Irritable Bowel Syndrome (IBS)

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Irritable Bowel Syndrome (IBS)
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We're so glad you're here. Scroll down to find some of the Crohn's conversations happening in our community. The more, the merrier—jump in anytime!

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10 reasons to join the Crohn’s and Colitis Support Group

1. It’s full of other people with connections to IBD.
2. It’s a safe forum to ask any and all IBD questions.
3. It’s a way to connect with others on the Mighty community.
4. I’m one of the group leaders (living with #UlcerativeColitis ), and I’m pretty cool.
5. We want to normalize talking about poop.
6. We do Q&As with partners like Girls with Guts.
7. It’s a small but “Mighty” community that we want to grow.
8. It’s supportive.
9. Why not?
10. Do it today!

You can search the groups to join. #CrohnsDisease #InflammatoryBowelDiseaseIBD #ChronicIllness #IrritableBowelSyndromeIBS

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The Mighty's Crohn's Disease community is 76,000+ people strong, but there's always room for more. Follow along or join in today—whatever is comfortable for you!
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What is something you wish people knew about living with Crohn's?

What is something you wish people knew about living with Crohn's?

Your response may be used in an article or video on The Mighty.

#CrohnsDisease #ChronicIllness

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Unseen Struggles: A Journey Through Chronic Pain

Chronic pain, a persistent and often misunderstood condition, affects millions worldwide. Unlike acute pain, which is temporary, chronic pain endures for months or even years, significantly impacting a person’s quality of life. This persistent discomfort can impair a person's ability to work, socialize, and maintain relationships.

In my practice, I often work with people who struggle with chronic migraines. I also work with a significant number of people who struggle with Irritable Bowel Syndrome (IBS), as well. The invisible nature of chronic pain often leads to misconceptions, exacerbating feelings of isolation and frustration for those affected. Beyond the physical toll, people can experience anxiety, depression, struggles within relationships -- chronic pain can impact the day-to-day and sexual functioning of relationships -- and an overall diminished quality of life.

The Emotional Impact

Living with chronic pain can have a significant impact on your emotional wellbeing. For example, you may experience feelings of frustration, anger, anxiety, or depression as you struggle to cope with persistent discomfort, as well as the threat of the next occurrence.

It is also common for relationships to suffer as partners may struggle to fully understand the extent of your chronic pain. Many have been told things such as, "Your migraine is just a headache," or, "It's all in your head," or even, "You would stop getting them if you really wanted to," and so on. These kinds of comments can leave people feeling ashamed, misunderstood, angry, and alone as they continue to struggle.

Common Myths Associated With Chronic Pain

If Your Pain is Invisible, You Must Be Fine

Chronic pain often lurks beneath the surface, invisible to the naked eye. You may appear fine externally, but internally, you’re battling constant discomfort. This disconnect between appearance and reality can lead to harmful misconceptions and judgments. People might assume that you can’t suffer that much if you don’t look like you’re in pain. These kinds of assumptions not only come from people out in the world, but often even from close family members.

If You Can Function, It Must Not Be Bad

Another pervasive myth is that if you can work or attend events, your pain can’t be severe. However, people with chronic pain often push through immense discomfort to maintain some semblance of normalcy. Every activity requires careful consideration, knowing there's a risk of the pain coming on or getting worse. The ability to function doesn’t negate the constant presence of pain. For the most part, people with chronic pain have essentially learned to function in spite of their pain.

The Idea that Chronic Pain is Only Physical

Chronic pain’s impact goes beyond the physical. It affects your mental health, intimate relationships, sex life, social relationships, and overall quality of life. It is important for people who struggle with chronic pain to not only receive support in these areas, but also that their supports are able to understand the ripple effect of chronic pain beyond the physical.

Chronic Pain is Medical Only

This is a myth that doesn't get enough attention. While some elements of migraines and certain other types of chronic pain can have medical bases, chronic pain is often caused and exacerbated by body responses to emotional struggles. For example, the impacts of old traumas carried with you over time, or recent or ongoing traumas can all have a significant impact on the mind and body. Anxiety, depression, and stress can also cause the body to physiologically respond with debilitating migraines, GI symptoms, back pain, and more. Unless there is a clearly identified medical basis for one's chronic pain, chronic pain has often shown to be interconnected between medical and mental health.

