Alyssa Hamblin

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09/06/2026

A whole different experience.

camera roll crumbs 📸🫶🏼
09/05/2026

camera roll crumbs 📸🫶🏼

Olive is off to her first day of pre-k!! 🥹🤍✨🪿🫶🏼 (she requested our porch goose be in the pics too 😆)
08/31/2026

Olive is off to her first day of pre-k!! 🥹🤍✨🪿🫶🏼 (she requested our porch goose be in the pics too 😆)

some camera crumbs from August 🫶🏼✨
08/26/2026

some camera crumbs from August 🫶🏼✨

08/23/2026

haha if you make it to the mirror part, ignore those 4 holes in the wall they are now filled and awaiting paint 🙃🤠

08/18/2026

This video was the night after Oscar was discharged.

I could tell countless stories about the medical things I’ve seen being his mom, but I don’t think it has ever hit me so hard that I am his voice, until he finds his, and it is up to me to make sure he gets what he needs.

I’m not a doctor. Trying to make decisions for him without ever having 100% certainty had me on the floor crying while 6+ nurses and doctors held Oscar down to place an NG tube and bridle.

I asked them to sedate him. They said a nasal sedative would be enough.

It wasn’t.

He ripped off the oxygen sensor, got the sedative pushed up his nose, ended up with a double nosebleed and blood coming from his mouth, and even once he was loopy it still took more than 6 of us restraining him.

They tried for around 30 minutes while he gagged and choked on blood before the tube was finally placed. Then came more probes up his nose for the bridle.

All of that just to get bowel prep into him.

And I had agreed to it because I knew we needed answers.

That part broke me.

Now we finally have answers: EGID & EoE.

But somehow, we’re still waiting for a plan.

I called yesterday thinking maybe I had missed something. Basically, they know what’s wrong with Oscar, but treating him isn’t straightforward because he isn’t a “typical” child.

He has fewer than 10 foods he’ll consider eating. He doesn’t communicate pain the way another child might. He may not tolerate the standard treatment or simply swallow a medication because it was prescribed.

And I can’t stop thinking about how backwards it feels that the kids who are hardest to study are often the kids we desperately need more research for.

The kids without voices.
The kids who can’t explain what hurts.
The kids who don’t fit neatly into the standard treatment plan.

We have answers.

EGID & EoE.

We just don’t have the next steps yet.

And I know there are so many families living in this exact in-between with us.

08/10/2026

Round 4 of Oscar’s stem cell journey update 🧩

We’re about 5 weeks out from Oscar’s 4th round, so here’s what we’ve noticed + a recap of each round.

🇮🇳 Round 1 Mumbai, India
This was our first time seeing noticeable cognitive gains. More communication, babbling, echolalia, awareness & engagement. But one of the BIGGEST gains was SLEEP. Oscar started sleeping through the night and still does years later. 🙌🏼 I recently heard a parent say their child was up 3am to 7am “per normal” and immediately flashed back to Oscar doing cannonballs into his ball pit for HOURS at night… or smearing 💩 everywhere. I remember those TRENCHES. 😣

🇲🇽 Round 2 Playa del Carmen, Mexico
His asthma basically disappeared. Before, we had 2 to 3 flares a MONTH with hospital visits, steroids & oxygen. Since then? Maybe 1 or 2 in YEARS. He did have a major respiratory illness right after treatment, so who knows for sure, but the difference has been amazing!

🇷🇸 Round 3 Belgrade, Serbia
Oscar started understanding & disliking being soiled, which was HUGE for potty training. His ABA clinic did the teaching, but that new awareness made a massive difference. Now if 💩 gets smeared it’s because he’s trying to wipe himself clean 🥲

🇮🇳 Round 4 Mumbai, India
This time we did a MUSE stem cell protocol. So far we’re seeing more reliable independent communication + new words/phrases, better attitude, improved attention & eye contact, easier transitions and decreased aggression. 🥹

I’m no scientist, I just love documenting what WE see and sharing our experience as clinics continue trialing new approaches.

And because nothing with Oscar is ever straightforward 😂 tomorrow we’re going inpatient for a feeding tube so he can complete bowel prep for an endoscopy + colonoscopy.

He hasn’t swallowed his own spit for 4 months+ and we still don’t know why. We’re hoping this gets us closer to answers. 🥲

This month he’s also switching speech providers so we can watch & learn + starting food therapy there too. 😅

If I ever ignore a text or call, just know I’m probably treading water in the trenches.

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Miles City, MT
59301

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