hot red face but cold everywhere else

i all. I've been diagnosed with crohns since 2009. I was blessed enough to also get the lovely add ons of this disease. rheumatoid arthritis, hiatal hernia, enlarged liver, and now, something new. I get very cold, but hot in face. my face gets red like I have sunburn, but just on cheeks. I have been getting this on n off for past 2 weeks. I'm at loss on this. my doctor can't explain why it's happening. I thought maybe side effects of meds, but he said no since I've been on them over 2 months it wouldn't start this late. I had no insurance, so I just dealt w issues of all parts of my illnesses for 5 years. I still have no insurance, but found dr that offers sliding scale, but he seams not interested in anything really. my sugar levels do fluctuate, but he said could be from simvastatin. anyone else get this symptom, or is it not crohns related??


simvastatin 40mg
folic acid 1mg
ondansetrom 4mg (prn nausea)
methotrexate 2.5 mg (3 tablets once a week)
tylenol (prn pain)
b-12complex
probiotic
peppermint pills
multi vitamins

just when I think I get something "under control" I get something else. most don't understand the constant pain in lower abdominal pelvic region, think it is "attention grabber" or something like that. I was in er week ago cause crohns related RA caused hip to give out when I was attempting to get out of bed, too make it to bathroom in time (woke to severe cramping n huge bout of diarrhea) I fell (again) n caused wrist injury. sporting stylish brace on left arm n sling, which hurts RA in shoulder, so its a win win thing here. I don't drink soda. haven't for YEARS. carbonated drinks cause bad gas. I get hives w one alcohol drink, so have not had booze of any kind in years also. I drink coffee n decaf herbal teas that are decaf. water or flavored water. I cut out lots of carbs, eat organic. limit red meats n pork. mostly seafood, or chicken. no sugar except for creamer used in coffee. (chocolate caramel from international delights. my one vice I refuse to let go of) hiatal hernia causes extreme pain at night, mid chest. esophageal area. enlarged liver csuses pain when I sit straight or lay on right side. I have issues sleeping cause of pain, and before all this medical issues I was a registered pharmacy technician (had to quit when RA caused me to drop everything, n crohns sent me to bathroom 20 times a day) I know what long term effects of pain meds can do. I want my life back. I use to go out, fishing n camping w kids. now I can't move some days, other days live in bathroom. I need walker on bad RA days n no joke, thinking diaper bad CD days. driving distances a chore in itself. gonna get graphic n sorry for visual, but coming home from outing, I got the chills, sweats, cramps of a flare, told boyfriend to stop asap, closest place was McDonald's n made it into store but not bathroom. it was crowded,n I left in tears. meds don't do anything but make me cough, tired n nauseous for 2 days. I go days w/o sleep. n now, I get red hot face on top of everything else. I hate going out. I'm afraid of not making it to bathroom, not being able to walk. I look like death knocking at my door some days. I get depressed n cry cause once upon a time I was vibrant n active and I now have huge medical issues that cause me to hurt by sneezing. I've done everything dr, CD organizations, and medical journals have said to do to relieve some of the effects, but nothing I do is working. I seem to lose more n more of who I was daily. n now I look like freak cause I have steroid mask w/o being on steroids.

I'm sorry the length n depressing tone of this post. I feel so lost. I hate that some think the pain of crohns not pain. that I have it all in my head. I'm lazy cause I can't do what I use to. I'd give up anything to go to work again. cause that would mean I'm not chained to the toilet anymore. that hands work w/o pain from RA n.I csn walk w/o fear of falling.