Living With and Working Through Chronic Pain

One of the things that people struggle with the most with chronic migraines is that they never know when the next migraine is going to strike. This goes to show that even the pain-free days can often hold the most anxiety, while the painful days are the most physically debilitating. Either way, it is all emotionally and physically exhausting and draining for people who struggle with chronic pain.

Much of what I do in my practice for chronic migraines and pain is help people work through the emotional side of the struggle -- both the emotional impacts of dealing with chronic pain, as well as what may be exacerbating it on a deeper level. I have seen people whose chronic pain has mostly (and even fully) subsided after working through deeper carried traumas. When the body can release stored tensions, anxieties, and the impact of painful experiences, it can lighten the weight of chronic pain with it.

#MentalHealth #ChronicPain #Headache #Migraine #Anxiety #Depression #Stress #IrritableBowelSyndromeIBS

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Diagnosis in your 70s?

I was diagnosed about 15 years ago with just so Neue hypoallergic pots gastroparesis and later on MCAS before that decades of what they called fibromyalgia con fatigue syndrome, many miscarriages, and a lot of what they call just happened to be bad luck medical situations. I was recently sent to a pain management Specialist by another pain management Doctor Who worked with my spine doctor. He wanted me to have a consult with this person this person went over my extensive medical history examined me, and I told him I do not have a history of being super flexible if anything always uncoordinated and clumsy While my some of my kids are very flexible and can do all those wrist and arm things that I cannot do he examined me as I’m dealing with yet another episode of a side joint syndrome and then looked at me and said you REDS you have been all this time Is this possible as for all these years the doctors have been trying to figure out where my just saw Denoia came from as mine has gotten worse and worse over the last few years I have many specialist, dealing with each part of my body for my gastroparesis for a neurologically, my proprioception and Gate and Balance And I’m very sensitive to all medication which I’ve been told could be my mass cell issues. I guess I’m just right now Steine after seeing so many doctors for so many years any input or thought would be very welcomed and appreciated. Bless you.

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About Pots,fibromyalgia,ehlers-danlos,&chronic-fatigue

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do you suffer from all 4..?? or have tips on how to manage them all at once?

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sue Lindsay

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Diagnosed EDS at 72 yrs ?

I’m still wondering if this is possible . I have dysautonomia diagnosed over 15 years ago, seen by some of the best was told I had pot hyper adrenergic form and a bunch of other initials. Fast forward a few years later the IBS was gastroparesis and the rashes were MCAS. Neurologically, they thought it was MS, but it wasn’t trouble with Balance gate and proprioceptor. Pain throughout my body has been as far back as I can remember. But having someone tell me this this far into the game now I’m just wondering is it really possible that no one picked it up until now or should I take this diagnosis with a grain of salt. I was referred to this specialist a pain management facility and this person has a special interest with EDS patients. Went over my complete medical history from childhood to now and had a family member take me and examine that person briefly who is very hyper flexible but I am not and that’s what always made me believe there could be no connection. Any opinions are appreciated. God bless you all.

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About Pots,fibromyalgia,ehlers-danlos,&chronic-fatigue

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do you suffer from all 4..?? or have tips on how to manage them all at once?

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Anniecom

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sue Lindsay

1m

Diagnosed EDS at 72 yrs ?

I’m still wondering if this is possible . I have dysautonomia diagnosed over 15 years ago, seen by some of the best was told I had pot hyper adrenergic form and a bunch of other initials. Fast forward a few years later the IBS was gastroparesis and the rashes were MCAS. Neurologically, they thought it was MS, but it wasn’t trouble with Balance gate and proprioceptor. Pain throughout my body has been as far back as I can remember. But having someone tell me this this far into the game now I’m just wondering is it really possible that no one picked it up until now or should I take this diagnosis with a grain of salt. I was referred to this specialist a pain management facility and this person has a special interest with EDS patients. Went over my complete medical history from childhood to now and had a family member take me and examine that person briefly who is very hyper flexible but I am not and that’s what always made me believe there could be no connection. Any opinions are appreciated. God bless you all.

