Undifferentiated Connective Tissue Disease

Create a new post for topic
Join the Conversation on
Undifferentiated Connective Tissue Disease
2.6K people
0 stories
251 posts
About Undifferentiated Connective Tissue Disease Show topic details
Explore Our Newsletters
What's New in Undifferentiated Connective Tissue Disease
All
Stories
Posts
Videos
Latest
Trending
Post

I'm new here!

Hi, my name is Standingtall77. I'm here because I have been diagnosed with Undifferentiated Connective Tissue Disease, Fibomyalgia and a long list of food allergies … I was already living with Asthma, Hypertension, Migraine, Tinnitus and Nasal allergies and now have few more to live with.. I don’t know anyone around me who has or knows about the auto immune disease or fibromyalgia… everything I have to read online … here it will help me understand and deal with my conditions better knowing that I am not alone ..

#MightyTogether #Migraine #Fibromyalgia

Most common user reactionsMost common user reactions 4 reactions 3 comments
Post

Incredible guiltTraumatizing my kids (19&21yo) I got toxic megacolon 3 wks ago, the drs saved my life w colectomy w ileostomy. I’m a single mom

Both my kids are persevering with multiple serious medical problems. I’m a single mom with very limited family, friend and community support. I’ve nearly died three times this year and 1-2 times every year for the past six years. My kids are very depressed about almost losing me again. My kids both have treatment resistant depression, CPTSD, endometriosis/ademomyosis,
rheumatoid arthritis, Crohn’s, epilepsy, polymigratory arthritis, degenerative spine disease, scoliosis, reynaud’s syndrome, cardiac issues, migraines and fibromyalgia, complex regional pain syndrome. The crushing guilt of being an ineffective mother, giving birth to two children who each have 5-6 illnesses inherited from me and their father who hurt them physically and emotionally especially when I was in the hospital getting 8 reconstructive spine surgeries with hardware, screws, plates in nine years covering most of my spine. My son is autistic spectrum disorder high functioning and affectionate. I’m so lucky to be here for my kids with my kids. I understand that without emergency surgery and a fully invasive opening, I wouldn’t be here today. I’m grateful to Gd for saving me. What have I done to my kids. I wasn’t so sick when I got pregnant. I didn’t know when I got pregnant that the kids father’s side has most of the same illnesses and there are many. Now both my kids, as they mature, their health diagnoses increase to longer terrifying lists of diagnoses including many of my dozens of disorders including from Crohn’s, epilepsy, an unspecified connective tissue disorders, immune modulatory disorder, endometriosis, interstitial cystitis, seronegative rheumatoid arthritis, primary immunodeficiency disorder, MGUS/multiple myeloma (monoclonal gammopathy of unknown significance), demyelinating syndrome like MS without known disease prognosis. This year I almost died three times from necrotic aspiration pneumonia with large abscesses in my lungs. I am eligible for the reversal ileostomy surgeries (2 surgeries- the first 8-10 hours is almost as devastating as the emergency colectomy. There’s a small window (4months) when surgeons can do this. It’s my only chance to get my life back to live w/o an ostomy. It’s a long process after surgery and the stoma is repaired in a follow up surgery. I need this surgery. It’s a long long recovery and major surgery with many complications. How can I do this to my family? I worry that my son & daughter can’t handle this much disruption, stress, sadness. We have such little support and no one called my kids to check on them as the plan we created was supposed to happen in emergencies. No one called. Every one gave excuses, so disappointing. Such a problem for future surgeries. I know they should be independent by now yet given their medical status, being an independent young adult is very challenging. I’m so thankful to my daughter who has been helpful beyond any thing I could have hoped for. She’s incredibly giving and loving to me. It’s hard to be here. Not functional, not effective.

#UndifferentiatedConnectiveTissueDisease #MixedConnectiveTissueDiseaseMCTD # primaryimmunodeficiencydisorder #PrimaryImmunodeficiency #AutoimmuneImmunodeficiency #CrohnsDisease #PTSD #ComplexPosttraumaticStressDisorder #ComplexRegionalPainSyndrome #CongenitalHeartDefect #Epilepsy #RheumatoidArthritis #DegenerativeDiscDisease #Scoliosis #InterstitialCystitis #Pneumonia #AspirationPneumonia
#necroticpneumonia
#Gastroparesis #gastrointesinlbleed #RheumatoidArthritis #singleparent #SjogrensSyndrome #DiffuseIdiopathicSkeletalHyperostosis #Diabetes #ComplexPosttraumaticStressDisorder #Ileostomy #Colectomy

Most common user reactionsMost common user reactions 23 reactions 10 comments
Post
See full photo

Exhausted

I feel tired. I feel weak. My body hurts. I've been on three rounds of steroids in the past month and two rounds of antibiotics. Between my UCTD (suspected lupus), the recurring GI issues that we're now suspecting as some form of IBD, and a bout of pneumonia, I'm worn. I'm exhausted. My mental health is great until I'm sick for weeks on end. How do you maintain mental wellness when your body seems to want to quit? #UndifferentiatedConnectiveTissueDisease #InflammatoryBowelDiseaseIBD
#Lupus

Most common user reactionsMost common user reactionsMost common user reactions 5 reactions
Post

I’m new here!

Hi, my name is Hanolo14. I'm here because I want to hear how others like me have stopped their illnesses from controlling their lives

#MightyTogether #Anxiety #Depression #UndifferentiatedConnectiveTissueDisease

Most common user reactions 1 reaction
Post

I'm new here!

Hi, my name is Peacheschuhuahua2018. I'm here because I would like answers on how to live with uctd. I am 69 years old.

#MightyTogether

Most common user reactions 9 reactions 3 comments
Post

Hello all. I have UCTD and am at my wits end. I’m just looking for others who may be more knowledgeable. I’m new to The Mighty. It seems to me that this disease is a mystery. Periodically, I do searches to see if there are any new articles. Maybe a breakthrough. Anyway, thanks for allowing me to join the group.

Most common user reactionsMost common user reactions 5 reactions 4 comments
Post
See full photo

Flare up cart ideas!

Do you have a flare up cart? If so what do you put in it so it’s easily accessible to you during bad days and flare days? #Flareup #Fibromyalgia #UCTD #AutonomicDysfunction

Most common user reactionsMost common user reactions 16 reactions 6 comments