Itching skin: Has anybody had any... - Encephalitis Inte...

Encephalitis International

704 members515 posts

Itching skin

Tuesando profile image
5 Replies

Has anybody had any experience with itching skin following encephalitis? In this case located to certain parts of he legs. This continues 6 months after hospital discharge. Wonder whether it is a neurological consequence of he encephalitis or drugs related (keppra/Lacosamide)

Written by
Tuesando profile image
Tuesando
To view profiles and participate in discussions please or .
5 Replies
vloaiza09 profile image
vloaiza09

I feel like I’m more itchier than normal after having encephalitis... BUT I do have eczema and I think my immune system is worse because of encephalitis therefore, making my eczema worse. Have you told your doctor? You should. Any rough dry, patches? If not then it could be the meds...

alpappy profile image
alpappy in reply tovloaiza09

do too mostly on my legs

KDJR profile image
KDJR

Hi - my son is 7 years old and this was something he complained about even before he had a formal diagnosis of autoimmune encephalitis. We call them "itchies" and they move to different spots on his body (often his arms and legs) and last for a short period of time. He recently had a flare and now that he is again receiving IVIG and steroids, he rarely complains of them. I am hoping that once he is off IVIG/steroids that his cellcept dose will control the "itchies". I was only aware that this can be a possible symptoms of encephalitis as I had read Brain on Fire by Susannah Cahalan (before he became ill). I don't know if this is helpful, but I hope it is. Best of luck with your recovery. As a mom of someone fighting this disease, I know how truly amazing you are. Warm Regards

Tuesando profile image
Tuesando in reply toKDJR

Thanks KDJR. I’ll read ‘Brain on Fire’. I think there is a connection with the encephalitis. Up until now I’ve been treating it with over the counter insect bite cream. It seems to alleviate the itching some.

KDJR profile image
KDJR in reply toTuesando

I'm happy to share - and really glad the info might help you. I think there is definitely a connection; Ryan's "itchies" don't go away until he receives steroids or IVIG and they are one of the symptoms I monitor and tell his specialists about. If you look up "neuropathic itch" it might provide some information that is helpful and allows you to better explain it to your doctors and hopefully get some treatment that works. Warmest Regards

Not what you're looking for?

You may also like...

Encephalitis missed by GP and By Eye casualty visit

hello to all in this society. I know very little about encephalitis but my Dad has just passed away...
Anjidav profile image

Wish there was an encephalitis group based in Miami, fl

One thing I learned in my dads recovery with viral encephalitis is it’s not mostly seen here is...
Catmom8727 profile image

Sobbing seizures?

Hubby was diagnosed with autoimmune encephalitis in January and has been on steroids and anti...
Kw55 profile image

Has anyone had viral encephalitis turn into autoimmune encephalitis??

My father is still in the new hospital we took him in for a second opinion his MRI showed small...
Catmom8727 profile image

Focal Aware Seizures

Hi I'm recovering from encephalitis and recently been getting focal awareness seizures, they...
Scots_dad profile image

Moderation team

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.