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Diagnosed EDS at 72 yrs ?

I’m still wondering if this is possible . I have dysautonomia diagnosed over 15 years ago, seen by some of the best was told I had pot hyper adrenergic form and a bunch of other initials. Fast forward a few years later the IBS was gastroparesis and the rashes were MCAS. Neurologically, they thought it was MS, but it wasn’t trouble with Balance gate and proprioceptor. Pain throughout my body has been as far back as I can remember. But having someone tell me this this far into the game now I’m just wondering is it really possible that no one picked it up until now or should I take this diagnosis with a grain of salt. I was referred to this specialist a pain management facility and this person has a special interest with EDS patients. Went over my complete medical history from childhood to now and had a family member take me and examine that person briefly who is very hyper flexible but I am not and that’s what always made me believe there could be no connection. Any opinions are appreciated. God bless you all.

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Dizzy from doctors 🥼

Hey. I’ll try to keep this short as it’s way too much if I go into details.
2 years ago began the start of the newest problems.
August 2024, they increased and got worst at a way faster rate.

Diagnosis:
Vitiligo
Recurrent staph/MRSA/cellulitis
Folliculitis/Eczema/Prurigo Nodularis
Anemia (most of my life)
Thickened endometrium
Hormone imbalances
Migraines
Spinal injuries
Mental health (ptsd/severe anxiety/depression)
Chronic swollen throat/tonsils/lymph nodes
Sinusitis
Chronic dry cough
Low BP
Recent deviated septum
Fatigue, malaise
Body aches/weakness
Carpal tunnel
Skin intolerance to hot/cold
Recurrent UTI’s
Fibromyalgia
Recurrent ear infections / ear staph
Eustachian tube dysfunction
Hearing loss
Uterine fibroids & cysts
Memory loss
ADHD
Severe Insomnia with nightmares
IBS/GERD
TMJ/Bruxism

Not yet diagnosed:
Raynauds (2 almost constantly blue toe nails, recently started in second, 1st has been present last two years off and on)
Chronic chills
Brittle nails
Hair loss (possibly medication related)

Recent testing:
A few genetic tests
Allergy testing
Several autoimmune panels

Current additional issues:
Oral thrush (due to long term antibiotic usage - close to four months now)
Ear pressure/fullness along with dark red/purple spot inside filled with liquid ? Also spots of white appearing pus that pop to drain
— can’t handle loud noise or cold air currently. Severe ear itching.
Eye itch and redness (not pink eye)
Muscle weakness and twitching - minimal long-term control in arm muscles

Pending:
Additional testing
Meeting hematology
CT of neck/throat/nose
Hysterectomy (paused until healthy)

Immediate Family history of:
Lupus (blood work shows low middle numbers not high enough to diagnose)
Celiac (ruled out by endo/colonoscopy)
Psoriasis
RA (ruled out by blood work)
Heart issues

All I can say is yes, I’m in pain. And yes, I’m exhausted. And frustrated. I’m not a crier and all I do is start crying all the time. I have 4 kids and I can’t be the best for them. I am failing everywhere in life and I just need to get this fixed or someone to finally step in and help because I can’t keep declining like this.

I am a veteran. I have little say in my health care. I can’t get a second opinion. Getting a rheumatologist seems to be impossible despite numerous doctors telling me I should see rheumatology. I’m feeling so defeated. If I could at least narrow things down it would help so much, so I could share my research with my doctors. I have several things on my list but I need to get a really good list. Please help if you can think of what may be causing all of this.

Thank you.

*** I would share many more pictures if I could 💕

#chronichealth #Pain #hurting #mother #Veteran #Desperate #pleaselisten #sick #someonegetmedrhouse #illeventakethegoofysidekickguy #ijustwanttofeelbetter #helpme #Genetics #hematology #labs #Skin #Dermatology #IBS #GERD #autoimmune #Disorder #PTSD #Fibro #Rheumatology

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