Please help! extreme fatigue
Posted , 11 users are following.
Can someone help me shed some light on why I feel so horrendous! I have been suffering with extreme fatigue and exhaustion for about 8/9 months now and its affecting my everyday living. Any exercise makes it worse and takes me 2/3 days to be able to do anything. Im a nurse so have a hectic work schedule and ive been forgetting things and not able to concentrate. I have pain in my muscles and a pins and needle sensation down my back
My eyelid twitches and I have blurred vision.
I have frequent mouth ulcers and water infections so my immune system is affected but ive had tests done including FBC ESR thyroid diabeties anaemia b12 dificiency iron HIV Hep B urine samples and bowel checks as I was diagnosed with IBS last august. All other Tests were normal.
My diet is healthy to accomodate my Ibs and I drink plenty of fluids, take multivitamins daily and no change. Im struggling as my doctors seem to be ignoring everything im saying. I have migranes now and disturbed sleep and my emotions are all over the place. I get irritated easily as im.so exhausted. Some days I cant physically get out of bed or do everyday activites like washing my hair. Im 22 and feel like im 82! If anyone can suggest something to do I would really appriciate it
Jess.
0 likes, 22 replies
lefteris54687 Jl26
Posted
I had significant improvement when I treated a small stomach ulcer. As you mentioned, I used to feel like 82 (sometimes I used to think that even old people can stand for sometime whereas I couldn't). I would suggest apart from treating the other deficiencies to treat your IBS. Perhaps it will help as the digestive system is responsible for converting food to energy. I wish complete and fast recovery.
Jl26
Posted
x
georgeGG Jl26
Posted
caitlin39841 Jl26
Posted
i'd say the first 'stop off' should be to sign on to one of the CFS/ME management programs if you're in the UK. they run 8 week programs over a longish period of time. they are helpful, especially when newly diagnosed. there are lots of books out there too as well as numerous forums like this one etc. etc.
there's the ME/CFS association. Action for me. Breakthrough research and any number of support groups throughout the country. the latter vary in quality, so you'll have to make the choice there
also, your place of work are obliged by disbaility/equality statute to make any necessary amendments to your work environment. this could include a quite place to rest/nap during the day i.e. a reclining chair, lights adjustment, supportive sitting arrangements etc.
depending on the severity of your mobility, you may qualify for mobility allowance.
educating the family, loved ones, partner and close friends will have to be on the 'to do list'.
i don't want to overwhelm you with infromation, so maybe that'll help for now.
all good wishes
Caitlin
caitlin39841
Posted
Caitlin
georgeGG caitlin39841
Posted
Nasteha85 Jl26
Posted
Mouth sores? that sounds like a folate deficiency.