 — Can Amfexa cause eczema or am I allergic?
Image 3 — Can Amfexa cause eczema or am I allergic?
▲ 2 r/ADHDMedsUK+1 crossposts

Can Amfexa cause eczema or am I allergic?

This is a lengthy post so I apologise in advance! I just want to preface that I am not 100% sure that this is being caused by my medication, but just wondering if this has happened to anyone else just in case.

Fast forward to now: I have been on Amfexa since end of Feb / early March and it has little to no side effects for me and I am really happy on it. I was previously taking Elvanse which caused me to lose a lot of weight and inevitably wasn’t sustainable to say on it.

(I was 9stone when I started meds and lost 1.5stones on Elvanse pretty rapidly and I’m currently 7stone 5lbs which leaves me with a BMI of 16.6 which is quite underweight as a 26yr old female 5ft6)

Current issue: At the start of March, I noticed a small red mark on my knuckle but no pain or cuts so assumed I had just knocked it and would clear, but it persisted for about 3 weeks and noticeably got larger and was quite swollen but still no pain. My GP gave me antibiotics incase it was an infection, but still didn’t clear and then I noticed a redness appearing on another finger on the same hand which was quite sore. I went back to the GP who prescribed a steroid cream and was pretty confident it would clear, but it didn’t. The redness had spread and again long story I went back to the doctors roughly 3 times up until now and had multiple steroid creams and blood tests. (Side note - I told every GP that I am taking Amfexa and no one seemed to take an interest in this or think it was connected). My bloods came back fine, and the steroid creams definitely reduced a lot of redness but didn’t clear the issues. At the start of May, my hand did start to clear up about 85% after a few days of not using any steroid cream but after about a week or so - which leads me to now, my hand is incredibly painful and massively flared up again.

It was only after racking my brains that I have thought that the only thing that I have changed since this started is my ADHD meds but would have never thought it could be connected as I am responding really well to Amfexa? I have been searching the last couple of days to see if anyone else has experienced this kind of reaction to Amfexa or any stimulant medication in general and saw a few posts saying it has either made people’s eczema worse or given them chilblains. I have Raynaud’s anyway and yes stimulants have made my hands/feet colder, but I have never experienced anything like this!

The main factors are: I am currently underweight and have had a lot of stress within these 3 months which I know can trigger dyshidrotic eczema but as no steroids seem to be helping - i’m left wondering am I having some weird allergic reaction to my medication?

I have a dermatology appointment next week as my GP has said it looks like dyshidrotic eczema/psoriasis (which I have never suffered with before) and I am hoping this will be more helpful to find out what is going on. I am currently in the process of my shared cared agreement being taken over by my doctors so I just wanted to see if anyone else has experienced this crazy side effect of their ADHD meds and did it go away? Or if this is totally a new separate eczema issue!!

u/CozyGremlinEnergy — 4 days ago
▲ 2 r/ADHDMedsUK+1 crossposts

Private titration with NHS diagnosis

I am heavily debating going private for my titration assessment. I already have an NHS diagnosis, I started the process in 2020, diagnosed 2022 now it’s 4 years later still waiting for a titration assessment. I am desperate for medication before I finish my degree (just finished my 2nd year, going into last) I’ve been looking at RTC but the waitlist is still so long..
My parents have some money saved and I have talked with my mum about paying for private titration/medication for a year, but we cant commit to paying large fees forever.
I’ve been seeing some people say they are on the RTC waitlist (maybe even NHS?) while actively paying for private treatment. Could I stay on the NHS waitlist or the RTC waitlist while getting treatment privately?

The waitlists with private are so much shorter than anywhere else, it seems like a no-brainer but I am worried about hidden fees.
If there’s any private clinics that allow straight to titration with an NHS diagnosis you would recommend please let me know!

Also, if anyone has any experience with Health Harmonie minds privately please let me know! Their package seems good and not too expensive comparatively but like I said I’m worried about being stuck with hidden costs.

If I think too hard about how long I’ve waited for treatment I tear up a little
God bless anyone else who is in the same position stuck waiting for meds we are in this together!!🙌

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u/Pickleds3 — 9 days ago

Intuniv and stimulants

Has anyone felt emotionally “less like themselves” on Intuniv/guanfacine?
I’ve been on 1mg Intuniv (guanfacine XR) for about 5 weeks alongside Attentin/dexamphetamine for ADHD and I’m really struggling to work out whether it’s helping me or not.
On the positive side:
I definitely feel less jittery/anxious physically

stimulants feel smoother

less adrenaline/wired feeling

less overstimulated overall

BUT…
I also feel:
less happy/fun

emotionally flatter

less verbal/articulate

more blunt/opinionated

more sensitive emotionally at work

less socially “myself”

kind of detached from my personality/spark

I’ve also had ongoing 3:30am wake-ups, sweating/overheating, bloating and body soreness, but I’m also in perimenopause/HRT territory so it’s hard to know what’s causing what.
My doctor suggested either:
increasing Intuniv to 2mg
OR

increasing stimulants instead

…but I’m very medication sensitive and honestly nervous to increase the guanfacine when I already feel emotionally different on 1mg.
Did anyone else experience:
emotional flattening?

personality changes?

feeling calmer physically but “less you” mentally?

early waking/sleep issues?

muscle/body soreness?

And if so:
did it improve with time?

improve after increasing?

or did you eventually stop it?

Would especially love to hear from women/perimenopause/people sensitive to meds because my nervous system seems ridiculously reactive to everything 😅

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u/misschanandlerbong83 — 11 days ago