Lower right abdominal pain

Not that I'm aware! I didn't have a HIDA scan. Could this be the problem?

You could ask for a report on your ultrasound to see if your gallbladder was scanned or ask your doctor to find out if it was.  Your doctor will also have the paperwork. Right sided pain can be associated with gallbladder problems and especially if you have pain between both your shoulder blades or your right shoulder blade along with severe stomach pain. It may be worthwhile checking this since everything else has come back normal.

I haven't had pain there though it's only been on my lower right side no where near rib cage and pain is only in right lower back

Have you been tested for H pylori and have you had any change in the frequency or consistency of your bowel movements?  IBS could be a possibility if everything else is normal.  I would also push for an endoscopy and colonoscopy to get any problems ruled out there.

Have you tried a food diary to see if any food is causing pain?  Have you eaten anything that you would not normally eat?  What about any medications you are on? 

I'm not sure what I was tested for! bowel movements completely normal.

I've been eating normally.

Don't take any medications apart from what they've given me which is codeine which isn't work and is now giving me tightening chest pains.

It's a never ending cycle.

Would a gall bladder problem cause LOWER right sided abdominal cramping pain?

My girl is in chronic constant lower abdominal right sided pain (as many here know by now, haha) and the gall bladder visually (MRI, laparoscopy) fine, a HIDA scan never suggested therefore and also told, that location was not the spot.

Perhaps ask to see gastroenterologist or change your doctor if you still can't get help.  I would still consider a food diary in case you have a food intolerance and don't realise it.

Did you find out what she has? Are her symptoms the same as mine? I'm still in pain and it's nearly 2 weeks now since it started. I've even been to see a homeopath and she didn't know what was wrong! I'm in desperate need to find out what's wrong and the right treatment rather than chucking all these pain killers down my throat!

Intermittent episodes for 4 months,

now chronic and 24/7 for 1.5 years!

Her pains:

severe abominal very localised right lower side cramping (10-30 second on/off intervals), can put finger on it!, rolling her up in a ball when severe, able to walk very slowly if moderate.

Physical activity always triggered the episodes or worsening of moderate to severe cramping. Odd, isn't it.

Constipation, never diarrhea.

Pain not better if constipation tackled successfully with laxatives.

Mild fever, sometimes facial flushing/blocked nose (mast cells come to mind),

nausea, vomiting different severeness,

but never gone, currently upon lying down instant retching (hernia?). (gastroparesis confirmed in gastric emptying study)

Multiple diets useless, except for going low fiber and avoid meat and graininess of grains, that make it worse, but nothing makes it better.

Sudden appearance of 1000s of striae from top to ankles without massive weight fluctuation.

Cramping staying even after a picosalax clean out for colonoscopy, so is not the constipation re pain.

Pain not better after toilet. 

Side effects: FOB or visible blood on stool due to straining.

Sorry to slash hope here a bit, we didn't think it wouldn't go away ever either.

But it is very rare.

Life has turned into a sad window watching, hardly school or social life, but replaced by pain and a financial disaster.

Went to ER 4 times, even rcommended by physician, only pumped full with narcotics, checked electrolytes and went home since obviously not dying, just in agony.

She is diagnosed with hEDS (connective tissue disorder), gastroparesis and borrelia.

Her MRI clearly showes an elongated, thin, hanging transverse colon but the radiologist did not mention it even. Pointing pic (as I always have all imaging and results as a copy) out to gastroenterologist who says 'some have that, no problem'. 

I am currently trying to find a gut motility center and hopefully get a colonic transit study, that will prove something.

First been through the normal usual mill of

scopes, appendectomy, useless pelvic ultrasounds,

bouncing to gynecologist who bounces back to gastroenterologist and taking 1.5 years to find out, that a gastroenterologist is not a motility expert even they trial gastroparesis drugs (that did not help), none would refer to a special motility department or doc! ......

Of course a 'cyst' must be the reason in the untrained eye of a gastroenterologist, the normal 2cm luteal cyst wasn't there when symptoms started and long gone now (actually on continuous bc pill to avoid additional mens pains) and gynecologist can just laugh about. Duh.

One has to be terribly proactive yourself. You know best!

You will need to go through the mainstream mill 

to narrow down possibilities as there are so many and do exist.

You need to observe what makes it better, or has no impact.

(We see a naturopathic trained western doc additionally for avoiding side effects of malabsorbtion and stress, got blood tested first (copper, zinc, vitamine levels) to not throw in contraindicated supplements. With homoeopathy I am not a big friend since I don't understand the work mechanism of diluted substances in water so much, that it is not there anymore. I like herbs, chemicals, minerals, but not homoepathy. Again self healing and belief is a huge huge gain, so it might work for those, who believe in it. I don't, since I made homoepathic diluted medicine....We also tried acupuncture and the lot, but not successful)

Best of luck!! Take care!