YOLA | FDN-P
Region: US
Friday 28 August 2026 03:36:31 GMT
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xXRuthieXx :
I had a breast ultrasound, they said I had dense breast tissue. I wonder if that's linked
2026-09-06 22:20:56
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whatsmyname :
this is helpful to hear. i have lipedema and suspect i’m hyper mobile (hEDS) but i had partially ruled it out since not all of my joints are hyper mobile. also, i am on a deep dive currently working on lymphatic drainage every day and on my fascia. i am hearing “hydrate fascia” but what are the things you’re being taught to do to hydrate it?
2026-08-31 16:52:42
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Cuillinbrose :
Hypermobility is an adjective which specifically describes lax joints. Joint Hypermobility is not in itself a Connective Tissue Disorder, it is a symptom - in fact it is a symptom of over 200 conditions. Over 20% of all adults (50% children) have one or more hypermobile joints - on its own it’s a natural human variance. There is a comorbid association between Lipoedema and a number of the CTDs, including hEDS and cEDS but also several other conditions.
2026-09-06 11:05:49
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wwwConfiLifeCoachingcom :
But doctors will try to tell you you need a genetic testing
2026-08-29 17:48:52
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sandy0811_v :
the more I learn the more I'm sure that eds, lipedima, autism/adhd and histamin intolerance are definitely connected.
2026-09-03 20:59:19
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SidSnowAngel :
Do you do seminars that educate other doctors? Many doctors aren’t educated on anything to do with any form of EDS. I felt like I had to go through 10 years of hell before I found a doctor that diagnosed.
2026-08-29 05:26:05
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Dawn May :
YESSSSSS!!!! Please and thank you!!! I have been diagnosing my Primary Care patients & I consider their joints based on age, injury history, chronic activities history, chronic pain history, whole body systems symptoms hystory… educating them and starting them on lifestyle modifications. These are all for at home therapy, as there are not any resources in our area… I would love to start up a clinic specifically for this spectrum of disorders & work on the functional health aspect of EDS.
2026-08-28 18:04:13
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@Librastellium_17 :
hEDS and lipedoma here 🥹
2026-08-28 14:08:05
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Special_Bae :
I would love to see some ultrasound images
2026-08-28 18:19:36
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Shiloh :
How do you get tested my dr said he was referring me to a rheumatologist
2026-08-28 22:30:11
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haleylunamaine :
Hmmmmm. Are ganglion cysts an indirect cause of this? I have several where some lose joints are.
2026-08-30 13:34:39
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Anita :
I have EDS & am not hypermobile. It’s nice to hear the distinction of “if you’re hypermobile or have EDS” bc believe it or not, the only joint I’ve dislocated is my skull from C1 & C2.
2026-08-30 04:01:21
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Snickers’ Doodles :
Who is the practitioner and where is the practice located?
2026-08-28 04:06:43
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random3🧩 :
What Dr is the one that can test you for connective tissue disorders?
2026-08-28 13:09:36
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Lauren Aardema Borrego :
I made an appt with Dr. Iker five months ago! Finally have it coming up on Tuesday this week!
2026-08-28 05:45:57
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Alician :
You treated my mom a year back and changed her life - thank you doctor
2026-08-28 21:36:41
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thequeenoffrance :
Just put it in the list 😩
2026-08-30 03:12:39
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Cora :
What type of doctor can diagnose lipedema? I have EDS with POTs already diagnosed by my geneticist. I’m seeing a vein surgeon who is removing bad veins on my legs just finished 2nd leg.
2026-08-28 15:39:15
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user123459876 :
I have them both and it’s not an easy life.
2026-08-29 04:58:56
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Meagan_Mye :
I have Heds & Lipodema on my upper thighs upper arms & the fat roll right under my boobs
2026-09-01 02:23:58
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Meagan_Mye :
@None-ya 👀
2026-09-01 02:22:45
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